QC Specialist

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 .

Summary: Responsible for supporting QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring, including data review/verification. Provide assistance with the method transfer, documentation, deviations, investigations, and continuous improvement efforts. Duties/Responsibilities Perform routine testing of in-process, final product and stability samples. • May perform method transfer/validation and routine testing of in-process, final product, and stability samples. Perform data verification, data review, and review of GMP documentation for general and complex methods. Perform document revision. Identify opportunities for continuous improvement. Identify and initiate deviations, CAPA’s and Laboratory Investigation. Train and mentor others on QC test methods, processes, and procedures. Perform other tasks as assigned. Qualifications - Education and Experience Bachelor’s degree or equivalent required, preferably in science. 2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment. Demonstrated experience in microbiological techniques (e.g. Gram Stain assays, sterility, environmental monitoring, endotoxin, growth promotion and aseptic technique). Knowledge, Skills, and Abilities Ability to understand, follow, interpret, and apply Global Regulatory and cGMP requirements accurately and completely. Experience in technical writing preferred. Problem-solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers about task status, roadblocks, and needs. Ability to work in a fast-paced environment, meet deadlines, and prioritize work. Knowledge of LIMS, ELN and laboratory data analysis 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.

Overview: Bothell - WA - US: $38.30 - $46.41per 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 in effect at the time and may require enrollment. Our benefits include: 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).