At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration, and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

QC Associate II

Sun-Wed 1pm to midnight Shift

This Position qualifies for a $10,000 Sign-on Bonus, $5,000 payable within 30 days of start date and $5,000 payable following 6 months of continuous employment. Payments are subject to a 1-year repayment agreement from date of payment issue. Applies to external hires only.

PURPOSE AND SCOPE OF POSITION:

The primary focus of the Associate II, Quality Control (QC) role will be to perform GMP testing to support product release and in-process testing. This role will also provide technical support and troubleshooting for analytical or microbiological tests.

REQUIRED COMPETENCIES:  Knowledge, Skills, and Abilities:

Education:

Bachelor’s Degree in Science or equivalent combination of education and experience

Experience

3+ years of regulated industry experience or equivalent combination of education and experience

DUTIES AND RESPONSIBILITIES:

• Perform GMP lot release and in-process testing for analytical and/or microbiological test methods and perform data analysis using various electronic instruments and computer systems
• Support assay transfer and method validation by executing validation protocols and generating data/results to support the final report
• Assist in the implementation of new assay methodologies and the associated instruments
• Operate and maintain analytical and/or microbiological instruments according to standard operating procedures
• Participate in cross-functional assay training
• Author and revise standard operating procedures and test methods
• Identify and facilitate continuous improvement projects
• Lead small scope projects