Manufacturing Operations Manager
2 days ago
Our client, a leading pharmaceutical company, is seeking a skilled Manufacturing Supervisor (DP) to join their dynamic team in Chicago, IL. As a Manufacturing Supervisor (DP), you will play a crucial role as a shift leader in their manufacturing operation, ensuring the production of high-quality products in compliance with regulatory requirements, operational plans, and company policies.
Key Responsibilities:- Production Oversight: Supervise and guide production floor personnel to ensure efficient use of equipment and materials for high-quality product outcomes in accordance with cGMP and production plan.
- Staff Development: Provide coaching, counselling, and development to direct staff, conducting annual performance reviews.
- Department Alignment: Maintain alignment with department goals and objectives.
- Compliance and Safety: Promote safe work practices and compliance with policies, environmental, health, and safety standards.
- Training and Development: Train personnel on equipment, processes, and SOPs.
- Packaging Scheduling: Develop and manage packaging schedules within budget.
- Project Management: Ensure timely project completion and participate in qualification and validation activities.
- Problem-Solving: Investigate and resolve problems, propose process improvements, and foster collaboration.
- Process Monitoring: Monitor processes, generate reports, and provide operational direction.
- Documentation: Review documentation for compliance standards and establish timelines.
- Team Collaboration: Participate in multi-functional project teams and perform additional tasks as required.
- Education: Bachelor's degree in engineering, pharmaceuticals, related life sciences, or equivalent with 4+ years of experience.
- Experience: Master's degree in engineering, pharmaceuticals, related life sciences, or equivalent with 2+ years of experience.
- Preferred Experience: Preferred experience in aseptic processing, manual visual inspection, and finished product packaging with serialization.
- Skills: Strong communication, leadership, and problem-solving skills.
- Technical Skills: Proficient in technical writing, MS Office applications, and leading operational teams.
- Regulatory Knowledge: Familiarity with FDA cGMPs and regulations.
- Work Environment: Ability to work in office and biotechnology manufacturing environments.
- Flexibility: Flexibility for different shifts, overtime, and travel.
The Global Life Science Hub is a niche Life Science headhunting firm. We place professionals across Europe and the US for a variety of Biotechnology, Pharmaceutical, and CRO companies ranging from small start-ups to large global organisations.
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