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Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
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The Analyst – QC Microbiology is part of the Microbiology team of the Quality Control department at BMS Boudry Site.
The main responsibilities of the position include performing and reviewing microbiological tests on raw materials, manufactured drug products and stability samples, performing Environmental Monitoring in cleanrooms, waters, and compressed gases, and performing peer review of raw data.
The analyst may also participate in projects related to laboratory safety or continuous improvement and participates to QC documentation changes.
The QC Analyst – Microbiology activities carries out her/his activities in compliance, always, with laboratory procedures and safety rules (EHS) as well as good documentation and good manufacturing practices (GDP and GMP).
Duties/Responsibilities
Microbiological testing of raw materials and drug products according to incoming testing, release, and stability specifications, and of manufacturing monitoring sampling and testing.
Microbiological testing of raw materials and drug products according to incoming testing, release, and stability specifications.
Microbiological validation activities: execution of validation
Environmental monitoring of cleanrooms (microbiological and particles tests), compressed air, and waters (microbiological tests, TOC, conductivity, nitrates)
Review of analytical raw data generated in the Microbiology Laboratory.
Release of culture Media (growth promotion testing) and material used in Microbiology laboratory.
Identifications of microorganisms.
Support QC Microbiology activities.
Support to maintenance/calibration of equipment and keeps relationship with suppliers. P1 Training of other members of Quality Control or other departments General laboratory tasks (sample management, waste disposal management, cleanings, etc.). Supply management of consumables, including purchase requisitions. Creation and update of procedures, work instructions and other QC documents. Print Worksheets as required, for the purpose of the assignment by Manager or delegate Participation in projects and implementation of continuous improvement actions in the laboratory. Participation and presentations at team meetings. Respect 5S principles and propose 5S improvements. Other responsibility assigned by the laboratory management.
Promotes safe practices and behaviors.
Report immediately incidents to Environmental Health and Safety department, participate in investigations and identify measures to prevent similar accidents in the future.
Demonstrate Bristol Myers Squibb values.
Qualifications
Specific Knowledge, Skills, Abilities:
Good knowledge on experience of environmental, water and gas monitoring.
Knowledge of good microbiological practices and contamination control concepts.
Knowledge of regulatory requirements related to microbiological testing and environmental monitoring.
Good organizational skills and good multi-tasking ability; ability to set and focus on priorities.
Strong attention to details
Ability to work independently for extended periods of time and collaboratively within a team.
Good knowledge of laboratory safety rules.
Ability to write business and technical documents (good technical writing skills).
Capable of independent problem-solving; informs management as appropriate.
Advanced computer proficiency (Windows and MS Office) and ability to use a LIMS.
Fluency in French and professional command of English (oral and written)
Ability to communicate effectively with peers (QC members, management, other departments).
Good knowledge of the LEAN and 5S concepts and methodologies.
Flexible, able to adapt to change.
Education/Experience/ Licenses/Certifications:
Federal Certificate of Capacity as Laboratory Technician or similar education.
At least 1 year of work experience in a GMP environment or regulated industry.
Experience with microbiological testing according to compendial harmonized methods.
Good knowledge and ability to apply GDP and GMP rules.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in 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.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
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