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.
- Valuable 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-(phone hidden)

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:
- Bachelor's (Preferred)

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

📌 APQR / DOCUMENTATION EXECUTIVE (Jejuri)
🏢 Inducare Pharmaceutical u0026 Research Foundation
📍 Jejuri