Pharmaceutical Production Lead

TSP talent; Irvine (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

TSP talent is seeking a Production Lead I (On-site) in Irvine to coordinate daily production activities in a pharma manufacturing setting. The role ensures compliance with cGMP, safety, and quality while meeting production targets.

You will organize staffing, verify batch documentation, and support deviation investigations, with opportunities for continuous improvement and team coaching.

Qualifications

• Demonstrated front-line leadership experience.
• Strong knowledge of cGMP expectations and compliance.
• Clear emphasis on safety and quality in production.
• Ability to review documentation and support investigations and corrective actions.

Responsibilities

• Coordinate line setup, production activities, and changeovers.
• Review and verify batch documentation for completeness and compliance.
• Support deviation investigations and corrective/preventive actions.
• Participate in continuous improvement initiatives.
• Coach, train, and develop operators; promote cross-team collaboration.
• Maintain a safe, compliant, and efficient manufacturing environment.

Skills

Front-line leadership

cGMP knowledge

Safety awareness

Quality focus

Documentation review

Investigations & CAPA support

Job description

Production Lead I (On-site) to support pharmaceutical Manufacturing & Production

Coordinate daily production activities to ensure compliance with cGMP, safety, and quality requirements while achieving production targets. Organize staffing and support effective execution of operations.

Key Duties

• Coordinate line setup, production activities, and changeovers.
• Review and verify batch documentation for completeness and compliance.
• Support deviation investigations and corrective/preventive actions.
• Participate in continuous improvement initiatives.
• Coach, train, and develop operators; promote collaboration across teams.
• Maintain a safe, compliant, and efficient manufacturing environment.

Qualifications/skills

Demonstrated front-line leadership, strong knowledge of cGMP expectations, attention to safety and quality, and the ability to review documentation and support investigations and improvement efforts.