Bristol Myers Squibb · 2 days ago
Sr Associate Scientist I - Microbiology
Indianapolis, IN
Full-time
Onsite
Mid, Senior Level
$82K/yr - $100K/yr
3+ years expBristol Myers Squibb is a company that transforms the lives of patients through science, and they are seeking a Sr Associate Scientist I - Microbiology to support testing activities related to radiopharmaceuticals. The role involves advanced laboratory analyses, troubleshooting, method validation, and ensuring compliance with regulatory requirements while maintaining quality standards for product release.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Perform routine microbiological assays including but not limited to bioburden, endotoxin, sterility, environmental monitoring, microbial identification and media qualification testing
Execute method qualification, verification and validation studies with minimal supervision
Troubleshoot assay related issues and perform out of trend analysis
Support investigations/deviations, including root cause analysis and CAPA development to ensure timely close-out
Ensure all assay documentation is audit ready
Prioritize workload to ensure timely completion of an on-time and right first time manner
Foster a positive and collaborative work environment within the lab and with external stakeholders both within the site and outside the site
Train team members on assays
Work with Manager and/or Investigation Writer to ensure any discrepancies are resolved in a timely manner
Support continuous improvement programs such as new technologies and improve data visibility
Identify other opportunities for process improvements and implement changes to increase quality and efficiency within the Quality Control laboratories
Participate in troubleshooting of issues and implement corrective actions to improve quality processes as a result of investigations or internal audits
Work with RSO and QA to ensure compliance with GMP regulations, safety guidelines, and quality standards (FDA, USP, NRC, EP, and other regulatory agencies as needed)
Weekend work, early starts, or late ending times may be required
Qualification
Required
BS in microbiology or related field with 3+ years of direct radiopharmaceutical experience or 4+ years of experience in pharmaceutical field, OR MS in microbiology or related field with 3+ years of experience in pharmaceutical field
A strong background in microbiology and aseptic manufacturing is required
Perform routine microbiological assays including but not limited to bioburden, endotoxin, sterility, environmental monitoring, microbial identification and media qualification testing
Execute method qualification, verification and validation studies with minimal supervision
Troubleshoot assay related issues and perform out of trend analysis
Support investigations/deviations, including root cause analysis and CAPA development to ensure timely close-out
Ensure all assay documentation is audit ready
Prioritize workload to ensure timely completion of an on-time and right first time manner
Foster a positive and collaborative work environment within the lab and with external stakeholders both within the site and outside the site
Train team members on assays
Work with Manager and/or Investigation Writer to ensure any discrepancies are resolved in a timely manner
Participate in troubleshooting of issues and implement corrective actions to improve quality processes as a result of investigations or internal audits
Work with RSO and QA to ensure compliance with GMP regulations, safety guidelines, and quality standards (FDA, USP, NRC, EP, and other regulatory agencies as needed)
Weekend work, early starts, or late ending times may be required
Highly motivated and organized professional with the ability to work independently or in a team environment
Attention to details and data integrity
Good organizational skills are required
Work with multiple computer systems, including Microsoft Office
Excellent professional ethics, integrity, and ability to maintain confidential information
Preferred
Experience in radiopharmaceutical field
Experience handling radioactive materials
Experience with software such as Sherpa or LIMs or equivalent data systems
Multi-disciplined scientist with GMP experience. Radiochemistry experience preferred
Experience with root cause techniques such as 6 M's, 5 Why's, fishbone, or similar preferred
Very personable with strong communication skills and cross-functional collaboration
Ability to multi-task and prioritize work based on multiple workflows
Benefits
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
10001+ employees
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
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