Document Control Specialist
Allendale, NJ, United States
Job Description
Clinical Research Document Control Specialist
GMP, Quality Assurance, Quality Control, Batch Record, SOP
- Document record(s) receipt in record location database
- Prepare record(s) for repository storage location
- File record(s) in assigned storage location
- Monitor record request inbox
- Respond to incoming record withdrawal requests
- Prepare requested record for distribution
- DMS (Document Management System)
- Train personnel for document authoring & reviewer/approver role within DMS
- Perform administrator duties in DMS
- Create/revise/manage document templates
- Create/revise quality documents in DMS
- Review documents in DMS for GDP compliance/template adherence
- Manage publishing documents process in DMS to support business initiatives
- Experience with e-DMS systems and e-QMS systems
- Relevant IT skills (Word and Excel) (Visio, Microsoft Project a plus)
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.
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Job Detail
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Job IdJD4292213
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationAllendale, NJ, United States
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EducationNot mentioned