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Validation Engineer

  • ... Posted on: Feb 23, 2026
  • ... Meet Life Sciences
  • ... DACH, null
  • ... Salary: Not Available
  • ... Full-time

Validation Engineer   

Job Title :

Validation Engineer

Job Type :

Full-time

Job Location :

DACH null United States

Remote :

No

Jobcon Logo Job Description :

Validation Engineer / Validation SpecialistLocation: DACH Region (Germany / Austria / Switzerland) Employment Type: Full-time, 1 year Contract Industry: Pharmaceuticals / Biotechnology / Medical DevicesAbout the RoleWe are looking for a motivated Validation Engineer / Validation Specialist to support commissioning, qualification, and validation activities within a regulated GxP environment. In this role, you will contribute to ensuring that systems, equipment, and processes meet regulatory, quality, and compliance requirements while supporting complex industrial projects on site.You will work in dynamic project environments, collaborating with cross-functional teams and applying your technical expertise to a variety of validation challenges across the DACH region.Key ResponsibilitiesPlan, prepare, execute, and document validation activities (DQ, IQ, OQ, PQ)Support commissioning and qualification of equipment, processes, utilities, and/or computerized systemsPrepare and review validation documentation, including validation plans, protocols, and reportsEnsure compliance with GMP, GxP, and applicable regulatory guidelinesCoordinate validation activities in line with project milestones and schedulesCollaborate with Quality, Engineering, Manufacturing, IT, and external vendorsSupport audits and inspections by internal and external regulatory authoritiesManage deviations, change controls, CAPAs, and risk assessments related to validation activitiesMonitor progress, report key deliverables, and contribute to issue resolutionYour ProfileBachelor’s or Master’s degree in Engineering, Life Sciences, Pharmacy, or a related technical fieldExperience in validation and/or commissioning within a regulated industry (pharma, biotech, medical devices)Solid understanding of GMP/GxP requirements and regulatory expectationsExperience with validation documentation in quality-managed environmentsStructured, detail-oriented, and analytical working styleStrong communication skills and ability to work in cross-functional teamsWhat We OfferChallenging and varied projects in a regulated, high-quality environmentOpportunities for professional development, training, and career growthCompetitive salary and benefits packageFlexible working models depending on project and locationSupportive, collaborative, and quality-focused work cultureInterested?If you are passionate about quality, compliance, and technical excellence and would like to contribute to high standards in regulated industries, we look forward to receiving your application.You can apply directly by sending your CV to

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Jobcon Logo Position Details

Posted:

Feb 23, 2026

Reference Number:

28140_4364558863

Employment:

Full-time

Salary:

Not Available

City:

DACH

Job Origin:

APPCAST_CPC

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Validation Engineer / Validation SpecialistLocation: DACH Region (Germany / Austria / Switzerland) Employment Type: Full-time, 1 year Contract Industry: Pharmaceuticals / Biotechnology / Medical DevicesAbout the RoleWe are looking for a motivated Validation Engineer / Validation Specialist to support commissioning, qualification, and validation activities within a regulated GxP environment. In this role, you will contribute to ensuring that systems, equipment, and processes meet regulatory, quality, and compliance requirements while supporting complex industrial projects on site.You will work in dynamic project environments, collaborating with cross-functional teams and applying your technical expertise to a variety of validation challenges across the DACH region.Key ResponsibilitiesPlan, prepare, execute, and document validation activities (DQ, IQ, OQ, PQ)Support commissioning and qualification of equipment, processes, utilities, and/or computerized systemsPrepare and review validation documentation, including validation plans, protocols, and reportsEnsure compliance with GMP, GxP, and applicable regulatory guidelinesCoordinate validation activities in line with project milestones and schedulesCollaborate with Quality, Engineering, Manufacturing, IT, and external vendorsSupport audits and inspections by internal and external regulatory authoritiesManage deviations, change controls, CAPAs, and risk assessments related to validation activitiesMonitor progress, report key deliverables, and contribute to issue resolutionYour ProfileBachelor’s or Master’s degree in Engineering, Life Sciences, Pharmacy, or a related technical fieldExperience in validation and/or commissioning within a regulated industry (pharma, biotech, medical devices)Solid understanding of GMP/GxP requirements and regulatory expectationsExperience with validation documentation in quality-managed environmentsStructured, detail-oriented, and analytical working styleStrong communication skills and ability to work in cross-functional teamsWhat We OfferChallenging and varied projects in a regulated, high-quality environmentOpportunities for professional development, training, and career growthCompetitive salary and benefits packageFlexible working models depending on project and locationSupportive, collaborative, and quality-focused work cultureInterested?If you are passionate about quality, compliance, and technical excellence and would like to contribute to high standards in regulated industries, we look forward to receiving your application.You can apply directly by sending your CV to

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