Job summary
Job post source
This job is directly from Bristol Myers Squibb
Job overview
The Sr. Manager, Quality Assurance for Quality Control at Bristol Myers Squibb oversees QC laboratory operations ensuring compliance with cGMP and supports quality assurance activities to maintain high standards in analytical and microbiological testing.
Responsibilities and impact
The role involves quality oversight of QC labs including investigations, method validation, equipment validation, change control, regulatory audit preparation, and continuous improvement projects to support manufacturing and product testing.
Compensation and benefits
The position offers a salary range of $124,449 to $150,800 plus incentive cash and stock opportunities, along with comprehensive benefits including medical, dental, vision, 401(k), paid holidays, vacation, parental leave, and wellness programs.
Experience and skills
Requires a bachelor's degree in engineering or life/physical sciences and 10+ years of relevant experience in analytical development, QC, or QA in regulated environments, with strong knowledge of GMP, regulatory requirements, and QC methodologies.
Career development
The company offers opportunities for growth through challenging projects, leadership roles, and exposure to cutting-edge biotechnology in a supportive environment.
Work environment and culture
Bristol Myers Squibb promotes a balanced and flexible work environment with a culture of passion, innovation, inclusion, and integrity, supporting employee well-being and diversity.
Company information
Bristol Myers Squibb is a global biopharmaceutical company focused on innovative therapies, including cell therapy and radiopharmaceuticals, with a strong commitment to transforming patient lives.
Team overview
The candidate will join the QC laboratory team at RayzeBio, a Bristol Myers Squibb company, working closely with high-achieving teams in a dynamic biotech setting.
Job location and travel
The role is based at the RayzeBio facility in Indianapolis with site-essential onsite work requirements and a moderate noise laboratory environment.
Application process
Applicants are encouraged to apply even if not perfectly aligned with the resume; accommodations are available for disabilities, and the company follows transparent recruitment and equal opportunity policies.
Unique job features
The job involves working with innovative radiopharmaceuticals in a regulated lab environment requiring protective gear and offers unique opportunities to impact cancer treatment development.
Company overview
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for serious diseases. They generate revenue primarily through the sale of prescription drugs, with a strong portfolio in oncology, immunology, cardiovascular, and fibrosis. The company has a rich history, including its merger with Celgene in 2019, which significantly expanded its product pipeline and research capabilities. Candidates should note Bristol Myers Squibb's commitment to scientific excellence and its strategic acquisitions to enhance its therapeutic offerings.
How to land this job
Position your resume to highlight your extensive experience in quality assurance and quality control within regulated environments, emphasizing your leadership in QC analytical and microbiological laboratory operations as described in the job posting for Bristol Myers Squibb.
Focus on showcasing your expertise in analytical method lifecycle management, including development, validation, and transfer, as well as your knowledge of cGMP regulations and regulatory authority interactions such as FDA and EMA audits.
Apply through multiple channels including the Bristol Myers Squibb corporate careers site, LinkedIn, and any other job boards listing the position to maximize your chances of visibility and consideration.
Connect on LinkedIn with current employees in the Quality Assurance or Quality Control divisions at Bristol Myers Squibb, using ice breakers such as commenting on recent company innovations in radiopharmaceuticals or expressing your enthusiasm for the company’s mission to transform patient lives through science.
Optimize your resume for ATS by incorporating keywords from the job description such as 'quality assurance,' 'quality control,' 'cGMP,' 'analytical method validation,' 'regulatory audits,' and 'laboratory operations' to ensure your resume passes initial automated screenings.
Utilize Jennie Johnson’s Power Apply feature to automate applying through multiple platforms, tailor your resume with relevant keywords, and identify LinkedIn contacts to network with, allowing you to focus your time on interview preparation and strategic job search activities.
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