Job Title: QA Specialist III
Location: Slough (Onsite)
Duration: 5 months contract
Job Description
- Setting up and assisting in the implementation of new DMS and quality records global systems, including clean-up activities, preparation work, validation and qualification support, enrolment in the online training program, and alignment with stakeholders to ensure a robust system implementation.
- Provide regular updates on the project realization to line manager and/or Senior leadership team where required.
- Monitoring internal quality records to ensure timely completion, where applicable.
- Perform and support deviation or investigation where applicable
- Performing all business related activities as reasonably requested and instructed by the line manager or senior management team.
- Taking personal responsibility for fostering a strong quality culture.
Qualifications
- Required: B.Sc or equivalent experience
- Field of Study: Life Science or QA discipline
Work Experience
- Area: Minimum 5 years’ experience in pharmaceutical or CDMO industry in QA relevant roles, Level: Advanced – 5-10 years
Area: Extended experience in PQS systems, deviation, investigations, Level: Advanced – 5-10 years
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