Job Description:

? Key Responsibilities

GMP Compliance

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

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

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

Documentation & Records

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

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Ensure proper documentation practices (GDP) are followed.

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

Training & Awareness

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Conduct GMP induction and refresher training for employees.

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Promote GMP awareness and hygiene practices on shop floor.

Deviation, CAPA & Change Control

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Assist in investigation of deviations, incidents, and OOS.

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Support root cause analysis and implementation of CAPA.

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Coordinate change control activities related to GMP systems.

Housekeeping & Hygiene

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Monitor housekeeping, sanitation, and personal hygiene practices.

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Ensure pest control and sanitation programs are followed.

Continuous Improvement

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Participate in GMP improvement initiatives.

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

? Qualification

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

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Additional training in GMP / Quality Systems preferred

?‍? Experience

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

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

? Skills & Competencies

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Strong knowledge of GMP & GDP

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Positive documentation and communication skills

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Hands-on experience in audits and compliance activities

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Ability to coordinate across departments

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Basic knowledge of regulatory standards and quality systems

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