Scientist, Upstream MS&T

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.

The Role

BMS Cruiserath Biologics is seeking to recruit a Scientist, Upstream MS&T as part of Manufacturing Science and Technology to support the commercial manufacturing of biopharmaceuticals in the area of cell culture. This is 12 month fixed term contract role. Responsibilities will include design, execution and analysis of thaw, shake flask and bioreactor and filtration experiments. Imperative to this role will be the ability to interpret data and transfer that knowledge for the benefit of GMP manufacturing

The successful candidate will be a key contributor to a dynamic and highly technical global team. This position will build collaborations with Process Development, Manufacturing, Manufacturing Support, Engineering, Quality Assurance and Global Regulatory Sciences groups. As part of MS&T, this position offers the opportunity to be a member of cross-functional teams addressing critical business objectives. 

Key Responsibilities:

• Support commercial and product technical transfers including late-stage process characterisation programs.
• Design and execution of experiments with an ability to interpret data in thaw, seed production, harvest and filtration unit operations to support NPI, process characterisation and site operations.
• Preparation of study protocols and reports.
• Participate in cross-functional teams and also work independently to meet highly visible critical business objectives. 
• Troubleshooting of manufacturing process-related events and evaluation of new process technologies through the design of scale-down studies and the evaluation of data from manufacturing.
• Interpretation of data to make risk-based decisions and communicate recommendations to technical and non-technical audiences.   
• Leads or contributes to cross functional teams (Manufacturing, QA, QC, Regulatory, Supply Chain, etc) for facility fit activities, specification changes, technical assessments, alternate vendor qualifications, change management.
• Knowledge of cGMP compliance, site and regulatory agency requirements.
• May provide process subject matter expertise for regulatory inspections, filings and other interactions with regulatory agencies, representing the Cruiserath site.
• Contributes to global network initiatives such as the evaluation of new technologies or the establishment of best practice approaches in area of responsibility.

Qualifications, Knowledge and Skills Required:

• A minimum of a BSc. in a Biological or Chemical Sciences/Engineering field is required with an MSc. in one of these fields preferred.
• 2-5 years of industry and/or academic experience. 
• Practical knowledge of cell culture and filtration techniques.
• Candidates must possess good organizational skills and strong attention to detail.
• Demonstrates ability to independently troubleshoot, interpret and discuss data with technical and non-technical audiences.
• Demonstrates ability to identify scientific/operational gaps and identify potential solutions.
• Be self-motivated and work independently under minimal supervision.
• Critical qualities include a high degree of initiative, independent time and project management, good verbal and written communication skills, and the ability to work in a team environment while being able to prioritize.

Why you should apply

• You will help patients in their fight against serious diseases
• You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
• You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym

#LI-Onsite

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 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.

R1602912 : Scientist, Upstream MS&T