Qc Associate Jobs

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 seeking a quality control professional to join our QC team, performing QC testing in support of biologics bulk drug substance manufacturing and Stability Studies using defined methods in a cGMP compliant laboratory. The QC Associate assures test results are accurately recorded and abnormal data or equipment/instrument malfunctions are promptly reported to supervisors. The works day shifts are Monday through Friday.

Major Duties And Responsibilities

• Perform routine testing and data review of batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant laboratory.
• Executes routine procedures based on methodologies/responsibilities, such as HPLC, UPLC, iCIEF, Capillary Electrophoresis (CE), and Gel Electrophoresis.

Education, Knowledge And Skills

• Demonstrated manual dexterity.
• Demonstrated ability to work independently as well as part of a team to complete assignments within defined time constraints.
• Experience in analytical test methods such as HPLC and Gel Electrophoresis highly preferred.
• Knowledge of lab software applications (e.g. LIMS, ELN (LES/SmartLab), Empower) preferred.
• Ability to interpret and apply cGMPs, USP, regulatory requirements and industry best practices.
• Demonstrates problem solving and analytical thinking skills.
• High attention to detail and demonstrated organizational skills.
• 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.
• A minimum of 0-2 years of experience in a Biologics QC laboratory or related biopharmaceutical cGLP or cGMP lab.

Contacts

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

Working Conditions

• Flexibility to work irregular hours and short notice overtime.
• 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.

Decision Making

• Incumbents normally receive detailed instructions on routine work and detailed instructions on new assignments.
• Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure.

BMSBL, BMSBLDMA, VETERAN

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.