Associate Director, Software Development Engineer
Associate Director, Software Development Engineer
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Job Description
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: Overview:
We are seeking a motivated and innovativeSoftware Development Engineer (SDE)to join our cell therapy technology team. In this role you will design implement and maintain software solutions that power advanced cell therapy manufacturing research and clinical workflows. You will collaborate with scientists engineers and cross-functional teams to develop robust applications that enable life-saving therapies for patients.
Key Responsibilities:
Design develop and maintain high-quality software modules for cell therapy platforms including automation data analysis and laboratory workflows.
Collaborate with biologists product managers and engineers to define software requirements and deliver user-centric solutions.
Integrate software with laboratory instruments robotics and imaging systems to support automated cell therapy processes.
Participate in the full software development life cycle (SDLC): planning analysis design implementation testing deployment and maintenance.
Develop and maintain documentation including specifications flowcharts and user manuals.
Ensure software quality through unit testing code reviews and adherence to regulatory standards (e.g. GMP GxP FDA IEC 62304) as applicable.
Troubleshoot debug and upgrade existing systems to enhance performance and reliability.
Work in an Agile environment participating in sprint planning daily stand-ups and retrospective meetings.
Support data management visualization and reporting for research and clinical studies.
Stay current with emerging technologies and propose innovative solutions to improve laboratory and manufacturing efficiency.
Required Qualifications:
Bachelors or Masters degree in Computer Science Engineering or a related technical field.
10 years of industry experience in software development; experience in life sciences medical devices or regulated industries is highly desirable.
Proficiency in object-oriented programming languages such as C# Java Python or C.
Experience with web-based distributed applications (front-end and back-end) REST APIs and relational databases.
Familiarity with laboratory automation image processing (e.g. OpenCV) or integration with scientific instruments is a plus.
Strong analytical debugging and problem-solving skills.
Knowledge of SDLC methodologies (Agile/Scrum) CI/CD and good documentation practices.
Excellent communication skills and ability to work collaboratively in multidisciplinary teams.
Desired Skills:
Experience with laboratory information management systems (LIMS) or bioinformatics platforms.
Familiarity with regulatory standards for medical software (GMP GxP FDA IEC 62304).
Experience in test-driven development and continuous integration.
Background in data science or statistical analysis using R or similar tools is a plus.
Experience with cloud platforms (Azure AWS) and DevOps tools is preferred.
The starting compensation for this jobis a range from $195000 - $220000 plus incentive cash and stock opportunities (based on eligibility).
The starting pay rate takes into account characteristics of the job such as required skills and where the job is performed.
Final individual compensation will be decidedbased on demonstratedexperience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits please visit subject to the terms and conditions of the applicable plans then in effectand may include the following: Medical pharmacy dental and vision care. Wellbeing supportsuch asthe BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability life insurance supplemental health insurance business travel protection and survivor -life programs include paid national holidays and optional holidays Global Shutdown Days between Christmas and New Years holiday up to 120 hours of paid vacation up to two (2) paid days to volunteer sick time off and summer hours caregiver bereavement and military leave. Family care services such as adoption and surrogacy reimbursement fertility/infertility benefits support for traveling mothers and child elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
If you come across a role that intrigues you but doesnt 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.
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 . Visit 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: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Required Experience:
Director
Employment Type
Full-Time
