- M.Sc. or B.Sc. in a relevant field
- Experience in Quality Assurance within an API plant
- Knowledge of wet lab analysis
- Expertise in raw material analysis
- Lab instrument calibration
- A well-established corporate group with over 50 years of industry experience
- A leading Indian manufacturer of pharmaceutical excipients, active pharmaceutical ingredients (APIs), and specialty chemicals
- Headquartered in Mumbai, with manufacturing plants in Gujarat and Maharashtra
- Global operations spanning North America, Europe, Asia, Africa, and South America
- Issue Batch Manufacturing Records (BMR), equipment cleaning records, logbooks, and analytical reports for raw materials, finished products, and packaging materials.
- Assist in drafting and preparing SOPs for various departments.
- Conduct plant rounds to verify documentation compliance with cGMP and GLP norms.
- Perform line clearance activities for manufacturing and packaging before processes begin.
- Issue deviation forms, change control forms, out-of-specification (OOS) forms, customer complaint forms, and out-of-trend (OOT) forms as requested by departments.
- Review and verify analytical and batch manufacturing records, ensuring proper filing and QA verification for product release.
- Prepare and monitor documentation and activities in accordance with SOPs.
- Manage the distribution, retrieval, and control of SOPs and records across departments.
- Participate in internal audits, customer audits, and regulatory inspections.
- Attend quality review (QR) meetings as scheduled.
- Ensure data integrity compliance as per established procedures.
- Review manufacturing, storage, and quality control activities.
- Prepare and maintain an approved vendor list and oversee vendor qualification.
- Conduct traceability activities.
- Maintain and update the CAPA log.
- Investigate deviations, product recalls, returned goods, customer complaints, OOS, and OOT cases, ensuring proper documentation and CAPA implementation.
- Collect data and prepare the annual product review.
- Witness and verify process validation, cleaning validation, and equipment qualification, preparing necessary protocols and reports.
- Investigate returned materials and maintain records.
- Investigate product complaints and maintain documentation.
- Ensure compliance with equipment maintenance and calibration schedules.
- Prepare templates and record formats as per SOP requirements.
- Develop and conduct training sessions on cGMP and GLP, including evaluation of training effectiveness.
- Provide job-specific training based on identified needs.
- Undertake additional assignments as directed by the Head of QA.
- Ensure proper waste disposal procedures are followed.
- Support environmental management initiatives and report progress to the department head.
- Investigate environmental deviations/incidents in coordination with the department head.
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· Job Description: · REQUIREMENTS · Education / Experience · Education: · Graduate / Post Graduate in Pharmacy or Chemistry · Experience: · 2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Reg ...
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As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. · ...
Bharuch3 weeks ago
- Work in company
Officer / Executive / Assistant Manager - Quality Assurance
Only for registered members
· Job Description: · REQUIREMENTS · Education / Experience · Education: · BSC / MSC Chemistry · Experience: · 2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements · JOB PUR ...
Bharuch6 days ago
- Work in company
Officer / Executive - Development Quality Assurance (DQA)
Only for registered members
· Job Description: · Qualification & Experience · M.Pharm / M.S / B.S in Chemistry, Pharmaceutics or related discipline · 3–5 years of experience in R&D (DQA) · Strong knowledge of GMP, GCP, GLP and 21 CFR 210/211 · Experience with dermatology products or medical devices is an a ...
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Ankleshwar ₹400,000 - ₹900,000 (INR) per year6 days ago
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Ankleshwar, Navsari, Rajkot1 month ago
Quality Assurance Officer - Ankleshwar - TalentEdge Recruitment Consultants
Description
Job Title: Quality Assurance Officer
Job Location: Ankleshwar, Gujarat
Industry: API / Pharma / Chemical Manufacturing
Experience Range: 2 to 5 years in Quality Assurance within an API manufacturing company
Qualifications & Required Skills:
About the Company:
Job Responsibilities:
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Quality Assurance Officer
Only for registered members Ankleshwar, Dahej
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Quality Assurance Officer
Only for registered members Ankleshwar
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Quality Assurance Officers
Only for registered members Ankleshwar, Dahej
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Quality Assurance Officer
Only for registered members Ankleshwar
-
Quality Assurance Officer
Only for registered members Anklesvar
-
Officer / Executive - Quality Assurance
Only for registered members Ankleshwar
-
Quality Assurance Officer
Only for registered members Bharuch, Dahej
-
Quality Assurance Officer
Only for registered members Panoli
-
Officer / Executive - Quality Assurance
Only for registered members Bharuch
-
Officer / Executive - Quality Assurance
Only for registered members Bharuch
-
Officer / Executive - Quality Assurance
Only for registered members Bharuch
-
Officer / Executive - Quality Assurance
Only for registered members Bharuch
-
G12B Senior Officer Quality Assurance
Only for registered members Bharuch
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Officer / Executive / Assistant Manager - Quality Assurance
Only for registered members Bharuch
-
Officer / Executive - Development Quality Assurance (DQA)
Only for registered members Bharuch
-
Quality Assurance Officer
Only for registered members Dahej
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Quality Assurance Manager
Only for registered members Ankleshwar, Bharuch, Dahej
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Executive - Quality Assurance (API)
Only for registered members Ankleshwar
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QA Officer
Only for registered members Ankleshwar
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Key Relationship Manager
Only for registered members Ankleshwar, Navsari, Rajkot
