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Global Life Science Hub

Night Shift Supervisor Job at Global Life Science Hub in Chicago

Global Life Science Hub, Chicago, IL, US


Job Description

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.