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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP)

Location: United States

Proclinical is currently recruiting for a QA Documentation Specialist with a biopharmaceutical company located in North Chicago, IL.

Job Responsibilities:

Provide QA support for manufacturing process
Documentation management
Ensure all products are in compliance with corporate and government regulations
Support of quality regulations
Conduct initial regulatory review and approval of quality documents
Perform QA review of product release

Skills and Requirements:

HS diploma or higher
1-4 years of experience
Past experience within pharma/biotech industry and QA
Excellent interpersonal skills
MS Office, especially Excel
Attention to detail is critical for processing
Experience with AttachePro would be a plus
Document management/control experience

If you are having difficulty in applying or if you have any questions, please contact Catherine Nguyen at 215-531-5643.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#LI-CN1

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