Aseptic Production Supervisor

2 weeks ago


Chicago, Illinois, United States Global Life Science Hub Full time
Job Overview

Global Life Science Hub is seeking a skilled Manufacturing Supervisor (DP) to oversee our aseptic production operations. This pivotal role involves leading a team to ensure the efficient and compliant manufacturing of pharmaceutical products. Your expertise will contribute significantly to our commitment to quality and regulatory adherence.

Key Responsibilities:

  • Direct and mentor production staff to optimize equipment and material usage, ensuring high-quality product outcomes in line with cGMP and operational plans.
  • Provide leadership and development opportunities for team members, including conducting performance evaluations.
  • Align departmental objectives with organizational goals to enhance productivity.
  • Champion safety protocols and ensure compliance with environmental, health, and safety regulations.
  • Educate staff on equipment operation, manufacturing processes, and standard operating procedures (SOPs).
  • Plan and manage packaging timelines while adhering to budget constraints.
  • Facilitate timely project delivery and engage in qualification and validation processes.
  • Analyze and troubleshoot production issues, recommend enhancements, and encourage teamwork.
  • Monitor production workflows, compile reports, and provide strategic operational guidance.
  • Review compliance documentation and establish project timelines.
  • Contribute to cross-functional project teams and undertake additional responsibilities as necessary.

Qualifications:

  • Bachelor's degree in engineering, pharmaceuticals, life sciences, or a related field with a minimum of 4 years of relevant experience.
  • Master's degree in engineering, pharmaceuticals, life sciences, or a related field with at least 2 years of relevant experience.
  • Preferred background in aseptic processing, manual visual inspection, and serialization in finished product packaging.
  • Excellent communication, leadership, and analytical skills.
  • Proficient in technical documentation, Microsoft Office Suite, and managing operational teams.
  • Knowledgeable about FDA cGMP regulations and standards.
  • Ability to thrive in both office and biotechnology manufacturing settings.
  • Willingness to adapt to various shifts, overtime, and travel requirements.


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