PSG Global Solutions Careers
Compliance Specialist II
PSG Global Solutions Careers, Meriden, Connecticut, us, 06451
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The Opportunity
Description
We're looking for a
Compliance Specialist II , working in
Pharmaceuticals and Medical Products
industry in
1000 Research Parkway, Meriden, Connecticut, 06450, United States .
Responsibilities: Performs audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation. Establishes auditing requirements, quality standards and test methods in accordance with FDA and GMP requirements. Conducts internal audits of manufacturing processes to ensure compliance. Conducts review of change controls, CAPA's, and deviations. Reviews document and ensures compliance commitment dates for audit responses.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Skills/Qualifications:
3-6 years experience CAPA review Compliance Audit Response Monitoring and Closure Deviation Management Root Cause Analysis
What Do You Think? Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
Compliance Specialist II , working in
Pharmaceuticals and Medical Products
industry in
1000 Research Parkway, Meriden, Connecticut, 06450, United States .
Responsibilities: Performs audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation. Establishes auditing requirements, quality standards and test methods in accordance with FDA and GMP requirements. Conducts internal audits of manufacturing processes to ensure compliance. Conducts review of change controls, CAPA's, and deviations. Reviews document and ensures compliance commitment dates for audit responses.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Skills/Qualifications:
3-6 years experience CAPA review Compliance Audit Response Monitoring and Closure Deviation Management Root Cause Analysis
What Do You Think? Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?