1357 Ipqa Jobs - Page 11

Role & responsibilities To supervise all IPQA/QMS function activity on daily basis and update. To conduct and participate in CAPA meetings and review summary report of the same within defined time period monthly. To do implementation of GMP, GDP practices and review of issues and impact of the same, if any, and take corrective actions. To do investigation for complaints and deviations and CAPA after reviewing instruments. To prepare, review, Implement and update SOPs according to current regulations systems. To review Master Batch Document (MBD) / Master Packing Document (MPD) and get approval in advance from Head of Department of Production & QA. To train/update about new procedures and cur...

Key Responsibilities Quality Engineering Support Assist Quality Engineers in the use and application of statistical tools within the workcell. Support Corrective & Preventive Action (CAPA) activities and ensure timely closures. Conduct defect analysis and prepare structured defect reporting. Support APQP activities and documentation requirements. Production & Process Quality Troubleshoot production issues and support resolution of defects on the line. Ensure capability studies are completed on critical processes and dimensions. Perform First Article Inspection (FAI); review and update inspection visual aids as required. Guide Quality Technicians in creating accurate visual inspection aids. M...

Role & responsibilities Responsible for monitoring of IPQA related activities at Fill Finish, DSP, Plasma Fractionation, and Warehouse. Responsible for ensuring the batch record review and perform the batch release, ensuring compliance with quality standard. Preferred candidate profile In-process monitoring, worked in shop floor, knowledge of the equipment operations, investigation skills, working in shifts

Austin Alloy Cast is looking for Manager Quality Assurance to join our dynamic team and embark on a rewarding career journey Team Leadership: Manage and lead a team of employees, providing direction, guidance, and support to achieve departmental or organizational goals Planning and Strategy: Develop strategic plans, set goals, and create action plans to accomplish business objectives Operations Management: Oversee day-to-day operations, ensuring efficient workflow, resource allocation, and adherence to policies and procedures Budgeting and Financial Management: Manage budgets, allocate resources, monitor expenses, and contribute to financial planning Performance Management: Set performance e...

1) Ensuring cGMP compliance on the production shopfloor in a pharmaceutical API company 2) Issuance & receipt of documents 3) BMR Review

Role & responsibilities : QC,QA & Production We are seeking a diligent and experienced candidates QC OFFICER TO EXECUTIVE (HPLC/GC/UV/RM/PM),LOGISTICS INCHARGE, PRODUCTION SR.OFFICER(OSD)(GRANULATION/COMPRESSION),QA(QMS/VALIDATION/IPQA)(DPI) Preferred candidate profile Quality control QA/QC/Production The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance (QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. The Saksham Success Enterprises Near Sunder Ayan by pass solan 17...

Role & responsibilities Responsible for in-process quality assurance activities in the OSD manufacturing area, including line clearance, batch record review, monitoring of critical process parameters, IPQC checks, sampling, deviation control, and ensuring GMP compliance throughout production.

Role & responsibilities : Experienced in In process-checks, Line clearance, sampling, Environment monitoring, Documentation, process monitoring, Strong knowledge of GMP, regulatory guidelines (e.g., FDA), and quality assurance practices. Excellent analytical skills and attention to detail

Job Title: Executive - Pharmacokinetics Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Responsibilities: Literature search and study design...

Job Title: Manager CMO Business Unit: Global Quality & Compliance Job Grade G10 -Manager-1 / G9B (SM-2) Location : Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Summary : To ensure that SUN Pharma Qual...

Job Title: Deputy Manager- Formulation Location: Govandi, Mumbai Working Days: Monday to Saturday(2nd and 4th Saturday off, 1st,3rd and 5th Saturday operational) Department: Corporate Quality Assurance Qualification, Experience and Technical Competency: 1. Masters Degree in Pharmacy or Science or equivalent scientific field. 2. Minimum 10 years experience in Pharmaceutical Industry (Strong background of Formulation industry with 2 to 3 years experience in Quality Control.) 3. Work experience in Regulatory Sites (USFDA, MHRA, EU GMP) 4. Knowledge of current Good Manyfacturing Practices (cGMP), Quality Management Systems (QMS) and regulatory guidelines. Key Requirements: Responsible for Qualit...

We are Hiring for Senior Engineer Quality Engineer for our Plastic Injection Molding Component in Chennai Irungattukottai Position: Senior Engineer Quality ( Plastic Injection Molding ) Location: Chennai Experience Required: 7+ Years Industry: Plastic Injection Molding Role Overview: The Senior Engineer Quality will be responsible for ensuring consistent product quality in plastic injection Molding operations. The role involves driving quality systems, supporting production with problem-solving, ensuring compliance with customer requirements, and leading continuous improvement initiatives. Key Responsibilities: Oversee quality assurance activities related to plastic injection Molding process...

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Responsibilities: * Collaborate with cross-functional teams on process improvements * Conduct IPQA activities during product development * Ensure compliance with regulatory requirements Annual bonus

Open Positions Microbiology (0 to 6 Years) (Qualification: M.Sc-Microbiology/Biotechnology) Experience in Disinfectant Preparation, Media Preparation, MLT, BET, Sterility Testing, Method Validation & Documentation Experience in Culture Handling and Environmental Monitoring Engineering (2 to 6 Years) (Qualification: ITI / Diploma / B.Tech) Hands-on experience in operating Lyophilizers Experience in Water System & HVAC operations Experience in Instrumentation activities Production (0 to 10 Years) (Qualification: ITI / Diploma / B.Sc / B.Pharm / M.Pharm) Skilled in operation and supervision of filling lines Ability to supervise packing lines Strong expertise in Production QMS Training supervisi...

You will be responsible for performing In-Process Quality Assurance (IPQA) activities at the shop floor during various stages of sterile manufacturing and packing. This includes conducting sampling at each stage or when necessary during product manufacturing, filling, and packaging processes. Additionally, you will be required to perform in-process checks of manufacturing, filling, and packaging activities. After the visual inspection of products, you will conduct Acceptable Quality Level (AQL) inspections. It will also be part of your duties to carry out audit trails, electronic data reviews batch-wise and as per the schedule. You will manage control samples and stability samples. Moreover,...

Role & responsibilities Quality Control-(Chemist to Executive): Perform High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and various wet chemical analyses to ensure product quality. Analyze raw materials, intermediates, and finished products as per established quality standards. Prepare SOPs in line with regulatory requirements, including stability studies and market sample analysis. Ensure GLP-oriented documentation and maintain accurate records for audits and compliance. Work proficiently on multiple laboratory software platforms to support analytical testing and reporting. Quality Assurance -(Officer to Manager): Ensure cGMP and regulatory compliance across all QA o...

Walk In Drive For Quality Assurance Sterile In Formulation Division - Kothur Department:- Quality Assurance Sterile Formulations Qualification :- B Sc | B Pharmacy | M Pharmacy| M.sc Experience :- 2 To 8 Years Skills :- Experience:- Manufacturing:- IPQA | Sterile Validations | AQA | Microbiology Division :- Formulation Interview Date:- 15-11-2025 Work Location:- MSN Formulation UNIT-2 Kothur | MSNF -V , China Chilkamarri Inteview Location :- MSN Formulation UNIT-2 Kothur Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out ...

Responsibilities: Perform in-process inspection of moulded parts as per approved standards and control plans. Verify critical dimensions, appearance, and functional requirements at regular intervals. Monitor process parameters and ensure production runs within specified limits. Identify and segregate defective or NG parts during production. Record inspection results in IPQC check sheets and maintain proper documentation. Communicate quality issues immediately to the production and quality engineers. Support line setup approval and first-piece inspection. Follow standard sampling plans and inspection frequency. Ensure 5S and discipline in the production area. Support continual improvement and...

As a candidate for the position, you will be responsible for handling the production area for Tablets and Capsules. This includes the preparation and filing of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Additionally, you will oversee the management of Men Power within the production area. Your role will also involve coordinating with the In-Process Quality Assurance (IPQA) team and Quality Control (QC) department. The ideal candidate should have 2 to 4 years of relevant experience in this field. For any further details, you can reach out to hrd@stravahealthcare.com. As a candidate for the position, you will be responsible for handling the production area for Tablets a...

* Responsible for in-process quality checks, line clearance & documentation review * Should have experience into QMS & Investigation * CAPA in the medical devices or pharmaceutical industry Required Candidate profile * Knowledge on Deviation Management, IPQA, Batch Release Testing * Ensuring GMP & ISO Compliance in manufacturing & packaging areas

Shift IPQA IN charge BMR/BPR review, GMP Compliance at shop floor

GLP & review of analytical data of raw material, finished product & stability sample analysis Knowledge of RCA & CAPA,Change control,Deviation,OOS,Failures,Incident,APQR,batch records,market complaint,line clearance,in-process checks & AQL procedures Required Candidate profile Must have good experience in quality assurance - cosmetics or Pharma industry Must have independently handled the QA documentation wrork Must be sincere and smart Can set new processes

Followings will be the responsibilities of the position holder: Compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance. Manufacturing and Packing process compliance in accordance with approved BMR/BPR. To carry out line clearance, In-process checks at the different stages of batch manufacturing and packing. Collection and management of control samples / stability samples / validation samples / other samples (as applicable) and maintain their record. Issuance of Batch records and review of executed batch documents. Issuance of controlled copies of Logbooks and formats. Compliance of IPQA related SOPs and records. Calibrati...

monitoring manufacturing processes to ensure real-time compliance with quality standards and regulations, verifying batch records, and performing line clearance checks