Manufacturing Associate I - Bothell WA
Company: Msccn
Location: Bothell
Posted on: April 4, 2026
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Job Description:
Job Description ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our
organization works with partner companies to source qualified
talent for their open roles. The following position is available to
Veterans, Transitioning Military, National Guard and Reserve
Members, Military Spouses, Wounded Warriors, and their Caregivers .
If you have the required skill set, education requirements, and
experience, please click the submit button and follow the next
steps. Unless specifically stated otherwise, this role is "On-Site"
at the location detailed in the job post. 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 and 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) • Executes transactions and process in all
electronic systems and adheres to business continuity processes •
Prioritizes safety of self and others • Reports safety events
within 24 hours • Immediately escalates 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, that
includes people, product, and material flow across multiple shifts
• Work within a control 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 regiment as required to meet global
Health Authority requirements • Continues to refine and improve
manufacturing process technique to improve individual operational
times. • Verifies 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 Additional
Qualifications/Responsibilities 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: • 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 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) Shift: Wed-Fri Alt
Sat 11am-1130pm BMSCART LI-ONSITE 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
Keywords: Msccn, Lakewood , Manufacturing Associate I - Bothell WA, Manufacturing , Bothell, Washington