Associate Scientist, Ct Qc Analytical Testing

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

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The QC Associate Scientist is responsible for supporting the analytical testing at QC Analytical Testing department at the Cell Therapy Operations (CTO) manufacturing facility during clinical and commercial phases. This department is responsible for flow-cytometry and molecular based testing for stability, validation, critical reagent qualification, training, and other critical support as needed. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot.

Responsibilities:

Perform testing of the QC Analytical Testing Department including:

• Complete all work in a timely manner.
• Capable of handling complex issues and solving problems with only general guidance.
• Prepare and present continuous improvement projects to management.
• Perform cell based in-vitro flow experiment, ELISA, qPCR to assess critical reagent concentration.
• Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment.
• Comprehensive understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents.

Perform peer review of testing data.

• Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
• Complete all reviews in accordance with required release timelines.
• Review all data in accordance with applicable procedures and cGMP requirements.
• Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required.

Support document revision, project, CAPA, and investigation/deviation tasks.

• Communicate effectively with management regarding task completion, roadblocks, and needs.
• Perform assigned tasks within a CAPA, deviation, or project.
• Take a leadership role, as required, for projects.
• Performs other tasks as assigned.
• Draft and review technical documents, such as SOPs and protocols/reports.
• Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.
• Participate in complex projects and continuous improvement efforts.

Knowledge & Skills:

• Advanced ability to accurately understand, follow, interpret, and apply Global Regulatory and cGMP requirements.
• Ability to represent the interests of the group on cross-functional teams.
• Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects.
• Advanced technical writing skills, problem-solving ability/mentality, technically adept and logical thinking.
• Ability to work with management locally and globally. • Advanced ability
• Advanced hands-on experience with various analytical techniques including flow-cytometry, molecular techniques and scientific knowledge in the characterization and transfer of pharmaceutical products.

Basic Requirements:

• Bachelor’s degree required, preferably in Science.
• 3 years of relevant analytical testing or QC experience.

Preferred Requirements:

• Advanced Degree preferred.
• 4-5 years of relevant analytical testing or QC experience.

Working Conditions:

• The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required.
• The incumbent will be working around biohazardous materials, including chemical agents up to six (6) hours per day.
• The incumbent will be working a laboratory setting up to six (6) hours per day.
• The incumbent must analyze numerical values on a daily basis.

BMSCART, #LI-Onsite

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

COVID-19 Information
To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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