Create, maintain, and revise, forms, standard operating procedures, batch records, and material specifications to improve efficiencies while enhancing company GMP compliance. Author and collaborate with authors/initiators of Manufacturing/Packaging/Laboratory Notice of Events (NOEs) and Investigations and subsequently identify appropriate Corrective and Preventative Actions (CAPAs).
Qualified candidates must be legally authorized to be employed in the United States. UPM does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Essential Duties and Responsibilites
Education/Experience:
Bachelor’s degree in a science/engineering related field and at least five years of pharmaceutical experience in a GMP environment, or equivalent combination of education and experience.Qualified candidates must be legally authorized to be employed in the United States. UPM does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
To apply, send resume and salary requirements to:
humanresources@upm-inc.com
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