{"id":3730968,"url":"https://alion.io/job/cambrex-analytical-development-technical-writer","title":"Analytical Development, Technical Writer","company":{"id":1965307,"name":"Cambrex","domain":"cambrex.com","url":"https://alion.io/company/cambrex","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"iCIMS","truth_index":null},"role":"Product","role_family":"Product","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Charles City, 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":"GMP","optional":false},{"name":"Windows","optional":false}],"status":"live","first_seen_at":"2026-11-04T08:14:16Z","employer_posted_date":"2026-11-04","last_verified_at":"2026-11-07T07:50:01Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"Company Information\nYou Matter to Cambrex.\nCambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services.\nWith over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.\nYour Work Matters.\nAt Cambrex, we strive to build a culture where all colleagues have the opportunity to:\nengage in work that matters to our customers and the patients they serve \nlearn new skills and enjoy new experiences in an engaging and safe environment\nstrengthen connections with coworkers and the community\nWe’re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!\nYour Future Matters.\nKnown for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!\nOverview:\nThe AD Technical Writer will be responsible for consistently generating high quality technical documents, such as test procedures, protocols, and reports based on data collected by other members of the Analytical Development department that meet the needs of other departments, clients, and regulators. Compliance with SOPs, cGMP, ICH, and other regulatory guidelines is required to perform most job tasks.\nResponsibilities:\nDrafting and revising controlled documents such as test procedures, method evaluation protocols, reports, and SOPs while following established guidelines for correctness, completeness, clarity, and format. \nCoordinate the approvals of these documents through the use of software such as MasterControl and TrackWise. \nCompile and present data from multiple sources such as laboratory notebooks and various laboratory instrumentation software. \nMaintain open communication with members of AD, QC, and QA to ensure timely delivery of high quality documents to support evolving business needs. \nContinuously improve documentation systems to increase efficiency and compliance with cGMP and/or other regulatory requirements. \nAll employees are required to adhere to EPA, DEA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.\nQualifications / Skills:\nAdvanced technical writing skills and the ability to communicate effectively with peers, department management, and cross-functional coworkers. \nFluent in written English. \nFamiliarity with compliance requirements within cGMP with an emphasis on method validation and reporting requirements preferred. \nDemonstrated excellence in advanced word processing using Microsoft Word. \nDemonstrated computer literacy, including spreadsheets, structural drawings, databases, and communication packages preferably in a Windows environment. \nAbility to work in a highly independent and self-directed work environment. \nEducation, Experience, and Licensing Requirements: (Text Only)\n- Bachelor’s degree in Chemistry or closely related field required. - Minimum of 2 or more years of experience in a cGMP regulated laboratory environment highly 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