Average salary: Rs416,080 /yearly
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- ...growth, make Actylis the ideal place to work and thrive. We hope you'll consider joining us! To assign and plan daily activity for the IPQA team. To ensure that line clearance are in place while executing operational activities for different departments like but not...SuggestedFlexible hours
Actylis
Ahmedabad10 days ago - ...logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc.. Calibration of IPQA instruments. Additional Responsibilities Real-time Monitoring and Compliance Reporting. Participation in Investigations....Suggested
Amneal Pharmaceuticals
Ahmedabad20 days ago - ...Process validation protocol and report , Review of Cleaning Validation protocol and report, Batch records, 4:Review of CPV data, 5:IPQA shop floors investigation. 1: Handling of JMP software for CPV and PQR, 2: Execute and monitor the Internal Audit programs to maintain...Suggested
Enzene Biosciences Ltd
Pune6 days ago - ...and revenue generation to fulfill employees' long-term aspirations. Role Description This is a full-time on-site role for an IPQA Specialist located in Yamunanagar. The IPQA Specialist will be responsible for day-to-day tasks associated with in-process quality assurance...SuggestedLong term contractFull time
Dev Staffing Solutions
Yamunanagar17 days ago - ...Qualifications & Experience Master's degree in Chemistry, Pharmacy, Biotechnology, or related field. Minimum 5 years of experience in IPQA within the food, herbal, nutraceutical, or related industry. Strong understanding of food safety systems and GMP requirements....Suggested
Natural Remedies Private Limited
Hosur19 days ago - ...affairs, to resolve quality-related issues and drive continuous improvement initiatives. Maintain accurate and up-to-date records of all IPQA activities and documentation, ensuring compliance with GMP (Good Manufacturing Practices) and other regulatory guidelines. Identify...Suggested
Pelltech Healthcare
Palghar19 days ago - ...calibration records and executed Batch Manufacturing and packaging Records and respective electronic records. To perform calibration of IPQA instruments. To ensure appropriate labelling during manufacturing and packaging. Storage, handling and dispensing of printed packing...Suggested
Amneal Pharmaceuticals
Ahmedabad20 days ago - Key Responsibilities JOB DESCRIPTION Environment monitoring Aseptic area behaviour and monitoring Handling of Instrument i.e NVPC and MAS. Personnel monitoring Trend analysis and reporting Sample handling Qualifications Qualification: M.Sc (Microbiology...Suggested
Amneal Pharmaceuticals
Ahmedabad20 days ago - Job Description Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain accurate records and documentation of environmental...Suggested
Amneal Pharmaceuticals
Ahmedabad20 days ago - Job Title: Executive / Senior Executive – QA (DSQA) Department: Quality Assurance Experience: 2–9 Years Qualification: M.Sc / M.Pharm Location: Pune Job Purpose To ensure cGMP compliance at the shop floor for Drug Substance (DS) manufacturing through effective...Suggested
Enzene Biosciences Ltd
Pune6 days ago - ...parameters and completion of the Log book and BMR of Granulation area. To provide machine for preventive maintenance. Co-ordination with IPQA/QC/Engineering department for smooth functioning of Production activities. To ensure proper use of Personnel Protective Equipment's...SuggestedShift work
SUN PHARMA
India19 days ago - ...generating a batch number assignment. 11. To review departmental Standard Operating Procedure and keep it updated by providing inputs for IPQA functions as per regulatory guidelines. 12. To maintain Bill of material, Creation of HALB code in JDE. 13. To review cross-...Suggested
Baxter Medical Devices
Ahmedabad3 days ago - ...Responsible for submission of qualification documents to RA as per requirement. Responsible for review of media fill BMR. Responsible for IPQA activities as per requirements. Responsible for review and approval of documents like Validation protocols, reports, QRM, SOPs etc.....Suggested
Amneal Pharmaceuticals
Ahmedabad20 days ago - ...process data. ~ Review open CAPA and ensure effectiveness. ~ Organize sample shipments to EU labs. ~ Approve license certificates and IPQA SOPs. ~ Manage IPQA lab instruments and CAPEX budgeting. ~ Monitor sample management and batch release status. ~ Review and...Suggested
SUN PHARMA
Paonta18 days ago - ...Work as a Quality Engineer / Sr. Engineer in the Quality Assurance Department. Capabilities to work in IGI (In-coming Goods Inspection), IPQA (In-Process Quality Assurance), FQA (Final Quality Assurance), OBA (Out Box Audit), PDI (Pre-Dispatch Inspections). New parts...Suggested
ideaForge
Navi Mumbai20 days ago - ...point for utilities & purified water system. Management of Site Qualification & Validation Master Plan In-Process Quality Assurance [IPQA] Review & Approval of Master Batch Records & executed Batch Records Review and Approval of logbooks. Line clearance in...Long term contractFor subcontractor
Sanofi
India6 days ago - ...reprocessing order in SAP, if required. To check the RM/PM received against the job assigned to workers. To take line clearance from IPQA for the job assigned, prior starting. To verify the tool used for filling/packing activity for cleanliness and contamination free....Flexible hours
Actylis
Ahmedabad10 days ago - ...CAPA, and risk assessments. Ensure timely review and release of products. Team Management Lead and mentor QA team members across IPQA, QMS, and documentation. Build capability through training and continuous improvement initiatives. Regulatory & Customer...Full time
- ...manufacturing environments. Strong knowledge of cGMP, QMS, validation, qualification, and regulatory guidelines. Experience leading IPQA and validation functions across multiple manufacturing units is preferred. Proficiency in electronic QMS platforms (e.g., TrackWise,...
Biotech Healthcare
Ahmedabad17 days ago - ...manufacturer with 4 GW cells & modules and 2 GW of ingots & wafers manufacturing capacities Job Purpose: The Shift Engineer - Cluster - IPQA conducts in-process quality inspections during shifts, monitoring production processes and identifying quality deviations. This role...Shift work
Adani Group
Mundra17 days ago - ...areas (temperature, pressure differentials, cleanliness). Ensure timely closure of deviations, CAPA, and change controls related to IPQA activities. Support technology transfer and validation activities from a QA perspective. Assist in review of batch...Traineeship
Amneal Pharmaceuticals
Visakhapatnam20 days ago - ...will find purpose and pride. Unique Opportunity Come join Baxter Healthcare Corporation as a Sr. Executive, Quality Assurance - IPQA, Production in our brand new manufacturing facility in Ahmedabad. This role offers an exciting chance to be at the forefront of ensuring...Shift work
Baxter International Inc.
Ahmedabad22 days ago - ...numbering, storage, and control of BPRs, analytical records, deviations, CAPA, OOS/OOT, change controls, and risk assessments. Perform IPQA activities Review and investigate laboratory incidents, deviations, market complaints, CAPA, and non-conformities. Ensure...Full time
- ...reviewing performance of Quality Assurance at regular frequency by Quality Head. 2.26 To prepare and review of SOPs pertaining to IPQA and review of SOPs pertaining to cross functional departments. 2.27 To assess the continuity of the process or activity in...Immediate startShift work
- ...laboratories & manufacturing/customer's and ensures to provide timely & necessary support to fulfil organizational requirements. Support IPQA, QA, Production, PDL, Regulatory, Stability Lab, API and Validation for microbiological requirements. Co-ordination for internal/...
SUN PHARMA
Dewas19 days ago - ...demonstrate a collaborative spirit, knowing that we 'Thrive together' and support each other's journeys.' Key Responsibilities To ensure IPQA activity during manufacturing and packing operation. To give the line clearance as per respective SOP, BMR/BPR checklist. To...Immediate start
SUN PHARMA
India19 days ago - ...Field 2: 2947 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: Formulation Others Travel Description: IPQA Expert with Basic knowledge of CV -PV-Qualification profile.
Dishman Carbogen Amcis Ltd
India19 days ago - ...Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Handling of Manufacturing Compliance i.e. IPQA Activity Handling of QMS Documents like CAPA, and OOS and Change control Handling of APQR Handling of Batch release activity...
Dishman Carbogen Amcis Ltd
India19 days ago - ...parameters and completion of the Log book and BMR of Coating Area. To provide machine for preventive maintenance. Co-ordination with IPQA/QC/Engineering department for smooth functioning of Production activities. To ensure proper use of Personnel Protective Equipment's...Shift work
SUN PHARMA
India19 days ago - ...calculation of equipment contact surface area. To Coordinate and perform the Visual inspection and swab sampler qualification of all the IPQA personnel involved in swab sampling activity. To ensure compliance and closure of the audit observations. To perform risk...
SUN PHARMA
Dewas19 days ago
