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QC Laboratory Manager

GSK
Full-time
On-site
Zebulon, NC
Operations

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Role Summary

QC Laboratory Manager who lead a team to ensure the highest quality standards in laboratory operations, overseeing regulatory compliance and good manufacturing practices, with a focus on development, continuous improvement, and cross-department collaboration.

Responsibilities

  • Develop and implement strategies to ensure laboratory compliance with regulatory standards and company policies.
  • Lead and mentor a team of laboratory professionals, fostering their growth and development.
  • Manage laboratory operations, including resource allocation, budgets, and equipment maintenance.
  • Oversee audits and inspections, ensuring adherence to safety and quality standards.
  • Drive continuous improvement initiatives to enhance efficiency, quality, and cost-effectiveness.
  • Collaborate with cross-functional teams to support production and new product introductions.

Qualifications

  • Bachelor’s degree in a scientific field such as chemistry, biochemistry, or related discipline.
  • 5+ years of experience in a GMP-regulated laboratory environment.
  • 5+ years of experience supervising or managing a team.
  • Experience with laboratory audits and inspections.
  • Preferred: Master’s degree in a scientific field.

Skills

  • Strong leadership and interpersonal skills.
  • Experience in analytical method validation and transfer processes.
  • Ability to prioritize and manage multiple tasks effectively.
  • Excellent verbal and written communication skills.
  • Familiarity with continuous improvement methodologies and tools.
  • Proven experience in a quality support role within the pharmaceutical or biopharmaceutical industry.
  • Strong knowledge of laboratory compliance and regulatory requirements.

Education

  • Bachelor’s degree in chemistry, biochemistry, or related field (required).
  • Master’s degree in a scientific field (preferred).

Additional Requirements

  • On-site role based in the United States.
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