Working with Us

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

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. Read more: careers.bms.com/working-with-us .

The Manufacturing Cleaning & Sanitization Manager leads and drives execution of routine and on demand facility cleaning and sanitization to support manufacture of cell therapies with Current Good Manufacturing Practices (cGMP's). The Manager is responsible for leading a team whose primary focus is on execution of routine cleaning and sanitization activities, maintaining a culture of compliance, innovation, and safety within their functional group. Managers are required to guide the personnel in their group with knowledge and technical knowledge to lead troubleshooting activities, provide investigation support, analyze process/equipment data, and identify and implement process improvements.

Duties and Responsibilities:

• Provides direct oversight of the completion of daily activities that contribute to cleaning and sanitization of GMP areas for CAR-T therapy manufacturing.

• Acts as an area/system owner - a point of contact for all work to be carried out in Cleaning & Sanitization and ensures proper communications with internal and external customers and stakeholders.

• Responsible for the health and safety of all personnel in areas of ownership- ensuring safety precautions are followed and safety hazards (including ergonomic risk) are reported and resolved in a timely manner.

• Willing to become certified as a safety event first responder and take action in emergency situations.

• Ensure all cleaning methods and materials are adequate, available, safe to use, and compliant with cGMP requirements.

• Takes an active role in hiring, managing, coaching and developing employees to ensure adherence to SOP's and cGMP.

• Fosters a collaborative and psychologically safe team environment. Leads daily huddles, resolves conflicts, and acts as a servant leader to meet the day to day needs of the staff.

• Drives continuous improvement initiatives, 5S, and standard work to improve safety, cost, and effectiveness.

• Is a role model for Quality/Right first time/Patient-focused culture by providing direct training, guidance, and problem solving as necessary.

• Monitors daily work coordination and distribution to maintain schedule adherence and cycle time.

• Builds trust relationships and productive partnerships with cross functional department teams including QA, Sterility Assurance, and Microbiology.

• Acts as a consultant to project teams to ensure impact to cleaning operations is considered.

• Supports compliance audits and deviation investigations. May own actions based on audit or deviation findings.

• This role is responsible for a team that works Night shift hours, 2x12 hour shifts, 7 days per week. Must be willing to work on site, with flexible hours but mainly on a swing shift schedule (2pm-10pm) Monday through Friday.

• This role is supported by shift leads but does require occasional on-call duty on weekends in instances of illness, emergency, or planned time off.

Qualifications:

• 5+ years of experience in pharma/GMP environment, preferably in a direct manufacturing setting.

• Minimum 1-2 years of leadership experience with demonstrated examples of leading and directing a team.

• Well-versed in GMP manufacturing requirements including good documentation practices, ALCOA+ principles, and sterility best practices.

• Associate's or Bachelor's degree in related field is preferred.

• Minimum of high school diploma and/or equivalent combination of education and experience is required.

The starting compensation for this job is a range from $92,000 to $121,000, plus incentive cash and stock opportunities (based on eligibility).

The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.

Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers Site (https://careers.bms.com/working-with-us) .

Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

BMSCART

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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/

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

Company: Bristol-Myers Squibb

Req Number: R1585212

Updated: 2024-12-14 01:40:30.342 UTC

Location: Bothell-WA

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.