Associate, Quality Control, Cell Therapy

Bristol Myers Squibb

Bothell, WAOn-siteFull time
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Pay
$35 to $43
an hour
Location
Bothell, WA
Work style
On-site
Job type
Full time
Posted
Oct 22
1 day ago
Career path

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About the company

Bristol Myers Squibb

Pharmaceutical Manufacturing · 10,001+ employees

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome.

Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients.

Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do.

Review our Social Media Community Guidelines at: https://www.bms.com/social-media-community-guidelines.html

Bristol Myers Squibb on LinkedIn

What you'll do

  • The Associate will perform GMP testing to support product release and in-process testing while providing technical support for analytical or microbiological methods.
  • They are responsible for managing samples, maintaining equipment, and initiating quality documentation such as Deviations and CAPAs.

What you need

  • Candidates must hold a Bachelor's degree or an equivalent combination of education and experience.
  • The role requires 0-2 years of experience in a regulated industry and demonstrated proficiency in laboratory techniques and safety practices.
  • Education: a bachelor's degree

Key skills

GMP testingSample managementProduct testingRaw material releaseEnvironmental monitoringEquipment maintenanceAssay transferMethod validationLaboratory investigationsAnalytical skillsCommunication skillsComputer proficiencyLaboratory safetyTroubleshooting

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Perks

  • Wellbeing support
  • Retirement benefits
  • Financial protection benefits
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life insurance
  • Disability insurance
  • Flexible Time Off
  • Paid company holidays
  • Paid sick leave
  • Paid volunteer days
  • Summer hours flexibility
  • Leaves of absence
  • Annual global shutdown

See full description on company page, apply now

Read the full posting here
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. The primary focus of the Associate, 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. Perform or support cGMP activities, such as but not limited to, sample management, product testing, raw material release, environmental monitoring sample collection and processing, and system and equipment maintenance support. Support sample management. Support assay transfer and method validation. Identify and facilitate continuous improvement projects. Identify and initiate Deviations, CAPA’s and Laboratory Investigations. Ensure timely completion of testing and tasks as assigned. Knowledge, Skills, and Abilities Demonstrated experience with basic laboratory techniques and laboratory safety practices. Detail oriented with ability to work in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. Strong analytical and communication skills Computer proficiency as well as the ability to master new software programs. Experience working a GMP environment is preferred. Education/Experience: Bachelor’s degree or equivalent combination of education and experience. 0-2 years of regulated industry experience, or equivalent combination of education and experience. Work hours: Wed-Sat (1330-0000) compensation will include additional 10% shift differential for working evening shift. We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. Compensation Overview: Bothell - WA - US: $35.29 - $42.77per hour 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. Benefits: Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working. Supporting People with Disabilities 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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.comwith the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1607736 : Associate, Quality Control, Cell Therapy

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