We at Inducare Pharmaceutical & Research Foundation set up a Public testing laboratory and manufacturing facility for oral solid dosage and external preparations at G-32 MIDC Jejuri, Dist. Pune 412303 has facilities for microbiological testing, instrumentation, testing stability Testing, wet laboratory, etc.
Hiring: APQR Documentation Executive
Company: Inducare Pharmaceuticals & Research Foundation
Location: Jejuri, Pune, Maharashtra
Position: APQR / DOCUMENTATION EXECUTIVE
Qualification
- B. Pharm / M. Pharm / M.Sc.
Experience
- 2-3 Years
- Experience in Pharmaceutical Manufacturing
Key Responsibilities
- Job Responsibilities:
- Preparation, compilation and review of APQR (Annual Product Quality Review) for pharmaceutical products.
Required Skills:
- Good knowledge of APQR preparation and documentation.
- Knowledge of GMP and pharmaceutical QA systems.
- Good documentation and analytical skills.
- Good knowledge of MS Word and MS Excel.
- Good communication and coordination skills.
- Ability to work with cross-functional teams.
Note:
2–3 years of experience in Documentation, APQR and other QA Compliance activities is required.
Candidates having only IPQA experience are not required.
- Collection and compilation of data related to:
- Batch Manufacturing Records (BMR)
- Batch Packaging Records (BPR)
- In-process and finished product testing
- OOS / OOT
- Deviations
- CAPA
- Change Control
- Market Complaints
- Product Returns / Recalls
- Stability Studies
- Yield and rejection trends
- Preparation, review and maintenance of QA documentation as per GMP requirements.
- Ensure timely completion and approval of APQR documents.
- Coordinate with Production, QC, QA, Warehouse and other departments for collection of required data.
- Review product quality trends and identify any significant deviations or recurring issues.
- Maintain proper documentation and records related to APQR and other QA compliance activities.
- Support internal audits, regulatory inspections and customer audits by providing required documentation.
- Follow cGMP, WHO-GMP and applicable regulatory requirements related to documentation and product quality review.
- Ensure proper control, filing and retrieval of QA documents and records.
Contact No-7709940354
Email Id:[email protected]
Interested candidates can apply through Indeed or share their updated resume.
Job Type: Regular / Permanent
Pay: ₹30,000.00 - ₹60,000.00 per month
Ability to commute/relocate:
- Jejuri, Maharashtra: Reliably commute or planning to relocate before starting work (Required)
Education:
Experience:
- • Knowledge of GMP and pharmaceutical QA systems: 3 years (Preferred)
- APQR preparation and documentation: 3 years (Preferred)
License/Certification:
- 2 years of exp. in Documentation, QA Compliance activities (Preferred)
Work Location: In person
