QC Laboratory Manager
GSK
Full-time
On-site
Zebulon, NC
Operations
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Role Summary
QC Laboratory Manager will oversee laboratory activities to ensure compliance with regulatory requirements and good manufacturing practices. You will lead a team, drive continuous improvement, and collaborate across departments to deliver impactful results.
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.
- Master’s degree in a scientific field. (Preferred)
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 a scientific field (Required).
- Master’s degree (Preferred).