Average salary: Rs416,080 /yearly
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- ...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
- ...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
Ahmedabad2 days ago - Roles & Responsibilities - IPQA & Manufacturing Oversight Perform line clearance activities for new batches, dispensing of raw materials, cell bank issuance, and handling of Drug Substance (DS). Provide in-process QA oversight during manufacturing operations to ensure...Suggested
Enzene Biosciences Ltd
Pune1 day 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
Palghar1 day ago - ...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
- 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
- Job Description : # Line clearance for production operations. # Review of BMR, BFR, BPR. # In - process QA functions. # Control sample management. # Collection of In process / Finished product and customer samples. # Compilation of APQR data with ...Suggested
Piramal Enterprises
Medak2 days ago - Job Title: Executive / Senior Executive – QA (DSQA) Department: Quality Assurance Location: Pune Experience: 2–9 Years Qualification: M.Sc / M.Pharm Job Purpose To ensure cGMP compliance at the shop floor for Drug Substance (DS) manufacturing through...Suggested
Enzene Biosciences Ltd
Pune1 day ago - 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
- Role Specification: Quality Leadership & Systems: Lead In-Process QA teams for Optical connectivity products, ensuring process compliance and continuous improvement. Ensure preparing and managing Quality Department plans and budgets. Drive adherence to SOPs and...SuggestedLong term contractTemporary work
STL - Sterlite Technologies Limited
Silvassa2 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
Ahmedabad2 days ago - ...that products are manufactured as per approved process, Ensure online documentation with respect to activity and execution. Ensure IPQA activities in Shop Floor. Planning & Management of Routine Activities during Production & Packing. Trained to IPQA & Validation Persons...Suggested
Promea Therapeutics
Secunderabad2 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
India2 days ago - ...for to adherence of cGMP in all activities performed and responsible for compliance. Responsible for planning and Execution of Shopfloor IPQA activities. Responsible for Inporcess Quality Assurance, Responsible for Authorizing the Line Clearance during the product change over...Suggested
Endo
Kanchipuram11 days ago - ...reliability. Key Stakeholders - Internal Cluster Manager - FQA Shift Engineer - Cluster - Incoming Shift Engineer - Cluster - IPQA Production Supervisor Maintenance Technicians Key Stakeholders - External Quality Control Auditors Packaging Suppliers...SuggestedShift work
Adani Group
Mundra2 days ago - ...State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Monitoring and review IPQA,Sampling,Batch record review, Line clearance and Review of log books. Retain sample management Job Segment: Quality
Dishman Carbogen Amcis Ltd
India2 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...
ideaForge
Navi Mumbai2 days ago - ...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....Full time
- ...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
India2 days ago - ...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
Dewas2 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
India2 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
India2 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
India2 days ago - ...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...Full timeContract workLocal area
- ...with Technical Trainers to develop QA training plans for MES users. Provide mentorship during on-the-floor manufacturing DS QA/ IPQA responsibilities such as support in PCO’s, line clearances, oversight activities, shop floor visit, vial issuances Qualifications...Relocation packageShift work
Dr. Reddy's Laboratories
Secunderabad5 days ago - ...internal and external audits by providing necessary records and compliance data. Assist in preparation and review of SOPs related to IPQA activities. Participate in training activities to stay updated with quality and compliance standards. Coordinate with QA, QC, and...Contract work
Amneal Pharmaceuticals
Dahej2 days ago - ...Job Description JOB DESCRIPTION The Officer – IPQA is responsible for performing in-process quality assurance activities during API manufacturing operations in compliance with cGMP requirements. The officer ensures proper line clearance, equipment cleaning verification...Shift work
Amneal Pharmaceuticals
Visakhapatnam2 days ago - .../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
Amneal Pharmaceuticals
Ahmedabad2 days ago - ...generating a batch number assignment. To review departmental Standard Operating Procedure and keep it updated by providing inputs for IPQA functions as per regulatory guidelines. To maintain Bill of material, Creation of HALB code in JDE. To review cross-functions...
Baxter International Inc.
Ahmedabad2 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
Dewas2 days ago
