Average salary: Rs416,080 /yearly
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- ...stages and collection of samples as per the protocol. # Documentation & Calibration : - Maintaining the all documents related to the IPQA like Semi finish sample register Validation sample register Rinse water register control sample register finish sample register and...SuggestedFull time
- ...inspections and training programs . Qualifications ~ / / (Microbiology Biotechnology Chemistry). ~2–5 years of experience in IPQA for sterile/injectable formulations . ~ Strong knowledge of cGMP WHO EU and USFDA guidelines . ~ Familiarity with aseptic techniques...SuggestedFull time
- In-process QA for liquid ointment and capsule BMR/BPR. Walk-in Interviews 11 AM to 6 PM Prior appointment mandatory Requirements Vacancies: 2 Qualification: / / / Experience: 23 years Salary:per month Required Skills: We are specifically looking...SuggestedFull time
- Perform line clearance and ensure readiness before batch production. In-process checks during manufacturing & packaging (e.g. weight variation hardness friability disintegration dissolution leak test etc.). Monitor critical stages of manufacturing : granulation compression...SuggestedFull time
- Key Responsibilities: Monitor in-process activities during food production to ensure compliance with GMP HACCP and company quality standards. Conduct real-time inspections of production lines including hygiene checks process parameters and product specifications. ...SuggestedFull timeShift work
- In-process QA for liquid, ointment, and capsule BMR/BPR. Walk-in Interviews 11 AM to 6 PM | Prior appointment mandatory Requirements Vacancies: 2 Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc Experience: 2–3 years Salary: ₹15,000 – ₹23,000 per month...SuggestedFull time
- ...choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: Job Summary IPQA activities. Warehouse QA activities MMaR S / MPaRs Review. Job Responsibilities Line clearance of Various in process stage...SuggestedFull timeWorldwide
- ...like Analytical Quality Assurance (Analytical Bioassay and Microbiology) Engineering Quality assurance Manufacturing Quality assurance (IPQA) Quality Management Systems Vendor Quality Management Audits and Compliance sections. The incumbent shall oversee quality operations...SuggestedFull timeContract workLocal area
- ...# Arrangement of sampling accessories & reserve sample and hold time sample cabinets. # Cleaning of sampling aids & accessories and IPQA cabinets. # Destruction of reserve samples. # Request receipt and submission of protocol logbooks to document cell. # Issuance of...SuggestedTraineeshipInternshipWorldwide
- ...Prepare and maintain Quality Assurance documentation including AQA APQR and IPQA records. Lead and support validation activities across manufacturing and testing processes. Conduct internal and external audits to ensure compliance with GMP and regulatory requirements....SuggestedFull time
- ...of Batch records and review of executed batch documents. 6. Issuance of controlled copies of Logbooks and formats. 7. Compliance of IPQA related SOPs and records. 8. Calibration of IPQA instruments and to maintain related records. 9. To assist investigation activities...SuggestedFull timeShift work
- ...led these audits directly. - Comprehensive understanding of QA and QC functions, including QC, stability, validation/qualification, IPQA, quality management systems, compliance, commercial releases, and vendor audits. - 3-6 years of experience at the QA Head or Compliance...SuggestedContract workImmediate startWorldwideOverseas
- ...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...SuggestedFull time