QA Documentation Specialist job in El Segundo, USA

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First Name*

Last Name*

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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: Permanent

Discipline: Good Clinical Practice (GCP), Good Laboratory Practice (GLP)

Location: United States

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

Proclinical is currently recruiting for a QA Documentation Specialist position with a globally leading pharmaceutical company in El Segundo, CA. A successful candidate will have experience working within the pharmaceutical/biotechnology industry and batch records.

Job Responsibilities:

Printing, compiling and issuance of Batch record documentation, in-process and final product labels for clinical and commercial product.
Collaborates with cross-functional departments to support activities for commercial and clinical launches.

Skills and Requirements:

Pharmaceutical/biotechnology experience
Experience with batch records

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 contact Catherine Nguyen at 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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