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 Apply Here vacanciesforyou.net
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