As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.
Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer.
We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
We are seeking an Engineer II - Documentation Specialist to support document lifecycle management, engineering standards control, version management, and governance processes for the Global CM Documentation & Industrialization Hub.
This role will help ensure that manufacturing documentation, supplier records, engineering templates, best practices, and technology transfer materials are controlled, organized, accessible, and maintained in accordance with defined governance and quality expectations.
Key Skills for This Role
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Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. DESCRIPTION:
We are seeking an Engineer II - Documentation Specialist to support document lifecycle management, engineering standards control, version management, and governance processes for the Global CM Documentation & Industrialization Hub.
This role will help ensure that manufacturing documentation, supplier records, engineering templates, best practices, and technology transfer materials are controlled, organized, accessible, and maintained in accordance with defined governance and quality expectations.
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Manage document lifecycle processes including creation, review, approval, release, revision, archival, and retirement of controlled documentation
Maintain version control, naming conventions, metadata standards, taxonomy, and repository structure for CM documentation libraries
Support governance of engineering templates, manufacturing standards, work instructions, playbooks, and best-practice documents
Coordinate document reviews and approvals with Engineering, Quality, Operations, Procurement, and external manufacturing stakeholders
Ensure documentation completeness, accuracy, traceability, and compliance with applicable internal procedures and quality expectations
Support audit readiness by maintaining organized document records, revision history, approval evidence, and retrieval processes
Identify documentation gaps, inconsistencies, duplicate content, and obsolete records, and drive corrective cleanup actions
Support CM Portal and documentation library administration from a content governance and document control perspective
Develop user guidance, training materials, and standard operating practices for documentation submission, retrieval, and change management
Track documentation KPIs including document aging, approval cycle time, compliance gaps, and repository health
Partner with analytics and knowledge management colleagues to improve content searchability, usability, and adoption
Minimum Qualifications
Bachelor's degree with 5+ years of experience or Master's degree with 3+ years of experience in Engineering, Technical Documentation, Quality Systems, Information Management, Operations, or a related discipline
Experience in document control, technical documentation, engineering documentation, quality systems, or records management
Working knowledge of document lifecycle management, change control, metadata, taxonomy, version control, and records governance
Experience with PLM, SharePoint, document management systems, eQMS, ERP, or controlled repository platforms
Ability to structure complex technical content into clear templates, libraries, and governance processes
Familiarity with audit readiness, quality systems, compliance documentation, and controlled document practices
Strong technical writing, editing, proofreading, and information organization skills
Strong attention to detail and ability to manage multiple document workflows concurrently
Effective communication and stakeholder coordination skills in a global environment
Key Competencies
Documentation governance discipline and attention to detail
Strong ownership of data integrity, version control, and compliance
Customer-focused content organization and usability mindset
Structured execution and follow-through
Cross-functional coordination and stakeholder support
Continuous improvement mindset for document processes
Accountability for accuracy, timeliness, and audit readiness
About Thermo Fisher Scientific
Pharmaceuticals & Biotech10,001+Founded 2006
Thermo Fisher Scientific supplies instruments, laboratory products, life sciences solutions and pharmaceutical services to customers in research, healthcare, industry and applied markets. The company was formed in 2006 through the merger of Thermo Electron and Fisher Scientific.