Production - QMS (Executive)

Department: Production QMS

Designation: Officer to Executive

Experience: 3 to 6 Years

Location: Bavla, Ahmedabad

Key Responsibilities:

Injectable Production Activities

• Carry out and monitor day-to-day manufacturing of injectable products (aseptic or terminal sterilized).
• Follow batch manufacturing records (BMRs) and SOPs during production.
• Coordinate with cross-functional teams like QA, QC, and Maintenance for smooth operations.

Quality System Support

• Handle QMS activities such as deviations, CAPA, change control, and documentation updates.
• Participate in investigation and closure of production-related quality events.
• Assist in risk assessments and implementation of preventive actions.

Compliance & Documentation

• Ensure proper documentation of all production operations.
• Adhere to data integrity and good documentation practices (GDP).
• Support SOP revisions and ensure they reflect current practices.

Audit Readiness

• Assist in preparation for internal and external GMP audits (USFDA, EU, WHO, etc.).
• Ensure compliance with cGMP, regulatory requirements, and company standards.

Training & Improvements

• Conduct or attend GMP and QMS training sessions.
• Suggest and implement improvements to increase process efficiency and quality.

Must Exposure in Parenteral Background

We wish to have association with people like you in our organization and you may confirm your interest by sending your detailed Resume on Recruitment@swiss.in