Technical Writer III at Thermo Fisher Scientific in Plainville, Massachusetts

Job Description:

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.

• 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.