Technical Writer

Job Summary:

The Individual is responsible for supporting GMP manufacturing operations through high‑quality technical documentation, deviation investigation ownership, and cross‑functional operational support for clinical and/or commercial drug product manufacturing. This role involves authoring, reviewing, and managing deviations, CAPAs, technical reports, SOPs, batch record updates, and manufacturing documentation to ensure compliance with cGMP regulations, principles, and internal quality standards. The candidate partners closely with Manufacturing, Quality Assurance, MS&T, Engineering, Validation, and Supply Chain teams to support timely investigation closure, process improvements, and manufacturing readiness.

Location:

Norwood, Massachusetts
Job Type: Contract
Salary: $60–$68 per hour

Work Hours:

9:00 AM – 5:00 PM

Education:

Bachelor’s degree (Master’s acceptable)

• Follow all relevant GMP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
• Practice and promote safe work habits and adhere to safety procedures and guidelines.
• Execute tasks precisely as defined in internal procedures, SOPs, and work instructions.
• Follow Good Documentation Practices (GDP) and Data Integrity requirements to ensure documentation accuracy, completeness, and inspection readiness.
• Author, revise, review, and manage manufacturing deviations, investigations, CAPAs, technical reports, and quality event documentation.
• Lead deviation investigations utilizing root cause analysis tools, including fishbone analysis, 5‑Why methodology, and risk assessments.
• Partner cross‑functionally with Manufacturing, QA, MS&T, Engineering, Validation, and Supply Chain to gather investigation data and drive timely closure of quality records.
• Support batch record review activities and identify documentation discrepancies, procedural gaps, and process improvements.
• Author and revise SOPs, work instructions, batch production records, protocols, and technical documentation to support manufacturing operations.
• Support implementation and effectiveness checks for CAPAs and continuous improvement initiatives.
• Ensure deviations and technical documents are written in a clear, concise, technically accurate, and compliant manner suitable for regulatory inspection.
• Track investigation metrics and support efforts to reduce deviation recurrence and improve closure timelines.
• Support audit and inspection readiness activities by providing documentation support and responding to quality system inquiries.
• Participate in operational excellence initiatives focused on process simplification, documentation standardization, and right‑first‑time execution.
• Provide on‑the‑floor support for investigations, fact‑finding activities, troubleshooting, and manufacturing assessments.
• Utilize manufacturing and quality systems as required, including but not limited to Veeva, SAP, Syncade, DeltaV, LIMS, CMMS, and Microsoft Office applications.
• Support training initiatives related to deviation writing, documentation practices, and GMP compliance expectations.

• Bachelor’s or Master’s Degree in Engineering, Life Sciences, Pharmaceutical Sciences, Chemistry, Biology, Biotechnology, or a related technical discipline.
• Senior/ Specialist: 5–8 years of experience in pharmaceutical, biotechnology, or medical device manufacturing within a GMP‑regulated environment.
• Specialist: 3–5 years of relevant GMP experience in deviation investigations, technical writing, manufacturing support, or quality systems.
• Position is site‑based; requires full‑time presence at Moderna’s site. Remote work is not eligible.

• Experience authoring and managing deviations, CAPAs, change controls, and GMP technical documentation.
• Strong understanding of GMP regulations, GDP, ALCOA+, and quality systems.
• Experience supporting aseptic processing, solid oral dose, biologics, or sterile drug product manufacturing preferred.
• Familiarity with electronic quality management systems (eQMS) such as Veeva, Track Wise, or similar platforms.
• Experience with root cause analysis methodologies and risk management tools.
• Demonstrated technical writing and editing proficiency.

• Medical, prescription, dental, vision, AD&D, and life insurance offerings.
• Short‑term disability.
• 401(k) plan (eligibility required).

Equal Opportunity

Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.