Manufacturing Associate I

Bristol Myers Squibb EU Policy · Bothell, WA · 3 wk ago

On-siteResearch$30.61–$37.09/hrPart-time

About the role

At Bristol Myers Squibb, we offer challenging, meaningful, and life-changing work that transforms the lives of patients and the careers of those who do it. You’ll have the opportunity to grow and thrive through uncommon opportunities in scale and scope, alongside high-achieving teams. 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.

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.

Responsibilities

Learn and execute Cell Therapy Manufacturing operations compliantly.
Execute operations as outlined in Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms).
Execute transactions and processes in all electronic systems and adhere to business continuity processes.
Prioritize safety of self and others.
Report safety events within 24 hours.
Immediately escalate any/all issues that may impact compliance or safety of self and/or others.
Complete documentation required by Source Governing Documents contemporaneously.
Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements including ALCOA+.
Complete training assignments prior to assigned due date to ensure necessary technical skills and knowledge.
Train for proficiency in process systems and some supporting business systems.
Execute the daily unit operations schedule, including people, product, and material flow across multiple shifts.
Work within a controlled cleanroom environment and execute aseptic processing procedures (as assigned).
Maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection as required.
Continue to refine and improve manufacturing process technique to improve individual operational times.
Verify training completion prior to performing any GxP tasks.
Author manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements.

Requirements

U.S. Associate or bachelor's degree in a related field is preferred. A minimum high school diploma and/or equivalent combination of education and experience is required.
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.
Excellent interpersonal skills, 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.

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 but 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).

Schedule

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

Pay

Bothell - WA - US: $30.61 - $37.09 per hour (full-time employee 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.

Benefits

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life Benefits:
- Paid Time Off for US Exempt Employees: flexible time off (unlimited, with manager approval), 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico, or Rayzebio employees).
- Phoenix, AZ, Puerto Rico, and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
- Additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs, and an annual Global Shutdown between Christmas and New Year's Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.