QA Compliance Specialist job in Syracuse, USA

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First Name*

Last Name*

Email*

Phone Number*

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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*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Good Manufacturing Practice (GMP), 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 Compliance Specialist with a leading pharmaceutical company located remotely. The role is an initial 6 month contract with a high probability of extension.

Job Responsibilities:

Review batch records, specifications, SOPs, data, and other supporting documentation related to the manufacturing, testing, packaging, and labeling processes to assess compliance with the regulatory submissions.
Determine source of any differences or issues found upon review of the documentation.
Collaborate with cross-functional departments to resolve discrepancies and ensure compliance.
Assess discrepancies for product impact and author justifications where possible.
Foster communication with key stakeholders in order to properly plan and prioritize workloads based on potential impact to supply.
Identify and implement continuous improvement initiatives.
Support QA project initiatives for a broad range of topics as the group evolves.
Perform other responsibilities as requested.

If you are having difficulty in applying or if you have any questions, please contact Max Kelly at (+1) 312-270-1613 or m.kelly@proclinical.com.

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-MK2

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