Who We Are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity The RA Associate I, under direct supervision, is responsible for the preparation and revision of high-quality US Gx labeling documents filed under an ANDA and/or 505(b)2, if required, while ensuring adherence to federal regulations and meeting deadlines driven by company goals. Candidate should possess a knowledge of US FDA labeling regulations and guidance to the level of applying them effectively to all work output in addition to developing compliant Structured Product Labeling (SPLs) files with complete drug listing information. How You’ll Spend Your Day Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents.Establish SPL for assigned projects. Ensure product data elements align with the required drug listing regulations.Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes, but is not limited to, the development of side-by-side comparisons, SPL, and other required submission materials, as necessary.Perform quality reviews of labeling and submission documents by proofreading established labeling files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT.Work with Regulatory Operations as well as in Teva’s publishing software to ensure assigned projects are submitted on time following the eCTD requirements related to labeling.Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling.Work in a team environment.Perform all other job-related duties as required by management and dictated by process changes. Your Experience And Qualifications Pharma Graduate/Postgraduate with a scientific or regulatory background, or an equivalent combination of education and experience.Bachelor’s in pharmacy/Master’s in science & Life sciences- 2-3 Years in the Pharmaceutical Industry.Master’s in pharmacy-1-2 Years in the Pharmaceutical Industry.Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry.1 to 3 years of pharmaceutical industry experience, specifically in Regulatory Affairs with a focus on US Gx labeling.Knowledge of SPL development and drug listing requirements. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Apply now » Regulatory Affairs Associate I, Labeling Date: May 12, 2025 Location: Navi Mumbai, India, 400706 Company: Teva Pharmaceuticals Job Id: 61890 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity The RA Associate I, under direct supervision, is responsible for the preparation and revision of high-quality US Gx labeling documents filed under an ANDA and/or 505(b)2, if required, while ensuring adherence to federal regulations and meeting deadlines driven by company goals. Candidate should possess a knowledge of US FDA labeling regulations and guidance to the level of applying them effectively to all work output in addition to developing compliant Structured Product Labeling (SPLs) files with complete drug listing information. How you’ll spend your day Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents. Establish SPL for assigned projects. Ensure product data elements align with the required drug listing regulations. Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes, but is not limited to, the development of side-by-side comparisons, SPL, and other required submission materials, as necessary. Perform quality reviews of labeling and submission documents by proofreading established labeling files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT. Work with Regulatory Operations as well as in Teva’s publishing software to ensure assigned projects are submitted on time following the eCTD requirements related to labeling. Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling. Work in a team environment. Perform all other job-related duties as required by management and dictated by process changes. Your experience and qualifications Pharma Graduate/Postgraduate with a scientific or regulatory background, or an equivalent combination of education and experience. Bachelor’s in pharmacy/Master’s in science & Life sciences- 2-3 Years in the Pharmaceutical Industry. Master’s in pharmacy-1-2 Years in the Pharmaceutical Industry. Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry. 1 to 3 years of pharmaceutical industry experience, specifically in Regulatory Affairs with a focus on US Gx labeling. Knowledge of SPL development and drug listing requirements. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Apply now » Regulatory Affairs Associate I, Labeling Date: May 13, 2025 Location: Navi Mumbai, India, 400706 Company: Teva Pharmaceuticals Job Id: 61889 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity The RA Associate I, under direct supervision, is responsible for the preparation and revision of high-quality US Gx labeling documents filed under an ANDA and/or 505(b)2, if required, while ensuring adherence to federal regulations and meeting deadlines driven by company goals. Candidate should possess a knowledge of US FDA labeling regulations and guidance to the level of applying them effectively to all work output in addition to developing compliant Structured Product Labeling (SPLs) files with complete drug listing information. How you’ll spend your day Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents. Establish SPL for assigned projects. Ensure product data elements align with the required drug listing regulations. Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes, but is not limited to, the development of side-by-side comparisons, SPL, and other required submission materials, as necessary. Perform quality reviews of labeling and submission documents by proofreading established labeling files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT. Work with Regulatory Operations as well as in Teva’s publishing software to ensure assigned projects are submitted on time following the eCTD requirements related to labeling. Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling. Work in a team environment. Perform all other job-related duties as required by management and dictated by process changes. Your experience and qualifications Pharma Graduate/Postgraduate with a scientific or regulatory background, or an equivalent combination of education and experience. Bachelor’s in pharmacy/Master’s in science & Life sciences- 2-3 Years in the Pharmaceutical Industry. Master’s in pharmacy-1-2 Years in the Pharmaceutical Industry. Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry. 1 to 3 years of pharmaceutical industry experience, specifically in Regulatory Affairs with a focus on US Gx labeling. Knowledge of SPL development and drug listing requirements. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Apply now » Regulatory Affairs Associate II, Labeling Date: May 13, 2025 Location: Navi Mumbai, India, 400706 Company: Teva Pharmaceuticals Job Id: 61885 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity The RA Associate II is responsible for preparing and revising high-quality US Gx labeling documents submitted under an ANDA and/or 505(b)(2), as required. This role ensures compliance with federal regulations, guidance documents, and internal procedures while meeting deadlines aligned with company objectives. The candidate must demonstrate the ability to work with minimal supervision and possess a thorough understanding of US FDA labeling regulations and guidance documents, applying this knowledge effectively across all work output. Additionally, they will be responsible for creating compliant Structured Product Labeling (SPL) files, ensuring complete drug listing information, and adhering to compliance requirements for importation, bulk listings, and related processes. How you’ll spend your day Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents. Develop US labeling documents needed for early development projects requiring a human factor or comparative analysis study and ensure established labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents with all relevant departments. Some experience in developing labeling content that requires carve-outs due to protected language associated with patents/exclusivities. Establish and maintain SPL for assigned projects. Ensure product data elements align with the required drug listing regulations and established SPL is submitted through FDA’s Electronic Submission Gateway. Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes, but is not limited to, the development of side-by-side comparisons, SPL, and other required submission materials, as necessary. Perform quality reviews of labeling and submission documents by proofreading established files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT. Work closely with external departments, including CMC and the Device team, to align with internal product/device strategy and process. Work closely with Regulatory Operations, as well as in Teva’s publishing software, to ensure assigned projects are submitted on time following the eCTD requirements related to labeling. Support products falling under Business Development deals, if required, from a labeling/artwork and drug listing perspective. Attend assigned project meetings to ensure labeling timelines are met. Maintain an accurate project tracker of all assigned projects with identified due date priorities and timelines of initial assignment, initiation, and completion of projects. Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling. Work in a team environment with minimal supervision. Perform all other job-related duties as required by management and dictated by process changes. Your experience and qualifications Pharma Graduate / Postgraduate with a Scientific or Regulatory background or equivalent combination of education and experience 3+ years of pharmaceutical industry experience, specifically in Regulatory Affairs with a focus on US Gx labeling and drug listing. Knowledge of SPL development and US FDA drug listing requirements. Bachelors in Pharmacy/Master in science & Life sciences- 4-5 Years in the Pharmaceutical Industry. Master in Pharmacy-3-4 Years in the Pharmaceutical Industry. Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Apply now » Finance Operation Admin III Date: May 8, 2025 Location: Bangalore, India, 560064 Company: Teva Pharmaceuticals Job Id: 61855 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. How you’ll spend your day Technical/functional knowledge in Accounting and fixed asset closing area Ensure that capitalization, maintenance, depreciation, amortization are properly recorded and analyzed Very well verse with lease accounting concept Preparation of Journal Entries, Supporting schedule & Roll forwards Perform monthly and quarterly FA closing activities of multiple entities Analysis of the various fixed asset accounts and variances per legal entities, obtain explanation on deviations and prepare a summarized reporting on a monthly basis within scheduled time Preparation & clearance of open reconciling item in account reconciliations Hands on experience in submission of trial balance in HFM Identify & drive standardization opportunities in processes and tasks across the team Acting as a key contact for local teams for fixed assets and lease related questions Ensuring that accounting books and records comply with accounting policies and regulations Provide supporting documents and explanations for all internal and external audit as and when required Participate in ad-hoc activities and projects Your experience and qualifications University education in Accounting or Finance required Minimum experience of 3+ years into managing fixed assets & leases register for large scale organization Preferably familiar with US GAAP Working knowledge of internal controls Good working knowledge of SAP Good understanding of accounting processes and can follow accounting policies Good analytical skills and have hands on experience in Fixed asset as well as Leases process Fluent verbal and written communication in English Experience in a multinational firm or within a GBS (Global Business Services) is preferred Hands-on and proactive; strong organizational skills Accustomed to working with deadlines, in a dynamic environment Results driven and service oriented to internal and external customers Excellent collaboration with colleagues within the local organization and with the colleagues of the global business service to support the overall Finance department’s goals and objectives Flexible and able to work in a changing environment Strong focus on improvement opportunities Want to work in a new (to be) established team Process documentations and certifications – will have to ensure that all process are appropriately documented and periodically certified by team members on regular basis Reports To Group Leader, Financial Operations. Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Job Details: Job Title: Manager Utility Location: Gajraula, UP Minimum Required Skills: Qualification: BE/B. Tech-Mechanical Experience: Twelve Years and above Key Skills: Good understanding of Safety procedures, Understanding of GMP and Technical Knowledge of Utility equipment Main Responsibilities: To ensure plaining and scheduling for annual preventive maintenance of all utilities installed in the plant. To attend and timely response for all emergency breakdowns of utility equipment in the plant. To ensure and implement GMP requirements in function. Aligning SOP corporate SOP and guideline. To ensure spare part inventory of the utility equipment items in Engineering Stores. To evaluate new utility equipment and ETP equipment proposals for Capex & modification and its procurement with timely execution. Support site project team for evaluation and timely completion for utility project. To ensure renewal of registrations and licenses related to Utility equipment for concerned Government Department as per Teva standards. To ensure the safety of persons, plant & Equipment while carrying out the maintenance job. Work procedure update and training. To critically analyze the expenditure on procurement of items and utility maintenance expenditure periodically and find out ways and means to control the same at optimum level. To review the planning and implementation of energy conversion schemes. To ensure timely closely of permanent change Control, temporary change control, deviation, CAPA and service calls of utility function. Is accountable for the performance and results of a team with own disciplined & Function. Defines Team operating standard and ensures essential procedure are followed based on knowledge of own disciplined, to ensure completion of assigned the training of self & Team members. Excretive limited management authority, sets employee performance objectives, conducts performance reviews and recommends pay actions. To ensure all the activities perform in own discipline for self and team should follow the compliance requirements. To support GFM for own discipline in colony and its execution.

Who We Are At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. The opportunity The Global Senior Category Manager - Direct Procurement is responsible for leading and implementing comprehensive procurement strategies across direct categories to drive value creation and achieve organizational objectives. This role involves developing and executing innovative procurement strategies, optimizing supplier relationships, drive cost efficiencies and ensuring alignment with business goals. The role requires a creative and energetic leader who can identify gaps, risks, challenges and drives process to ensure the successful implementation of strategic projects across countries. By leveraging deep market insights, this position will identify opportunities to enhance cost efficiency, ensure supply chain resilience, and promote sustainable practices. The role requires close collaboration with cross-functional teams and senior stakeholders, fostering a culture of excellence and continuous improvement in procurement processes and strategy development. How You’ll Spend Your Day Develop and Manage Procurement Initiatives: Oversee and lead key procurement strategy initiatives such as tenders, procurement process optimizations, category supplier consolidation, cost reduction programs, sustainable sourcing,contractig strategy,etc. Market Knowledge: Provide expert-level knowledge of the API, raw materials' supply base, and global intermediates market (suppliers, prices, technology, etc.). Develop Strategic Plans: Create comprehensive strategic plans that align with TAPI's global objectives and drive growth within the procurement category. Identify Opportunities: Analyze market trends and identify new business opportunities to enhance procurement strategies and supplier relationships. Lead Strategic Initiatives : Manage strategic initiatives from conception to execution, ensuring alignment with overall business goals. Collaborate with Teams: Work closely with cross-functional teams to ensure effective implementation of strategic projects and initiatives. Report and Present: Prepare and present strategic reports, presentations and recommendations to senior management, providing insights and actionable plans. Problem-Solving : Address complex challenges and develop solutions to optimize procurement processes and drive cost efficiencies. Monitor and Adjust: Continuously monitor the effectiveness of strategic initiatives and make necessary adjustments to achieve desired outcomes. Negotiation: Lead raw materials negotiations with suppliers to achieve aggressive savings targets, aligned product costs and with TAPI's strategic goals. Risk Management: Proactively identify, assess, and mitigate procurement risks to ensure business continuity, compliance, and strategic alignment. Supplier Relationship: Foster strong, strategic supplier relationships to drive collaboration, ensure reliable supply, and achieve mutual long-term value creation. Market Research: Conduct thorough market research and competitive analysis to inform strategic decisions and identify potential risks and opportunities. Your Experience And Qualifications At least 10 years' experience in Pharma, API, Intermediates, Raw materials Procurement. Experience in other areas such as supply chain, project management, commercial operations is an advantage. Master's degree in natural sciences, chemistry, pharmaceutical sciences, biotechnology or equivalent is mandatory. In addition, MBA is an advantage. Advanced competency in Microsoft Excel for data analysis and reporting. Strong interpersonal skills including cross-functional teamwork, A proactive and positive approach to challenges, demonstrating a willingness to take on new tasks and find solutions. Ability to work autonomously, make decisions and resolve/follow up issues quickly Flexibility to thrive in a fast-paced, dynamic environment and adapt to changing conditions. Ability to draw strategic insights from analysis and effectively summarize and present insights Sensitivity and awareness of cultural differences to effectively collaborate with global teams and stakeholders. Fluent English (both written and verbally) Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon! Reports To Director Global Category Head Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Who We Are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity Regulatory Affairs associate I – RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the Regulatory Affairs Associate How You’ll Spend Your Day Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada. Exposure in handling post approval submissions publishing and transmitting quality submissions to agency. Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents as per the agency guidance. Collaborate with scientific personnel for planning, preparation and publishing. Maintain working knowledge of internal and external publishing standards. Basic knowledge of ICH and eCTD related specification/guidelines governing regulatory submissions (eCTD, NeeS, paper) Must be aware of Technical systems like Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, Lorenz Validator Your Experience And Qualifications B. Pharm, M. Pharm, or a Master's in Life Sciences Experience required: 1–3 years of experience required for the role (preferably with regulatory publishing experience in the EU and US markets). Strong command of spoken and written English Sensitivity to the cultural diversity of a global organization. Good understanding of regulatory IT systems Reports To Manager – Regulatory Submission Management Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Who We Are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity The Role Of GRO Regulatory Data Analytics Is To Manage Teva’s data in accordance with requirements for xEVPMD in order to maintain Teva’s Article 57 compliance Provide a Central Data Service for the creation and maintenance of GRA product registration data in line with the global needs of Teva Global Regulatory Affairs. Provide SME services for data management in current and future regulatory data systems The primary purpose of this position is to execute the operations and services applicable to the GRO Regulatory Data Analytics role in line with business goals and objectives. How You’ll Spend Your Day Responsible for executing GRO Regulatory Data Analytics operations in line with Work Instructions and SOPs. Primarily will be Regulatory Data Analytics Service related to product registration data management (includes the procurement of data from source regulatory documentation which requires a thorough understanding of the structure and contents of a regulatory dossier, and a thorough understanding of the data structures applicable to registration data and the related system workflows). Operationally hands-on in terms of carrying out data management activities as an individual contributor. This will require a thorough understanding of the structure and contents of a regulatory dossier (i.e. will be fluent in navigating and understanding the contents of a dossier). Registration data management will require a thorough understanding of the registration data structures, workflows, and applicable work instructions etc. Perform Quality Control (QC) and data integrity checking, as part of the Regulatory Data Analytics operation, to confirm the accuracy and completeness of the Teva Global Registration database. Represent GRO Regulatory Data Analytics across the wider Global Regulatory Affairs community. Must be proficient at building effective working relationships with all stakeholder and customer groups. Responsible for providing effective business project contributions for projects focused on improving regulatory data quality, the provisioning of regulatory data for internal re-use via system integration, or the implementation of any business or technology change that impacts regulatory data or the regulatory technology landscape. Your Experience And Qualifications Minimum Educational Qualifications: Required: Bachelor's or Master's degree in Life Sciences or Information Technology. Preferred: MS in a scientific or information technology discipline Minimum Years Of Work Experience Required: 1–3 years (preferably with experience in regulatory operations/affairs). Required Job Knowledge and Skills Interest in pharmaceutical regulatory affairs. Aptitude for regulatory data management. Preferred Experience in the pharmaceutical industry with direct involvement in regulatory affairs, demonstrating a strong understanding of the pharmaceutical regulatory process. Experience in managing regulatory product registration data, ideally within a regulatory information management environment Reports To Manager, Regulatory Data Analytics Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Responsible on-Site product transfer & New Product transfer, scale-up, proposals, Capex evaluations & Process Engineering calculations Improvement in the yield, efficiency and cost effectiveness of developed API’s by introducing new Technologies and further development of process fine tuning Extensive experience in API manufacturing with a deep understanding on Scale-up. Troubleshooting the plant related problems, to overcome the process related difficulties for smooth production Contribute novel ideas by way of participation during technical discussion with superiors/ Colleagues Cycle time reduction, Capacity enhancement and making capacity increase proposals with the support of site CFT members/ leads. Ability to manage 4-5 Engineers coaching, career development and build high performing, engaged and effective teams through motivation and inspiration Person will be expected to support chemistry projects to develop the process engineering knowledge and lead the transfer from lab to scale-up lab and further to production scale Experience on handling CDMO products will be an advantage Person will have demonstrated expertise in the scale-up and process understanding of chemical process unit operations in the manufacture of APIs, intermediates and raw materials. Experience in Quality by Design, process safety, technology transfer and commercial production would be advantageous. Person will be responsible to execute trial and validation batches and support in related activities at plant in the time of scale up In-depth, hands-on expertise and up-to-date knowledge of a wide range of chemistry unit operations such as reactions, distillation, separation, filtration and drying. Strong scientific track record, ability to handle several projects in different stages of development at the same time. Person will be responsible to Investigate and troubleshoot in case of issues in scale up/validation and support troubleshooting activities in case of issues in scale up/validation batches Responsible to use process modelling tools like Dyno Chem, VISMIX for reaction, crystallization, filtration, solubility and mixing studies Good knowledge on solvent recovery & recycle by using latest technologies etc Your Experience And Qualifications B. Tech/ M. Tech Chemical (Regular from reputed Institute) 14-16 Years experience & 5 years in people management Excellent communication skills to interact internally with project teams and externally with customers Good project management and supervisory skills. Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. A team player & Competent in the use of key process engineering and modelling software packages Equivalent experience in a Process, Synthetic Chemistry or Manufacturing environment. Experience in working to GMP. Experience in the application of Process Safety to the design of chemical processes Reports To Associate Director, MS&T Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Who We Are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. How You’ll Spend Your Day Complete knowledge of E2E invoice processing/ accounting impact of the process, including 3 way/ 2 way match concepts and deeper understanding of the Vendor payment procedure & other governing policy guidelines. Oversee the processing of invoices, resolving Invoice discrepancies by holding regular follow-up meetings with the business users thereby ensuring all payments are made accurately and on time for multiple countries in scope for GBS. Proficiency in VAT, India GST, TDS and APAC Tax rates Monthly books closure activities including closing of Invoice booking, open GRIR analysis, reporting OPEX, Vendor advances, CAPEX payables and Accruals preparation. Ensure all approvals/ supporting are suitably documented. Work closely with internal teams (e.g., procurement, legal, operations) to resolve payment-related discrepancies or issues. Prepare and present reports on Accounts payable activities, including payment forecasting. Lead & independently manage the transitions from local countries, including creation/ monitoring of a transition plan and documentation of SOP. Positively and creatively influence change and champion mission critical change initiatives Ensure compliance with company policies, financial regulations and internal controls. Supervise and mentor a team of Accounts payable specialists, providing guidance and support to ensure efficient workflow and high performance. Provide training and development opportunities for team members to enhance their skills and knowledge. Your Experience And Qualifications Master’s degree in accounting. 10+ years of working experience in Accounts payable process (E2E Strong knowledge of accounting principles, proficiency in Microsoft Office (Advanced excel, Word, PPT) and experience with SAP for Accounts payable modules. Working and implementation experience of E-invoicing solutions (includes vendor portal) Excellent verbal and written communication skills, with the ability to interact effectively with internal and external stakeholders. Good interpersonal skills to establish and maintain effective working relationships with a diverse population; ability to interact professional and courteously. Strong analytical/ problem-solving and time-management skills. Flexible and adaptable to change, with the ability to work under pressure to meet deadlines in a fast-paced office environment. Detail-oriented with a high level of accuracy and attention to detail Reports To Group Leader, Accounting Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, The opportunity The Treasury Analyst role includes technical or transactional responsibilities primarily in payments, cash and liquidity management, inter-company funding, cash forecast and banking as well as more strategic and business partnering requirements, Communication and (internal) stakeholder management with higher management levels within the Global Teva organization is required in this process How Youll Spend Your Day Supporting day-to-day treasury operation activities, including preparing daily cash position, investigations and monitoring payments process initiated by Operations Tracking and settle inter-company receivables and payables and manage activities across in-house banking Supporting FX conversions and derivatives operation activities, Playing an active role in promoting an advanced risk management culture, including awareness of the various foreign exchange exposures, ensuring timely & accurate booking of FX exposures (performed by accounting), awareness of translation differences on cash, etc Preparing and supporting Guarantees and Letter of Credits when needed, according to the relevant policy The implementation of, and compliance with, all Treasury Policies & guidelines Support and lead complex and international ad-hoc projects and ad-hoc reporting Support systems implementation and modification to existing system and ensure timely delivery of all system testing and validation, Process documentations and certifications will have to ensure that all process are appropriately documented and periodically certified by team members on regular basis, Working on cash forecasting and working capital projects Your Experience And Qualifications University education in Accounting or Finance required CA Inter qualified is must, Minimum 1 year of relevant treasury experience is good to have Well versed with Finance world, latest trends, technology & best practices in the industry Experience in fast-paced multinational matrix organization Strong change management, communication and influencing skills Fluent verbal and written communication in English Hands-on and proactive; strong organizational skills Results driven and service oriented to internal and external customers Ability to work effectively under pressure Reports To Associate Director Treasury Already Working @TEVA If you are a current Teva employee, please apply using the internal career site available on "Employee Central" By doing so, your application will be treated with priority You will also be able to see opportunities that are open exclusively to Teva employees Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well If you have trouble accessing your EC account, please contact your local HR/IT partner, Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience, Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,

Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, The opportunity Researches, develops, plans, designs, maintains and implements policies and programs that enhance the organization's relations with the community, the public, government and regulatory authorities, and shareholders, Coordinates media relations and prepares strategy for external communications, Plans, prepares and relays information concerning the organization to the press and government authorities to gain understanding and acceptance for the organization, Develops and maintains healthy relations with government authorities, law maker, media, community influencers and other external audience groups, Design, implement and monitoring of countrys Corporate Social Responsibility programmes, How Youll Spend Your Day Policy & Regulatory Research: Research support on various regulatory and policy matters such as upcoming policies, new regulations and notifications, Prepare recommendations on draft policy/regulations for submission directly or through industry associations, Include research from journals/ newsletters/ online research/ social media such as twitter, and other relevant platforms, Tracking of news/notifications/ union budget/election results/political & economic updates etc and preparation of its related summary communication for dissemination to concerned internal stakeholders, Tracking national / international developments related to TAPI business, Timely coordination with team for preparation and circulation of Monthly reports to leadership, documents for important and other meetings, Preparation of monthly policy and regulator monitors, annual policy report, Preparation of whitepapers, reports, leadership advisories etc Engagement support in policy outreach with relevant external stakeholders Partnering With Sites & BU Leads Support the unit location teams on projects, government communications, monthly reports, trackers, strategy documents, stakeholder mapping, briefing books etc Coordinate for projects including business transfer, major approvals, special projects etc Timely support to the international business team for meeting with external stakeholders, pending payment issues, information on FTAs etc Extend support for coordination with personnel involved in liasoning / dealing with authorities from site, Engagement With External Stakeholder And Industry Associations Ensuring positive external stakeholder engagement on relevant business matters and regular engagement with Industry Associations Engage in policy outreach for key policy/regulatory matters with relevant external stakeholdersIndustry associations, government officials, Track and ensure participation in key industry events/ forums / state level investment summits It will include identification of thought leadership forums and evaluation of same (for Tava leadership and relevant businesses) with a focus on Teva's priority areas, Providing support in management of critical legal issues in conjunction with the legal team, Community Development Programs / Corporate Social Responsibilities Identifying the initiatives for community development as part of the overall strategy and within the purview of the applicable laws and norms Partner with NGOs / agencies and implementation partners for program effectiveness Validate, qualify and propose projects to the committee for approvals and implementation, Administer the progress of key performance indicators and publish periodic reports, Guide the site teams on the overall strategy and ensure adherence with the global donation policy, Conduct periodic audits to ensure effectiveness of the programs and utilization of the funds, Ensure adequate documentation and process governance, Single point of contact for all community development related queries and solutions, Your Experience And Qualifications Masters in Mass Communication / Business Administration / Economics or any other Master Degree, 15 to 20 years (Corporate Affairs)in Pharmaceutical industry and Manufacturing business, Reports To Sr Director Head of Develop api R&D, Global R&D Tevas Equal Employment Opportunity Commitment TAPI is the leading international supplier of active pharmaceutical ingredients (APIs) With the industry's broadest portfolio including over 350 API products We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service, Our employees are at the core of our success Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market, Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,

Who We Are At TAPI, we are not just a company?we are a community committed to advancing health from the core As the worlds leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies With a legacy spanning over 80 years and a portfolio of more than 350 products, were shaping the future of health worldwide, Our strength lies in our people?a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India Together, we innovate, solve problems, and deliver excellence Join us and be part of a mission that transforms lives, The opportunity We are seeking a highly motivated, energetic, and skilled Financial Systems Expert to join our Corporate Accounting team in a key role that will focus on group reporting and consolidated financial statements This role will report to the Director Global Head of Accounting If you are enthusiastic about driving accuracy in financial reporting and have experience working in the headquarters of a multi-national corporate, we would love to hear from you How Youll Spend Your Day Group Consolidation System: Responsibility for setup, maintenance, and ownership of group consolidation system Automation of consolidation process and implementation of a new system Ensure FX setup; rates are accurate for global transactions, Consolidated Financial Statements: Timely and accurate consolidation of the groups monthly, quarterly, and yearly financial statements Lead the consolidation process, including intercompany eliminations, equity elimination, foreign currency translations, unrealized profit on inventory, allocation of corporate costs to group entities, and top-side adjustments, Group Reporting: Business implementations lead for both managerial and statutory reporting including requirement gathering, testing, and implementation Prepare periodic financial reporting for internal and external purposes, ERP implementation: Finance lead for ERP implementation, bringing legal entities onto one IT platform Identify and resolve gaps in global system blueprint against target country requirements Partner with target countries to ensure smooth process mapping, data conversion, go-live support, post-go live hyper care activities, Financial Analysis: Conduct thorough analysis of consolidated financial data to provide insights into the companys performance, trends, and potential financial risks Analyze fluctuations and trend of balance sheet / income statement and be able to identify and communicate potential misstatements Collaborating with FP&A and providing insight on budgeting and forecasting variances, Projects: Prepare and develop financial reports for other stakeholders (investors, banks, etc ) Preparation of ad-hoc analyses and special projects as requested, Internal Controls: Establish and maintain a robust internal controls environment, and supporting documentation, for key balance sheet and income statement accounts Develop and document business processes and accounting policies to maintain and strengthen internal controls, Continuous Improvement: Seek and perform continuous improvement in financial and management reporting processes, increasing efficiency, and reducing errors, Audit Support: Assist in internal and external audits of TAPI Consolidated Financial Statements, providing necessary documentation and responding to audit queries as required, Your Experience And Qualifications Qualified Accountant (Chartered Accountant / CIMA / CPA/ACCA), Minimum of 5 years of experience in group reporting, intercompany transactions, multi-currency consolidations within a multi-national corporate environment, ERP System Implementation and integration experience, Bridge the gaps between business finance and IT organization, Experience of working with consolidation software tools and ERP systems, Proficiency in Microsoft Office; advanced excel knowledge, Finance Process Change Management, Integration, and Process Improvements experience, Reports To Director, Accounting Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,

Who are we? Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity As a Sr Manager HRBP, you will have an integrated role to develop actionable insights that support the implementation of People Strategy. You will adopt a data-driven methodology to evaluate the effectiveness of optimization, capabilities, talent development, and employee experience across GBS functions. How you’ll spend your day This position will be responsible for guiding, overseeing, and ensuring the implementation of all HR programs as per organizational guidelines. Focus on the quality of hire, onboarding experience, and building capability and competency through planned interventions. Drive initiatives to provide an employee-oriented, high-performance, high-quality culture across teams. Drive employee experience and wellbeing initiatives across locations. Support alignment within the leadership team on people strategy imperatives. Adopt a data-driven methodology to evaluate the effectiveness of optimization, capabilities, talent development, and employee experience. Analyze trends and metrics (hiring, attrition, training schedule adherence, FTE utilization, talent gaps, etc.) to develop solutions for the respective business. Ensure timely delivery of talent MIS and key insights. Provide strategic counsel and legal advice on people matters. Your experience and qualifications Master’s degree in Human Resources Management is mandatory. 8+ years of experience in all aspects of human resources management and staff development. Excellent analytical, critical thinking, and strategic problem-solving skills. Maturity and ability to work in a matrix environment. Personal integrity; learning agility; open and transparent. Stakeholder management. Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site. The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Equal Opportunity Statement Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Start making a difference with Teva today If you believe you’re ready to make a difference with us, we’d love to hear from you. Visit https://www.tevapharm.com/your-career/ to find out more about us or click the link below to apply now. Show more Show less

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. The opportunity This role is responsible for leading the Indirect Procurement team of TAPI India. Responsibility includes management of 2 Procurement Managers who support all TAPI Indirect Procurement activities in India. This includes working with the relevant TAPI stakeholders to identify and optimize all Indirect Procurement needs in India, implementation of the global Indirect category strategies, supplier sourcing and management, contract negotiations, risk management, stakeholder engagement and ongoing continuous improvement activities. This role strives to generate and deliver ongoing value through year-over-year savings, to maintain excellent customer satisfaction and to ensure the supply of required Indirect goods & services for TAPI. How You’ll Spend Your Day Manage a team of 2 Procurement Managers. Support Head of Indirect Procurement in development and implementation of global and regional Procurement strategies, goals and objectives. Execute Indirect category strategies for all spend under its responsibility. Establish and maintain collaborative relationships with the relevant TAPI stakehoders. Manage supplier relationships (SRM) for all suppliers under its responsibility. Accountable to achieve Indirect categories objectives – most notably for savings generation, supplier risk management and uninterrupted plant operations and services. Conduct supply market research to provide category intelligence and benchmarks on industry dynamics, trends and best practices. Source the right suppliers to support and deliver business needs. Lead supplier negotiations and contracting, including management of tender and bids Your Experience And Qualifications Education Required: Bachelor’s Degree Degree in Engineering, Business, Logistics, Law is an advantage but not mandatory. Understanding of Industrial manufacturing environment is highly desirable. Experience Required: at least 7 years of indirect procurement management experience preferably in a large industrial company. Functional Skills: Strong leadership skills. A team player with capability to influence stakeholders while working in cross functional teams. Excellent communication and presentation skills, both written and verbal – the ability to gain senior leadership support. Strong Interpersonal/Relationship Management Skills. Ability to work in a dynamic and demanding work environment. Strategic mindset with demonstrable capabilities of executing assignments in Indirect Procurement. Excellent command of ERP systems like SAP / ARIBA etc. is a must. Language requirements: Proficiency with spoken and written English Travel Requirements – Once every quarter to TAPI sites in India. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Overhauling & replacing faulty parts of process & utility equipment. Trouble shooting in case of any abnormality/breakdown & diagnosing the troubles. Responsible for undertaking maintenance, repairs, minor improvement works across the site Recording all maintenance records & reports for future reference Execute preventative and corrective maintenance of equipment’s. Ensure work compliance as per job orders/work permits. Responsible for getting the material from Engineering Store for the respective work to be carried out. Ensure preventive maintenance has been carried out within schedule date. Ensure compliance of job order and closure of work permits. Responsible to check the breakdown/maintenance work pending from previous shift and report it. To maintain all document pertaining to maintenance. Responsible for Preventative maintenance of equipment &Documentation as per SOP of the site. Responsible for Safety CAPA execution at site. Handling all documentation as per GMP. Person should have computer skill to handle Maintenance related work. Knowledge of all safety norm as per industries. Knowledge of all safety work permit system as per industries standard. Your Experience And Qualifications Qualification: ITI - Mechanical Experience: Minimum 7-15 Years Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

Apply now » Operator III - TAPI Date: May 29, 2025 Location: Gwalior, India, 477117 Company: Teva Pharmaceuticals Job Id: 61733 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Carrying out dispensing activities as per applicable procedure. Responsible for recording the observation of reaction parameters on the batch card as per approve procedure. Filling of all the batch card ( production cleaning) as per approved instruction Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipment, update the equipment. Report accident and irregularities at the work station to the Shift Officer. To prepare the production batch card, protocol and other relative document of production ERP operation related to Production activities. Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production. Coordinating with QA for Online compliance of GMP at shop floor. All other Production related activities advised by the Superiors from time to time. Your experience and qualifications B.Sc./M.Sc. (Chemistry) / Diploma (Chemical Engineering) 5+ years Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Apply now » Maintenance Engineer II - TAPI Date: May 27, 2025 Location: Gwalior, India, 477117 Company: Teva Pharmaceuticals Job Id: 62085 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day 1. Overall responsible for New Project, Modification jobs activity in the plant as per requirement of site. 2. Project management and execution of new and expansion project from Design to till handing over to plant. Also closing of project with capitalization. 3. Responsible for execution of project with given time line. 4. Compliance of all statutory & GMP requirement in new project. 5. Design & compliance of safety practices at site and to ensure zero reportable incidents. 6. Coordination with consultant for technical aspect. 7. Evaluation of Design, drawing, technical specification as per Teva Standards. 8. Procurement assistance to SCM for project. 9. Installation and commissioning of project as per standard/ Teva guidelines. Indenting of material and technical evaluation of vendors. 10. Coordination with all vendor/ consultant for deliverables. 11. Responsible for project result, forecasting and controlling-project schedule & cost. 12. Preparations of budget estimate for proposed/ new project. 13. Manpower & Contract Management 14. Responsible for attending/rectification of mechanical breakdowns in the plant through job orders/permits. 15. Responsible for preventive maintenance of equipment’s as per schedule& closer in ERP system. 16. Co-ordinate with other service team for problem rectification in plant. 17. Responsible to overall maintenance of production block. 18. Responsible to carry out the preventive maintenance/overhauling of cGMP Equipment, critical equipment and its subparts etc. as per schedule. 19. Responsible for spare part main 20. Preparation of Equipment Layout, Plant Layout, P & ID (Piping & Instrumentation Diagram), PFD (Process Flow Diagram). 21. Responsible for Permit issuance & safety compliance of assigned plant. 22. Responsible for GMP& EHS CAPA and deviation closure and updation. Your experience and qualifications B.E. / B.Tech(Mechanical) 8+ Years of experience Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Apply now » Team Leader Production - TAPI Date: May 29, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62165 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team. Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives. Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills. Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR) Coordination of production tasks to meet assigned schedule Your experience and qualifications Requires a B.Tech Chemical / Msc -Chemistry. or equivalent Requires a minimum of 3 - 5 years of relevant experience in a regulated industry Prefer previous experience in a leadership role Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »