QA Documentation Specialist job in El Segundo, USA

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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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?*

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a QA Documentation Specialist for a globally leading pharmaceutical company located in El Segundo, CA. Successful candidate will have past experience working in a GMP environment and with batch records/SOPs.

Job Responsibilities:

Printing, compiling, and issuing batch record documentation, in-process and final product labels for clinical and commercial products
Collaborate with cross-functional departments to support activities for commercial and clinical launches
Other duties as needed

Skills and Requirements:

Experience working in a GMP environment and with batch records/SOPs.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please Catherine Nguyen at (+1) 215-531-5643 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

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
#Compliance/Quality

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