{"id":2136985,"url":"https://alion.io/job/biogen-sr-associate-i-quality-control-microbiology","title":"Sr Associate I, Quality Control Microbiology","company":{"id":449685,"name":"Biogen","domain":"biogen.com","url":"https://alion.io/company/biogen-2","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":79,"open_postings":18,"ghost_share":0,"stale_share":0.833,"repost_share":0,"time_to_fill_p50_days":33,"computed_at":"2026-10-21T05:46:15Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Research Triangle Park, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":81000,"max":105000,"currency":"USD","period":"year","gross":null,"usd_annual":105000},"salary_estimate":null,"experience_years_min":4,"visa_sponsorship":false,"relocation_package":false,"has_equity":true,"technologies":[{"name":"GMP","optional":false},{"name":"LIMS","optional":false},{"name":"GLP","optional":true},{"name":"Veeva","optional":true}],"status":"live","first_seen_at":"2026-10-08T00:00:00Z","employer_posted_date":"2026-10-08","last_verified_at":"2026-10-21T16:03:39Z","board_verified":true,"closed_at":null,"days_open":13,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":13},"description":"Schedule: This onsite position operates on 10-hour shifts from Sunday through Wednesday during the first shift (8AM-6PM), with some occasional support required outside of those hours.\nAbout This Role\nWe are seeking a highly motivated QC Microbiology Sr Associate I to support microbiological testing of in-process and raw materials, and environmental/utilities monitoring at RTP drug substance manufacturing facility. The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory. The Sr. Associate I performs and trains other team members on the microbial testing of all in-process drug substance, EM/UM, and raw materials samples. Additionally this role is responsible for method qualification and projects as assigned.\nWhat You’ll Do\nReview test data in LIMS\n\nPrepare quarterly EM/UM reports\n\nSupports testing for all qualification and study directed testing\n\nTroubleshoot complex assays\n\nPerform microbiology testing (e.g. Bioburden, Endotoxin, plate reading, and microbial identification) following standard procedures\n\nConduct routine Environmental Monitoring (viable and non-viable) in controlled manufacturing areas\n\nCollect and process utility and compressed gas samples\n\nComply with SOPs and controlled documents under minimal supervision\n\nMaintain laboratory cleanliness, equipment readiness, and inventory\n\nPerform investigations (i.e. laboratory and deviations)\n\nFollow site safety and contamination control policies\n\nWork overtime as required by business needs\n\nPerform other assigned duties\n\nWho You Are\nSomeone who demonstrates strong attention to detail and analytical skills, along with a solid commitment to maintaining data integrity and quality\n\nYou possess a collaborative approach and work effectively across manufacturing and facilities teams\n\nRequired Skills\nBachelor’s in Microbiology, Biology, or related field\n\nMinimum 4 years’ experience in pharmaceutical microbiology and GMP-regulated manufacturing\n\nLIMS experience, including using electronic notebooks\n\nDemonstrated knowledge of microbiological assays (bioburden, endotoxin, environmental monitoring), aseptic techniques, and general laboratory techniques\n\nExperience with document control including reviewing and editing technical documents\n\nIntermediate familiarity with fundamental statistical tools to analyze data in relation to trends results\n\nAble to follow procedures and complete technical tasks\n\nCan meet cleanroom and aseptic gowning requirements\n\nPhysically able to stand long periods, bend, move carts, and lift 25 lbs\n\nStrong written and verbal communication skills, along with proficiency in Microsoft Word and Excel\n\nExcellent organizational skills with the ability to prioritize, follow through on tasks, and meet deadlines\n\nPreferred Skills\nAdvanced knowledge of Microbiology testing and Microbiology theory\n\nPrior experience in utilities monitoring, including gas monitoring\n\nPrior training experience, including classroom training\n\nProficient in using LIMS systems, Veeva, Kneat, and Microsoft software\n\nKnowledgeable in GMP, GLP, and GDP requirements\n\nAdvanced knowledge of all compendial test methods (Bioburden, Endotoxin, Sterility testing)\n\nLEAN lab and Six Sigma training and/or certification\n\nAdvanced experience with microbial ID systems, ability to troubleshoot complex equipment and instrumentation (MALDI, MicroSeq)\n\nExperience performing EM/UM excursion investigations\n\nJob Level: Professional Additional Information\nThe base compensation range for this role is: $81,000.00-$105,000.00Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.\nRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.\nIn addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:\nMedical, Dental, Vision, & Life insurances\nFitness & Wellness programs including a fitness reimbursement \nShort- and Long-Term Disability insurance\nA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)\nUp to 12 company paid holidays + 3 paid days off for Personal Significance \n80 hours of sick time per calendar year\nPaid Maternity and Parental Leave benefit \n401(k) program participation with company matched contributions\nEmployee stock purchase plan \nTuition reimbursement of up to $10,000 per calendar year \nEmployee Resource Groups participation\nWhy Biogen?\nWe are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.\nAt Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.\nAll qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. 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