Director, Operational Quality

GSK

Pennsylvania, United States
Quality assurance/operations
Cgmp compliance
Regulatory inspections
As the Third Party Quality Director, you will be responsible for the quality leadership of third party contract operations of both Large and Small Molecule, including new business developments, while supporting the performance of third party contract manufacturing companies

Job Summary

  • As the Third Party Quality Director, you will be responsible for the quality leadership of third party contract operations of both Large and Small Molecule, including new business developments, while supporting the performance of third party contract manufacturing companies.
  • This role will provide YOU the opportunity to lead key activities to progress YOUR career, including providing leadership for securing new products and managing development and performance objectives for a team of Quality professionals.
  • GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together, aiming to positively impact the health of 2.5 billion people by the end of the decade.

Matching Summary

As the Third Party Quality Director, you will be responsible for the quality leadership of third party contract operations of both Large and Small Molecule, including new business developments, while supporting the performance of third party contract manufacturing companies.

Skills & Requirements

Must-have

  • Quality Assurance/Operations
  • cGMP compliance
  • Regulatory inspections
  • Quality Management Systems (QMS)
  • Corrective and Preventive Actions (CAPA)

Nice-to-have

  • Analytical problem-solving skills
  • Data-driven decision making
  • Flexibility and adaptability
  • Team player

Key Requirements

  • Bachelor's Degree
  • 7+ years pharmaceutical industry experience
  • Project management experience
  • Team leadership experience

Work Rights

Not specified

Tailored Resume

Cover Letter