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Temporary- Associate Compliance

Billerica, Massachusetts · Biotech/Pharmaceutical
We are seeking a Temporary Associate, Compliance to support product quality complaint investigations in a regulated pharmaceutical environment. This role involves working closely with quality teams to review, document, and investigate product complaints while ensuring compliance with current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
The ideal candidate is detail-oriented, organized, and able to manage multiple tasks in a fast-paced setting. Strong writing skills and experience in pharmaceutical or medical device environments are preferred. If you meet these qualifications and are looking for an opportunity to contribute to a quality-driven team, we encourage you to apply.

Full-time Onsite
Contract 
Pay Rate: DoE


Job Summary
The Temporary- Associate Compliance provides support in the evaluation and investigation of product quality complaints.
 
Ensures compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and Quality Management System Standard Operating Procedures related to product complaint handling.

Area Of Responsibility
  • 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.
  • Other duties as assigned

Qualifications
  • BS in a scientific field a plus
  • Minimum 3 years related experience in a pharmaceutical/medical device manufacturing regulated environment
  • Superior internal customer service/people skills
  • Ability to manage multiple responsibilities in a fast-paced environment, while performing in an efficient manner
  • Working knowledge of cGMPs (current Good Manufacturing Practices) and GDP’s (Good Documentation Practices)
  • Strong working knowledge of MS Word software
  • Must have exceptional writing skills to document the evaluation and investigation processes completed.
  • Experience evaluating and investigating drug/device product complaints a plus
  • Experience using the Trackwise complaint module a plus

About ProStaff Workforce Solutions
We are a fast growing and successful agency that treats all its clients and candidates with a personal touch. ProStaff Workforce Solutions is a group of industry experts—many hailing from larger agencies—who know their business well and enjoy working in a more hands-on and flexible environment, with attention to detail. Our mission is to match quality people with quality jobs and quality companies to maximize productivity and profitability. We develop long-term relationships and provide a level of customer service and expertise that instill confidence and trust in our client companies and candidates.

Our Values
• Integrity
• Commitment
• Quality
• Diversity


Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.


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