Symbio Generics is a reputed name in the pharmaceutical industry, specializing in API (Active Pharmaceutical Ingredient) manufacturing. With a commitment to quality and compliance, Symbio offers dynamic career opportunities for professionals in the pharma sector. This role is based at VPL Chemicals, a facility known for its adherence to global regulatory standards.
Job Description
We are seeking an experienced Executive – Production Documentation to oversee critical documentation processes in API production.
Key Responsibilities:
- Prepare Batch Manufacturing Records (BMR), SOPs, and cleaning records.
- Handle Quality Management System (QMS) documents, including:
- Change control
- Deviation reports
- OOS (Out of Specification) and OOT (Out of Trend) investigations
- Review BMRs and logbooks with checklists.
- Ensure audit compliance and support regulatory inspections.
- Proficiency in MS Office and SAP is required.
Eligibility Criteria
Education:
- B.Sc/M.Sc in Chemistry
- Diploma/B.Tech in Chemical Engineering
Experience:
- 3-5 years in API Pharma Production Documentation.
Skills:
- Strong documentation and compliance knowledge.
- Familiarity with GMP, QMS, and audit processes.
- Technical proficiency in MS Office & SAP.
How to Apply
Interested candidates meeting the eligibility criteria can share their updated CV and referral forms to:
Email: careers@symbiogenerics.com
(Note: Only shortlisted candidates will be contacted. Pharmabharat.com does not charge any fees for job applications.)
