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Associate I, Manufacturing

Associate I, Manufacturing

Bristol-Myers SquibbKenmore, WA, US
12 days ago
Job type
  • Full-time
  • Part-time
Job description

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. 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 .

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.

Duties / Responsibilities

  • Learn and execute Cell Therapy Manufacturing operations
  • Perform patient process unit operations and complies with operations described in standard operating procedures and batch records
  • Executes transactions and process in all electronic systems
  • Prioritizes safety of self and others
  • Reports safety events within 24 hours
  • Escalates any / all issues that may impact safety of self and / or others.
  • Complete documentation required by governing controlled documents and batch records
  • Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements
  • Complete training assignments to ensure necessary technical skills and knowledge
  • Train for proficiency in process systems and some supporting business systems
  • Execute the daily unit operations schedule, that includes people, product, and material flow across multiple shifts
  • Maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements
  • Continues to refine and improve manufacturing process technique to improve individual operational times.
  • Ensures training completion prior to production

Reporting Relationship

Manager / Supervisor

Qualifications

Education :

  • 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
  • Experience :

  • 0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education
  • Proven experience working on teams where 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 is critical to success
  • Possess excellent 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 preferred
  • Shift :

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

    Days - Thu - Sat (alt. Wed) 0500 - 1730,

    Swing - Sun - Wed (alt. Sat) 1100 - 1130

    Swing - Wed - Fri (alt. Sat) 1100 - 1130

    Nights - Sun - Wed (alt. Sat) 1700 - 0530

    Nights - Wed - Fri (alt. Sat) 1700 - 0530

    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)
  • 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.

    Compensation Overview :

    Bothell - WA - US : $30.61 - $37.09per hour

    The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. 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 https : / / careers.bms.com / life-at-bms / .

    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.

    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 a supportive culture, promoting global participation 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 an 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 / 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.

    Required

    Preferred

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    Manufacturing Associate • Kenmore, WA, US

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