1357 Ipqa Jobs - Page 3

JOB PROFILE Designation and Department - Sr. Executive Quality Assurance Experience - 5-8yrs Address - Savanur, Hubli. Qualifications - M Pharma, B Pharm, M. Sc, B. Sc Job Responsibilities: To carry out the in-process activities at Warehouse, Manufacturing, Primary Packing & Secondary Packing Areas & complete the documentation works online. To allocate, check and monitor the In Process Quality Assurance work to all IPQA Personnels in absence of IPQA Manager. To collect analysis sample like in-process, finished products, validation sample, control sample, stability samples (but not limited to), customer sample and submit to QC for analysis. To withdraw & charge the Stability Samples as per th...

WALK-IN DRIVE @ HYDERABAD We are pleased to announce a walk-in drive for various positions at our Matoda manufacturing facility . If your experience aligns with any of the openings listed below, we invite you to attend with your updated resume. 1. ENGINEERING (Instrumentation / QMS / Plant Maintenance / Qualification) Roles: Senior Executive / Executive / Senior Officer Experience: 3 10 Years Qualification: BE / B. Tech 2. ANALYTICAL DEVELOPMENT FORMULATION Roles: Research Associate / Sr. Research Associate Experience: 3 8 Years Qualification: B. Pharmacy / M. Pharmacy / M.Sc. 3. FORMULATION DEVELOPMENT INJECTABLE & OSD Roles: Research Associate / Sr. Research Associate / Research Scientist ...

We are looking for a highly skilled and experienced professional to join our team as an Executive Quality Assurance Operations at APOTEX PHARMACHEM INDIA PRIVATE LIMITED. The ideal candidate will have a strong background in quality assurance operations and a proven track record of ensuring compliance with regulatory requirements. Roles and Responsibility Develop and implement quality control processes to ensure compliance with regulatory standards. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve quality-related issues and improve overall process efficiency. Analyze data to identify trends and opport...

Responsible for DS (MCM and CCM) IPQA activities. Primary Responsibility (Strategic, Operational, People, Financial responsibilities) Strategic: 1. Maintain data integrity in all activities at site and ensure appropriate and adequate traceability. 2. Preparation, review and implementation of Standard operating procedures, Protocols etc., pertaining to Quality Assurance department, in line with Global GMP compliance regulations and industry practices related to Biopharma industry. 3. To ensure all time readiness for customer and regulatory audits and inspections. 4. To ensure the Quality Compliance of DS manufacturing, DS Warehouse and Engineering area activities. Operational: 1. Involving in...

A Quality Assurance (QA) job involves ensuring products/services meet standards by designing tests, identifying defects, documenting issues, and collaborating with teams to fix them, focusing on reliability, performance, and customer satisfaction,

Maithri Drugs Private Limited is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and ...

Maintaining GRNs Register updating. Raw material and Packing material receiving and ATRs raised to QC. Material issue updating in BIN cards. Raw materials Receipts, dispensing and updating Dispensing logbooks, Temperature Balance Calibration records, Housekeeping / Tools cleaning, records. Raw Material and solvents approved status updating. Hazardous material handling. Identification of the Re-test due materials and update details in logbook. Responsible for Raw Materials and Packing materials. To follow the cGMP And Safety Norms in the Warehouse. Responsible for Internal units materials transfers and dispatches. To Co-Ordinate our colleges and all over department. Re-test and Rejected logbo...

Handling of QMS actives, Change control Deviations market complaints BPR review Process validation review Cleaning validation review APQR preparation Qualification Groups Graduation B.Sc Post Graduation M.Pharma Post Graduation M.Sc Graduation B.Pharma Graduation D Pharmacy

Handling of QMS activities Change controls, Stability data review QC analytical data review Qualification Groups Graduation B.Sc Post Graduation M.Pharma Post Graduation M.Sc Post Graduation M.Tech Graduation B.Pharma Graduation D Pharmacy

Our world is transforming, and PTC is leading the way.Our software brings the physical and digital worlds together, enabling companies to improve operations, create better products, and empower people in all aspects of their business. Our people make all the difference in our success. Today, we are a global team of nearly 7,000 and our main objective is to create opportunities for our team members to explore, learn, and grow – all while seeing their ideas come to life and celebrating the differences that make us who we are and the work we do possible. TBD Life at PTC is about more than working with today’s most cutting-edge technologies to transform the physical world. It’s about showing up ...

As a leading IPQA (In Process Quality Assurance) Team, your role will involve assigning tasks to IPQA chemists for day-to-day activities. You will participate in, review, and approve protocols and reports for various studies such as user requirement specifications, qualifications, validations, risk assessments, and other site-related activities. It is crucial to ensure that all commitments to regulatory authorities are fulfilled for the concerned batch and to actively contribute to the design, development, approval, and implementation of quality systems at the manufacturing site. Your responsibilities will include participating in external inspections of the manufacturing site, preparing CAP...

job responsibility - IPQA Sterile (7-10 years experience) Perform real-time IPQA monitoring of sterile manufacturing and aseptic operations. Review and ensure accuracy of BMR/BPR documentation and GMP compliance. Conduct line clearance for aseptic areas and verify equipment readiness. Oversee environmental monitoring activities and review EM data trends. Monitor aseptic practices during filling, filtration, and media fill operations. Handle deviations, OOS/OOT, and support root cause analysis and CAPA implementation. Participate in validation activities including sterilization and process simulation. Ensure adherence to contamination control strategies and data integrity (ALCOA+). Support re...

Dear Candidate, Greetings from Intas Pharmaceuticals Ltd.! Intas Pharmaceuticals is a leading, vertically integrated global pharmaceutical company headquartered in Ahmedabad, India, with a strong presence in over 85 countries. Driven by innovation and quality, Intas is committed to developing and manufacturing affordable medicines that improve lives across the world. We are pleased to announce a Walk-In Drive for our SEZ Plant for professionals experienced in Quality Assurance IPQA Lab Q.A. Documentation Cell Quality Control Micro Chemical Experience Required: - 3 to 12 Years Qualification Required: - M.Pharm./M.Sc./B.Pharm. Walk-In Drive Details: - Date: Sunday, 7nd December 2025 Time: 09:3...

Opening for Pharma Lifescience. Role & responsibilities : Candidate is having knowledge of OSD Formulation Plant. Depth knowledge of In Process Quality Assurance . Third Party Manufacturing Knowledge. Candidate is Ready for Within City Travelling for who are Manufacturing our Medicine. Qualification:-M-Pharma-QA or B-Pharma. Interested candidates shared resume on snehal@topgearconsultants.com

REQUIRED IPQA OFFICER FOR A OSD, INJECTABLE AND EXTERNAL LIQUID MANUFACTURING COMPANY

Line clearance activities for Washing, Filling, Sealing, and Visual Inspection. Perform Environmental Monitoring in Grade A, B, C, and D clean room areas. Execute in-process checks and ensure compliance with GMP procedures.

Dishman Carbogen Amcis is looking for Officer Formulation QA to join our team Roles and Responsibility Develop and implement quality control processes to ensure compliance with regulatory requirements. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve quality-related issues. Analyze data to identify trends and opportunities for process improvements. Develop and maintain documentation of quality control procedures and protocols. Ensure all products meet required quality standards before release. Job Requirements Bachelor's degree in a relevant field. Minimum years of experience in formulation quality a...

Job Title: Senior Executive Business Unit: Global Operations Job Grade G11B Location: Sikkim, Unit II Sr. No. Responsibilities 1 To execute/supervise Production activities machine wise at Coating/Capsule/Nutraceutical-I area & documentation. 2 Handling of change control, deviation, CAPA, Product Quality Complaint investigation and other QMS documents in Production. 3 To accomplish the responsibilities of Departmental Training Coordinator by coordinating and conducting training (online/offline) on manufacturing employees and workmen in department and maintain the training related document. 4 Preparation of PPT, daily, weekly and monthly reports. 5 To ensure the online training of new employee...

Job Title: Senior Officer Business Unit: Global Operations Job Grade G12B Location: Sikkim, Unit II Sr. No. Responsibilities 1 To execute/supervise Production activities machine wise at Granulation area. 2 Online checking of In-process parameters and completion of the Log book and BMR of Granulation area. 3 Handling of change Control, Deviation, CAPA, Product Quality Complaint Investigation and other QMS related documents in Production. 4 To check and make availability of machine as per Preventive Maintenance schedule. 5 Co-ordination with IPQA/QC/Engineering/IT and MSTG department for smooth functioning of Production activities. 6 Handling of SAP and Track wise related work in Production. 7...

Job Title: Technician Business Unit: global Operations Job Grade 301 Location: Sikkim, Unit II At 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 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. Sr. No. Responsibilities 1 Online Checking of in-process parameters and completion of the ...

Job Title: Junior Technician 1 Business Unit: Global Operations Job Grade 301 Location: Sikkim, Unit II Sr. No. Responsibilities 1 Online Checking of in-process parameters and completion of the Log book and BMR of Compression area. 2 To provide machine for preventive maintenance. 3 Co-ordination with IPQA/QC/Engineering department for smooth functioning of Production activities. 4 To ensure proper use of Personnel Protective Equipment s (PPEs) in area. 5 To maintain cGMP practice in production area. 6 To fill documentation as per GDP and maintain data integrity in Production area. 7 To do calibration/verification of balances in Production area. 8 Proper shift hand-over to the next shift tech...

Job Title: Officer (Quality Assurance) Business Unit: Global Quality And Compliance Job Grade G12C Location: Sikkim, Unit II At 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 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. Sr. No. Responsibilities 1.To ensure IPQA activity during ma...

Job Title: Officer Business Unit: Global Operations Job Grade G12C Location: Sikkim, Unit II Sr. No. Responsibilities 1 To execute/supervise Production activities machine wise at Granulation area. 2 Online checking of In-process parameters and completion of the Log book and BMR of Granulation area. 3 Handling of change Control, Deviation, CAPA, Product Quality Complaint Investigation and other QMS related documents in Production. 4 To check and make availability of machine as per Preventive Maintenance schedule. 5 Co-ordination with IPQA/QC/Engineering/IT and MSTG department for smooth functioning of Production activities. 6 Handling of SAP and Track wise related work in Production. 7 To fil...

Job Title: Officer Business Unit: Global Operations Job Grade G12C Location: Sikkim, Unit II Sr. No. Responsibilities 1 To execute/supervise Production activities machine wise at Granulation area. 2 Online checking of In-process parameters and completion of the Log book and BMR of Granulation area. 3 Handling of change Control, Deviation, CAPA, Product Quality Complaint Investigation and other QMS related documents in Production. 4 To check and make availability of machine as per Preventive Maintenance schedule. 5 Co-ordination with IPQA/QC/Engineering/IT and MSTG department for smooth functioning of Production activities. 6 Handling of SAP and Track wise related work in Production. 7 To fil...

Job Title: Management Associate (Grade 2) Business Unit: Global Operations Job Grade 299 Location: Sikkim, Unit II Sr. No. Responsibilities 1 Online Checking of in-process parameters and completion of the Log book and BMR of Compression area. 2 To provide machine for preventive maintenance. 3 Co-ordination with IPQA/QC/Engineering department for smooth functioning of Production activities. 4 To ensure proper use of Personnel Protective Equipment s (PPEs) in area. 5 To maintain cGMP practice in production area. 6 To fill documentation as per GDP and maintain data integrity in Production area. 7 To do calibration/verification of balances in Production area. 8 Proper shift hand-over to the next...