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
Valuable 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
🏢 SDP HR Solution
📍 Vapi