Senior Validation & Quality Lead (Hybrid)

GSK

Zebulon (NC)

Hybrid

USD 95,000 - 125,000

Full time

14 days+
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Job summary

GSK in Zebulon, North Carolina is seeking a qualified Validation Lead for a crucial hybrid role. You will oversee validation lifecycle management, ensure compliance with GMP regulations, and lead validation projects in a team-oriented environment.

The ideal candidate has over 10 years of experience in the pharmaceutical industry, including extensive validation expertise. Strong analytical skills and the ability to manage diverse teams are essential for success.

Qualifications

  • Minimum 10 years of experience in the pharmaceutical industry.
  • Proven experience managing validation projects.
  • Experience with analytical equipment and methods.

Responsibilities

  • Drive all aspects of Validation Life Cycle and Change Control.
  • Manage the development and oversight of validation protocols.
  • Collaborate with business clients to meet objectives.

Skills

Analytical skills
Validation project management
Technical expertise in chemical theory
Leadership in validation teams

Education

Bachelor’s degree in Chemistry, Engineering, or related field

Tools

Analytical equipment
Laboratory instrumentation

Job description

GSK in Zebulon, North Carolina is seeking a qualified Validation Lead for a crucial hybrid role. You will oversee validation lifecycle management, ensure compliance with GMP regulations, and lead validation projects in a team-oriented environment.

The ideal candidate has over 10 years of experience in the pharmaceutical industry, including extensive validation expertise. Strong analytical skills and the ability to manage diverse teams are essential for success.

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