Thermo Fisher Scientific
Technical Operations, Technical Writer II
Thermo Fisher Scientific, Plainville, Connecticut, United States
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Work Schedule Standard (Mon-Fri)
Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing efficiency in their laboratories, we are here to support them. At Viral Vector Services (VVS) a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources to help clients deliver innovative gene therapies.
Job Title: Technical Writer II Location/Division Specific Information : US - Massachusetts – Plainville (on-site)
How will you make an impact? As
RSO,
you’ll play a key role in supporting our GMP manufacturing operations by developing and maintaining high-quality documentation. Your work directly impacts the consistency, safety, and compliance of the treatments we help bring to market. A day in the Life:
Partner with subject matter experts (SMEs) to create and revise GMP-compliant documentation, including SOPs, logbooks, batch records, and technical reports Manage documentation workflows, ensuring content accuracy, version control, and adherence to formatting standards Additional responsibilities may include administrative duties to manage and process-controlled documents for the manufacturing processes Keys to Success:
Education
Associates degree with 3-4 years of experience Bachelor’s degree with 1-2 year of experience Experience
Proven experience conducting interviews or meetings with SMEs to gather technical information Hands-on experience structuring, drafting, and editing GMP-compliant technical documents Demonstrated ability to review and analyze documents for completeness, accuracy, and compliance Knowledge, Skills, Abilities
Excellent written and verbal communication skills; able to translate technical concepts into clear documentation Strong collaboration skills with the ability to engage SMEs and gather information through interviews and meetings Proficient in Microsoft Office and document management systems Detail-oriented with a strong sense of quality and accuracy Able to analyze, structure, and format technical content in a logical, user-friendly way Understanding of GMP principles and ability to assess documents for compliance Willingness to gown aseptically for cleanroom access if needed Physical Requirements / Work Environment
Role is 100% onsite in a GMP manufacturing environment May require periodic cleanroom entry and the ability to gown per sterile manufacturing protocols
]]>
Work Schedule Standard (Mon-Fri)
Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing efficiency in their laboratories, we are here to support them. At Viral Vector Services (VVS) a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources to help clients deliver innovative gene therapies.
Job Title: Technical Writer II Location/Division Specific Information : US - Massachusetts – Plainville (on-site)
How will you make an impact? As
RSO,
you’ll play a key role in supporting our GMP manufacturing operations by developing and maintaining high-quality documentation. Your work directly impacts the consistency, safety, and compliance of the treatments we help bring to market. A day in the Life:
Partner with subject matter experts (SMEs) to create and revise GMP-compliant documentation, including SOPs, logbooks, batch records, and technical reports Manage documentation workflows, ensuring content accuracy, version control, and adherence to formatting standards Additional responsibilities may include administrative duties to manage and process-controlled documents for the manufacturing processes Keys to Success:
Education
Associates degree with 3-4 years of experience Bachelor’s degree with 1-2 year of experience Experience
Proven experience conducting interviews or meetings with SMEs to gather technical information Hands-on experience structuring, drafting, and editing GMP-compliant technical documents Demonstrated ability to review and analyze documents for completeness, accuracy, and compliance Knowledge, Skills, Abilities
Excellent written and verbal communication skills; able to translate technical concepts into clear documentation Strong collaboration skills with the ability to engage SMEs and gather information through interviews and meetings Proficient in Microsoft Office and document management systems Detail-oriented with a strong sense of quality and accuracy Able to analyze, structure, and format technical content in a logical, user-friendly way Understanding of GMP principles and ability to assess documents for compliance Willingness to gown aseptically for cleanroom access if needed Physical Requirements / Work Environment
Role is 100% onsite in a GMP manufacturing environment May require periodic cleanroom entry and the ability to gown per sterile manufacturing protocols
]]>