CMC Technical Writer (Contract)
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What you'll do
- Translate data, parameters, and results from various CDMOs in various disciplines (analytical, drug substance, drug product) into scientific reports with appropriate scientific summaries and conclusions to support regulatory content and submissions.
- Review, revise, and finalize technical reports from CDMOs in support of program deliverables.
- Assist with document finalization and final source document organization, including but not limited to analytical methods, validation reports, method development summaries, batch records, and campaign/production reports.
- Partner with Quality on specification and retest/expiry/shelf-life documentation, as well as close coordination with Clinical Supply for investigational medicinal product documentation and alignment with Regulatory on documents for modules and submissions.
What they're looking for
- 12+ years of pharmaceutical or biotechnology industry experience with broad CMC expertise across Drug Substance, Drug Product, Analytical Development, and Regulatory CMC.
- Scientific background with strong technical writing and communication skills
- Understanding of phase-appropriate documentation to support CMC development, including regulatory guidelines and filing requirements
- Ability to simplify complex scientific terminology into high-level take home narratives for ease of review
- Proficient with document management tools
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX750) – is being developed for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.
Headquartered in Boston, Massachusetts, Centessa was recognized as a Great Place to Work® in 2026.
Description of Role
The CMC Technical Writer role will critically review data, methods, batch records, and various development, campaign, and production reports from external CDMOs to finalize source documents for analytical, drug substance and drug product. The CMC Technical Writer should also then be able to write scientific and regulatory content and author and prepare report summaries and conclusions from the source documents for final document repository.
Key Responsibilities
- Translate data, parameters, and results from various CDMOs in various disciplines (analytical, drug substance, drug product) into scientific reports with appropriate scientific summaries and conclusions to support regulatory content and submissions.
- Review, revise, and finalize technical reports from CDMOs in support of program deliverables.
- Assist with document finalization and final source document organization, including but not limited to analytical methods, validation reports, method development summaries, batch records, and campaign/production reports.
- Partner with Quality on specification and retest/expiry/shelf-life documentation, as well as close coordination with Clinical Supply for investigational medicinal product documentation and alignment with Regulatory on documents for modules and submissions.
Qualifications
- 12+ years of pharmaceutical or biotechnology industry experience with broad CMC expertise across Drug Substance, Drug Product, Analytical Development, and Regulatory CMC.
- Scientific background with strong technical writing and communication skills
- Understanding of phase-appropriate documentation to support CMC development, including regulatory guidelines and filing requirements
- Ability to simplify complex scientific terminology into high-level take home narratives for ease of review
- Proficient with document management tools
Compensation
The hourly range for this position is $120.00 to $140.00 per hour. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge.
Contractors engaged through Centessa are employed through a third-party agency that serves as the employer of record and provides access to a comprehensive benefits package. Eligible contractors may enroll in medical plans, including PPO and EPO options, as well as dental and vision coverage after 30 days. Additional perks, such as a 401(k), wellness programs, and other discounts, may also be available to eligible contractors.
Position: Temporary, non-exempt
Work Location
The CMC Technical Writer (Contract) role is a based in the US - Remote
EEOC Statement: Centessa Pharmaceuticals, a wholly owned subdisary of Eli Lilly and Company believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. We will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.
Company
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