{"id":1684169,"url":"https://alion.io/job/abzena-analytical-services-contractor","title":"Analytical Services Contractor","company":{"id":2138905,"name":"Abzena","domain":"abzena.com","url":"https://alion.io/company/abzena","size_band":"201-500","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":{"grade":"B","score":75,"open_postings":5,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-12T06:55:09Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":"contractor","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":[],"countries":[],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":86000,"max_usd":163000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":958},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-06-23T19:54:21Z","employer_posted_date":"2026-06-23","last_verified_at":"2026-10-12T21:20:39Z","board_verified":true,"closed_at":null,"days_open":111,"trust":{"level":"stale","repost_count":0,"flags":["stale"],"days_open":110},"description":"We are seeking a highly skilled and detail-oriented Analytical Services Contractor to support our Analytical Serviceswith documentation and data review activities. The ideal candidate will possess strong technical expertise in separation-based analytical techniques (e.g., HPLC, GC, CE-SDS) and have a solid understanding of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).\nThis individual will play a critical role in reviewing laboratory notebooks, ensuring data integrity, assessing suitability of the methods with AD management oversight, and supporting GMP-related documentation including method reviews, protocol/report reviews, and Certificates of Testing (CoT) for development batches.\nQualifications\nBachelor’s degree or higher in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.\n5+ years of industry experience in analytical development or quality control within a regulated (GMP) biopharmaceutical or pharmaceutical environment.\nStrong working knowledge of separation-based analytical techniques, particularly HPLC, GC, and CE-SDS.\nDemonstrated experience in reviewing laboratory notebooks, technical reports, and GMP documents.\nFamiliarity with method development and qualification principles.\nExcellent attention to detail, strong organizational skills, and the ability to manage multiple priorities.\nEffective communication and collaboration skills for cross-functional teamwork.\nProficiency in document management systems is a plus.\nPreferred Skills:\nExperience with stability testing and strong familiarity with ICH guidelines, including but not limited to: ICH Q1A-Q1E (Stability), ICH Q2(R2) (Analytical Method Validation), ICH Q3A/B (Impurities in Drug Substances and Products)\nSolid understanding of regulatory expectations for early-phase clinical development, including appropriate analytical data packages to support IND-enabling studies.\nPrior experience supporting IND filings is a plus.\nFamiliarity with analytical data trending, specification setting, and interpretation of development and stability data in alignment with regulatory and internal 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