Manufacturing Associate II Bothell - WA - US R1603015

## Manufacturing Associate IIBothell - WA - USFind out how well you match with this job
** 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:
** 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 (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms)
* Demonstrate strong practical and theoretical knowledge
* 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 the necessary technical skills and knowledge
* Trains for proficiency in process systems and some supporting business systems, and maintains trainer qualifications
* Collaborate with support groups on recommendations and solving technical and operational problems
* Train others on Source Governing Documents to successfully complete manufacturing operations
* Execute daily unit operations schedule, that includes 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 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
** 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 requiredNetherlands
• 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…