
Website Pfizer
Job Description:
The position will support the Pfizer Sanford, NC Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, validation, and stability. Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; assist QC authors with document formatting/template updates, review, and approval processes; conduct manual holder tasks; perform administrative training tasks; and initiate noncomplex change controls.
Job Responsibilities:
- provide tracking and metrics for documents processed
- initiates noncomplex change controls
- conducts manual holder tasks
- assists QC authors with document formatting/template updates, review process, and approval processes
- APRR authoring and reviewing
Job Requirements:
- Intellectual capability to perform complex mathematical problems and perform complex data analysis.
- Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets
Qualification & Experience:
- Experience in Quality Operations
- Laboratory experience, including Cell Culture, Bioassay, Aseptic Technique, and ELISA
- 4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.
- A BS/BA Degree in Science/related field with experience in biotech or pharmaceutical industry is preferred; however, other appropriate combinations of education and/or experience in the biotech or pharmaceutical industry are suitable.
Job Details:
Company: Pfizer
Vacancy Type: Full Time
Job Location: Fayetteville, NC, US
Application Deadline: N/A
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