3772 Pharma Jobs - Page 38

Role Summary: As a Senior IT Analytics Specialist at a 100% cloud-based pharma startup in Mumbai, you will be responsible for driving data-driven decision-making, AI-powered automation, and cloud-based analytics across all business functions. Your primary focus will be on utilizing data from ERP, SFA, DMS, LIMS, HRMS, and Chemist Software to generate actionable insights, predictive analytics, and AI-driven forecasting tools for pharma operations. You should have hands-on experience in BI tools, AI/ML adoption, cloud analytics, API integrations, and data governance. Additionally, you will collaborate with outsourced vendors to ensure seamless data flow, security, and analytics-driven business intelligence. Key Responsibilities: - Collaborate with AI & Data Science teams to drive real-time analytics adoption. - Implement AI-driven forecasting tools for pharma sales, inventory, and demand planning. - Develop and support LLM-powered chatbots for customer service, sales insights, and operational automation. - Ensure seamless data lake connectivity for advanced cloud analytics and BI tools (Power BI, Qlik, Tableau). - Serve as the single point of contact for all data analytics vendors and AI partners. - Negotiate SLAs, contracts, and performance benchmarks for outsourced IT analytics services. - Oversee system performance, data accuracy, and security updates for all analytics platforms. - Focus on data visualization, defining KPIs for each function, and ensuring analytics serve as a business enabler. Desired Candidate Profile - Must-Have Qualifications: - 6-8 years of experience in IT analytics, cloud BI, and AI-driven decision-making. - Expertise in data pipelines, ETL workflows, and API integrations for enterprise systems. - Strong knowledge of BI tools (Power BI, Qlik, Tableau), SQL, Python/R for data analytics. - Experience in cloud-based analytics (AWS, Azure, GCP) and data governance. - Knowledge of AI-driven insights, predictive modeling, and NLP-driven analytics tools. Good-to-Have: - Experience in pharma, healthcare, or regulated environments. - Familiarity with data privacy laws (HIPAA, GDPR, DPDP Act India). - Certifications in AWS, Azure, ITIL, CISSP, or AI/ML technologies. Required Qualification: - Bachelor of Engineering - Bachelor of Technology (B.E./B.Tech.)- IT/ CS/ E&CE/ Bachelor of Computer Applications (B.C.A.) Please note that this position is based in Mumbai and offers the opportunity to work in a 100% cloud-based pharma setup as part of a giant Indian Conglomerate.,

As a Key Accounts Manager you will be responsible for the development and performance of all sales strategies in assigned market. Further you will drive primary sales, secondary sales and ensuring brand presence in defined markets. You will supervise/manage the distributor network to achieve desired sales objectives thereby ensuring achievement of financial and ethical objectives of the division as per the business strategy. To achieve this you will have authority to develop your customer management plan, approve expiry products issue credit note for distributors under your control, recommending appointment and credit limits of distributors, develop, execute & plan your resource utilization and participate in Strategy Execution review meetings to ensure alignment. You have a very important role to play in Divisions success. Area Business Planning: Plan for monthly and quarterly business. Plan for Trade activation business and over all sales Plan demand generation and fulfillment Monitor actual Sales and mid course corrections and inputs to reduce variance against expectations Prescription audit for Abbott brands and other competitors brands To create and update customer list having specified number of doctors / chemist (Trade) as per the therapy / product requirement and maintain the same in physical / electronic format. Identifying potential town and appointing distributor and customers (trade) in line with business philosophy Business generation & development: Achieve monthly, quarterly, half yearly and yearly Sales target by promoting companies product ethically to customers as per the business plan Having science base discussion with Doctor and chemist for promotion of product in clinic and at chemist place Organizing Camps (CME) as per the division strategy and customers need To carry out activations across trade and clinics for brand visibility To plan and conduct merchandising and sampling activity as per Division strategy. Facilitate the process of successful new product / products launch in the territory by undertaking correct identification and targeting customers for the new product, meet them at pre determined intervals, effective in clinic / trade promotion and feed back to the company Execute the customer management plan to ensure that all the customers are covered as per the plan and meet minimum KPIs as follows: a. 100% coverage of Doctors. b . Customer Call average as per the customer management plan of the division / therapy. c. Market intelligence collection, retailer level inventory management calls as per the product profile and marketing strategy of the therapy / division. Brand Management: Ensuring the visibility of Abbott brands on retailers outlet as a part of brand promotion strategy To plan and attend Retail meets, Market Blitz etc for sales growth

MAIN PURPOSE OF ROLE Conduct market research and feasibility studies to analyze the viability of alternative business development opportunities. MAIN RESPONSIBILITIES Collect, compile, verify, and analyze financial, competitive, sales, marketing, and other information about potential business partners, new markets, products and services, or other business opportunities so that senior management has accurate and timely information for making strategic and operational decisions. Prepare documents and materials (for example, reports, presentations, information packages) for meetings and negotiations with potential clients and business partners so that the information provided is accurate and appropriate for external distribution. QUALIFICATIONS Associates Degree ( 13 years)

Job Description: Applications are invited for the post of Project Research Scientist - I (Non-Medical) for the ICMR New Extramural (First in the World Challenge) grant in the Centre for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT). (No. EM/Dev/FIW/00252/2024 (E-Office-227016)). Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have a first-class postgraduate degree, including the integrated PG degrees, relevant to nano technology, nano-delivery, biological therapeutics, pharmaceutical sciences, Biotechnology. Stipend: Rs. 56,000 + 10% HRA (Rs. 61,600) per month, stipend will be as per Institute norms. Sponsoring Agency: ICMR, New Delhi Duration: 3 years Principal Investigator: Dr. Natarajan Chandrasekaran, Professor, Higher Academic Grade, Centre for Nanobiotechnology (CNBT), Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu Co-Principal Investigator: Dr. George Priya Doss C, Professor Grade 1, Department of Integrative Biology School of Bio Sciences and Technology Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc on or before (10/06/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

To support and maintain a robust, inspection-ready Quality System in alignment with global regulatory standards, ensuring operational excellence, data integrity, and continuous improvement in GxP environments. This role encompasses management of key quality processes including Change Control, Product Quality Reviews, and Risk Management. Principle Responsibilities: Maintain an efficient, compliant, and inspection-ready Quality System aligned with applicable GxP regulations and industry best practices Oversee the end-to-end change control process, ensuring timely assessment, approval, and implementation in compliance with applicable regulations. Coordinate and ensure timely completion of PQRs for all marketed products, including data collection, trending, evaluation, and final review. Support the implementation and monitoring of quality metrics and KPIs to assess system performance and identify areas for improvement. Provide governance for quality risk management processes and ensure timely escalation of significant issues to senior management. Manage Quality Risk Escalation and Quality Council meetings Identify and drive continuous improvement initiatives in quality systems and processes. Regularly report quality system metrics, status of change controls, and PQRs to the Head of Quality Compliance. Prepare dashboards and presentations as needed. Qualifications and Education Requirements Bachelor s or Master s degree in Life Sciences, Pharmacy, or a related discipline. Minimum 5 years of experience in pharmaceutical/biotech quality systems or quality assurance roles. Experience in PQR and change control management. Excellent communication, leadership, and problem-solving skills. Experience with quality audits and regulatory inspections is an advantage.

The ideal candidate will have a consistent record of leadership in technology-driven environments using 3DEXPERIENCE Cloud platform and has a passion for fostering innovation and excellence in the biotechnology industry. Additionally, collaboration with cross-functional and global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a strong background in the end-to-end software development lifecycle and a Scaled Agile practitioner, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational critical initiatives, foster a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Roles & Responsibilities: Maintain strategic relationships and strong communication with the leadership team about IS services and service roadmaps to ensure that all the customers feel informed and engaged Lead and manage large, diverse teams within a matrixed organization. Collaborate with geographically dispersed teams, including those in the US and other international locations. Foster a culture of collaboration, innovation, and continuous improvement. Develop talent, motivate the team, delegate effectively, champion diversity within the team and act as a role model of servant leadership. Responsible for managing, growing, and developing the Amgen Technology team in India, ensuring global ways of working are imbedded in the local organization Understand the decision-making process, workflows, and business and information needs of business partners and collaborators Contribute and define business outcomes + requirements, technology solutions, and services Improve activities being measured by crafting, monitoring, and optimizing relevant feedback loops through test & learn activities Work with Product Owners, Service Owners and/or delivery teams to ensure that delivery matches commitments, acting as an escalation point and facilitating communication when service commitments are not met Ensure communication of key performance metrics and analysis of unmet needs Participate in collaborator and other leadership meetings, working with other parts of the organization, and functional groups to ensure successful delivery Ensure ongoing alignment with strategy, compliance, and regulatory requirements for technology investments and services Facilitate standard process sharing, ensuring ongoing alignment with the Technology & Digital strategy Provide education to new partners with regards to IT service offerings Remain accountable for ensuring overall organizational compliance to quality/compliance requirements such as GXP and Privacy Basic Qualifications: Doctorate degree / Masters degree / Bachelors degree and 12 to 17 years of experience in Business, Engineering, IT or related field . Preferred Qualifications: Functional Skills: Must-Have Skills: Strategize, plan, and implement various phases of PLM roadmap using Dassault Systemes 3DEXPERIENCE platform and integrating with key enterprise platforms Strong Technical/Functional experience solutioning and supporting GMP applications across Engineering, Clinical, Commercial and Quality functions. Demonstrated hands-on experience in managing technology solutions involving one of the leading PLM solutions (Windchill, Teamcenter or 3DEXPERIENCE). Experience integrate PLM with enterprise systems such as Data Fabric, Veeva vault, SAP, MES and SCADA systems. Experience in people management and leading highly skilled matrixed teams, passion for mentorship, culture and fostering the development of talent. Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment. Exceptional collaboration, communication and interpersonal skills to effectively manage collaborator relationships and build new partnerships. Experience in applying technology standard process methodologies: Scaled Agile (SAFe) Good-to-Have Skills: Experience in a leadership role within a pharmaceutical or technology organization Experience with configuring and customizing solutions for Requirements, CAD, Risk, EBOM, MBOM, Configuration/Variants, Recipe, MPP, Document and Change management. Experience leading data migration from various sources to 3DEXPERIENCE platforms. Experience creating solutions using Enterprise Integration Framework and usage of middleware systems such as Mulesoft, Boomi or Tibco. Extensive experience in software development lifecycle. Experience using and adoption of Scaled Agile Framework (SAFe) Strong analytic/critical-thinking and decision-making abilities. Ability to work effectively in a fast-paced, dynamic environment. Established business partnerships and IS governance practices involving senior business stakeholders Broad working knowledge of key IS domains and layers Professional Certifications: Scaled Agile Framework (SAFe) for Teams (preferred) Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Excellent analytical and troubleshooting skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams

You ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. What you will do Let s do this. Let s change the world. In this vital role you will Support the R&D quality Audit and help to build quality into everything Amgen does. Data entry into Amgen s Quality System of approved audit responses Audit resourcing/planning Quarterly Investigator Site audit planning including identifying audit resourc es t hrough risk assessment of audit targets on a regular basi s Yearly planning of other audit types including internal process/Service Provider and Affiliate Audits Updating Audi t tracking and accountability t ools and distrib uting/communicatin g all ocations to the audit teams Compiling Audit reporting metrics and communication Manage Audit documentation and filing Supporting outsourced audits by: Supporting outsourced audit resourcing/planning for Audits Provide necessary tools, reports/documentation, and access to systems for outsourced Audits Review initial draft audit reports, audit responses and debrief slides. Schedule and facilitate Quality Lead (pre-audit meetings) and audit debrief meetings QC Data entry into AMS of audit findings Confirming data entry into RDCS of approved audit responses Oversee timelines met for issuance of Initial audit reports; review of audit responses and issuing Final Audit Reports Provide guidance and resolve queries from external Audit vendors Weekly Meeting with external audit vendor to review tasks and status of audits Communicate noncompliance to Manager Administrative Support (includes maintaining & updating distribution lists and templates) Data entry/QC in to the Audit Management System (Trackwise) of audit findings Administrative support for audit resourcing/planning Manages Audit documentation and filing Ensures that the Audit Archive is updated with Final audit reports and closure memos and Plans/Agendas where applicable Follow up with CAPA Owners for completion dates and objective evidence Review and Append Objective evidence in Amgen s Quality System and close record What we expect of you We are all different, yet we all use our unique contributions to serve patients. The Quality professional we seek has a can do approach with these qualifications. Basic Qualifications: Master s degree in Life sciences or related field Preferred Qualifications: Minimum of 3-5 years in biopharmaceutical industry experience in Quality Management, Quality Assurance, or other relevant areas of the pharmaceutical/biotech industry where risk-based quality and quality by design are a core responsibility. Experience supporting regulatory authority inspections of clinical research, and/or pharmacovigilance activities Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Track wise. Quality Assurance Qualification/Certification (preferred)

The Manager in the Global Regulatory Intelligence team is a hands-on contributor responsible for gathering and organizing regulatory intelligence under the guidance of the RI Director. This role often has a technology and data focus , managing the tools and information that drive the intelligence process. Key Responsibilities: Intelligence Gathering & Analysis: Assist in monitoring and analyzing the global regulatory landscape, and in developing intelligence reports and updates as directed by the RI Director. A core duty is to collect and synthesize new or updated local regulatory requirements obtained from Amgen s local regulatory teams, for the Manager s assigned areas of responsibility. This information feeds into the group s centralized knowledge base. The Manager helps execute the regulatory intelligence workplans by preparing agreed deliverables - for example, compiling monitoring reports, bulletins, and landscape summaries that highlight regulatory changes or requirements relevant to upcoming filings. They ensure that these deliverables are coherent and actionable, providing clear recommendations or insights where appropriate . Tools & Data Management: Take ownership of the tools, databases, and documentation that support intelligence gathering and dissemination. The Manager is responsible for facilitating and maintaining these systems on a day-to-day basis. This includes ensuring that repositories of regulatory requirements and intelligence reports are up-to-date and accessible to stakeholders. Importantly, the Manager may also be expected to build or modify new tools and databases as needed, not just use existing ones. (For example, if a new tracking database or dashboard is required to capture regulatory changes, the Manager would play a key role in its development or configuration. ) Emphasizing this in the job description sets clear expectations that the role involves technical initiative in improving intelligence systems. Cross-Functional Support: Work closely with other members of the Regulatory Policy & Intelligence team and with regulatory staff in various functions to ensure intelligence is applied effectively. The Manager engages with policy analysts, product regulatory leads, and other cross-functional team members to share findings and gather input. While the Manager may not lead cross-functional projects independently, they support these efforts by providing the necessary data or analysis. For instance, if a cross-product regulatory strategy project is underway, the Manager might supply the compiled country requirements or recent regulatory changes needed for decision-making. They help ensure that agreed intelligence deliverables are executed on time and that any intelligence requests from internal stakeholders are addressed promptly. Progress Tracking & Improvement: Monitor the progress of intelligence-gathering activities against the team s objectives and timelines. The Manager tracks their assignments (e. g. , monitoring tasks or updates due) and regularly reports status to the RI Director. If there are delays or obstacles in obtaining information, the Manager flags these and helps troubleshoot solutions. Additionally, the Manager contributes to process improvement discussions - identifying any inefficiencies in how intelligence data is collected or shared and suggesting enhancements. They participate in continuous improvement of the function s processes and tools, helping to refine workflows for greater efficiency and reliability. Knowledge & Skills: Regulatory Knowledge: A solid grounding in regulatory affairs processes and requirements is needed. The Manager should understand regulatory submission guidelines and procedures across different regions (major markets and smaller markets) and have familiarity with how local regulations impact drug development and filings. While they may rely on senior staff for deeper analysis, the Manager must be able to interpret regulatory documents or health authority guidance and extract key points. The ability to handle complex information and distill it into clear summaries is crucial - often the Manager will be the first to review new regulations and must highlight what matters to Amgen s products. Attention to Detail and Analytical Skills: The role requires strong analytical abilities and attention to detail. The Manager will be dealing with regulatory texts, tracking changes, and inputting data into intelligence systems - so accuracy is paramount. They should be skilled at comparing regulatory requirements and spotting differences or trends. At the same time, they need to maintain a big-picture view to recognize how a particular change might affect Amgen s global filing strategy. Being able to propose practical solutions or escalate important findings is part of this analytical skill set. Technical and Project Skills: Proficiency in using information systems and databases is important, as this role often acts as the power user of regulatory intelligence tools. Experience with managing or configuring databases, spreadsheets, or tracking tools will be useful. The Manager should also have good project coordination skills - capable of managing their own workstreams, meeting deadlines, and juggling multiple intelligence requests or projects. Strong written and oral communication skills are needed to draft clear reports and to communicate findings to the team or other stakeholders. Additionally, a willingness to learn and even create new technical solutions (e. g. , leveraging an internal SharePoint site or an intelligence software platform) is highly valued in this position. Qualifications: Education & Experience: It is recommended that candidates have at least a Bachelor s degree in a relevant discipline (such as life sciences or regulatory affairs) plus relevant experience in regulatory or drug development roles. An advanced degree ( Master s or higher) in a related field is a plus. While Amgen s internal templates for similar roles have sometimes listed lower educational minima ( e. g. associate degree or high school with significant years of experience), for a Regulatory Intelligence Manager it is preferable to require a Bachelor s degree as the minimum qualification . This ensures the candidate has a sufficient foundation to grasp complex regulatory information. In terms of experience, a few years of hands-on regulatory affairs or regulatory operations experience (for instance, ~3-5 years with a Bachelor s degree ) would likely be expected, given the need to work independently and with understanding of the regulatory context. Preferred Background: Relevant industry experience in pharmaceutical/biotech regulatory affairs or compliance is strongly preferred. Experience specifically with regulatory intelligence or policy tracking - whether in a prior role or via project work - would allow a new hire to hit the ground running. Familiarity with regulatory intelligence tools or subscription databases (such as Tarius or similar services) and experience interacting with global regulatory colleagues would also be advantageous . The ideal candidate will be one who not only has the technical skills to manage data and tools, but also the curiosity and insight to understand why regulatory changes matter and how to communicate those insights effectively.

Title: Manager / Sr. Manager - Production (Peptide Block) Business Unit: API : Peptide Job Grade G10 / G9B Location : Ahmednagar, M. H. Key Responsibilities At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Job Profile- To plan and execute peptide manufacturing activities as per the schedule and Budget by optimum utilization of plant capacity To ensure the sustainable quality production with optimum utilization of plant capacity. Monitoring and reduction in process TRT, Cleaning TRT, number of preps per batch on Prep HPLC, Improve yields. Improve the process of Synthesis & Analytical Section. Co-ordinate with Purchase, Planning department to deliver the goods in time. To ensure every day interaction with each department for smooth functioning Compliance of waste water disposal as per IN-HOUSE policy To ensure grooming of disciplined workforce and staff to meet the planned growth charts. Developing different innovative practices to increase productivities and up gradation of work culture. To maintain Good Documentation Practices and Good Laboratory Practices Review of batch process record, Standard Operating procedure and cGMP documents Investigation of Deviation, Change Control & OOS Implementation & follow all safety instruction & practices Travel Estimate Low Job Requirements Educational Qualification M. Sc. (Chemistry) / B. E. (Chemical) / B. Tech (Chemical) Experience 15-20 yrs experience in Peptide API plant Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together!

To write, review and manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of To write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide authoritative documentation-related consultancy to other line functions. To coach/mentor and/or train less experienced writers. Major accountabilities: To author, review and/or independently manage high quality clinical and safety documents: complex Clinical Study Reports (CSR), Risk Management Plans (RMP), complex CTD submission documents (clinical overviews, summaries of clinical efficacy and safety, summaries of clinical pharmacology and biopharmaceutics), other documents for health authorities (e. g. , Briefing Books, answers to questions). Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for clinical portions of the CTD, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. Ad-hoc member of Clinical Trial Team (CTT) / extended member of Safety Management Team (SMT). Core member of multiple Clinical Submission Teams (CST). Extended member of Global Clinical Teams (GCT). Input into planning of data analyses and presentation (statistical analysis plan review and meetings) used in CSRs, submission documents and/or answers to questions. Documentation expert in GCTs and CSTs to ensure compliance to internal company standards and external regulatory guidelines. Provide content and strategic expertise for clinical portions of the CTD. Program Writer for large and/or complex programs ensuring adequate medical writing resources are available for assigned program and consistency between documents. Lead process improvement in RWS and cross-functional initiatives and/or activities. Can identify training needs to foster high level of performance within RWS. Coach and/or mentor less experienced writers. Leader in cross-functional communication to optimize feedback and input towards high quality documents. Maintain audit, SOP and training compliance. Key performance indicators: Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards, according to RWS metrics. Completion of an adequate volume of work (taking into account complexity) per year in accordance with the Key Performance Indicators. Work Experience: 6 years medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus expert knowledge of medical writing processes. Expert knowledge of and repeat experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). Expert knowledge, extensive experience, and demonstrated record of accomplishment in global registering of drugs. Excellent communication skills (written, verbal, presentations) Expert knowledge of biostatistics principles. Proven ability to prioritize and manage multiple demands and projects. Demonstrated ability to define and solve complex problems ( Problem-solver ) Broad knowledge and future oriented perspective Proven ability to drive and manage organizational and team performance across cultures. Proven track record in matrix environment Repeat experience in managing global, cross-functional teams or complex global projects. Demonstrated ability to motivate and coach people.

Development of marketing and promotional plans for products to support the end consumer s need Monitor business performance and support the portfolio with the help of regular tracking Market intelligence through primary research and customer connect Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs; initiating and coordinating marketing activities and projects Presentation to staff and training field staff for the same Visiting national and international congresses, hospitals, and key opinion leaders (KOLs); Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy; Discussion partner for first, second, and third-line professionals such as general practitioners, medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies; Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations. Collaboration with internal & external media to ensure the proper execution of strategies WHO YOU ARE: Experience: 3 to 4 years of experience in Pharma Marketing Qualification: B. Pharma + MBA - Marketing OR Pharma. Management Therapy Exposure: Cardio-Diabetes Skills: Able to foster collaborative relationships Proven track record of launching and managing successful products Strong analytical and problem solving skills Proficiency in product management tools Good in communication and presentation Science driven marketing strategies

We are currently seeking a Clinical Data Science Programmer to join our diverse and dynamic team. As a Clinical Data Programmer at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. What you will be doing Develop and implement programs and scripts to support data processing, validation, and analysis in clinical trials. Collaborate with cross-functional teams to design and optimize databases and data collection systems. Perform data manipulation, transformation, and quality control activities to ensure accuracy and completeness of clinical data. Generate and maintain documentation related to programming activities, ensuring compliance with regulatory requirements and industry standards. Contribute to the development and validation of statistical analysis programs and tools to support clinical study reporting. Your profile Bachelors degree or higher in Computer Science, Statistics, or a related field. Previous experience in clinical data programming within the pharmaceutical, biotechNlogy, or CRO industry. Proficiency in programming languages commonly used in clinical research, such as Rave + Custom Function . Familiarity with CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines. Strong analytical, problem-solving, and communication skills with a keen attention to detail and accuracy. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Clinical Data Science Programmer- Office based- Chennai/ Trivandrum We are currently seeking a Clinical Data Science Programmer to join our diverse and dynamic team. As a Clinical Data Programmer at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. What you will be doing Develop and implement programs and scripts to support data processing, validation, and analysis in clinical trials. Collaborate with cross-functional teams to design and optimize databases and data collection systems. Perform data manipulation, transformation, and quality control activities to ensure accuracy and completeness of clinical data. Generate and maintain documentation related to programming activities, ensuring compliance with regulatory requirements and industry standards. Contribute to the development and validation of statistical analysis programs and tools to support clinical study reporting. Your profile Bachelors degree or higher in Computer Science, Statistics, or a related field. Previous experience in clinical data programming within the pharmaceutical, biotechNlogy, or CRO industry. Proficiency in programming languages commonly used in clinical research, such as Rave + Custom Function . Familiarity with CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines. Strong analytical, problem-solving, and communication skills with a keen attention to detail and accuracy.

Career Category Quality Job Description Let s do this. Let s change the world. In this vital role you will collaborate closely with cross-functional teams to ensure that the PLM solutions follow the required validation processes, documentation, and comply with Amgen s standard operating procedures, policies, and guidelines. Your expertise will be instrumental in ensuring quality and adherence to required standards so that the engineering teams can build and deploy products that are compliant. Roles & Responsibilities: The ideal candidate will be accustomed to working in Web applications and should be actively involved in various types of testing such as Functional, System, Stress, Performance, Integration, Regression, and Beta. Develop and maintain comprehensive test plans for 3DExperience platform modules and application Lead, mentor and coach junior Quality and Validation engineers in their activities Analyze test results, collaborate and communicate effectively with the product teams and Dassault to pursue issue resolution. Develop validation documentation such as Validation Plans, Validation Protocols (IQ/OQ), Validation Reports, deviations, change control, non-conformance and other Computer System Validation (CSV) documents. Ensure validation strategies meet regulatory requirements and company standards. Guide junior validation engineers in writing the CSV documents and verify their output for completeness, accuracy and quality. Stay updated on relevant changes to Amgen s SOPs and ensure validation practices are aligned with evolving standards. Lead test automation scripting, framework maintenance, and CI/CD integration. Develop and execute automated test suites across various modules in 3DEXPERIENCE. Analyze test automation results, identify failures or inconsistencies, and assist in root cause analysis. Collaborate with cross-functional teams, including quality assurance, system owners, business owners, RunOps, engineering, and platform teams to drive validation activities and meet project deadlines. Ensure timely and effective completion of all validation activities in line with project objectives and schedules. Involve actively in release planning and estimate test efforts. Identify opportunities for process improvements in validation activities. Stay current on new technologies, validation trends, and industry best practices to improve validation efficiencies. Basic Qualifications: Doctorate degree / Masters degree / Bachelors degree and 8 to 13 years of Software Quality and GMP Validation . Must-Have Skills: Experience in Quality Assurance (QA) testing with at least 6 years of experience specifically working on the 3DEXPERIENCE platform or similar PLM/enterprise software solutions. Strong experience in manual and automated testing for complex applications, especially in the 3DEXPERIENCE platform. Experience in Computerized System Validation in a GMP-regulated environment (pharmaceutical, biotech, medical devices, etc. ). Experience in QA & Test Automation is expected. Experience leading software validation projects. Proficiency in developing and executing validation protocols (IQ, OQ, PQ), reports, and related documentation. Hands-on experience executing and analyzing automated test suites Familiarity with computer system validation and software validation is a plus. Strong problem-solving and analytical skills. Good-to-Have Skills: Understanding of 3DExperience platform architecture, modules, and integration points Experience with automated and computer-controlled systems validation (21 CFR Part 11) Soft Skills: Excellent analytical and troubleshooting skills. Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented, with a focus on achieving team goals. Ability to learn quickly, be organized and detail oriented. Strong presentation and public speaking skills.

As a Sr. Digital Product Manager within Enterprise Data Strategy and Engineering (EDSE), youll play a key role in unlocking the power of data and intelligence to enable Amgen s mission of accelerating breakthrough therapies. You will help shape and deliver Data and AI products and capabilities that support Amgen s strategic goals. Working closely with capability leads, business key collaborators, and engineering teams, you ll define solution roadmaps and set go-to-market strategies that drive adoption and measurable outcomes. This role is ideal for someone who enjoys shaping product direction, scoping new opportunities and delivering measurable outcomes. Youll contribute to the broader data strategy by ensuring that products and capabilities are positioned effectively and adopted meaningfully. Lead product discovery with internal customers to surface problems worth solving and define valuable, feasible solutions Shape product strategy and roadmap aligned to enterprise priorities and capability vision Own go-to-market strategy, driving adoption and engagement across the business Use AI tools and rapid iteration methods to prototype, validate, and define product requirements Translate insights into clear, actionable specs that engineering teams can complete Measure and track product outcomes, not just output, to ensure continuous value delivery Partner with business and technical leaders to position internal capabilities effectively Mentor Product Analysts and help build strong internal product practice as the team grows Define product and capability roadmaps aligned to business needs and enterprise data strategy Work with delivery teams to ensure timely execution and solution alignment As the function scales, you ll also play a key role in building and leading a team of Product Analysts, contributing to a growing internal product management practice What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Doctorate degree / Masters degree / Bachelors degree and 12 to 17 years of experience in Information/Tech Systems Proven ability to lead product lifecycle end-to-end, from strategy through execution Demonstrated ability to innovate by leveraging AI tools to enhance product impact and accelerate outcomes Strong experience crafting and implementing go-to-market strategies Excellent communication skills and ability to work across business and technology functions Familiarity with data, analytics, and AI platforms or related technologies Agile delivery experience in a matrixed environment Excellent project management skills with a record of building strong partnerships across multi-functional teams and managing diverse workloads to meet deadlines. Ability to work autonomously with minimal guidance and know when to seek input, combined with a collaborative approach to align with and support project goals Preferred Qualifications: Relevant experience, with overall experience in above mentioned range, in a product management role preferably in Data, AI and related platforms. Experience in leading products, defining roadmap and tracking the success of the product. Develop and align product strategy to the organizational strategy. Experience with Agile methodologies (Scrum/SAFe). Excellent critical thinking, problem solving, and communication skills Preferred Qualifications: Familiarity with cloud technologies, data platforms, and business intelligence (BI) tools and solutions Ability to work and lead effectively across matrixed organizations and collaborate between data and AI teams. Passion for technology and product success, particularly in driving innovative AI and data solutions. Experience in technology products related to data and AI products is a plus, and familiarity with biotech/pharma is beneficial. Soft Skills: Strong presentation and public speaking skills with experience communicating to Sr. leaders Excellent analytical and solving skills. Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to handle multiple priorities successfully. Team-oriented, with a focus on achieving team goals

As an Architect at Quest Global, you will play a crucial role in managing complex, exciting, and innovative building construction projects in the Concept/Basic and Detail Design phases. Your expertise will be instrumental in developing sophisticated solutions for a wide variety of building typologies, leading the project team, and ensuring the success of the project. You will serve as the central point of contact for clients, user representatives, and the design team, and your communication skills will be key in delivering precise, binding, and result-oriented solutions. To be successful in this role, you should have a degree in Architecture and a minimum of 10 years of professional experience in design and implementation planning. Experience in using Autodesk Revit is an advantage. We expect you to have a high level of architectural design standards and technical competence. Assertiveness, entrepreneurial thinking, and acting are essential qualities for this position. Additionally, strong social skills and the ability to work independently are highly valued. Your ability to communicate precisely, bind stakeholders together, and deliver result-oriented solutions will be crucial to your success in this role. Experience from the EPCM industry is preferred, but we also highly value experience from the High Tech Industry, such as Semiconductor, Pharma, Lifesciences, Data Center, Battery/Automotive Production. If you are a highly skilled and experienced Architect looking for an opportunity to work on complex and innovative projects in the EPCM industry, Quest Global is the place for you. Join our team and be part of our journey towards becoming a centenary company. Work Experience - Bachelors degree in Architecture - Minimum of 5 years of experience in architecture BIM - Experience in the High Tech Industry, preferably in Semiconductor, Pharma, Lifesciences, Data Center, Battery/Automotive Production - Proficiency in Autodesk Revit and Revizto Responsibilities: - Collaborate with Sr. Architects understand the architectural needs and requirements - Develop and present architectural designs, plans, and proposals - Ensure compliance with building codes, regulations, and safety standards - Coordinate with project teams, including engineers and contractors, to ensure successful project completion - Stay updated with the latest industry trends, technologies, and best practices Qualifications: - Strong attention to detail and excellent problem-solving skills - Exceptional communication and interpersonal skills - Ability to work independently as well as in a team environment - Proven track record of delivering high-quality architectural projects on time and within budget - Strong proficiency in Autodesk Revit and Revizto Note: Only shortlisted candidates will be contacted for further evaluation.

The Senior Solution Architect at SailPoint begins by l everag ing their experience to build a deep understanding of our SaaS and/or Software solutions. Within a month or two, they are serving as a technical lead on customer engagements and cases where they will employ their client and partner communication skills, as well as their industry knowledge to share organizational best practices for SailPoint products and identity governance. After their first six months, Senior S olution Architects will have established themselves as both technical and consultative experts within the Professional Services organization, and by the end of their first year they will have become a trusted advisor to customers, partners, leadership and to less experienced team members. Responsibilities As a trusted advisor, provide strategic direction to customers and implementation partners for a successful Identity Security Program Perform assessment on customer s current Identity landscape and build out their future identity road map Build out customers Identity role based access control and application onboarding program Ensure SailPoint best practices are followed through the project for a successful project delivery Advise and provide direction to junior resources on the project implementation Provide pros & cons to customers for building custom tools to meet their unique & complex business goals Maintain healthy business relationship with customers and partners Work with other advisory services leads, program managers and provide recommendations on any changes needed for the program. Work with other cross functional teams to understand the product roadmap, product limitations and advise strategic direction to the customers Document and present SaaS product adoption gaps Recommend areas where SaaS products consumption can be improved Manage, mentor, and coach direct reports (if any) Requirements : 8+ years of experience in technical consulting role Effective communication and presentation skills needed to perform identity security program assessments and provide a road map Strong organizational, leadership and multi-tasking skills Excellent analytical and problem-solving abilities Documentation management and ability to use project management tools Attention to details even under pressure Time management skills with the ability to meet deadlines Experience with any SailPoint governance products Experience with networking, directory servers, databases Experience with PAM (Privileged Access Management) software Experience with Web based APIs Nice to have: IdentityIQ or IdentityNow Certification is a plus Experience with Object Oriented Programming Experience with Azure, AWS or GCP Experience with scripting framework (Angular, TypeJS , etc.. ) Education : Bachelor of Science in Computer Science or Engineering. Preferred Certifications (optional): CISSP (Certified Information Systems Security Professional) or CCSP (Certified Cloud Security Professional) or CISM (Certified Information Security Manager).

Job Title: Manager - 1 Business Unit: Sun Global Operations Manager Title: Sr. General Manager Function: Engineering & Projects Sub-Function: Civil Execution & MEP Coordination Job Classification Label: Civil Projects Job Family: Engineering & Projects Sub-Job Family: Engineering & Projects Location: Mumbai Key Responsibilities At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Position Summary - Candidate should have experience and possess core competency in planning of civil construction, interiors, planning, estimating, budgeting, project coordination. Pharma background mandatory . Strong hold in execution of on-site Civil construction activities. Ensuring projects are delivered within timeline while maintaining quality and safety. Should be able to control project costing and ensuring works are completed within approved budget. Should be able to Coordinate and manage consultants/ contractors and monitor and resolve onsite design and execution issues. Monitoring & controlling project progress through various types of progress reports. Should have strong hand in preparation and verification of reconciliation statements. Contractors bill verification & certification Travel Estimate Across sites as per the requirement Job Scope Internal Interactions (within the organization) Inter-departmental & within department External Interactions (outside the organization) Coordination with Consultants, Contractors, Architects etc. Geographical Scope Global Job Requirements Educational Qualification B. Tech / B. E. (Civil) Skills Behavioral skills: Decision-Making Communication Adaptability Collaboration Functional skills: MS-Project, Auto-CAD, MS-office with proficiency in Excel and Power Point. Experience 10-15 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together!

Responsibility for Chemical/ Instrumental testing of Raw materials sample. Responsible for assure the quality of Sun s products manufactured at Sun Pharmaceutical Industries Ltd for the domestic market as well as export to emerging markets. Responsible for system up-gradation as per CQ and regulatory guidelines To analyze and report the stability sample & FG sample if needed. Monitoring of gowning and sanitation practices in area of operation. Monitoring of compliance of standard operation procedure for operation of analytical instrument. To operate the analytical equipment in quality control as per the allotment works in shift. To follow the procedure of good documentation and recording of result as per SOP on GDP and good execution of laboratories practices. To support the internal audit/Regulatory/FDA audit with best of practices Following all regulations of cGMPs as per schedule M. To maintain the safety procedure in handling analytical equipment and hazards. Completing the training assigned as per the training need identified by participating in trainings organized or self-reading. To calibrate the analytical equipment s as per the calibration procedure for assigned responsibility of calibration. To maintain the analytical equipment s and laboratories in good state of operation To maintain the stock of working standard, column, reagent, chemicals, glass ware etc. To follow procedure for non-conforming result as it is applicable in SOP of OOT, Lab Incident & OOS. To follow the administrative procedure of compliance with respect to term and condition for attendance, leave and other benefits.

Job Requirements As an Architect at Quest Global, you will play a crucial role in managing complex, exciting, and innovative building construction projects in the Concept/Basic and Detail Design phases. Your expertise will be instrumental in developing sophisticated solutions for a wide variety of building typologies, leading the project team, and ensuring the success of the project. You will serve as the central point of contact for clients, user representatives, and the design team, and your communication skills will be key in delivering precise, binding, and result-oriented solutions. To be successful in this role, you should have a degree in Architecture and a minimum of 10 years of professional experience in design and implementation planning. Experience in using Autodesk Revit is an advantage. We expect you to have a high level of architectural design standards and technical competence. Assertiveness, entrepreneurial thinking, and acting are essential qualities for this position. Additionally, strong social skills and the ability to work independently are highly valued. Your ability to communicate precisely, bind stakeholders together, and deliver result-oriented solutions will be crucial to your success in this role. Experience from the EPCM industry is preferred, but we also highly value experience from the High Tech Industry, such as Semiconductor, Pharma, Lifesciences, Data Center, Battery/Automotive Production. If you are a highly skilled and experienced Architect looking for an opportunity to work on complex and innovative projects in the EPCM industry, Quest Global is the place for you. Join our team and be part of our journey towards becoming a centenary company. Work Experience - Bachelors degree in Architecture - Minimum of 6 years of experience in architecture - Experience in the High Tech Industry, preferably in Semiconductor, Pharma, Lifesciences, Data Center, Battery/Automotive Production - Proficiency in Autodesk Revit and Revizto Responsibilities: - Collaborate with clients and stakeholders to understand their architectural needs and requirements - Develop and present architectural designs, plans, and proposals - Ensure compliance with building codes, regulations, and safety standards - Coordinate with project teams, including engineers and contractors, to ensure successful project completion - Stay updated with the latest industry trends, technologies, and best practices Qualifications: - Strong attention to detail and excellent problem-solving skills - Exceptional communication and interpersonal skills - Ability to work independently as well as in a team environment - Proven track record of delivering high-quality architectural projects on time and within budget - Strong proficiency in Autodesk Revit and Revizto Note: Only shortlisted candidates will be contacted for further evaluation.

Rockwell Automation is a global technology leader focused on helping the world s manufacturers be more productive, sustainable, and agile. With more than 28, 000 employees who make the world better every day, we know we have something special. Behind our customers - amazing companies that help feed the world, provide life-saving medicine on a global scale, and focus on clean water and green mobility - our people are energized problem solvers that take pride in how the work we do changes the world for the better. We welcome all makers, forward thinkers, and problem solvers who are looking for a place to do their best work. And if that s you we would love to have you join us! Job Description As a professional services provider, our people are our greatest asset. We are looking for the absolute best to join our world-class team. If you believe you have the skills and qualities we are looking for, even if you dont meet every requirement listed in the job description, we encourage you to apply. We would rather have a conversation and determine if you are a good fit than never meet at all. Consulting is an apprenticeship-based business, and many of the skills you need to master are acquired on the job. You will report to Technical Director of the function and will work from our Electronic City, Bengaluru Office in Hybrid work model. Your Responsibilities: Lead end-to-end project management from strategic planning through execution and delivery, ensuring projects are completed on time and within scope. Coordinate cross-functional teams including developers, analysts, and domain experts to lead effective collaboration and execution. Ensure agile methodologies are followed, overseeing sprint planning, daily stand-ups, and retrospectives to maximize team velocity and adaptability. Analyse project risks and develop mitigation strategies, incorporating stakeholder input and maintaining regular communication on project health. Communicate project progress and performance to senior management and stakeholders, highlighting achievements, bottlenecks, and recommendations. Apply technical acumen to engage meaningfully with teams using technologies like Python, Java, Angular, React, SQL, Big Data, or AI, based on project needs. Continuously improve project performance, using KPIs and post-project reviews to refine methods and outcomes. The Essentials - You Will Have: 8-10 years of hands-on experience. Education qualification UG/PG (B. E/B. Tech/M. Tech/MCA) Must have experience of working with Project Management Tools like JIRA, Scrum or Azure. Good to have any of the Skillsets - Python/Java/Tech Stalk / Angular / React / SQL / Bigdata / Data Science/AI. Must have critical thinking and problem-solving skills to analyse and develop procedures for Project. Must have experience of developing a detailed execution plan and track (Resource Planning, Implementation, Delivery) Must have experience Risk Management, Stakeholder Management and Agile Methodologies. Develop, implement and track project performance goals. Communicate progress against deliverables. Worked on conceptualizing, modelling and communicating common Enterprise Program Management processes. Facilitate communications at the management level about issues, performance and recommendations. The Preferred - You Might Also Have: Good to have Domain exposure - Pharma/ Manufacturing/ Environmental What We Offer: Our benefits package includes Comprehensive mindfulness programs with a premium membership to Calm Volunteer Paid Time off available after 6 months of employment for eligible employees. Company volunteer and donation matching program - Your volunteer hours or personal cash donations to an eligible charity can be matched with a charitable donation. Employee Assistance Program Personalized wellbeing programs through our OnTrack program On-demand digital course library for professional development At Rockwell Automation we are dedicated to building a diverse, inclusive and authentic workplace, so if youre excited about this role but your experience doesnt align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right person for this or other roles. #LI-Hybrid #LI-JS2

You shall be the first point of contact for our prospects. Prospect new leads alongside your inside sales representative, via tailored and relevant outreach campaigns (social, email and cold calling) Ability to connect with Senior leaders of a Pharma and life sciences organisation. Build, develop and manage your sales pipeline Determine the exact needs and resolve issues or objections presented by the prospects Schedule appropriate next steps for the leads Lead and communicate effectively with customers Travel to customer locations and marketing events as needed Achieve or exceed monthly quotas of qualified opportunities

The Cloud + DevOps team consists of professionals dedicatedto optimizing software development and deployment processes through automation, continuous integration, and cloud infrastructure management. They specialize inconfiguring scalable cloud environments, streamlining CI/CD pipelines, andensuring system reliability and security. By leveraging tools like Docker, Kubernetes, Jenkins, and leading cloud platforms such as AWS, Azure, and GoogleCloud, the team ensures high availability, faster releases, and efficientinfrastructure management to support business growth. Responsibilities Strong knowledge of DevOps methodology including serverarchitecture, operating systems and networks Ability to diagnose and resolve complex technical issueseffectively and efficiently. Analyse problems that L1 could not resolve andapply their deeper technical knowledge to find solutions. Understanding customer requirements and project KPIs Implementing various development, testing, automation tools, and IT infrastructure Setting up tools and required infrastructure Defining and setting development, testing, release, update, and support processes for DevOps operation Have the technical skills to review, verify, and validatethe software code developed in the project Troubleshooting techniques and fixing the code bugs Selecting and deploying appropriate CI/CD tools Strive for continuous improvement and build continuousintegration, continuous development, and constant deployment pipeline ( CI/CD Pipeline)

Find a Career With Purpose at Teva Keyword Location Select how often (in days) to receive an alert: Regulatory Affairs Associate II Date: Jul 9, 2025 Location: Navi Mumbai, India, 400706 Company: Teva Pharmaceuticals Job Id: 62743 Who we are How you ll spend your day Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards. Responsibility for MA compliance with both legislation and business needs. Prioritise, plan and monitor submission for allocated procedures while documenting and informing involved parties of progress. To give regulatory support to project teams, stake holders and European Units for defined product responsibilities. Support the development and implementation of regulatory strategies for defined projects. Communicate with other Teva departments across Europe and European Agencies regarding proposed and pending submissions. Maintain and develop awareness of current/pending regulatory legislation and guidelines. Support the defined processes within the department and provide input where improvements can be made. Awareness of current/pending regulatory legislation and guidelines Your experience and qualifications Required Degree/Master in Pharmacy or Master in science/life sciences Relevant years of experience required for the role: 4 to 6 years in Regulatory affairs with EU post approval Overall Pharma industry experience: 4 to 6 years Desirable to have EU member state experience and knowledge of European regulatory procedures. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas 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.

JOB DESCRIPTION Designation: Associate Manager Proposal Management (Research Services) Job Location: Bangalore Department: Commercial About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngenes clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation. The Proposal Management team is crucial in securing new business opportunities by efficiently preparing and presenting compelling project proposals to potential clients. Job Purpose: The role will contribute to creating and delivering high-quality proposals within the Research Services Business Unit. Key Responsibilities: Take complete end-to-end responsibility for the quality of proposals submitted in the Research Services space (Discovery Services and Translational & Clinical Research), taking cognizance of the scope and time commitments. Accountable for the timely delivery of high-quality proposals to the business development team. Work with the technical & business development teams to create competitive pricing. Work on the request for information and the response to be submitted to the customer. Take inputs on the scope of work, assumptions, and effort from the technical business unit team. Liaises with third-party vendors for quotations or information as and when required. Update the deal tracker on the status of the deals being worked on. Coordinate the execution of contractual agreements on time. Help transition newly awarded deals to the project management team. Contribute to the content library by submitting new content or updates to existing content using the official content submission process. Follow workplace environment, health, and safety (EHS) requirements to ensure individual and lab/plant safety. Ensure environment, health, and safety (EHS) measures are imparted via training and adhered to within the team. Educational Qualification: M. Tech/Masters degree in Biotechnology or Life Sciences, MBA desirable Technical/Functional Skills: Good knowledge and experience working in the Research Services space Excellent customer service skills, attention to detail, and ability to get the task accomplished in a time-bound manner Demonstrated computer skills - requiring Microsoft Office experience (specifically Excel, Word, Outlook) Proven capability in planning, multitasking, and prioritizing, showcasing effective teamwork. Excellent English communication (both written and verbal) and strong organizational skills. Ability to communicate appropriately and effectively with internal stakeholders, clients, and Syngene senior management Knowledge of the pre-sales/proposal management function Possess the knowledge and exposure to environment, health, and safety (EHS) practices. Experience: 08 to 12 years of experience in Pharma Contract Research Organization (CRO/CDMO) with an inclination to the commercial aspect of business. Experience in Proposal/Project management or Pre-sales functions is desirable. Behavioral Skills: Attention to detail Team management Pro-active team working capability Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.