{"id":3853878,"url":"https://alion.io/job/planet-pharma-scientist-6","title":"Scientist","company":{"id":4467183,"name":"Planet Pharma","domain":"planet-pharma.com","url":"https://alion.io/company/planet-pharma","size_band":null,"is_staffing_agency":true,"employer_type":"agency","is_intermediary":false,"listed_via":null,"ats_vendor":"Schema","truth_index":{"grade":"B","score":80,"open_postings":11,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":15,"computed_at":"2026-11-07T05:47:08Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":null,"employment_type":"contractor","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"inferred_payroll_markers","remote_working_hours":null,"hiring_geo_confidence":"inferred","locations":[],"countries":[],"hiring_countries":["US"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Chromatography","optional":false},{"name":"PCR","optional":false}],"status":"live","first_seen_at":"2026-11-06T05:02:06Z","employer_posted_date":"2026-11-06","last_verified_at":"2026-11-07T21:27:49Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Target PR Range: 27-37/hr DOE\nBiopharmaceutical leader founded on discovering, developing, manufacturing, and delivering innovative human therapeutics. Attribute Sciences group within Process Development is seeking a Scientist.\nThe Scientist role in Commercial Process Development will be part of the global method implementation team responsible for method transfer and method validation strategies, statistical analysis, and documentation for implementing methods in Quality Control for pivotal and late stage programs. The role will provide technical support for critical large projects. Strong familiarity with the following method platforms is highly preferred: Chromatography, Bioassay, Device, PCR, Microbiology, Immunoassay, CE/Gel, Viral, and General. Protocol and report authoring according to regulatory and industry guidelines (i.e., ICH) and data analysis will be a core activity in this role. Strong technical writing and data review skills required. This individual may support clinical and commercial programs and locations throughout the company under the guidance of project leads.\nBasic Qualifications: Pharma or Biotech\n* Masters degree and 2 years of Operations or Scientific experience OR Bachelors degree and 4 years of Operations or Scientific experience\nPreferred Qualifications:\n* Bachelor’s in Biochemistry, Analytical Chemistry, Physical or Life Sciences\n* Strong understanding of methods within the following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device, Viral, and General (compendia)\n* Direct experience with method transfer and method validation processes from a Pharmaceutical or Biotechnology Company.\n* Knowledge of analytical methods/technologies used in biologic and synthetic development and manufacturing\n* Excellent written and oral communication skills for the timely coordination of scientific results in a fast-paced, multi-disciplinary, team-based environment\n* Excellent 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