We're looking for a Quality Compliance Specialist, working in the Biotechnology/Medical Devices industry in Minneapolis, Minnesota, United States.
Analyzes, reviews, and approves testing reports to ensure that the data is reliable.
Reports any inconsistency or incorrect result observed during review reporting.
Initiates an investigation.
Interfaces with internal clients to meet requirements for quality and timeliness of results.
Ensures compliance with regulations.
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
Bachelors degree in Chemistry or related field with 3+ years of experience, or Masters degree with 0+ year of experience
Exposure to laboratory and manufacturing environment
Demonstrated practical application of chemistry knowledge and laboratory skills to analyze/characterize drug products and polymer materials
Experience in data reviewing and approval process
Experience in Lab OOS/OOT and investigation techniques
Experience in execution of CAPAs
Experience conducting Quality Assurance tasks
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
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? Apply here.