Average salary: Rs422,515 /yearly
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- ...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
- ...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
Rs 5 - 9.5 lakhs p.a.
...Key Responsibilities Execute IPQA (In-Process Quality Assurance) activities during production Conduct sampling of finished products and cleaning validation samples as per protocol Perform regular plant rounds to monitor process adherence and quality compliance Ensure...Suggested- ...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
- ...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
- ...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
- ...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
- ...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
- 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
- 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
- About the Company Biocon Biologics Limited, a subsidiary of Biocon Limited, is a fully integrated global biosimilars organization. It is leveraging cutting-edge science, innovative tech platforms and advanced research & development capabilities to lower treatment costs while...SuggestedWorldwide
- 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
- ...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....SuggestedFlexible hours
- ...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...SuggestedLong term contractFor subcontractor
- ...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
- .../practice monitoring of operators (while working inside aseptic process area) during each aseptic batch (GMP batch) as per SOP. Qualifications Education: B.Sc., B.Pharma, M.Sc., M.Pharma Total Experience - 2 - 7 Year in IPQA Department of sterile manufacturing plant
- ...documents and logbooks. Ensure daily and monthly calibration of balances as per cGMP requirement. Coordinate with dispensing, warehouse, IPQA team for timely execution of batches as per schedule. Carry out manufacturing activity as per BMR instruction. Verify and cross‑...Contract workCasual workShift work
- ...proper execution of QMS activities, including document management and software use (e.g., TrackWise). Participate in line clearance and IPQA (In-Process Quality Assurance) activities as needed. Prepare and review GMP (Good Manufacturing Practice) documents such as SOPs,...
- ...Internal Audits and Inspections - Proficient cGMP and Compliance Review - Proficient Manufacturing Activity Supervision - Proficient IPQA Instrument Calibration - Proficient Specialized Knowledge: Licenses: About Us Amneal is an equal opportunity employer. We do...Immediate start
- ...during 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
- ...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
- ...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
- ...documents and logbooks. Ensure daily and monthly calibration of balances as per cGMP requirement. Coordinate with dispensing, warehouse, IPQA team to execute batches as per schedule. Perform packing activity as per batch packing record instruction. Cross check dispensed...Contract workImmediate startShift work
- ...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
- ...documents and logbooks. Ensure daily and monthly calibration of balances as per cGMP requirement. Coordinate with dispensing, warehouse, IPQA team to execute batches as per schedule. Perform packing activity as per batch packing record instruction. Cross check dispensed...Contract workShift work
- ...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-...
- ...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 Qualifications...
- ...standards. Quality Monitoring ~ Monitor production processes to identify quality issues, reporting findings to the Cluster Manager - IPQA. Assist in implementing corrective actions to address in-process quality deviations. Calibration & Validation ~ Validation of...Shift work
- ...department heads to ensure resource availability (e.g., operators, shift plans, changeover times). • Quality Assurance (QA): Ensure IPQA approvals and validations are coordinated with the line schedule to avoid interruptions. 6. Machine Changeovers and Preventive...Shift work
- ...book and BMR of Coating area. To check and make availability of machine as per Preventive Maintenance schedule. Co-ordination with IPQA/QC/Engineering/IT and MSTG department for smooth functioning of Production activities. To fill documentation as per GDP and maintain...Shift work
