Specialist, Associate Scientist, QC Microbiology

Posted 9 days ago
Main Location
New York City, NY, United States

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.

2nd Shift - Wednesday - Saturday


  • Carry out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws.
  • Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory requirements at all times.
  • Follow directions properly, work cooperatively as an individual contributor and as a team member.
  • Communicate effectively with QC peers, cross-functional peers and management.
  • Assist in troubleshooting and solving problems that may come up in the day to day operation of the department.
  • Participate in Aseptic Process Validations/ Media Fills.
  • Perform Sterility Testing and sample aliquoting.
  • Perform Viable and Non-Viable air monitoring viable surface monitoring.
  • Perform and lead Environmental Monitoring Performance Qualification and Aseptic Qualifications.
  • Perform Environmental Monitoring on routine basis.
  • Perform microbial identification via polymerase chain reaction (PCR).
  • Perform microbial isolation techniques and perform gram stains.
  • Send out samples to contract labs and track results/reports.
  • Evaluate environmental/personnel monitoring samples and create NOEs for action levels.
  • Support Endotoxin and Mycoplasma assays as needed.
  • Performs general laboratory cleaning/wipe-down.
  • Perform routine maintenance of lab equipment.
  • Maintain lab inventory and order lab supplies and materials.
  • Receives and stock test reagents, lab supplies and test media.
  • Document laboratory test results on worksheets, forms and logbooks utilizing Good Documentation Practices.
  • Support continuous improvement projects related to QC.
  • Assist in special projects as needed.
  • Author and revise controlled documents such as Standard Operating Procedures and Controlled Forms.  Author non-routine Protocols/Validation Plans/ reports in support of projects.
  • Assist in investigations &CAPAs associated with QC Microbiology Department.
  • Support data trending and tracking of results.
  • Perform all other duties as assigned by Management.


  • Fosters teamwork and promotes an environment that motivates others to achieve our goals.
  • Requires Bachelor’s degree in Microbiology, Molecular Biology, or related discipline and minimum 3 years of experience working in a regulated manufacturing environment. Environmental Monitoring and Microbiology lab experience strongly preferred. An equivalent combination of experience/education is acceptable.
  • Have a good understanding of USP, EP, JP, and FDA microbiology testing requirements.
  • Good knowledge of Microsoft Word and Excel.
  • Responds to challenges and additional workload in an understanding, professional and objective manner. 
  • Adaptable to dynamic conditions, work practices, project timelines and changing schedules.
  • Ability to multitask, prioritize workload, document properly and interpret data accurately.
  • Able to communicate effectively with GDPO functional areas and external agencies.
  • Flexible and willing to do all assigned tasks with positive attitude.
  • Primary responsibilities will be Environmental Monitoring related tasks.

Working Conditions

  • The incumbent will be required to wear uniform/ PPE for long durations in the manufacturing or

                 laboratory environment.

  • The incumbent may be required to stand and walk for extended amount of time.
  • The incumbent may be required to work hazardous materials and areas with magnetic and electric fields.
  • Flexibility with schedule (weekends, holidays, extended hours and rotating/staggered shift) is an absolute must.
  • Change to work timings and assigned tasks may occur at a very short notice to support business needs.
  • Shift days and hour may change to accommodate the business needs.


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. 

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 any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

We're a community of women leveraging our connections into top companies to help underrepresented women get the roles they've always deserved. Simultaneously, we work to build truly inclusive hiring processes and environments where women can thrive and not just survive.
Are you hiring? Join our platform for diversifiying your team
Specialist, Associate Scientist, QC Microbiology
Bristol Myers Squibb