QC Specialist

Bristol Myers Squibb•Bothell, WA

1d•Onsite

About The Position

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Position Summary: Responsible for testing of incoming raw materials, sampling, labeling tracking and shipping of samples. Performance of appearance for drug product.

Requirements

Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Apply scientific principles to analytical testing and the proper use of laboratory equipment.
Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
Attention to detail and demonstrated organizational skills.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Bachelor's degree preferred in science. Associate degree with equivalent combination of education and work experience may be considered.
0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.

Nice To Haves

Prior experience in analytical testing (e.g., pH, Osmolality, FTIR, HPLC, etc.) is preferred.
Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.

Responsibilities

Perform routine testing of raw materials and perform sampling of retains.
Ship samples to outside testing labs, as needed.
May review GMP documentation and perform data verification.
Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
May train others on general job duties.
Perform other tasks as assigned.

Benefits

wellbeing support
retirement and financial protection benefits
insurance offerings (medical, dental, vision, life and disability)
Flexible Time Off (FTO)
11 paid company holidays
160 hours of paid vacation annually for new hires
3 optional holidays
paid sick leave
up to two paid volunteer days per year
summer hours flexibility
leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
annual Global Shutdown between Christmas Day and New Year's Day