Full-Time Pharmaceutical Manufacturing Supervisor

Hader Solutions; Irvine (CA); In loco; USD 80.000 - 110.000; Tempo pieno

Descrizione del lavoro

Hader Solutions is seeking a Production Lead I for on-site work in Irvine, CA. The role oversees daily production activities in pharmaceutical manufacturing, ensuring schedule adherence and product quality on-site.

You will coordinate staffing, line setups, and changeovers while reviewing batch documentation and supporting deviation investigations. A focus on continuous improvement and team coaching will drive a compliant, efficient manufacturing environment.

Competenze

• Leadership and team management abilities.
• Knowledge of cGMP, safety, and quality standards in pharmaceutical manufacturing.
• Excellent organizational and communication skills.
• Ability to support deviation investigations and process improvements.

Mansioni

• Coordinate daily production operations to meet schedule and output goals.
• Ensure compliance with cGMP, safety, and quality standards.
• Organize staffing, line setup, and changeovers for production lines.
• Review batch documentation and support deviation investigations.
• Promote continuous improvement initiatives.
• Coach and train operators to ensure skilled and compliant team performance.
• Foster a collaborative, safe, and efficient manufacturing environment.

Conoscenze

Leadership

cGMP knowledge

Safety & Quality

Communication

Descrizione del lavoro

Role:

Production Lead I in pharmaceutical manufacturing, responsible for overseeing daily production activities on-site.

Key Responsibilities

• Coordinate daily production operations to meet schedule and output goals.
• Ensure compliance with cGMP, safety, and quality standards.
• Organize staffing, line setup, and changeovers for production lines.
• Review batch documentation and support deviation investigations.
• Promote continuous improvement initiatives.
• Coach and train operators to ensure skilled and compliant team performance.
• Foster a collaborative, safe, and efficient manufacturing environment.

Qualifications & Skills

• Strong leadership and team management abilities.
• Knowledge of cGMP, safety, and quality standards within pharmaceutical manufacturing.
• Excellent organizational and communication skills.
• Ability to support deviation investigations and process improvements.