Process Validation Engineers - Pharmaceuticals - 3–6 Months initially

Are you looking for your next contract, and fancy the opportunity to work in Washington State? Our client, a global biotechnology organisation, are recruiting for a Process Validation Engineers to join their team in the construction of their new biopharmaceutical production plant. This new build facility will be vital vehicle in helping our client continue global access to life changing therapeutics.

Responsibilities include:

Generate Process validation documentation such as PVMP, PPQ and Process Validation deliverables and studies
Support PV studies and PPQ report generation
Generate Governance policies and related SOPs for Process Validation
Generate and execute individual Process validation study documentation for PPQ supporting studies such as: Mixing studies, hold time studies, impurity clearance, E&L, filter validation, container closure integrity.
Conduct project meetings as needed to discuss Process Validation strategy and timelines.
Trach each project deliverable. Manage and coordinate execution of Process Validation Activities
Collaborate with MSAT team member to ensure completeness and approvals of validation documentation.
Able to use process and templates to support Process Validation Activities.

If this role is of interest, please apply now!

#LI-CO1

We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.

Engineering Director
Global Pharmaceutical firm

List #1

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Process Validation Engineers

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