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Quality Control Associate
2 months ago
SUMMARY
***100% onsite*** ARI QC
Admin / Standard hours M-F (8am-5pm)
ENTRY LEVEL but would like some lab experience additional to lab experience obtained on an educational level.
Raw materials USP/EP experience is a plus.
Ideal candidate: Some lab experience. Good attitude and work ethic.
Nice to have: Compendial lab experience
The Associate Quality Control (QC) position will provide general support to Quality Control laboratories at Client Rhode Island. The role will be based out of Client Rhode Island and will work under the guidance of the hiring manager. It is an administrative 100% onsite shift, Monday through Friday 8:00AM – 5:00PM.
The Quality Control team provides analytical expertise in testing of drug substance and raw materials to meet Client specifications and ensure a constant supply of raw materials for Client products.
Top 3 Must Have Skill Sets:
Strong Analytical Skills – Ideal candidate will have at least 4 years of experience performing analytical testing
Attention to Detail – Ideal candidate will be thorough and deliver polished work product.
Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site.
Day to Day Responsibilities:
Responsibilities will include, but are not limited to:
• Performing analytical testing for general chemistry (IDs, LODs, pH, osmolality, appearance, etc.),
• Interacting cross-functionally with a wide variety of people and teams;
• Troubleshoot, solve problems and communicate with stakeholders.
• Participate in initiatives and projects that may be departmental or organizational in scope.
• Evaluate lab practices for compliance and operational excellence on a continuous basis.
• Daily responsibilities will be focused on executing analytical testing of raw materials in a GMP laboratory.
