ResponsibilitiesResponsible for laboratory activities including sampling, testing, and release of raw materials, packaging materials, and finished products. Review and approve analytical results and Certificates of Analysis (CoA), ensuring timely material disposition in SAP. Manage quality systems including OOS/OOT, deviations, change controls, and Annual Product Quality Reviews (APQR). Ensure compliance with cGMP, GLP, and regulatory requirements across all QC operations and documentation (SOPs, STPs, DMS). Oversee laboratory operations including instrument qualification/validation, calibration, stability studies, and reagent/chemical management. Support audits, regulatory inspections, vendor management, and coordination with external laboratories. Develop continuous improvement initiatives while ensuring adherence to EHS standards. Qualification & ExpeirneceDegree in Pharmacy, Chemistry, or a related Life Sciences discipline. 1-3 years Strong experience in Quality Control within pharmaceutical or regulated manufacturing environments. In-depth knowledge of cGMP, GLP, and quality systems (OOS, deviations, change control, APQR). Hands-on experience with analytical techniques and laboratory instrumentation (e.g., HPLC, GC, UV, dissolution).

ResponsibilitiesLead end-to-end supplier quality processes such as Vendor Change Notifications (VCNs), Supplier Quality Agreements (QAAs), and supplier complaints to ensure timely and compliant handling Evaluate supplier changes and requests using risk-based and analytical decision-making to protect product quality and supply continuity Review and approve supply chain records (VSCI) governing the use of materials, services, and equipment across the Lonza network Collaborate with cross-functional teams (Manufacturing, QC, Procurement, MSAT, Planning) to assess impact and manage risks effectively Maintain accurate supplier documentation, ensuring compliance with quality management systems, regulatory requirements, and data integrity standards Monitor and report key performance indicators (KPIs) related to supplier quality processes, identifying risks and driving continuous improvement Act as a global point of contact for supplier quality topics, supporting audits, inspections, and alignment across internal and external stakeholdersQualification & ExpeirneceExperience in the pharmaceutical or life sciences industry, preferably within quality, compliance, or supply chain functions Strong knowledge of cGMP regulations, quality systems, and regulatory requirements Proven analytical, problem-solving, and risk assessment capabilities Ability to manage complex workflows and make sound decisions in dynamic, cross-functional environments Strong communication and stakeholder management skills across global teams Degree in a scientific discipline such as Biochemistry, Chemistry, Pharmacy, Microbiology, or Biotechnology (or equivalent) Business fluency in English

ResponsibilitiesTo approve analytical COA & test plan in LIMS.  Responsible to review Audit trail of laboratory instruments and software like EWS, Empower, LabX etc. To release/Approval of the RM/PM in SAP HANA and Analytical technology transfer/validation /development etc. Responsible to provide a data of OOS/OOT/Lab Event/FAR/OOC/CAPA/Recall for Quality Council/ R&D Team as applicable. Responsible to provide analytical data for annual quality review as applicable. Responsible for verification of qualification and training record of Laboratory Analysts. Trending of QA observations from raw data review and suggest for improvement. Approval of stability protocol, Method Transfer protocol/report, Method Validation Protocol / report, stability summary report. To review Pharmacopeia – Evaluation and Equivalence Report. To perform the trend analysis of OOS/OOT/Lab Event/QA of QC observation and evaluate the CAPA effectiveness for repetitive Deviation and internal quality observations. To actively participate in cross functional investigation. Review of regulatory query response. To provide technical training with respect laboratory function.  Issuance of template/documents /log books etc. Qualification & ExpeirneceQualification M. Pharmacy /B. Pharma , M,Sc chemistry Experience 10+ years

Responsibilities Manage, control, and maintain all Quality Assurance (QA) documents, records, and logs in compliance with GMP requirements.  Ensure timely issuance, retrieval, archival, and destruction of controlled documents according to approved procedures.  Maintain document revision history and ensure only current, approved versions are available for use.  Coordinate document review, approval, and distribution processes with QA, Production, QC, and other departments.  Monitor compliance with document control procedures and support internal audits and regulatory inspections.  Maintain electronic and physical document management systems, ensuring data integrity and confidentiality.  Track periodic review schedules for Standard Operating Procedures (SOPs), specifications, forms, and quality manuals.  Support change control activities by updating and distributing revised documents as per approved changes.  Prepare document control metrics, reports, and status updates for management review.  Ensure all documentation practices comply with applicable regulatory guidelines, including GMP, WHO, FDA, MHRA, and company quality standardsQualification & ExpeirenceB. Pharm B. Pharm - Required M. Pharm M. Pharm - Preferred Experience: 2 years or more in 2 - 5 Years

ResponsibilitiesTo perform QC activities in order to ensure quality of products and services and maintain related documentation to adhere to quality operations and regulatory requirements. Qualification & ExperiencePOST GRADUATE IN CHEMISTRY/PHARMACY Experience: 3-5 years in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities

ResponsibilitiesManage, with the FvP , the implementation and maintenance of an appropriate quality system covering primarily all GxP regulated activities related to development, manufacturing, distribution and commercialization of health care goods and their associated services and solutions. To perform quality lifecycle management for dedicated products for Swiss market. To take all necessary actions to secure the quality of the products and patient safety. Main Accountabilities And Duties Quality system management Implement and maintain a local quality system applying primarily to SwissMedic-regulated activities related to the import and distribution of products and controlled substances Assure compliance with local regulations in Switzerland, international GDP / GMP requirements and the company Write SOPs and relevant documents, manage them in eDMS (electronic Document Management System) and support in implementation by training employees QA GMP, systems: GMP and process trainings, personal file maintenance Providing support to ensure inspection readiness and participation on internal audits and HA inspections QA POs executions in Fiori Product Quality Management Preparation of Market release of purchased or repacked products for Swiss Market:

ResponsibilitiesServe as initial point of contact for Veeva Global GxP business questions related to QMS and EDMS processes. Act as a primary business liaison with IT support (FAS) for operational support activities Lead updates to system-specific SOPs, WIs, CBTs as driven by business needs. Review and approve master data requests as needed. Assist with triage and review of system standard releases, new feature requests, and business enhancement requests for feasibility with IT. Participate in system change request/release review and prioritization meetings (Change Advisory Boards) with IT, Compliance, sites, and other internal functions as needed. Support Global Business Owners during enhancement/change request reviews, including managing global business reviews and compiling feedback Ensure ongoing operational activities for the Veeva Global GxP system are aligned with global processes and standards. Support various Veeva Global GxP program phases with project activities as needed (e.g. data migration and cleansing, testing, etc. Conduct additional business training as needed post go-live to support site adoption Partner with appropriate functions (Business, IT) to provide issue resolution. Escalate issues to management as needed Participate in system periodic and user access reviews. Act as backup Global Business Owner for system validation activities for operational changes as needed (e.g. assist with gALM reviews/approvals as needed) Provide updates in Quality Global/regional/leadership meetings as needed. Any other tasks assigned by the management for smooth functioning of the team.Qualification & Expeirnece5 to 8 years of relevant experience Master’s degree in pharmacy or other natural sciences or bachelor’s degree in pharmacy or other natural sciences Good knowledge in Veeva Global GxP, QMS and EDMS processes. Good knowledge of Computerised Systems. Experienced with primary business liaisoning with IT support (FAS) for operational support activities

ResponsibilitiesEnsures that the review of CMC documentation is completed in timely & compliant manner as per Teva CORP standards and related Guidance’s. Review of Method Development/Validation Protocols & Reports, Stability Protocols & Reports received from various Teva contracting sites, R&D units, Method Development & Stability Testing Centres. Review of Instrument/Equipment Qualification records. Review of BMR. Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva’s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system Liaising with third party contract manufacturers and QA/QC/Technical support personnel located globally for data collection and arranging responses. Recommend actions and professionally communicate to sites/ Quality units for continuous improvement in quality of products Receives guidance from Supervisor, Group Leader, Manager Global Quality Services, Associate Director Global Quality GBS, other Managers in Quality Strategy & Shared Services, EMSO Quality affiliates, Commercial Quality EU & IM, TGO sitesQualification & Expeirnece2 to 8 years of experience in QA / QC function in the pharmaceutical industry Master’s Degree in Pharmacy or other natural sciences or Bachelor Degree in Pharmacy or other natural sciences Basic knowledge on worldwide cGxP regulations Good English language skills, other language skills could be helpful Good communication skills

ResponsibilitiesDesign and implement, in support of EXM Procurement launching SRM programs, an analytic capability that covers financials, operational metrics, risk factors, regulatory, and ESG metrics Align with EXM Procurement LT, a supplier segmentation (based on aligned criteria) and develop over a multi-year roadmap expansion of reporting capabilities across strategic suppliers in the categories Establish standardized processes for segmentation refresh, reporting metric updates and dashboarding capabilities Implement solutions and processes for consistent reporting of supplier risks in partnership with Global Procurement Risk management COE Team (e.g., financial health, supply disruption signals, compliance risks) Work with EXM Procurement teams to track risk mitigation plans for high-risk and critical suppliers Support data tracking of cross-functional response to supplier risk events and escalations, with intent to assess improvement of risks through reporting In partnership with EXM Procurement teams, support development of structured supplier performance management approach (scorecards, KPIs, review cadence) Work with EXM Procurement teams to define performance metrics across key dimensions and enable tracking by creating data capture and reporting templates (cost, quality, delivery, service, innovation, ESG) Support consistency in performance evaluation across categories and business units by work with EXM Procurement teams and Suppliers Review segmentation strategy with EXM Procurement leaders 1-2 times per year (e.g., strategic, preferred, transactional suppliers) Develop and prepare data reporting used in strategic supplier relationships executive business reviews (EBRs/QBRs) Support Supplier Relationship Management (SRM) programs to drive long-term value by ensuring data captured and reported is done with consistency Partner with Procurements Risk COE Team to develop risk and performance dashboards for EXM Procurement (prioritized suppliers)

ResponsibilitiesDrafting and Authoring of Annual Monitoring and Certification report for incoming materials.  Drafting / Negotiation (if applicable) and Archival of Quality Assurance Agreement with Suppliers/Service providers. Evaluation and Management of Supplier Change Notifications (SCN) and Initiation of quality record for the applicable SCN. Drafting and Evaluation of Supplier’s incoming materials Specification.  Performing Quality Risk Assessment (QRA) for existing and new Suppliers / Service providers.  Management of Supplier/ Material qualification and supplier related documentation.  Preparation of regulatory statement for materials and finished products.  Management Quality records, Support the Service Delivery team (SDT) with quality topics and 3rdPAP Management in TPRM (Third Party Risk Management) tool.  Co-ordination with stakeholders in SIM (Supplier Information Management) approval process for Quality deliverables.  Evaluation of change control tasks/ deviations related to supplier quality management.  Coordination in handling Discrepant Materials.  Audit preparation support, QARP and FURP Role for audit and CAPA Management.  End to end deliverables for supplier quality management activities as per the delegated task from the business partner. Qualification & Expeirence Around 8 Years Education - M Pharma / B Pharma / MSc or Equivalent from Reputed university.