QC Microbiology Associate III

Location
Bothell, WA, United States
Posted
Sep 25, 2020
Ref
R1530253
Required Education
Bachelors Degree
Position Type
Full time
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

This is a Wed - Sat AM Shift (6a - 4:30p)

The primary focus of the QC role will be to provide lab support functions within Juno's Quality Control Operations group. This role will be responsible for ensuring continual operations of the QC labs through preparation of reagents and solution, ordering of material and consumables, equipment maintenance, and assist in sample receiving.

Qualifications

BS Degree in Life Science and 3+ years of GMP/industry experience
  • Strong technical writing skill set and be able to critically review reports while effectively inputting and expressing Quality principles.
  • Innovative, proactive, and resourceful; committed to quality and continuous improvement.
  • Ability to work effectively at a fast pace with cross functional departments to finalize time-sensitive deliverables.
  • Able to manage multiple priorities.
  • Strong project planning skills.
  • Strong computer skills with MS Office (e.g. Word, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System)
  • Previous work experience in the following: quality assurance, CAPA, change control, deviation management, compliant handling and compliance.
  • Experience interacting with FDA or other regulatory agencies
  • Must complete tasks independently, notify supervisor of decisions outside of established processes and the ability to build an internal network.
  • Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationshipswithin CTDO
  • Preferred Qualifications:
    • Background in Protein Biologics or Cell Therapy Manufacturing
    • Experience in continuous improvement, operational excellence and six-sigma
  • 4+ years of quality systems experience.


BMSCART

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.