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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*

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Are you an employer or a jobseeker?*

Message

First Name*

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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 Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP)

Location: United States

Proclinical is currently recruiting for a QA Associate with a biotechnology company located in Durham, NC.

Job Responsibilities:

Issuance of Batch Production Records, Solution Lot Records, Labels, and Logbooks.
Review and approve site-specific GMP documents and records. This includes, but is not limited to, document creation, revision, review, change control guidance/review/approval, document issuance oversight, and document maintenance.
Contribute to oversight of quality systems and GMP activities, as well as site performance monitoring systems.
Identify and implement Quality System improvements.
Develop and support training on basic GxP quality systems.
Prepare for and support site inspections and audits.
Review changes to existing Quality Systems and GMP processes, identify gaps in existing Quality systems and propose solutions to site management.
Gain knowledge and understanding of quality systems, contribute to oversight of quality systems, and maintain GMP activities at the facility.
And other job duties that may be assigned from time to time.

Skills and Requirements:

Bachelor of Bachelor of Arts/Science Degree in Life Science or other technical discipline preferred with 0-2 years related experience.

If you are having difficulty in applying or if you have any questions, please contact Jarred Fetterman at 215-531-5593.

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-JF2

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