Process Validation Engineers
- North America, United States
- Contract
- Life Sciences
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.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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Caroline
I manage this role.