What are the responsibilities and job description for the Validation Specialist position at Akkodis?
Akkodis is seeking a Validation Specialist for a Contract job with a client in Swiftwater PA (Onsite).
The ideal candidate must have knowledge of GMP and Process Validation.
Validation Specialist
Key Responsibilities:
- Write protocols, reports, procedures, and memos as needed to support Adjuvant manufacturing activities related to engineering, investigational, definition, development, and process validation runs.
- Support execution and documentation of engineering, development, and/or validation studies and lead or supervise groups and/task forces in the planning of engineering, investigational, definition, development, and process validation runs.
- Input to design space/DOE studies through establishment of scale-up/scale-down parameters utilizing engineering fundamentals (mixing, mass/heat transfer, modeling, dimensionless parameters, etc.) and process control strategies.
Desired Qualifications:
- BS or MS in basic sciences, math, engineering, or pharmacy with 2 years' experience in biological processes or analytics in a cGMP environment.
We offer a competitive hourly rate based on experience, education, geographic location, and other factors. Benefits include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan.
Akkodis is an Equal Opportunity Employer/Veterans/Disabled. We will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements.
