Principal Safety Scientist
$124K - $150K/yr
The Principal Safety Scientist is responsible for conducting hazard evaluations of processes involved in the manufacture of strategic materials, chemical intermediates, active pharmaceutical ...
$124K - $150K/yr
The Principal Safety Scientist is responsible for conducting hazard evaluations of processes involved in the manufacture of strategic materials, chemical intermediates, active pharmaceutical ...
$124K - $150K/yr
The Principal Safety Scientist is responsible for conducting hazard evaluations of processes involved in the manufacture of strategic materials, chemical intermediates, active pharmaceutical ...
The Director, Patient Safety Scientist independently performs core signal detection activities and elevates program or portfolio issues impacting key SMT programs, priorities, resources, and ...
The Director, Patient Safety Scientist independently performs core signal detection activities and elevates program or portfolio issues impacting key SMT programs, priorities, resources, and ...
The Director, Patient Safety Scientist independently performs core signal detection activities and elevates program or portfolio issues impacting key SMT programs, priorities, resources, and ...
The Director, Patient Safety Scientist independently performs core signal detection activities and elevates program or portfolio issues impacting key SMT programs, priorities, resources, and ...
As a Safety Scientist III, you will be responsible for the planning, coordination, and delivery of signal detection and product safety scientist activities, with a focus on tasks that are low to high ...
As a Safety Scientist III, you will be responsible for the planning, coordination, and delivery of signal detection and product safety scientist activities, with a focus on tasks that are low to high ...
To utilize medical knowledge and operational expertise to ensure patient safety by performing medical assessment of adverse events, assembling up-front safety information, collecting quality ...
To utilize medical knowledge and operational expertise to ensure patient safety by performing medical assessment of adverse events, assembling up-front safety information, collecting quality ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
They must exhibit a solid knowledge of safety databases with regards to data entry, workflow ... Requirements: * BS in health science field, Pharmacy, CRA, biomedical sciences with 2 years of ...
They must exhibit a solid knowledge of safety databases with regards to data entry, workflow ... Requirements: * BS in health science field, Pharmacy, CRA, biomedical sciences with 2 years of ...
A global biopharmaceutical company is seeking an Associate Director, Safety Scientist, in Boston. This leadership role involves managing safety scientist activities, collaborating on regulatory ...
A global biopharmaceutical company is seeking an Associate Director, Safety Scientist, in Boston. This leadership role involves managing safety scientist activities, collaborating on regulatory ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
Serve as the lead safety scientist for assigned projects * In collaboration with CSPV physician, author, review and provide critical feedback to relevant sections of study documents including ...
Serve as the lead safety scientist for assigned projects * In collaboration with CSPV physician, author, review and provide critical feedback to relevant sections of study documents including ...
A leading pharmaceutical company is seeking an Associate Director, Safety Scientist to lead risk management in Global Patient Safety. This role involves managing safety scientist activities across ...
A leading pharmaceutical company is seeking an Associate Director, Safety Scientist to lead risk management in Global Patient Safety. This role involves managing safety scientist activities across ...
Basking Ridge, NJ · On-site
$242K - $404K/yr
Job Summary The Senior Director, Clinical Safety Science is a key leadership role responsible for shaping and advancing global safety strategy across the product lifecycle--from early development ...
Basking Ridge, NJ · On-site
$242K - $404K/yr
Job Summary The Senior Director, Clinical Safety Science is a key leadership role responsible for shaping and advancing global safety strategy across the product lifecycle--from early development ...
Basking Ridge, NJ · On-site
$242K - $404K/yr
Senior Director, Clinical Safety Scientist Job Requisition ID: 1430 Posting Start Date: 4/28/26 At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through ...
Basking Ridge, NJ · On-site
$242K - $404K/yr
Senior Director, Clinical Safety Scientist Job Requisition ID: 1430 Posting Start Date: 4/28/26 At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through ...
Serve as the lead safety scientist for assigned projects * In collaboration with CSPV physician, author, review and provide critical feedback to relevant sections of study documents including ...
Serve as the lead safety scientist for assigned projects * In collaboration with CSPV physician, author, review and provide critical feedback to relevant sections of study documents including ...
Basking Ridge, NJ · On-site
$201K - $302K/yr
Job Summary The Director, Clinical Safety Scientist, will handles aspects of signal identification, evaluation, and risk mitigation across therapeutic areas, in collaboration with product safety ...
Basking Ridge, NJ · On-site
$201K - $302K/yr
Job Summary The Director, Clinical Safety Scientist, will handles aspects of signal identification, evaluation, and risk mitigation across therapeutic areas, in collaboration with product safety ...
The Associate Director Safety Scientist is part of a team that performs high quality and timely scientific and operational safety analysis. This position works closely with the Safety Science group ...
The Associate Director Safety Scientist is part of a team that performs high quality and timely scientific and operational safety analysis. This position works closely with the Safety Science group ...
$201K - $302K/yr
Job Summary The Director, Clinical Safety Scientist, will handles aspects of signal identification, evaluation, and risk mitigation across therapeutic areas, in collaboration with product safety ...
New
$201K - $302K/yr
Job Summary The Director, Clinical Safety Scientist, will handles aspects of signal identification, evaluation, and risk mitigation across therapeutic areas, in collaboration with product safety ...
New
Senior Manager/Associate Director, Global Safety Scientist, MSRM Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one ...
Senior Manager/Associate Director, Global Safety Scientist, MSRM Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one ...
Senior Manager/Associate Director, Global Safety Scientist, MSRM Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one ...
Senior Manager/Associate Director, Global Safety Scientist, MSRM Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one ...
South San Francisco, CA · On-site
$155K - $202K/yr
Provides safety science input to cross-functional teams on patient safety and risk management topics. Supports the implementation of pharmacovigilance processes and contributes to continuous ...
South San Francisco, CA · On-site
$155K - $202K/yr
Provides safety science input to cross-functional teams on patient safety and risk management topics. Supports the implementation of pharmacovigilance processes and contributes to continuous ...
$30.53 - $36.17
4% of jobs
$36.17 - $41.81
17% of jobs
$43.32 is the 25th percentile. Wages below this are outliers.
$41.81 - $47.44
15% of jobs
$47.44 - $53.08
1% of jobs
$53.08 - $58.72
11% of jobs
The median wage is $60.48 / hr.
$58.72 - $64.36
8% of jobs
$64.36 - $70
19% of jobs
$70.15 is the 75th percentile. Wages above this are outliers.
$70 - $75.63
9% of jobs
$75.63 - $81.27
1% of jobs
$81.27 - $86.91
2% of jobs
$86.91 - $92.55
13% of jobs
$30
$61
$92
| Aspect | Safety Scientist |
|---|
| Required Credentials |
|---|
| Bachelor's or higher in safety, environmental science, or related field; certifications like ASP or CSP often preferred |
| Work Environment |
|---|
| Research labs, corporate safety departments, or regulatory agencies |
| Employer & Industry Usage |
|---|
| Used across manufacturing, healthcare, and chemical industries focusing on safety research and policy development |
| Comparison Summary |
|---|
Safety Scientists focus on researching and developing safety protocols, policies, and compliance strategies, often working in labs or policy settings. Safety Engineers, on the other hand, are more involved in designing and implementing safety systems on the ground, such as safety equipment and procedures. Both roles require safety certifications and work within similar industries, but Safety Scientists emphasize research and policy, while Safety Engineers focus on practical safety system implementation.

$124K - $150K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 3 days ago
8.1
Based on 50 frontline employees who took The Breakroom Quiz
32nd of 74 rated pharmaceutical
Working with Us
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. Take your career farther than you thought possible.
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. Read more: careers.bms.com/working-with-us.
Job Description
The primary responsibility of the Principal Safety Scientist is to conduct safety studies and evaluations that support internal and external process development and scale-up activities. The individual will collaborate with external testing laboratories and oversee the work conducted by vendor process safety testing groups.
Job Responsibilities
The Principal Safety Scientist is responsible for conducting hazard evaluations of processes involved in the manufacture of strategic materials, chemical intermediates, active pharmaceutical ingredients, and addressing dust hazards associated with excipient blends and other BMS materials. This work is carried out through experimentation, data collection, and interpretation. The scientist collaborates extensively across teams to identify potential safety issues and guide process design toward intrinsic safety.
Results from evaluations and studies are organized and communicated both orally and in writing to various groups and management levels within BMS, as well as to external partners.
The scientist utilizes a diverse range of instruments and techniques to support process research and development. All safety evaluation tests are conducted following standardized procedures, with customization as necessary to achieve project objectives.
Within a team environment, the individual takes initiative in problem solving, facilitates collaboration, and leads through generating ideas and evaluating potential outcomes of various project directions. Solutions based on literature are employed as appropriate.
The role includes coordinating safety testing efforts among internal and external laboratories, including vendor safety testing labs, to support the introduction of processes into a global integrated development and manufacturing network.
A testing strategy is developed and implemented to support chemical registrations, such as REACH, across different regions worldwide.
The scientist manages multiple projects and activities simultaneously, ensuring adherence to established priorities and effectively managing project prioritization as required.
Qualifications
PhD in Chemistry or Chemical Engineering with 4-6 of relevant industrial experience in process development or hazard evaluation, Master's with 6 - 9 year's experience or Bachelor's with 9 - 12 year's experience.
Experience in the pharmaceutical industry is preferred.
Strong technical skills in chemistry, chemical processing equipment, and calorimeters are desired. Prior experience in safety testing, hazard evaluation, plant operations, process development and scale-up, as well as clinical material manufacturing, is also preferred.
Excellent problem-solving abilities, verbal and written communication skills, and the capacity to manage multiple assignments effectively are essential.
The candidate must be able to work independently with minimal supervision.
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.
Compensation Overview:
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
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.
Work-life benefits include:
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
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 a supportive culture, promoting global participation 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 an 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.
Supporting People with Disabilities
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.
Candidate Rights
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/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1601204 : Principal Safety ScientistGet the full story on Breakroom
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Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.
Scientific research and development services and pharmaceutical and medicine manufacturing
10,000+ Employees
New York, NY, US