{"id":3768997,"url":"https://alion.io/job/seran-bioscience-quality-control-scientist-ii-swing-shift","title":"Quality Control Scientist II, Swing 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":"2026-11-08T05:47:12Z"}},"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":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"HPLC","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-11-04T19:06:06Z","employer_posted_date":"2026-11-04","last_verified_at":"2026-11-08T22:41:01Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"Serán BioScience is searching for an experienced Quality Control Scientist II to support an extended manufacturing schedule. This role would support all testing functions for Quality Control, primarily focused on in-process control lab methods to ensure manufacturing excellence. The Scientist II needs to exhibit experience and confidence within a cGMP laboratory with proficiency in analytical equipment operations and data record management.\nThe swing shift is a consistent weekly schedule of four 10-hour shifts, Monday - Thursday from 2:00 pm - 1:00 am. A shift differential of 10% of base salary will be applied. Salary is commensurate with experience.\nDuties and Responsibilities\nAdheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies\nPerforms routine extractions for dissolution, assay, and impurities testing\nPerforms routine testing using analytical equipment including but not limited to KFC, dissolution apparatus, water activity, FTIR, etc.\nConducts appearance testing, raw materials sampling, solution preparation, and pH measurements\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\nConducts peer review of routine testing at the discretion of management\nPerforms hypothesis testing or investigative work for OOS results under management and SME guidance\nTrains and mentors staff on established processes and procedures\nDemonstrates cross-functional support capabilities with other QC teams\nResponsibilities may increase in scope to align with company initiatives\nPerforms other related duties as assigned \nRequired Skills and Abilities\nProven analytical instrumentation experience (preferably HPLC) with at least 1-2 years in a cGMP pharmaceutical industry laboratory \nCommunicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company\nFollow detailed written and oral instructions\nDemonstrated ability to collaborate and work in cross-functional teams\nStrong organizational skills and attention to detail\nMultitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs\nStrong analytical and problem-solving skills\nAccepts feedback from a variety of sources and constructively manages conflict\nAbility to prioritize tasks and to keep leadership apprised of performance to timelines\nExperience with Empower preferred\nProficient with Microsoft Office Suite or related software\nEducation and Experience\nBachelor’s degree in a scientific discipline or related field\nMinimum of 3 years of dedicated lab experience \nRequires 2 years of GMP experience \nPhysical Responsibility\nProlonged periods of sitting or standing at a desk and working on a computer.\nProlonged periods of standing or sitting while monitoring laboratory equipment.\nMust be able to lift up to 15 pounds at times.\nAdheres to consistent and predictable in-person attendance.","description_format":"text","description_chars":3085,"description_truncated":false,"requirements":{"experience_years_min":3,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["CRO & CDMO Services","APIs & Drug 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