Validation Engineer Pharma
Listed on 2026-07-21
-
Pharmaceutical
Pharmaceutical Manufacturing, Pharma Engineer, Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
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.
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
- 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
- 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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