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Validation Engineer Pharma

Job in 5830, Boxmeer, North Brabant, Netherlands
Listing for: Oxford Global Resources
Full Time position
Listed on 2026-07-21
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Pharma Engineer, Quality Engineering
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 4680 - 6400 EUR Monthly EUR 4680.00 6400.00 MONTH
Job Description & How to Apply Below
Overview   Are you interested in working at the intersection of pharmaceutical manufacturing, process validation, and sterile production? We are looking for a  Validation Analyst  to support a large-scale validation project within  MSD Animal Health . In this role, you will contribute to ensuring compliance, product quality, and reliable sterile manufacturing processes within a highly regulated GMP environment.

Job Description    MSD Animal Health  is a global leader in the pharmaceutical industry, where quality, compliance, and continuous improvement are at the heart of operations. This newly created project-based role focuses on the validation and optimization of sterilization and filtration processes within a sterile manufacturing environment.
In this position, you will investigate and evaluate filtration processes to ensure they meet sterilization and regulatory requirements. You will develop, execute, and document validation activities, including protocols, reports, and technical assessments in accordance with GMP standards.

This role offers the opportunity to make a direct impact on critical manufacturing processes within an international and highly regulated pharmaceutical environment.
Responsibilities     Investigate, analyze, and optimize filtration and sterilization processes
Develop, execute, and document validation protocols, reports, and technical assessments
Ensure GMP compliance throughout all validation activities
Support process improvements within a sterile manufacturing environment
Collaborate with Engineering, Manufacturing, Quality, and other cross-functional stakeholders
Identify, assess, and implement improvements related to filtration and sterilization processes
Profile     Degree in Pharmaceutical Sciences, Chemical Engineering, Life Sciences, Biotechnology, or a related field
5-6 years experience within the pharmaceutical industry
Proven experience writing validation protocols, statements, reports, and GMP documentation
Strong knowledge of GMP regulations and validation principles
Understanding of filtration and sterilization processes
Strong analytical and communication skills in English is required
Employment Conditions     Contract Type:
Employment through Oxford Global Resources
Duration: 12 to 18 months
Salary Range: €4,680 - €6,400 gross per month

Working Hours:

40 hours per week
Region:
Boxmeer
Reference: 27440

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Position Requirements
5+ Years work experience
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