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Document Control Specialist

Document Control Specialist

Job Description


- Maintaining the flow of quality documentation in an FDA and GMP compliant manner
- Maintaining document control logs, validation logs, engineering drawings/specification logs, etc.
- Coordinating change control processes, and investigating CAPA’s related to documentation and document control
- Maintaining all quality records, work instructions, templates, forms and procedures related to the Quality Management System

Duration: 6 month contract to direct

Job Requirements


- BS Life Sciences
- 2-3 years of experience in a document control role for a medical device company
- Prior experience coordinating document control function and providing training for Quality Management Systems (QMS)
-  Working knowledge of US and European Medical Device Regulations, FDA, GMP, and international quality system regulations,  and ISO standards (Ideally ISO 13485 or 21 CFR Part 820 compliance)


Joulé offers competitive compensation and benefits including; medical, dental and vision benefits, holiday pay, company matching 401K plan, referral bonuses and more...

Job Snapshot

Employment Type Contractor
Job Type Science, Pharmaceutical
Education 4 Year Degree
Experience 2 to 4 years
Manages Others Not Specified
Industry Pharmaceutical, Medical Equipment
Required Travel Not Specified
Job ID 1150-JV-DCIV
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Document Control Specialist

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