GSK

Senior Validation Engineer

GSK$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 8+ years of relevant technical experience with 5+ years in validation within a regulated environment.
  • Bachelor's degree in engineering, life sciences, computer science, or related field; or associate’s degree with 8+ years technical experience.
  • Experience with Microsoft Windows OS configuration, process control systems, and executing validation protocols.
  • Strong background in hardware/software validation including IQ, OQ, PQ protocols.

Responsibilities

  • Lead validation test activities and drive resolution of deviations.
  • Coordinate cross-functional teams and maintain validation project plans.
  • Mentor junior staff to ensure consistent execution of validation standards.
  • Oversee development and approval of validation studies and protocols.
  • Guide development of specifications and ensure regulatory compliance.
  • Create and update policies and procedures related to computer system validation.
  • Set priorities and ensure timely completion of validation activities across departments.

Benefits

  • Opportunities for career growth and skill development.
  • Visibility through high-impact projects and initiatives.
  • Focus on meaningful work and continuous learning.
  • Commitment to diversity and inclusion within the workplace.
Full Job Description

Position Summary:

This role will be responsible for understanding modern computer systems and control/digital systems within the facility.It is important for the individual to have a background that will enable appropriate decision making to ensure the success of the facility. You will lead and execute validation projects for equipment, facilities, utilities, and computerized systems. You will write and review validation protocols, run or supervise testing, analyze results, and author final reports. You will work closely with engineering, quality, operations, and IT teams. We value practical problem solving, clear communication, and a focus on continuous improvement. This role offers growth, visible impact on regulated manufacturing, and alignment with our mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities:


This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Lead validation test activities, collect and analyze data, and drive timely resolution of deviations. Plan, write, and execute validation protocols and final reports for equipment, utilities, facilities, and computerized system.

  • Coordinate cross-functional teams, vendors, and contractors to meet project timelines. Maintain and update validation project plans and the Site Validation Master Plan.

  • Mentor and coach junior validation staff to build capability and consistency in execution. Support audits and regulatory inspections by preparing documentation and responding to findings.

  • Oversee the development of, and participate in, required validation studies and protocols for analytical equipment and computer systems and lead the effort to approve protocols and associated reports.

  • Assist and guide the development of specification documentation to ensure it complies with current validation standards and QMS methodologies, and systems are able to be adequately validated.

  • Development of procedures, practices, and policies related to computer system validation. Monitor and update the Validation Master Plan to ensure that it complies with appropriate regulatory guidelines and standard practices.

  • Provide leadership in setting priorities, fulfilling customer needs, defining timelines, and tracking projects.  Ensure team deliverables are met within defined timelines. Interface with other departments to coordinate resources and complete validation activities in a timely manner.

  • Development of Validation Project Plans to support major changes to the site and develop the team to become proficient in validation activities (e.g. analytical equipment qualification and computer system validation).



Basic Qualifications:


We are seeking professionals with the following required skills and qualifications to help us achieve our goals.

  • 8+ years of relevant technical experience with a minimum 5 + years’ hands-on validation experience in a regulated environment (equipment, facility, utilities, or computerized systems).

  • Bachelor’s degree in engineering, life sciences, computer science, or a related technical field or associate's degree in engineering, life sciences, biology with 8 plus years of technical experience.

  • Experienced required with hardware, software, specifically, Microsoft Windows operating system settings and configuration, process control systems, databases, writing and executing IQ, OQ, PQ or equivalent validation protocols.

Preferred Qualifications:


If you have the following characteristics, it would be a plus:

  • Advanced degree in engineering, life sciences, or related discipline.

  • Experience leading projects or supervising small technical teams.

  • Experience with computerized system validation, including lifecycle documentation and 21 CFR Part 11 concepts.

  • Familiarity with commissioning and qualification of utilities and automation systems.

  • Training in Lean, Six Sigma, or continuous improvement methods.

  • Strong interpersonal skills and experience working with cross-functional stakeholders.


What we offer:


You will join a team focused on meaningful work and continuous learning. You will gain visibility through high-impact projects and expand your technical and leadership skills. If you want to grow your career while helping deliver high-quality, compliant operations, we want to hear from you.

Apply now and tell us how your experience can help the team move forward. We encourage applications from people with diverse backgrounds and experiences who value inclusion and teamwork.

#LI-GSK

#GSKCareers

Please visit  to learn more about the comprehensive benefits program GSK offers US employees.

About GSK

GSK is a British multinational pharmaceutical company that specializes in researching, developing, and manufacturing a wide range of prescription drugs and vaccines. The company was founded in 2000 through the merger of Glaxo Wellcome and SmithKline Beecham. GSK's products are used to treat a variety of conditions including respiratory diseases, HIV/AIDS, and cancer. The company operates in over 150 countries and has a workforce of over 99,000 employees. GSK is headquartered in Brentford, England and is listed on the London Stock Exchange and the New York Stock Exchange.
Learn more about GSK
Size
90,096 employees
Market Cap
$71.6 billion
Industry
Net Income
$5.7 billion
Founded
1929
5 Year Trend
+4.1%
Revenue
$34 billion
NASDAQ

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