Validation Analyst III

Orion Group Life Sciences are looking for a Validation Analyst III for our Multinational Pharmaceutical client based in Boxmeer. Initial 12-month contract, with possibility of extension. This is an onsite position but is flexible to work max one day from home.

Main Responsibilities of the role

• Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilization validation).
• Authoring project validation master plans.
• SOP and documentation updates.
• Authoring validation protocols and final reports, executing validation studies, analysis of validation data.
• Resolving technical issues encountered during study execution.
• This individual will be required to work in a cross-functional team (in and external at our client) in a highly regulated environment.
• Works independently to accomplish validation project objectives.

Required Qualifications and skills

• Engineering or scientific background.
• (Chemical / Pharmaceutical) Equipment Validation and Sterilization Validation.
• Sterile filtration of complex oily / water mixtures.
• Strong technical writing and oral communication skills.
• Experienced in GMP and EU GMP Annex 1 rules and regulations.
• He or she has some experience with filters, and/or PUPSIT.
• Works with moderate to low work direction.
• easily adapted to IT systems.
• Has experience in change management.

If you would like to have a confidential conversation regarding this opportunity, please reach out to Tim Browaeys, [email removed] or contact Tim on [phone removed]

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