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Our client, a leading life sciences company based in Leiden, is seeking an experienced Validation Expert to support ongoing equipment periodic reviews and Computer System Validation (CSV) activities. As the Validation Expert, you will play a crucial role in ensuring GMP compliance across critical systems and equipment within the site.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Expert will be varied; however, the key duties and responsibilities are as follows:
1. Execute and document periodic reviews of GMP-regulated equipment in accordance with internal validation and quality standards.
2. Support and contribute to Computer System Validation (CSV) activities as needed across the site.
3. Review existing validation documentation and ensure alignment with current regulatory and internal standards.
4. Collaborate with Quality, Engineering, and IT departments to ensure timely and compliant execution of validation tasks.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Validation Expert we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Extensive industry experience in a GMP-regulated validation environment, preferably within pharmaceuticals or biotechnology.
3. A working knowledge and practical experience with equipment validation and periodic review processes.
Key Words: Validation Expert / GMP compliance / Computer System Validation / CSV / equipment validation / life sciences / pharmaceuticals / biotechnology / GAMP 5 / data integrity / 21 CFR Part 11
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Our client, a leading life sciences company based in Leiden, is seeking an experienced Validation Expert to support ongoing equipment periodic reviews and Computer System Validation (CSV) activities. As the Validation Expert, you will play a crucial role in ensuring GMP compliance across critical systems and equipment within the site.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Expert will be varied; however, the key duties and responsibilities are as follows:
1. Execute and document periodic reviews of GMP-regulated equipment in accordance with internal validation and quality standards.
2. Support and contribute to Computer System Validation (CSV) activities as needed across the site.
3. Review existing validation documentation and ensure alignment with current regulatory and internal standards.
4. Collaborate with Quality, Engineering, and IT departments to ensure timely and compliant execution of validation tasks.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Validation Expert we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Extensive industry experience in a GMP-regulated validation environment, preferably within pharmaceuticals or biotechnology.
3. A working knowledge and practical experience with equipment validation and periodic review processes.
Key Words: Validation Expert / GMP compliance / Computer System Validation / CSV / equipment validation / life sciences / pharmaceuticals / biotechnology / GAMP 5 / data integrity / 21 CFR Part 11
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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