G&H Staffing Companies (Temp-Secure Staffing and LSE Staffing)
Compliance Specialist
G&H Staffing Companies (Temp-Secure Staffing and LSE Staffing), Billerica, Massachusetts, us, 01821
Our client in Billerica, MA is looking for a Compliance Specialist to join their team. This is a long term contractor opportunity onsite.
Responsibilities
Ensures compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and Quality Management System Standard Operating Procedures related to product complaint handling. Support and assist the QA Complaint Coordinator and the QA Compliance Head on the evaluation and investigation of product quality complaints. Work directly on technical investigations relating to Product Quality Complaints. Document the evaluation and investigation of Product Quality Complaints within the Trackwise system. Qualifications
3+ years working as a Compliance Specialist, Doc Control Specialist, Compliance Associate. Ability to manage multiple responsibilities in a fast-paced environment, while performing in an efficient manner. Minimum 3 years related experience in a pharmaceutical/medical device manufacturing regulated environment. Working knowledge of cGMPs (current Good Manufacturing Practices) and GDP’s (Good Documentation Practices) Strong working knowledge of MS Word software. Experience evaluating and investigating drug/device product complaints a plus
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Ensures compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and Quality Management System Standard Operating Procedures related to product complaint handling. Support and assist the QA Complaint Coordinator and the QA Compliance Head on the evaluation and investigation of product quality complaints. Work directly on technical investigations relating to Product Quality Complaints. Document the evaluation and investigation of Product Quality Complaints within the Trackwise system. Qualifications
3+ years working as a Compliance Specialist, Doc Control Specialist, Compliance Associate. Ability to manage multiple responsibilities in a fast-paced environment, while performing in an efficient manner. Minimum 3 years related experience in a pharmaceutical/medical device manufacturing regulated environment. Working knowledge of cGMPs (current Good Manufacturing Practices) and GDP’s (Good Documentation Practices) Strong working knowledge of MS Word software. Experience evaluating and investigating drug/device product complaints a plus
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