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(Hybrid) Document Control Specialist
| Hours | Full-time, Part-time |
|---|---|
| Location | Woburn, Massachusetts |
About this job
The team is looking for a Document Control Specialist to support their medical device engineering team with design controls, change controls, etc.
- Design Controls are housed in:
- TrueVault (Veeva).
- Trackwise (heavy change controls come from here).
- Must be Project Management oriented to ensure the team gets documents completed per QMS (design control).
- Must have experience with Risk Management Activities (DHFs, etc.).
- Attention to detail.
- Ability to work independently and be proactive.
- Work with technical drawings and specifications.
- Engineering experience ideal – working with Technical Drawings.
- Medical Device experience is preferred.
- GDP, GMP not required, but would be helpful.
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.