Job Description: Key Responsibilities

GMP Compliance

- Ensure effective implementation of GMP guidelines across production, QA, QC, warehouse, and utilities.

- Monitor day-to-day GMP activities and identify non-conformances.

- Support GMP audits (internal, customer, and regulatory).

Documentation & Records

- Prepare, review, and control GMP documents such as SOPs, formats, logs, and registers.

- Ensure proper documentation practices (GDP) are followed.

- Maintain training, deviation, CAPA, and change control records.

Training & Awareness

- Conduct GMP induction and refresher training for employees.

- Promote GMP awareness and hygiene practices on shop floor.

Deviation, CAPA & Change Control

- Assist in investigation of deviations, incidents, and OOS.

- Support root cause analysis and implementation of CAPA.

- Coordinate change control activities related to GMP systems.

Housekeeping & Hygiene

- Monitor housekeeping, sanitation, and personal hygiene practices.





- Ensure pest control and sanitation programs are followed.

Continuous Improvement

- Participate in GMP improvement initiatives.

- Support compliance with ISO, FSSC, or customer audit requirements (as applicable).

Qualification
- B.Sc / M.Sc (Chemistry) / B.Pharm / M.Pharm / Diploma or Degree in Chemical

- Additional training in GMP / Quality Systems preferred

‍ Experience
- 2–5 years of experience in GMP / QA / Quality Systems

- Exposure to chemical / pharma / food / specialty chemical manufacturing preferred

Skills & Competencies
- Solid knowledge of GMP & GDP

- Good documentation and communication skills

- Hands-on experience in audits and compliance activities

- Ability to coordinate across departments

- Basic knowledge of regulatory standards and quality systems

📌 Chemist / Officer / Senior Officer - Quality Assurance (GMP) (Vapi)
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📍 Vapi