Manufacturing II Operator – 3rd Shift

About the role

The Manufacturing II Operator supports pharmaceutical product finishing and packaging on the 3rd shift. You will work with semi‑automated equipment to assemble, inspect, and package finished medicines while ensuring compliance with strict quality and safety standards.

Key responsibilities

• Perform manual assembly and inspection of commodities and components to meet GMP specifications.
• Operate semi‑automated manufacturing equipment to produce finished pharmaceutical products.
• Conduct and document in‑process quality checks to ensure batch record specifications are met.
• Move material to and from production lines to maintain efficient workflow.
• Adhere to safety guidelines and proper PPE gowning practices.
• Execute basic line changeover activities and verify component labeling.
• Set up and close out work orders, including lot line clearances and documentation audits.

Required profile

• Leaving Certificate or equivalent.
• Minimum 2 years of experience in a pharmaceutical production environment.
• Knowledge of applicable regulations such as CFR 210/211 and cGMP.
• Familiarity with documentation practices and batch record review.

Required skills

• Operation of semi‑automated manufacturing equipment.
• Manual assembly and product inspection.
• In‑process quality checks and documentation.
• Line changeover procedures.
• Work order setup and closeout.
• Knowledge of cGMP and CFR 210/211 regulations.

What we offer

• 3rd‑shift schedule: 23:30 – 07:30 Monday‑Thursday, 17:30 – 23:00 Friday (39 hours/week).
• Equal opportunity employment with a focus on integrity, innovation, and community impact.