CMC Technical Writer - Tech Transfer & Process Chemistry

Eurofins PSS Insourcing Solutions

Boston (MA)

Hybrid

USD 55,000 - 68,000

Full time

20 hours ago

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Benefits offered by this job

Medical coverage

Dental and vision

Life insurance

Disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions seeks a CMC Technical Writer to support Late-Stage Lipids Technical Transfer and Process Chemistry. You will translate small molecule synthesis data into clear, scientifically rigorous reports and maintain documentation for regulatory readiness.

The role requires a strong science background, cGMP experience, and the ability to produce first drafts with minimal SME input. Excellent communication and teamwork are essential.

Qualifications

B.S./M.S./PhD with 2+ years (MS) to 6+ months (PhD) of industry process chemistry or related experience.
Strong written and verbal English communication.
Knowledge of cGMP documentation standards and ICH guidelines relevant to process development.

Responsibilities

Draft conclusion-driven process development reports from protocols and SME input.
Structure reports per internal templates and late-stage CMC documentation standards.
Transform raw data into tables, figures and summaries for reports.
Produce complete first drafts requiring minimal SME revision.
Maintain traceable, inspection-ready source documentation for submissions.
Collaborate across process development teams to align reporting and workflows.

Skills

English fluency

cGMP knowledge

Attention to detail

Written communication

Independent work

Project coordination

Education

B.S. in chemistry, engineering or related field

M.S. in chemistry, engineering or related field

PhD in chemistry, engineering or related field

Tools

MS Word

Excel

Veeva Vault or Documentum EDMS

Job description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

Job Description

As a CMC Technical Writer, you will have an integral role in Late-Stage Lipids Technical Transfer and Process Chemistry supporting novel gene editing products. The successful candidate will possess a solid understanding of small molecule synthesis and purification processes, enabling effective engagement with project teams and the translation of technical progress into clear, concise, and scientifically rigorous documentation. The documentation will serve as a critical foundation for late-stage process characterization and regulatory readiness. The successful candidate will be responsible for driving the documentation and scientific narrative of process characterization efforts in parallel with the process SMEs. Their ability to independently develop high-quality, conclusion-driven reports and capture process knowledge in a structured manner will meaningfully expedite development timelines, improve documentation efficiency, and contribute significantly to overall project success.

Key Responsibilities:

Independently draft conclusion-driven process development reports from protocol objectives and minimal SME input, translating key findings, observations, and outcomes generated by CDMOs into clear scientific narratives.
Develop and structure reports in alignment with internal templates and late-stage CMC documentation standards, incorporating appropriate scientific rationale, data presentation, references, and well-supported conclusions.
Transform raw experimental data (in-process controls, yield/purity results, scale comparisons, and equipment parameters) into coherent tables, figures, and summaries without requiring process SME to pre-develop the report storyline.
Produce substantively complete first drafts that require minimal SME revision, reducing review cycles and enabling efficient documentation of development activities.
Maintain traceable and inspection-ready source documentation to support regulatory submissions, process knowledge management, and lifecycle documentation requirements.
Collaborate across broader process development functions to establish best Documentation practices, support process characterization initiatives, and align reporting approaches and work packages across diverse modalities and programs.

Minimum Required Qualifications:

B.S. degree in chemistry, engineering, or related scientific field with 4+ years of industry process chemistry experience. M.S. degree in chemistry, engineering, or related scientific field with 2+ years of industry process chemistry experience. PhD in chemistry, engineering, or related scientific field with 6 months+ of industry process chemistry experience.
Strong written and verbal communication skills, with professional fluency in English.
Working knowledge of cGMP documentation standards, 21 CFR Part 211, and ICH Q guidelines relevant to process development and manufacturing.
Proficiency in MS Word, Excel; experience with at least one EDMS platform (Veeva Vault, Documentum, or similar).
Experience in process characterization, process chemistry, and process development including purification chromatography and scaling design.
Strong foundation in compliance expectations for late-stage characterization work.
Attention to detail, critical analysis of data/reports, and troubleshooting abilities.
Proven ability to take initiative to achieve results, keep projects on timeline, and find solutions as needed to ensure that project deliverables are met.
Excellent interpersonal communication skills and previously demonstrated the ability to interact within a multi-disciplinary team.
Ability to meet deliverables with little supervision, manage priorities independently, highly organized, and self-motivated.
Ability to work in the United States indefinitely without sponsorship or restriction

Preferred Qualifications:

Experience in RNA-LNP process chemistry and process development is preferred.
Experience with RNA-LNP process characterization is highly desirable.
Familiarity with process characterization activities, including risk assessments, design of experiments (DOEs), process performance evaluation, and late-stage CMC documentation practices.

Additional Information

Position is Full Time, Monday-Friday, 8am-5pm. Hybrid schedule with a minimum of three days per week onsite. Specific days onsite will be determined by business needs and subject to change. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.

Excellent full-time benefits include: