Cleaning Validation Specialist
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Sjælland / Denmark
Engaging, representing, being Black Swans
Your Life Science Career Partner
A vital role ensuring patients’ safety never gets compromised, by maintaining qualified cleaning processes and procedures, as well as designing and implementing new cleaning procedures. Essentially you aspire to be a specialist in everything relating to aseptic behavior and protocol.
Maintain and ensure equipment qualification and validation by cleaning and taking samples as well as risk assessments. You’ll establish evidence that cleaning processes for manufacturing equipment prevent product contamination. You’ll be responsible for documentation to demonstrate Current Good Manufacturing Practice (CGMP) for finished pharmaceuticals. You’ll work on-site with customers, making it valuable that you’re service-minded.
A small consulting agency ensuring compliance in pharma, biotech, and medical devices. You’ll have close involvement in decision-making along with a flexible setup, and ample opportunities for growth and development. This company values quality over quantity, preferring a small workforce of 15 skilled and talented employees where everyone is acquainted with each other. They are placed in beautiful, rural surroundings.
- Solid experience composing cleaning validation strategies and documentation
- Experience with validation and qualification on equipment and processes
- Experience with risk assessment, GMP and QMS
- An educational background in either engineering or chemistry
- A flexible, enterprising and problem-solving approach to your work
If you want to hear more about this opportunity and the company, or if you have any questions regarding the position, please do not hesitate to contact us. If you wish to apply for the position, please send an updated version of your CV, together with what questions you might have, and we will get in touch with you soon.