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Scientist Biopharma Manufacturing Quality Control Analyst II Microbiology SFD-TC, Quality Control - NC

Astellas Pharma · NC
Full-timeGeneralMid Level$69,790–$99,700/yr
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About the Scientist Biopharma Manufacturing Quality Control Analyst role

Scientist Biopharma Manufacturing Quality Control Analyst positions focus on delivering results in their domain. This page aggregates open Scientist Biopharma Manufacturing Quality Control Analyst roles and what employers typically expect.

**Scientist Biopharma Manufacturing Quality Control Analyst II Microbiology SFD-TC, Quality Control – NC** **About Astellas** Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com. **Are you driven to make a real difference in the lives of patients?** We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. **Purpose & Scope** This resource will be part of the Quality Control Microbiology team located at the Sanford TC in Sanford, NC, and will be responsible for environmental and utility sampling and testing, as well as additional lab functions as needed. This role will support QC testing for any products manufactured at the Sanford TC. The Analyst II, Quality Control Microbiology will be responsible for implementing and executing microbiological testing in support of clinical and commercial products in compliance with GMP requirements. This role will also support testing for stability studies, method validation studies and equipment validation. **Role and Responsibilities** - Schedule Environmental and Utility Monitoring, ensuring all samples are collected as required - Perform Environmental and Utility Monitoring - Author/revise technical reports and laboratory procedures - Author/review electronic database improvements - Assist in data trending and summarization - Participate in deviation and OOS investigations - Perform plate reading and generate microbial isolates - Receive, unpack and organize supplies for QC areas - Perform routine cleaning, schedule equipment preventative maintenance, and organization of laboratory areas in accordance with cGMP *Other duties as required:* - Perform release, stability, and in-process testing supporting production activities. Testing includes, but is not limited to bioburden, endotoxin, pH/conductivity - Perform growth promotion/media qualification - Perform testing in support of method transfer/validations - Participate in equipment qualification/validation studies - Perform QC lab support activities including but not limited to sample management, reagent preparation, instrumentation maintenance, and instrument calibration **Required Qualifications** - B.S. Degree in Microbiology, or other science-related degree, with 0-2+ years’ relevant industry experience in a quality control role. - Demonstrated experience of aseptic technique and common microbiological and environmental monitoring testing. - Knowledge of relevant compliance and guidance documents. - Must be able to gown into cleanrooms in support of testing and manufacturing activities. - Good documentation and data organization. - Detail oriented and willingness to learn. - Strong interpersonal skills which contribute to a supportive and positive work environment - Proven history of working in a fast-paced team environment, time management, and meeting deadlines. - Highly collaborative team player with the ability and willingness to support other colleagues in the Quality Control department. - Flexibility to cover off-shift work (e.g., weekends) will be required. **Preferred Qualifications** - Experience in a small company and high growth, fast-paced environment - Experience in qualification of analytical equipment, including those with computerized systems - Experience in method validation/qualification/verification/transfer **** **Location and Working Environment** - This position is based in Sanford, NC and will require on-site work in a cGMP regulated manufacturing facility. - This role frequently requires long peri…

Salary estimate

$69,790 – $99,700/yr
Provided by the employer.

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