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Supervisor, QC Microbiology, Cell Therapy

Employer
Bristol Myers Squibb
Location
Bothell, Washington, US
Salary
Competitive
Closing date
Aug 19, 2022

View more

Sector
Consultancy/Private Sector
Field
Conservation science
Discipline
Biology
Salary Type
Salary
Employment Type
Full time
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.

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.

Shift:

Sun-Wed PM

Department and Location:

QC Microbiology Bothell, WA

GENERAL SUMMARY

The QC Microbiology Supervisor is a full-time position. This role is responsible for the day to day operations associated with the in-process and release testing of clinical and commercial autologous cell therapy product. The QC Supervisor will be a key leader responsible for GMP operations and meeting critical business goals.

MINIMUM REQUIREMENTS
  • BS in a scientific discipline.
  • Manager: 7+ years with regulated industry experience or equivalent


Knowledge, Skills, and Abilities
  • Strong working knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.
  • Demonstrated experience building, mentoring and leading exceptional teams
  • Ability to apply Lean, Six Sigma and Risk Management concepts and tools is preferred.
  • Ability to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects.
  • Strong analytical and communication skills as well as sound judgment, with the ability to work effectively with others.
  • Demonstrated success working in a high-performing, business results-driven environment.

Key Responsibilities
  • Provide supervision of Quality Control (QC) associates and oversees the day to day activities related to in-process, final release and stability testing of drug product.
  • Develops and manages a daily work plan for QC associates.
  • Hire, mentor and develop exceptional QC personnel.
  • Identifies and mitigates risks in QC labs that could negatively impact the safety, identity, strength purity or quality of the product.
  • Assists in the design, implementation and continuous improvement of Quality Control systems that are technically sound, promote effective and efficient operations, and comply with cGMP requirements.
  • Provides leadership support during trouble shooting of assay performance and equipment as it relates to ensuring the quality and compliance of the product.
  • Ensures deviations, CAPA, change controls, process transfers, and other business drivers are supported in a compliant manner.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

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

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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