QC Associate

Profile

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.

Performs routine testing and data review of in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment. Executes routine procedures based on methodologies/responsibilities of the specific QC sub-team. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).

Knowledge of science generally attained through studies resulting in a BS in the physical or life sciences, a related discipline, or the equivalent in related experience.

Knowledge of basic laboratory techniques such as pH, volumetric measurement, pipetting, analytical weighing and basic laboratory safety practices preferred.

Attention to detail and demonstrated organizational skills.

Demonstrated manual dexterity.

Knowledge of basic electronic systems (email, MS Office, etc.)

0-2 years experience with one or more of the following methodologies: ELISA, qPCR , and B7 binding Biacore methods

Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within QC, in order to exchange information regarding testing completed, in process and planned.

Daily contact with her/his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions.

Occasional contact with other line management staff relating to specific project responsibilities may be expected.

Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials.

Overtime work may be required on weekdays, weekends, holidays, and during adverse weather conditions in support of manufacturing facility.

Flexibility to work irregular hours and short notice overtime.

Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure.

Incumbents normally receive detailed instructions on routine work and detailed instructions on new assignments.

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 the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com