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QA Operations Supervisor

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Company :
American Regent, Inc.

Location :
New Albany, Pennsylvania

Expiry Date :
Fri, 05 Feb 2021 23:59:59 GMT

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Description :
American Regent, Inc., a Daiichi Sankyo Group Company, develops, manufactures, and supplies high quality sterile injectables for healthcare providers, clinics, hospitals and veterinary practices across the United States and Canada. We have locations in New York, Ohio, and Pennsylvania and sales territories nationwide. Nature and Scope This position, reporting to the QA Manufacturing Operations Manager, is responsible for leading QA Operations activities at a sterile manufacturing site. Essential Duties and Responsibilities Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. – Supervise QA Technicians to assure timely and quality oversight of daily production activities including materials receipt/release, manufacturing/filling and packaging. – Lead on-site QA activities in investigating deviations or compliance issues associated with daily manufacturing operations. – Identify and facilitate the resolution of quality issues including deviations, investigations and CAPA in conjunction with senior QA staff. – Identify and facilitate quality process improvements to increase efficiencies and performance of systems, operations and personnel. – Write and revise SOP’s and other GMP documentation. – Ensure all work is performed and documented in accordance with existing Company policies and procedures, as well as cGMP and health and safety requirements. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. – Associate’s or Bachelor’s Degree in Life Sciences, Business or related field is required. – Minimum of 2 years of work experience in QA, Regulatory, Compliance or Pharmaceutical Operations in a cGMP environment is required. – Minimum of 1 year supervisory experience required including managing day-to-day activities of subordinates, contributing to annual reviews and supervising projects – Experience in sterile pharmaceutical manufacturing preferred. – Extensive knowledge of cGMPs and other regulatory standards for Finished Product manufacturing. – Demonstrated success in managing multiple activities at the same time and producing outstanding results. – Excellent organizational, interpersonal and communication skills (oral and written). Physical Environment and Requirements – Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees. – Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. ##Job Category: Quality Affairs## We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.