
Production QMS Officer
18 hours ago
Responsibilities:
- Ensure compliance with QMS protocols in production and packing areas.
- Review and maintain batch records, SOPs, and documentation as per USFDA standards.
- Support deviation investigations, CAPA, and change control processes.
- Coordinate with cross-functional teams to uphold GMP and regulatory requirements.
Key Skills:
- Knowledge of QMS and GMP in pharmaceutical manufacturing.
- Experience in USFDA-audited facilities preferred.
- Strong documentation and communication skills.
Proffered Candidate Profile:
- Bachelors or Masters degree in Pharmacy or related field.
- 2–4 years of experience in pharmaceutical production or packing, preferably in a USFDA-audited facility.
- Strong understanding of QMS, GMP, and regulatory compliance.
- Experience handling documentation, deviations, CAPA, and change controls.
- Familiarity with ointment or topical dosage manufacturing is a plus.
** Immediate Joiner is preferred **
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