Micro Associate, Quality Control, Cell Therapy

Biopharma Careers; Bothell (WA); On-site; USD 4,863,000 - 5,892,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Flexible Time Off

11 paid holidays

Vacation time

Global Shutdown

Job summary

Bristol Myers Squibb in Bothell, WA is seeking a QC Micro Associate to perform GMP testing to support product release and in-process testing, and to provide technical support for microbiological assays.

The role includes data analysis, environmental monitoring, sample collection and data entry, and collaboration across teams to drive quality and process improvements. Shift: Sun–Wed 6AM to 4:30PM.

Qualifications

• Bachelor’s degree or equivalent combination of education and experience.
• 0-2+ years of regulated industry experience or equivalent combination of education and experience.
• Perform GMP lot release and in-process testing for analytical and/or microbiological test methods and perform data analysis using various electronic instruments and computer systems.
• Quality Control and Environmental Monitoring of environmental and microbiological testing.
• Complete sample collection, incubation, transferal, and data entry supporting facility monitoring.
• Support document revisions, projects, CAPA and deviation/investigation related tasks and departmental continuous improvement efforts.
• Assist in the implementation of new assay methodologies and the associated instruments.
• Perform ad hoc tasks as assigned.
• Sample Management duties as assigned.

Responsibilities

• Perform GMP lot release and in-process testing for analytical and/or microbiological methods.
• Conduct quality control and environmental monitoring of testing.
• Collect, incubate, transfer, and enter data for facility monitoring.
• Support CAPA, deviations, and related investigations.
• Assist in implementing new assay methodologies and instruments.
• Handle ad hoc tasks and sample management as needed.

Skills

GMP testing

Microbiological testing

Data analysis

Environmental monitoring

CAPA & deviation tasks

Education

Bachelor’s degree

Tools

Electronic instruments

Laboratory data systems

Job description

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.

QC Micro Associate

Sun-Wed 6AM to 430PM Shift

PURPOSE AND SCOPE OF POSITION:

The primary focus of the Quality Control (QC) Micro Associate, 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 microbiological tests.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

Education:

Bachelor’s Degree or equivalent combination of education and experience

Experience

0-2+ yearsof regulated industry experience or equivalent combination of education and experience

• Perform GMP lot release and in-process testing for analytical and/or microbiological test methods and perform data analysis using various electronic instruments and computer systems.
• Quality Control and Environmental Monitoring of environmental and microbiological testing.
• Complete sample collection, incubation, transferal, and data entry supporting facility monitoring.
• Support document revisions, projects, CAPA and deviation/investigation related tasks and departmental continuous improvement efforts.
• Assist in the implementation of new assay methodologies and the associated instruments.
• Perform ad hoc tasks as assigned.
• Sample Management duties as assigned.

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 workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustment prior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail] . 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 [e-mail] with 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.

R1605820 : Micro Associate, Quality Control, Cell Therapy