We use cookies. Find out about cookies here. By continuing to browse this site you are agreeing to our use of cookies.

Quality Control Analyst Laboratory (Temporary Assignment), Boudry, Nebraska

Created10/05/2020
ReferenceR1528896
CategoryQlty Assurance Methods
Job typeFull-Time
CountrySwitzerland
StateNebraska
CityBoudry
SalaryCompetitive

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.

Celgene (a wholly owned subsidiary of Bristol-Myers Squibb) is a global biopharmaceutical company committed to changing the course of human health through bold pursuits in science, life-enhancing therapies, and a promise to always put patients first. At the core of that mission are the talented individuals who contribute their unique skill sets to help us drive innovation and deliver truly life-changing drugs for our patients. As we continue to pursue that mission, we're looking for talented professionals like you to join our team

In this role, you are responsible to perform all type of analytical testing that is required for release of raw and packaging materials, final product and stability samples as well as all IPC testing. Additional responsibilities can be the support of stability studies, handling of deviations and change controls.

As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory:
  • Perform analytical testing according to raw material and product release specifications (HPLC, GC, UV/VIS, IR, dissolution, pH, conductivity, TOC, titration, weighing, wet chemistry experiments etc.)
  • Perform review of analytical data
  • Perform basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs etc.)
  • Support management supply of consumables
  • Support maintenance/calibration of equipment and keeps relationship with suppliers
  • Support stability studies (set up, sampling, testing, coordination)
  • Writes specific standard operations procedures (e.g. operation and maintenance of equipment)
  • Participate in method transfer and method validation activities
  • Support selection, purchase and commissioning of new equipment
  • Handling of deviations and change controls


Your Profile:
  • Federal Certificate of Capacity as Laboratory Technician or similar education
  • 2 - 3 years of work experience in a GMP environment
  • Solid knowledge in HPLC and GC techniques and CDS
  • Knowledge of dissolution, UV/VIS and IR techniques
  • Knowledge of analytical method transfer and analytical method validation
  • Experience of doing analytical testing according to Ph. Eur. and USP prescriptions
  • Good writing skills in French & English
  • Excellent team spirit !
  • Knowledge of most common office software


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.
EmployerBristol-Myers Squibb

Get new jobs by e-mail