Downstream Processing Supervisor (NIGHT SHIFT)
Global Life Science Hub
Chicago, illinois
Job Details
Full-time
Full Job Description
Supervisor, Downstream Processing (Night Shift)
Location: Chicago, IL
Global Life Science Hub is recruiting on behalf of a prominent biopharmaceutical company for a Supervisor, Downstream Processing, to lead their night shift operations (10:00 PM – 6:30 AM) in Chicago, IL. This full-time role involves managing critical downstream processing activities and ensuring the delivery of high-quality pharmaceutical products in line with cGMP standards. You will oversee a dedicated team, ensuring efficient operations while maintaining safety and compliance throughout the shift.
Key Responsibilities:
- Supervise downstream processing activities, ensuring effective use of equipment and resources to meet production goals.
- Train and mentor staff on downstream processes, SOPs, and equipment, promoting safety and regulatory compliance.
- Manage the night shift operations, ensuring all production schedules are met and team members perform efficiently.
- Ensure adherence to cGMP standards and environmental, health, and safety regulations during all production activities.
- Lead investigations into any deviations, collaborating with cross-functional teams to implement corrective actions (CAPAs).
- Maintain accurate documentation, review batch records, and report on production performance.
- Drive continuous process improvements and identify opportunities for operational efficiency.
- Provide ongoing performance feedback, conduct reviews, and foster team development.
Key Requirements:
- Education:
- Bachelor’s degree in Life Sciences, Biotechnology, Engineering, or a related field with 5+ years of experience, or
- Master’s degree with 2+ years of relevant experience.
- Experience:
- Strong experience in downstream processing within a cGMP-regulated environment.
- Prior supervisory experience in pharmaceutical or biotechnology manufacturing preferred.
- Skills:
- In-depth knowledge of downstream processing technologies and cGMP regulations.
- Proven leadership, communication, and problem-solving skills.
- Proficiency in MS Office applications.
Additional Information:
This role operates in a biotech manufacturing environment with a night shift schedule (10:00 PM – 6:30 AM), and occasional overtime may be required. The ideal candidate must thrive in a fast-paced, deadline-driven setting, ensuring smooth operations and high standards of compliance throughout the shift.