Manufacturing Associate II

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.

Position Summary
Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy. Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times.

BMS Values
Our values move us toward our mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

Candidates must exemplify the BMS values of Passion, Integrity, Inclusion, Accountability, Innovation, and Urgency.

Duties/ Responsibilities

Learn and execute Cell Therapy Manufacturing operations compliantly

Execute operations as outlined in Source Governing Documents (includingbut not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms)

Demonstrate strong practical and theoretical knowledge

Executes transactions andprocessin all electronic systems and adheres tobusiness continuity processes

Prioritizes safety of self and others

Reportssafety events within 24 hours

Immediatelyescalatesany/all issues that mayimpactcompliance or safety ofself and/orothers.

Complete documentation required by Source Governing Documentscontemporaneously

Perform alltasks in a mannerconsistent with the safety policies, SOPs,quality systems, and GMP requirements including ALCOA+ Complete training assignments prior to assigned due date to ensure thenecessary technical skills and knowledge

Trains forproficiencyin process systems and some supporting businesssystems, andmaintainstrainer qualifications

Collaborate with support groups on recommendations and solving technicaland operational problems

Train others on Source Governing Documents to successfully completemanufacturing operations

Execute daily unit operations schedule, that includes people, product, andmaterial flow across multiple shifts

Work within a controlled cleanroom environment and execute asepticprocessing procedures (as assigned). Maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels percontrolled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements

Continues to refine and improve manufacturing processtechniquetoimprove individual operational times.

Verifies training completion prior to performing anyGxPtasks

Reporting Relationship

Reports to Manager, Manufacturing Operations

Qualifications
Education:

U.S.

Associate or bachelor's degree in related field is preferred

A minimum high school diploma and/or equivalent combination of education and experience is required

Netherlands

MBO, 3 of 4 in science related field and/or equivalent

Experience:

1+ years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education

Proven experience working on teams where combined contribution, collaboration, and results were expected

Proficiency in common computer tools such as word processing, spreadsheet and web-based applications

Meticulous attention to detail and personal accountability are critical to success

Demonstrated good interpersonal skills, is attentive and approachable

Maintain a professional and productive relationship with area management and co-workers

Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is required

Preferred Experience:

Experience in cell therapy manufacturing, including Cell washing, Cell Expansion processes and automated equipment. Cell separation techniques and automated equipment. Cryopreservation processes and equipment.

Working Conditions:

Must be able to stand/walk for extended periods of time

Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as assigned), which require gowning and personal protective equipment (PPE), including by not limited to: safety shoes, safety glasses, aprons, face shields, powered air purifying respirators (PAPR), lab coats, full body gowns, hairnets, gloves, and hearing protection.

Required to carry and/or lift up to 30 pounds / 15 kg, several times a day, while handling production equipment and/or materials

Required to push and/or pull up to 50 pounds / 25 kg, several times a day, while handling production equipment and/or materials

Work in areas that may have strong magnets

Must be able to work in a BSL2 / ML1 work environment handling human blood components Work in areas with exposure to vapor phase liquid nitrogen

Must be able to work assigned shift (Day, Evening, Night, Weekends and/or Holidays)

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Shifts available:

Days – Sun – Tue (alt. Wed) 0500 – 1730

Days – Thu – Sat (alt. Wed) 0500 – 1730

Swing – Sun – Tue (alt. Wed) 1100 – 2330

Swing – Thu – Sat (alt. Wed) 1100 - 2330

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: $33.67 - $40.80per 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

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 (

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 View email address on manufacturingworkers.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:

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 .

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 View email address on manufacturingworkers.com 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.

R1603015 : Manufacturing Associate II

Req Number:

R1603015

Location:

Bothell - Washington - US

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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