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Bristol Myers Squibb
Devens - MA - US; Devens - MA
Source: Bristol Myers Squibb careers · View original posting
From Bristol Myers Squibb's posting. “We” and “our” refer to the employer.
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Subject matter expert in bioanalytical techniques leading method transfer/validation and routine testing of in-process, final product, and stability samples. Conceptualize and lead complex projects, CAPAs, deviations, and continuous improvement efforts. Represent department in product review boards, regulatory inspections, and author responses to regulatory requests. Apply technical knowledge, regulatory requirements, and scientific principles to independently perform complex troubleshooting and problem solving.
Duties/Responsibilities
Subject matter expert in bioanalytical techniques (e.g., cell-based assays, ELISA, qPCR, flow cytometry) leading method transfer/validation and routine testing of in-process, final product, and stability samples.
SME for training and mentoring team on multiple complex QC test methods, processes, and procedures.
Independently develop, write, and execute methods, protocols, reports, and other related documents aligned with regulatory and corporate guidelines.
Represent the department in product review boards, regulatory inspections (internal and external audits). Own and author responses to regulatory requests.
Review and approve laboratory investigations.
Champion and foster a positive and successful collaborative quality culture.
Conceptualize and lead complex projects, CAPAs, deviations, and continuous improvement efforts.
Own sections of APQR. • Represent QC interest on cross functional/ cross-site teams and communicate and collaborate effectively.
Apply technical knowledge, regulatory requirements, and scientific principles to perform troubleshooting and problem solving for nonroutine complex issues.
Perform other tasks as assigned.
Compensation
Devens - MA - US: $124,590 - $150,977
 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws.
Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.
LAYIQ is an independent job-discovery service. This listing does not imply a partnership with or endorsement by the employer. Review the original posting for current details and availability.
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