Document Control Specialist I
$20 - $21 per hourPrimary Talent Partners
Primary Talent Partners has a new contract opening for a Document Control Specialist I with our healthcare client in Round Lake IL. This is a 3-month contract with a potential for extension.
Pay: $20.00 - $21.33/hr ;W2 contract no PTO no Benefits. ACA-compliant supplemental package available for must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship. Schedule: 1st Shift - 8AM to 5PM - Wednesday to Sunday Description:This section focuses on the main purpose of the job in one to four sentences.
- Review and approve GMP/GLP Manufacturing and related documentation to support timely product and system release.
- Conduct internal audit of SOPs training records and other document types on an as needed basis.
- Assist and guide engineering in the preparation of product documentation product configuration and document change request package development.
- Responsible for activities related to providing required documentation and implementing related documentation systems.
- Assist in providing training on documentation and labeling processes and systems.
- Participate on project teams as needed.
- The incumbent will perform other duties assigned.
- Document configuration and product data management Aid in the execution of user acceptance testing Aid in the creation/writing of training materials Assist in training internal and external personnel on documentation and labeling related processes and systems.
- Maintain and own internal documents
- Review documentation for accuracy and compliance to procedures.
- Route release or reject as appropriate.
- Ensure all document and system elements are identified accurate and assembled for review and approval.
- Maintain proof read and change as needed.
To perform this job successfully an individual must be able to perform each essential duty satisfactorily. List knowledge skills and/or abilities required:
- Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
- Product/document configuration.
- Intermediate level and document management (e.g. Word)
- Software skills
- Project Management Skills
- Must have excellent conceptual analytical written and verbal configuration skills
- Comprehension of design methodology product configuration and complex manufacturing processes
- Ability to work under strict deadlines and changing priorities with minimal supervision
- Strong interpersonal skills and great attention to detail are necessary
- Must be a strong team player with good problem solving and good verbal and written communications skills
- Must be able to handle multiple projects concurrently have computer experience and have knowledge of FDA Regulations Applications of Good laboratory Practices and Application of Good Manufacturing Practices
- B.A. or B.S. and 3-5 years related experience (in-house or acquired outside).
- Ability to discuss normally encountered technical or project management issues both verbally and in written form.
- Knowledge of product/document configuration management.
- Working knowledge of related business systems.
Required Experience:
IC
Vacancy posted 1 day ago
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