Job Information
ThermoFisher Scientific Technical Writer III in Plainville, Massachusetts
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Job Description
Are you ready to make a significant influence on a global scale? As a Technical Writer III at Thermo Fisher Scientific Inc. in Plainville, you will be at the forefront of groundbreaking cell and gene therapy solutions. This role plays a crucial part in delivering innovative gene therapies that can cure genetic, rare, and otherwise untreatable diseases. Join us in our mission to build a healthier, cleaner, and safer world by providing world-class expertise and resources.
Responsibilities
Collaborate with area SMEs or technical specialists to build or revise existing procedures or documents for manufacturing.
Acquire and verify the accuracy of technical details, lead documentation workflows, and proofread drafts to meet established quality standards.
Perform administrative duties related to controlling document life cycles from issuance to archival with Quality Assurance.
Maintain the GMP manual of SOPs and manage logbooks for manufacturing operations.
Train junior associates on established writing standards for documentation design and quality.
Participate in initiatives supporting innovation, continuous improvement activities, and improved adherence to quality procedures and regulations.
Requirements
Minimum High School Diploma with 6-8 years of related experience.
Associate's Degree or equivalent experience with 4-6 years of industry-related experience.
Bachelor's Degree or equivalent experience with 2-4 years of industry-related experience.
Strong interpersonal and communication skills, both written and oral.
Ability to work effectively with diverse constituencies in various areas.
Proficiency in eliciting technical details from subject matter specialists through meetings and interviews.
Experience developing logical structures for technical documents, content, and illustrations.
Diligence in proofreading documents for accuracy and completeness.
Ability to recognize and respond to situations requiring further evaluation and report to senior specialists or management.
Familiarity with GMP compliance and operational documents.
Capability to gown aseptically and/or sterile gown as needed.
Expertise in multiple systems (e.g., upstream, downstream) and support and coordinate critical and non-routine operations.
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.
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