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Job Details


Biogen

Associate II, Quality Assurance (Swing Shift)

Life, Physical, and Social Science

All

Yearly

Full Time

No

Research Triangle Park, North Carolina, United States

Job Description About This Role The incumbent will perform a wide variety of activities to ensure the quality and safety of our products. Primarily, this role provides on-the-floor quality oversight of GMP manufacturing activities. Those activities include review of batch record pages, logbooks, equipment reports, and directly collaborating with Manufacturing Associates to assist with problem resolution. Additionally, activities include, but not limited to, the following: Data and Documentation Review and Analysis, Batch Record Review, and Deviations. This role will mirror the parenteral facility (PF) manufacturing operation in that it will follow a 12-hr/day shift schedule. *Please note that this is a Swing Shift position and will work a traditional "2-2-3 Manufacturing Rotation from 6am to 6pm, on a 12hr/shift schedule”. What You’ll Do Provide quality oversight during batch manufacturing Primary point of contact for issues that need immediate corrective action plans, product impact assessments and decisions with respect to batch discrepancies Responsible for compliance monitoring of the manufacturing area Reviews documents (e.g., production records, test methods, raw data, and certificates of analysis) for compliance and determines acceptability for use in GMP production activities and/or release of product for further processing and/or distribution Assesses criticality of exceptions/investigations for product impact Performs thorough reviews of the investigations and provides feedback to the department owner Collaborates with associated departments to determine the appropriate CAPA Responsible for controlling master production records and issuing working copies of these records according to the production scheduled Records are printed and verified to be accurate prior to issuance Assures compliance against applicable PRCD’s providing QA controlled document creation, revision, retirement, and issuance requirements Who You Are You enjoy drug production activities with a passion to build strong collaborative partnerships with cross functional teams. You have an enthusiasm for learning new technological skills and being solutions oriented. Qualifications Required Skills Minimally BA/BS in Life Sciences with 1-2 years of relevant industry experience required. Attention to detail Good organizational skills Developing ability to multi-task and coordinate multiple activities in parallel with a sense of urgency Ability to prioritize, plan and schedule Strong oral and written communication skills Investigative decision-making skills Problem identification and resolution skills Flexibility supporting schedule and manufacturing activities Additional Information Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.