{"id":3768998,"url":"https://alion.io/job/seran-bioscience-quality-control-scientist-iii-in-process-control-day-shift","title":"Quality Control Scientist I/II, In-Process Control- Day Shift","company":{"id":686143,"name":"Serán Bioscience","domain":"seranbio.com","url":"https://alion.io/company/seranbio","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":{"grade":"A","score":95,"open_postings":12,"ghost_share":0,"stale_share":0,"repost_share":0,"time_to_fill_p50_days":101,"computed_at":"2026-11-09T06:03:00Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bend, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GMP","optional":false},{"name":"HPLC","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-11-04T19:03:14Z","employer_posted_date":"2026-11-04","last_verified_at":"2026-11-10T04:01:06Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"description":"Serán BioScience is looking for a scientist with laboratory experience to support manufacturing of pharmaceutical drug products within our In-Process Control group. As a scientist within the Quality Control department you will work alongside a team of scientists and operators to ensure the highest quality product by testing raw materials and production equipment within GMP manufacturing and laboratory environments. Qualified candidates will demonstrate expertise in utilizing specialized laboratory equipment, techniques, and methodologies for technical assessments and data analysis purposes. Preference will be given to those with experience in GMP environments and technical data review specific to the pharmaceutical industry.\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\nDuties and Responsibilities\nAdheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies \nPerforms routine testing using analytical equipment including but not limited to HPLC, GC, KFC, Disso, etc. \nConducts appearance testing, solution preparation, raw material sampling, and pH measurement\nDrafts stability tables, sets-up stability studies, logs-in samples and standards\nCleans lab and glassware and disposes of analytical waste appropriately\nParticipates in process improvement and other non-routine projects\nEnters clean spaces with appropriate PPE to collect various samples\nIs familiar with introductory analytical equipment (e.g., HPLC, GC-HS, TOC, FT-IR)\nIs familiar with raw materials testing requirements (compendial and client testing)\nConducts peer review of routine testing at the discretion of the relevant supervisor\nPerforms technical writing and reporting including but not limited to: incident reporting, laboratory investigations, CAPAs, SOPs, trend reports, risk assessments, etc.\nPerforms hypothesis testing or investigative work for OOS results under management and SME guidance \nDemonstrates cross-functional support capabilities with other QC teams\nResponsibilities may increase in scope to align with company initiatives\nAll other related duties as assigned\nRequired Skills and Abilities\nHands-on lab experience in HPLC, CG-HS, TOC, FT-IR\nHands-on lab experience with raw materials testing\nStrong verbal and written communication skills\nDemonstrated ability to collaborate and work in cross-functional teams\nStrong organizational skills and attention to detail\nFollows detailed written and oral instructions\nStrong time management skills with a proven ability to meet variable and competing deadlines\nStrong analytical and problem-solving skills\nCommunicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company\nMultitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs\nAccepts feedback from a variety of sources and constructively manages conflict\nAbility to prioritize tasks and to keep leadership apprised of performance to timelines\nAbility to function well in a high-paced and at times stressful environment\nProficient with Microsoft Office Suite or related software\nEducation and Experience\nBachelor's degree in related scientific discipline\n3 years of hands-on laboratory experience required, cGMP preferred\nMinimum of 2 years of GMP experience required to be considered for Scientist II\nPhysical Requirements\nProlonged periods of sitting or standing at a desk and working on a computer\nProlonged periods of sitting or standing in laboratory environment\nMust be able to lift up to 25 pounds at times\nAdheres to predicable in-person attendance\nMotor skills required for basic laboratory 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