Thermo Fisher Scientific
Technical Operations, Technical Writer II
Thermo Fisher Scientific, Plainville, Massachusetts, us, 02762
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
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.