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Senior Consultant @ CPL Life Sciences - Contract Engineering UK/EU
CPL Life Sciences is working with a global Biotechnology organization to recruit a QA Validation Specialist for a 12-month contract in Visp.
Responsibilities include:
* Ensuring GMP compliance regarding equipment, facilities, and systems, aligned with regulatory guidelines.
* Understanding qualification & validation duties.
* Performing QA oversight of validation review and qualification activities.
* Conducting change control assessments.
* Understanding manufacturing equipment, autoclaves, clean utilities, shipping validation, temperature mapping, controlled storage rooms, and equipment.
* Developing validation protocols based on validation plans.
* Reviewing and approving SOPs, protocols, reports, change controls, deviations, and other records.
* Managing Quality Systems activities, including DMS, LIMS, Kneat, and Trackwise systems (change control, deviations, CAPA, etc.).
Qualifications:
* Bachelor's degree in science or technical field.
* Pharma industry experience (2-6 years).
If interested, please apply directly or email megan.smyth@cpl.com for further discussion.
Additional Details
* Seniority level: Mid-Senior level
* Employment type: Contract
* Job function: Quality Assurance
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