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Validation Engineer II, GMP

Thermo Fisher Scientific

Validation Engineer II, GMP

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Are you ready to advance your career with a world-class team? At Thermo Fisher Scientific, we seek an ambitious, highly skilled Validation Engineer II for our validation department in Tilburg. You will ensure flawless execution of equipment, utilities, facilities qualification, and process validation activities. You will work closely with technical, development, quality, and production teams to meet world-class validation standards.

Job Description:

  • Proven hands-on experience in Commissioning & Qualification and Validation gained in a highly regulated environment within a pharmaceutical setting or equivalent

  • Demonstrates expertise in crafting new equipment, changing processes, growing production, and successfully implementing new products

  • Co-drafts User Requirement Specifications (URS) with suppliers and the multi-disciplinary team

  • Drafts validation plans and performs implementation of protocols for C&Q/IQ/OQ/PQ related to equipment, utility, facilities, including final reports and advice on periodical review frequencies

  • Ability to extract information from systems and generate Periodic Review Reports for critical equipment/utilities/processes, including Continued Process Verification (CPV)

  • Provides validation technical support within other departments

  • Drafts, reviews, and amends procedures, Validation Master Plan, and other validation audited documents

  • Responsible for ensuring the validated status of all cGMP-critical automated process applications and quality systems

  • Remains abreast of current developments and regulations for the pharmaceutical industry

  • Acts as a validation SME for internal and external audits

Qualifications requirements:

Preference for candidates with a bachelor's degree or equivalent experience in technology, science, or a related field, and a willingness to learn. Prior experience in validation, GMP, or pharmaceutical manufacturing is required. This role offers an outstanding opportunity for learning and growth in various areas.

Personal:

Integrity, Intensity, Innovation, and Involvement are core characteristics we expect of all members of our organization. If you enjoy leading change and working within a matrix organization to improve internal processes, you will discover happiness in this role!

Locations

  • Tilburg, Netherlands

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Commissioning & Qualification (C&Q)intermediate
  • IQ/OQ/PQ protocolsintermediate
  • User Requirement Specifications (URS)intermediate
  • Periodic Review Reportsintermediate
  • Continued Process Verification (CPV)intermediate
  • GMP validationintermediate
  • Pharmaceutical regulationsintermediate

Required Qualifications

  • Bachelor's degree or equivalent in technology, science, or related field (experience)
  • Prior experience in validation, GMP, or pharmaceutical manufacturing (experience)

Responsibilities

  • Draft validation plans and implement protocols for equipment/utilities/facilities
  • Co-draft URS with suppliers and teams
  • Generate Periodic Review Reports
  • Provide validation support to departments
  • Draft/review procedures and Validation Master Plan
  • Ensure validated status of cGMP-critical systems
  • Act as validation SME for audits

Benefits

  • general: Opportunity for learning and growth
  • general: Work with world-class team

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Thermo Fisher Scientific logo

Validation Engineer II, GMP

Thermo Fisher Scientific

Validation Engineer II, GMP

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Are you ready to advance your career with a world-class team? At Thermo Fisher Scientific, we seek an ambitious, highly skilled Validation Engineer II for our validation department in Tilburg. You will ensure flawless execution of equipment, utilities, facilities qualification, and process validation activities. You will work closely with technical, development, quality, and production teams to meet world-class validation standards.

Job Description:

  • Proven hands-on experience in Commissioning & Qualification and Validation gained in a highly regulated environment within a pharmaceutical setting or equivalent

  • Demonstrates expertise in crafting new equipment, changing processes, growing production, and successfully implementing new products

  • Co-drafts User Requirement Specifications (URS) with suppliers and the multi-disciplinary team

  • Drafts validation plans and performs implementation of protocols for C&Q/IQ/OQ/PQ related to equipment, utility, facilities, including final reports and advice on periodical review frequencies

  • Ability to extract information from systems and generate Periodic Review Reports for critical equipment/utilities/processes, including Continued Process Verification (CPV)

  • Provides validation technical support within other departments

  • Drafts, reviews, and amends procedures, Validation Master Plan, and other validation audited documents

  • Responsible for ensuring the validated status of all cGMP-critical automated process applications and quality systems

  • Remains abreast of current developments and regulations for the pharmaceutical industry

  • Acts as a validation SME for internal and external audits

Qualifications requirements:

Preference for candidates with a bachelor's degree or equivalent experience in technology, science, or a related field, and a willingness to learn. Prior experience in validation, GMP, or pharmaceutical manufacturing is required. This role offers an outstanding opportunity for learning and growth in various areas.

Personal:

Integrity, Intensity, Innovation, and Involvement are core characteristics we expect of all members of our organization. If you enjoy leading change and working within a matrix organization to improve internal processes, you will discover happiness in this role!

Locations

  • Tilburg, Netherlands

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Commissioning & Qualification (C&Q)intermediate
  • IQ/OQ/PQ protocolsintermediate
  • User Requirement Specifications (URS)intermediate
  • Periodic Review Reportsintermediate
  • Continued Process Verification (CPV)intermediate
  • GMP validationintermediate
  • Pharmaceutical regulationsintermediate

Required Qualifications

  • Bachelor's degree or equivalent in technology, science, or related field (experience)
  • Prior experience in validation, GMP, or pharmaceutical manufacturing (experience)

Responsibilities

  • Draft validation plans and implement protocols for equipment/utilities/facilities
  • Co-draft URS with suppliers and teams
  • Generate Periodic Review Reports
  • Provide validation support to departments
  • Draft/review procedures and Validation Master Plan
  • Ensure validated status of cGMP-critical systems
  • Act as validation SME for audits

Benefits

  • general: Opportunity for learning and growth
  • general: Work with world-class team

Target Your Resume for "Validation Engineer II, GMP" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Validation Engineer II, GMP. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Validation Engineer II, GMP" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Validation Engineer II, GMP @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.