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Night Shift Supervisor

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.

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