Project and Documentation Coordinator, R&D

Novanta, Inc.

Mukilteo, WA

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JOB DETAILS

JOB TYPE

Full-time, Employee

SKILLS

3D Printing, Auditing, Code of Federal Regulations, Communication Skills, Data Quality, Detail Oriented, Document Control, Document Management, Documentation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Healthcare, ISO 9001, Industry Standards, Legal Standards, Maintain Compliance, Manufacturing, Microsoft Excel, Microsoft Word, Office Equipment, Organizational Development/Management, Organizational Skills, Presentation/Verbal Skills, Procurement Planning, Product Development, Product Documentation, Product Management, Product/Service Launch, Productivity Management, Project/Program Coordination, Prototyping, Records Management, Regulations, Research & Development (R&D), Robotics, Safety/Work Safety, Source Code/Configuration Management (SCM), Standard Operating Procedures (SOP), Systems Engineering, Team Player, Technical Drawing, Technical Support, Time Management, Willing to Travel, Writing Skills

LOCATION

Mukilteo, WA

POSTED

30+ days ago

Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing-improving productivity, enhancing people's lives and redefining what's possible. We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications-from minimally invasive surgery to robotics to 3D metal printing.

Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific. Looking for a great place to work? You have found it with a culture that embraces teamwork, collaboration and empowerment. Come explore Novanta.

Summary

The Project and Documentation Coordinator, R&D manages the organization, distribution, and integrity of a company's internal documentation and facilitates the R&D activities for new product development. This includes overseeing the document lifecycle from creation and approval to revision and archival, verifying that all records comply with regulatory, legal, and organizational standards.

This position plays a key role in maintaining version control, tracking approvals, and ensuring access to accurate information across teams such as engineering, quality, manufacturing, or compliance. Whether supporting audits, new product development, or safety programs, document control specialists are essential to operational accuracy and regulatory readiness.

Primary Responsibilities

Organize and maintain controlled documentation, including SOPs, technical drawings, specifications, and records
Implement and enforce version control and document retention policies
Process document and change requests and track approval workflows
Provide access control to confidential or regulated documents
Prepare documentation packages for audits or compliance reviews
Work with internal stakeholders to collect, distribute, and update required documents
Set and update user access levels in Arena PLM
Report out on key metrics related to the document control process
Ensure timely completion of New Product Integration (NPI) documentation for new product development
Ensure all parts are documented (rev control), quoted and ordered on time for prototype through first production builds.
Coordinate across the organization including engineering, product management, purchasing, planning, manufacturing, and quality to ensure the product meets company and customer requirements.

Required Experience, Education, Skills, Training and Competencies

High school diploma or equivalent required
5+ years of experience in document control or records management
Proficiency with document management systems (e.g., Arena, Oracle, SAP)
Knowledge of version control practices and document lifecycle workflows
Experience in regulated environment, document auditing and compliance tracking capabilities. Experience supporting audits or regulatory inspections
Highly organized and detail-oriented
Solid understanding of product development processes
Proactive and strong verbal and written communication skills
Solid MS Word and Excel skill and experience
Previous experience working in ISO (ISO 9001/ 14001/ 45001) preferred
Familiarity with industry standards such as GMP, FDA 21 CFR Part 11

Travel Requirements

None

Physical Requirements

Ability to work in a standard office setting and to use standard office equipment, including a computer.

Compensation Information

The rate for this role will range from $26.50 to $36.00 per hour based on full-time employment. Compensation offers are based on a wide range of factors including but not limited to location, relevant skills, training, experience, education, etc.
Certain roles may be eligible for performance-based incentive compensation and/or long-term incentives. Incentives could be discretionary or non-discretionary depending on the plan.
Novanta supports all aspects of your life's needs. This position provides a full range of medical, financial, and other benefits to make your quality of life better.

Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.

Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.

Equal Opportunity Employer – minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity.

About the Company

Novanta, Inc.

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