104 Jobs in Gajraula - Page 2

Company Description 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. Job Description We’re seeking a hands-on production expert with deep GMP knowledge, ISO Class 8 compliance, ERP proficiency, and operational expertise in powder processing equipment, documentation, safety. Key Responsibilities: Expertise in operating powder processing equipments involved in API process (micronizer, sifter, fitz mill and others). Execute batch manufacturing as per Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs). Complete knowledge of clean area standards, specifically adhering to ISO class 8 requirements . Handle raw materials, intermediates, and finished products safely and efficiently Maintain accurate documentation of process parameters, deviations, and cleaning records Ensure compliance with cGMP, EHS, and regulatory standards during operations Coordinate with maintenance and quality teams for equipment troubleshooting and process deviations Participate in training programs and continuous improvement initiatives Preparation of batch card, qualification protocol, report & other GMP related documents. Carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures. Skills & Competencies: Good understanding of Production procedures . Fam Understating of GMP & Safety Good communication and teamwork skills. ✅ Preferred Experience: Prior experience in regulated environments (USFDA, WHO-GMP, etc.) Exposure to API manufacturing in pharma. What We Offer: Competitive salary. Opportunity to work in a world-class API facility Training and career development programs Safe and inclusive work environment Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.Sc./ M.Sc./ Diploma (Chemical) or B.E. / B.Tech. in Chemical Engineering . Experience: 1 to 3 years of experience. Additional Information 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!

Job Title : .NET Developer Experience : 3+ Years Location: Shri Venkateshwara University, Gajraula, Uttar Pradesh Salary : Maximum 5.50 LPA Education Qualification: Bachelors or Masters Degree in Computer Science, IT. Industry Preference : Experience in University or Medical College setting preferred Job Summary We are seeking a skilled .NET Developer with 3+ years of hands-on experience to join our IT team at SVU, Gajraula . The ideal candidate should have a strong background in .NET technologies and experience working in educational or healthcare institutions. You will be responsible for developing, maintaining and supporting web-based applications that support academic and administrative functions. Key Responsibilities Design, develop, test, and deploy web applications using .NET (C#, ASP.NET, MVC) Maintain and enhance existing applications and systems Work with SQL Server for database design, queries, and stored procedures Collaborate with academic and administrative departments to gather and define software requirements Ensure application performance, scalability, and security standards Troubleshoot and resolve application issues and bugs Prepare technical documentation and user guides Required Skills Proficiency in C#, ASP.NET, MVC, and .NET Framework/Core Strong experience with SQL Server, including stored procedures and database optimization Knowledge of front-end technologies (HTML, CSS, JavaScript, jQuery, etc.) Experience with version control tools like Git Ability to write clean, maintainable, and well-documented code Excellent problem-solving and debugging skills Preferred Qualifications Experience working in a University, Medical College, or educational institution environment Familiarity with ERP or academic management systems Understanding of IT workflows in academic or healthcare settings How to Apply Interested candidates may send their CV to svuhr@svu.edu.in

Lead full plant operations, including production, quality, maintenance & supply chain. Drive efficiency, cost control, and safety. Ensure compliance and implement Lean/Six Sigma for continuous improvement.

Role & responsibilities: : 1. Complete knowledge of clean area standards, specifically adhering to ISO Class 8 requirements. 2. Expertise in operating powder processing equipment, including Micronizer, Sifter, Fitz Mill, and others. 3. Batch details put in ERP system. 4. Preparation of batch card, qualification protocol, report & other GMP related documents. 5. Preparation of safety work permits to carry out maintenance activities in shift. 6. Report accidents and irregularities at the work station to the Shift Officer. 7. Carrying out process and sampling activities during the production of Intermediate /APIs according to the approved batch cards. 8. Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations & parameters in the batch card. 9. Ensure verification of weigh balances and all daily documents as per applicable procedures. 10. Carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures. 11. Follow Standard operating procedure (SOP), Safety and cGMP guideline. 12. Ensure housekeeping of plant and cleanliness of the equipment/ area, update the equipment status board, use log book, other documents as per applicable procedure. Requirement - *API experience is required* Interested candidate can share their resume on jasleen.kaur@tapi.com or connect on 8076954558.

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. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. 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 equipments, update the equipment Report accidents and irregularities at the work station to the Shift Officer. 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 Coordination of production tasks to meet assigned schedule Your Experience And Qualifications 2 to 3 years – Msc. ( Chemical) 0 to 2 years B.Tech / B.E / Diploma(Chemical) 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.

Ensure plaining and scheduling for annual preventive maintenance of all mechanical and utility installations in the plant. Attend and timely response for all emergency breakdowns of mechanical and utility installations in the plant. Implement GMP requirements in function. Aligning SOP corporate SOP and guideline. Ensure spare part inventory of the mechanical and utility equipment items in Engineering Stores. Evaluate new equipment/facility proposals for Capex & modification and its procurement with timely execution. Support site project team for evaluation and timely completion of project. Renewal of registrations and licenses related to Utility & Mechanical equipment for concerned Government Department as per standards. Ensure the safety of persons, plant & Equipment while carrying out the maintenance job. Work procedure update and training. Critically analyze the expenditure on procurement of items and overall equipment and utility maintenance expenditure periodically and find out ways and means to control the same at optimum level. Review the planning and implementation of energy conversion schemes and maintenance excellence schemes. Timely closely of permanent change Control, temporary change control, deviation, CAPA and service calls. 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

Company Description 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. Job Description 🚀 We’re looking for a proactive engineering leader with a passion for capital project execution and GMP excellence—if you thrive in high-impact environments, this opportunity is for you. 📋 Key Responsibilities 🧩 Project Management & Execution Lead end-to-end execution of capital projects, ensuring they are delivered on time, within budget, and in line with business objectives Own and track the annual capital spending plan for the site Drive cost optimization and execution excellence through industry best practices Align projects with Global Engineering policies, procedures, and governance frameworks Provide design oversight for new processes, equipment, and facilities to ensure FDA and internal compliance Contribute to long-term planning for strategic product and manufacturing initiatives 👥 Talent & Procurement Collaboration Identify gaps in the project team’s expertise and support skill enhancement or hiring Collaborate with procurement to finalize capital equipment orders, including techno-commercial bid analysis Monitor and report Capex cash flow, forecasts, and monthly budget utilization Develop and maintain Capex governance tracking Prepare and analyze Annual Operating Plans (AOP) and Long Range Plans (LRP) for capital investment Finalize Capital Expenditure Requests (CERs) and manage global approval workflows ⚠️ Safety, Compliance & EHS Oversight Ensure full implementation of safety and HR compliance protocols for internal and contractor teams Meet local and global EHS KPIs consistently Conduct regular Safety GEMBA walks and lead risk assessments Ensure availability of Emergency Response Team (ERT) and first aid-trained personnel across all shifts 🔄 Miscellaneous Perform any additional tasks as assigned by the Department Head. Must Have Good understanding of Project procedures. Understanding of GMP. Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.E. / B.Tech. in Mechanical or Chemical Engineering. Experience: Minimum 12 years of experience in Engineering Site Project management. Additional Information 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!

Company Description 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. Job Description We’re looking for a proactive engineering leader with a passion for capital project execution and GMP excellence—if you thrive in high-impact environments, this opportunity is for you. Key Responsibilities: Project Management & Execution Lead end-to-end execution of capital projects, ensuring they are delivered on time, within budget, and in line with business objectives Own and track the annual capital spending plan for the site Drive cost optimization and execution excellence through industry best practices Align projects with Global Engineering policies, procedures, and governance frameworks Provide design oversight for new processes, equipment, and facilities to ensure FDA and internal compliance Contribute to long-term planning for strategic product and manufacturing initiatives Talent & Procurement Collaboration Identify gaps in the project team’s expertise and support skill enhancement or hiring Collaborate with procurement to finalize capital equipment orders, including techno-commercial bid analysis Monitor and report Capex cash flow , forecasts, and monthly budget utilization Develop and maintain Capex governance tracking Prepare and analyze Annual Operating Plans (AOP) and Long Range Plans (LRP) for capital investment Finalize Capital Expenditure Requests (CERs) and manage global approval workflows ️ Safety, Compliance & EHS Oversight Ensure full implementation of safety and HR compliance protocols for internal and contractor teams Meet local and global EHS KPIs consistently Conduct regular Safety GEMBA walks and lead risk assessments Ensure availability of Emergency Response Team (ERT) and first aid-trained personnel across all shifts Miscellaneous Perform any additional tasks as assigned by the Department Head. Must have: Good understanding of Project procedures. Understanding of GMP. Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.E. / B.Tech. in Mechanical or Chemical Engineering . Experience: Minimum 12 years of experience in Engineering Site Project management. Additional Information 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!

Role & responsibilities : Accountable for Assigned capital projects to be delivered on schedule and budget and to meet customer/business requirements. Provides leadership for the planning, development, and ongoing tracking of annual capital spending plan for the specified site. Integrates cost reduction, best project management skills, and ongoing execution improvement into capital projects. Ascertains the Global Engineerings rules, policies and procedures when appropriate. Consults on the engineering design of new facilities, processes, and equipment for compliance with Global standards and FDA regulation. Provides engineering input into long-range planning efforts for key products, processes and long-range development of company manufacturing initiatives. Identify gaps in expertise and develops plans to upgrade skills of current project management personnel or develops plans to recruit personnel with necessary skills. Close working with procurement for finalizing the orders for capital equipment Techno commercial bid analysis & recommendations. Provide analytical Capex cash flow & effectively monitor Capex spends and forecasts. Responsible for Capex monthly reporting. Analyze & Prepare Capex Annual operating plans (AOP) Long Range Plan (LRP) for Capital projects. Develop Capex governance tracking mechanism. Finalize Capital expenditure Requests (CER) & take approvals from Global to execute the project. Responsible for implementation of all Safety guideline in department & also at contractor end while on job including HR compliance part also. Ensure that local and global EHS KPIs are met without any delay. Perform Safety GEMBA walks. Ensure the availability of ERT Emergency Response Team) trained members and first aid members in each shift. Participate in Risk Assessment and implement the recommendations Preferred candidate profile: Qualification: B.E./B.Tech (Mechanical/Chemical) Experience: 12 Years Key Skills: Good understanding of Project procedures, Understanding of GMP.

Roles and Responsibilities Ensure quality management system (QMS) conforms to ISO standards through internal audits, external audits, and certification body audits. Develop and implement QMS procedures, work instructions, SOPs, and forms aligned with legal and customer requirements. Conduct regular audits to ensure compliance with QMS policies and regulations. Identify areas for improvement and implement corrective actions to address non-conformities. Collaborate with cross-functional teams to drive continuous improvement initiatives. Desired Candidate Profile Strong understanding of IFS, Procedures, Policies, SOPs, Work Instructions, and Formats in line with legal and customer requirements.

Role & responsibilities Greeting customers when they enter store and coaching the team to do the same Displaying commitment towards providing exceptional Customer Service and ensuring that Lenskart associates also treat Customer Satisfaction as a priority Dealing with customer service issues such as queries and complaints at store level and ensuring this is consistent with the team Driving sales vs. plan (Attrition Control) Cash & Inventory management Supervision SOP adherence & implementation Store upkeep & maintenance Preferred candidate profile Minimum qualification: Graduate Ability to act as a link between strategy and execution Ability to develop and inspire people to achieve their best Ability to build rapport and trusting relationships Ability to understand stated and unstated needs of the customer and offer solutions Clear communication and active listening skills Ability to adapt to a changing environment and openness to learn Proactive task ownership, result-orientation, and customer-orientation Ability to multitask and organize activities based on priority Whatsapp your CV - 9680019364

Join L&T Finance and Build a Career in Financial Services! Are you energetic, self-driven, and ready to work in the field? We’re looking for Micro Loan Officers to help us connect with customers, promote micro loan products, and manage loan processing and collections. This role is ideal for individuals who are passionate about customer interaction and career growth in the finance industry. Role Overview: As a Micro Loan Officer, you will: Promote and process micro loans for individual clients Build and maintain strong customer relationships Ensure timely repayment and follow-up on collections Work in the field to reach potential customers and drive loan growth Who Can Apply: Education: Any graduate Preferred Age Group: 20 to 30 years Additional Preferences: Must own a two-wheeler Hold a valid driving license (DL) Have a smartphone for field communication and updates Salary Package: Monthly salary: ₹16,500 – ₹19,500 (based on experience and qualifications) Additional field incentives and performance-based benefits Why Work With Us? Be part of one of India’s top finance companies Competitive salary with extra field allowances Training, mentorship, and career growth opportunities Ready to start your journey in finance? Apply now and grow your career with L&T Finance! Job Type: Full-time Pay: ₹16,500.00 - ₹19,500.00 per month Work Location: In person

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 Analysis of stability samples & working standard qualification activity as per defined procedure & monograph. Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation. Maintaining a system of methods and specification for all materials and products. Data filling and maintaining the log books, certificate, stability report and stability data in archive. Monitoring of stability studies with respect to ICH Q-1 and conducting analytical method validation activity according to ICH Q-2. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity. Qualifications of all analytical instruments should be maintained in stability Section. Follow the defined safety procedure during day to day activity in laboratory. Any other job assigned by Manager Quality Control. Your Experience And Qualifications Bachelor/Master of Science/ B. Pharmacy One Years 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. 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 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 for issuance of raw material from warehouse as per production requirement. Storage and labeling as per applicable procedure Assisting the Team leader in ensuring proper storage of raw materials, intermediates and finished goods in designated areas and labeling as per applicable procedures Carrying out dispensing activities as per applicable procedure & carrying out process and sampling activities during the production of Intermediate/API’s according to the approved batch cards Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations & parameters in the batch card Ensure verification of weigh balances and all daily documents as per applicable procedures & carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures Follow Standard operating procedure (SOP), Safety and cGMP guideline Ensure housekeeping of plant and cleanliness of the equipment/area, update the equipment status board, use logbook, other documents as per applicable procedure Complete knowledge of clean area standards, specifically adhering to ISO Class 8 requirements & expertise in operating powder processing equipment, including Micronizer, Sifter, Fitz Mill, and others Preparation of batch card, qualification protocol, report & other GMP related documents and adding batch details in ERP system Preparation of safety work permits to carry out maintenance activities in shift & report accidents and irregularities at the workstation to the Shift Officer Your Experience And Qualifications B.Sc./M.Sc./Diploma (Chemical)/B.Tech (Chemical)/B.E (Chemical) 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.

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 Analysis of stability samples & working standard qualification activity as per defined procedure & monograph. Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation. Maintaining a system of methods and specification for all materials and products. Data filling and maintaining the log books, certificate, stability report and stability data in archive. Monitoring of stability studies with respect to ICH Q-1 and conducting analytical method validation activity according to ICH Q-2. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity. Qualifications of all analytical instruments should be maintained in stability Section. Follow the defined safety procedure during day to day activity in laboratory. Any other job assigned by Manager Quality Control. Your Experience And Qualifications Bachelor/Master of Science/ B. Pharmacy One Years 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. 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 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 for processing and oversight of changes through the generation, justification, impact assessment, modification, review, approval, and implementation workflow. This includes but is not limited to SOPs, production records, test methods, specifications, protocols, reports, equipment, processes, material suppliers, facilities, computer systems etc. Responsible for review and approval of all continual improvement projects affecting quality at a site Responsible for processing of documents through the generation, modification, review, and approval workflow. This includes but is not limited to SOPs, production records, test methods, protocols, reports, labeling, etc. also, archival of records Responsible for Review of regulatory and quality compliance requirements and divisional policy, performance of gap assessments, and establishment or improvement of SOPs covering all areas of applicability. Development and monitoring of corrective action plans where needed Ensuring quality support to regulatory affairs as it relates to updates/changes to market authorizations Review of all documentation (i.e. LIR, OOS, Change Controls, etc.) Ensuring quality interface with internal and external customers when dealing with activities such as service requests, issue resolution, complaints, product information, or for movement of materials, products, or process from site to site Responsible for management of regulatory authority and other external compliance audits (e.g. Customer audits) including communication, tracking and resolution of observations. Management of communications with regulatory agencies including required reporting and resolution of any actions required by the agencies Responsible for Performing, reporting of observations and verification of compliance reports of internal audit Your Experience And Qualifications M.Sc. or B.tech chemical Minimum 10 Years of experience required 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.

Cnc plasma machine operator required. Experience at least of 3 yr to 8 yr. AutoCAD knowledge must . Cutting the plate with accuracy and quality. Shifting of plate on bed is also a key responsibility of operator. Reading technical drawings of cad. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Commuter assistance Internet reimbursement Paid sick time Schedule: Morning shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Work Location: Remote

Apply now » Quality Control Technician II - TAPI Date: Jul 4, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62341 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 Analysis of stability samples & working standard qualification activity as per defined procedure & monograph. Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation. Maintaining a system of methods and specification for all materials and products. Data filling and maintaining the log books, certificate, stability report and stability data in archive. Monitoring of stability studies with respect to ICH Q-1 and conducting analytical method validation activity according to ICH Q-2. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity. Qualifications of all analytical instruments should be maintained in stability Section. Follow the defined safety procedure during day to day activity in laboratory. Any other job assigned by Manager Quality Control. Your experience and qualifications Bachelor/Master of Science/ B. Pharmacy One Years 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 »

Role Description This is a full-time on-site role for a Marketing Executive located in Meerut. The Marketing Executive will be responsible for conducting market research and planning, communicating with stakeholders, customers and team members, and managing sales and marketing activities. The role involves developing marketing strategies, executing marketing plans, analyzing market trends, and identifying opportunities for growth. Qualifications Market Planning and Market Research skills Strong Communication skills Experience in Sales and Marketing Excellent analytical and problem-solving skills Ability to work independently and in a team Bachelor's degree in Marketing, Business Administration, or related field Experience in the education sector is a plus

Oversee the end-to-end procurement process for goods and services, ensuring timely and cost-effective purchasing aligned with institutional policies. Prepare and process purchase orders, requisitions, and tender documents according to the university/medical colleges guidelines. Evaluate quotations and negotiate contracts with suppliers and service providers. Maintain an up-to-date database of vendors, suppliers, market rates, and product specifications relevant to academic and medical requirements. Coordinate with department heads to identify procurement needs and budget constraints. Manage import procedures and documentation where necessary (especially for specialist medical or laboratory equipment). Track deliveries and resolve issues concerning order discrepancies, delays, or returns. Proactively seek and assess new sources and products for better institutional value. Prepare regular MIS reports on procurement activities, expenditures, and budget utilization for management review. Support internal and external audits related to procurement, inventory, and vendor payments. Familiarity with medical equipment, laboratory consumables, and academic supplies is highly desirable. Experience in procurement, preferably in a university, medical college, or healthcare institution is preferred Preferred candidate profile Excellent command on MS Excel and any ERP or procurement software is must Vendor management and development Contract negotiation and management Documentation and record-keeping Regulatory compliance (education/healthcare sector) Teamwork and cross-functional collaboration Good negotiation, communication, and interpersonal skills. High attention to detail and problem-solving ability. Ability to work independently and collaboratively in a fast-paced academic or medical environment. How to Apply? Please confirm your Interest by sending your updated resume to recruitment@svu.edu.in then you may call on 9368731732 / Neeraja

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Ingrevia Limited JubilantIngreviaisnowamemberoftheeliteGlobalLighthouseNetwork(GLN) oftheWorldEconomicForum(WEF) Celebrating our Culture and People. We are proud to be aGreat Place to Work certified! Jubilant Ingrevia history goes back to 1978 with the incorporation of VAM Organics Limited, which later became Jubilant Organosys and then Jubilant Life Sciences and now demerged to an independent entity as Jubilant Ingrevia Limited, which is listed in both the stock exchanges of India. Over the years, company has developed global capacities and leadership in chosen business segments. Ingrevia is born out of a union of ‘Ingredients’ and ‘Life’ (‘Vie’ in French). Jubilant Ingrevia Limited is committed to offering high-quality and innovative life science ingredients to enrich all forms of life. Jubilant Ingrevia, a global integrated Life Science products and Innovative Solutions provider serving, Pharmaceutical, Nutrition, Agrochemical, Consumer and Industrial customers with our customised products and solutions that are innovative, cost-effective and conforming to excellent quality standards. Jubilant Ingrevia Limited offers a broad portfolio of high-quality ingredients that find application in a wide range of industries. Jubilant Ingrevia’s portfolio also extends to custom development and manufacturing for pharmaceutical and agrochemical customers on an exclusive basis. Ourbusinessissplitacross3businessverticals,withgloballeadership acrossourkeyproductlines. Speciality Chemicals: The Specialty Chemical business of Jubilant Ingrevia manufactures Pyridine, Picolines and its forward integration derivatives, which finds application in agrochemicals, pharmaceuticals, dyes, solvents, metal finishes, fine chemicals, semiconductors etc. We have also launched new platform of Diketene & its value-added derivatives for multiple industry use. We are an established ‘partner of choice’ in CDMO, with more investment plans in GMP & Non-GMP multi-product facilities for Pharma, Agro and Semi-conductor customers. Chemical Intermediates: The Chemical Intermediates business has acetic anhydride and value added anhydrides and aldehydes catering to various industries. Nutrition & Health Solutions: The Nutrition & Heath Solutions business unit offers B3 & Picolinates (Chromium & Zinc) which are fully backward integrated. Our ingredients find application in animal nutrition, human nutrition, personal care, etc. We provide high-quality feed & food additives having application in poultry, dairy, aqua & pet food industry. In Human Nutrition & Health Solutions, we offer food ingredients & premix solutions to nutrition. Jubilant Ingrevia Limited is supported by five state-of-the-art manufacturing facilities in India. We practice world-class manufacturing processes in our day-to-day operations, assuring our customers with unmatched quality and timely delivery of products through innovations and cutting-edge technology. Transforming Manufacturing for Operational Excellence & Sustainability with “zero tolerance to any non-compliance” is the core focus of Jubilant Ingrevia Manufacturing. We have 5 world-class manufacturing facilities i.e. One in UP at Gajraula, Two in Gujarat at Bharuch and Savli, Two in Maharashtra at Nira and Ambernath. Environment Sustainability The company is committed to environmental sustainability and supports green chemistry by prioritising the use of bio inputs in manufacturing. Jubilant is one of the world’s largest producers of Acetaldehyde from the bio route. Find out more about us at www.jubilantingrevia.com The Position Organization : - Jubilant Ingrevia Limited Designation & Level: - Senior Research Associate- Chemical Research Location : - Gajraula Reporting Manager: - Sr. Group Leader Job Summary The Senior Research Associate in Research & Development will be responsible for implementing cost reduction and process improvement initiatives, managing lab operations and safety, and supporting scale-up and plant commissioning activities. Job Responsibilities Cost Reduction and Process Improvement of Existing Products: Identify and implement cost-saving measures and process optimizations for existing products. Conduct root cause analysis and troubleshoot process issues to enhance efficiency and reduce waste. Continuous improvement on the key projects to keep them cost competitive Collaborate with cross-functional teams to streamline operations and improve product quality. Data Entry and Document Preparation: Ensure accurate and timely data entry for all R&D activities. Prepare and maintain comprehensive documentation, including experimental protocols, reports, and regulatory submissions. Develop and implement standard operating procedures (SOPs) for data management and documentation. The Person Qualifications: Ph.D. or master’s in chemistry, Chemical Engineering, or related field. 2-5 years in R&D within the fine chemicals industry. Proficient in data management and lab safety. Skills: Project management and organizational skills. Design of Experiments for process optimization What’s on Offer: Opportunity to work with a leading company in the chemicals sector. Competitive salary and benefits package. Career growth opportunities in a rapidly evolving industry Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, please visit our LinkedIn page: https://www.linkedin.com/company/jubilant-bhartia-group/

knowledge of sheeting machine and z & c profile machine operation and maintenance , along with computer work and software data entry, adjustment of size of sheeting ect

Maintain day-to-day entries in tally, sale & purchase ect. Knowledge of GST & TDS etc. Making invoicing and e-way bill, maintain the workers attendance & prepare the salary of worker and staff,

Supervise production processes of structure fabrication to ensure efficiency and quality standards are met. Interpret the auto-cad, technical drawings, and specifications to guide fabrication tasks, meet production goals and resolve issues, ect

Apply now » Senior Manager Maintenance/Engineering Date: Jun 26, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 60951 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 Ensure plaining and scheduling for annual preventive maintenance of all mechanical and utility installations in the plant. Attend and timely response for all emergency breakdowns of mechanical and utility installations in the plant. Implement GMP requirements in function. Aligning SOP corporate SOP and guideline. Ensure spare part inventory of the mechanical and utility equipment items in Engineering Stores. Evaluate new equipment/facility proposals for Capex & modification and its procurement with timely execution. Support site project team for evaluation and timely completion of project. Renewal of registrations and licenses related to Utility & Mechanical equipment for concerned Government Department as per standards. Ensure the safety of persons, plant & Equipment while carrying out the maintenance job. Work procedure update and training. Critically analyze the expenditure on procurement of items and overall equipment and utility maintenance expenditure periodically and find out ways and means to control the same at optimum level. Review the planning and implementation of energy conversion schemes and maintenance excellence schemes. Timely closely of permanent change Control, temporary change control, deviation, CAPA and service calls. 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 Your experience and qualifications BE/B. Tech-Mechanical 14+ years of experience Reports To Director Site Engineering 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 »