Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description

Job Description: Maintain compliance requirements for established QMS processes and procedures. Provide support to product disposition process by reviewing completed batch documentation and verifying GxP requirements are met. Train and maintain proficiency in using electronic quality systems for managing change control deviations CAPA etc. Complete analysis identify issues and provide recommendations for compliance improvements if applicable help remediate processes and systems in accordance with company standards and regulatory requirements. Participate on projects or assignments and ensure objectives are appropriately set and met.

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 Experience in Quality Systems Effective time management, attention to detail, organizational skills, teamwork, and collaborations Ability to gown and gain entry to manufacturing areas Ability to work a 12-hour rotating shift and every other weekend, including some holidays Ability to lift 10 lbs

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?