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Job Details

Bristol-Meyers Squibb, Co.

Engineer II, Single Use Technology (R1553158-en-us-1)





Devens, Massachusetts, United States

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today. With therapies only in their infancy and BMS’s continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.

The Development Engineering & Automation group within the Cell Therapy Development (CTD) organization is focused on novel technology development. The team combines the skills of engineers and scientists to demonstrate the feasibility and robustness of next generation manufacturing equipment and process technologies. We are seeking an Engineer II who will support the development and implementation of process equipment for next generation cell therapy manufacturing, with a primary focus on single-use systems.

The Engineer II will be responsible for leading cross-functional teams across the BMS cell therapy network to design and qualify single-use assemblies for pipeline programs, continuous improvement initiatives, and new manufacturing technologies.

The successful candidate will:

  • Interact effectively with the end user community of development scientists and engineers to understand user requirements and provide technical guidance for material/supplier selection and qualification testing
  • Be capable of translating user requirements into single-use design drawings and specifications
  • Collaborate with internal partner functions to ensure a phase-appropriate approach to meeting technical, quality, and supply chain requirements and to ensure the delivery of robust materials that are suitable for clinical and commercial manufacturing
  • Engage with suppliers to communicate user requirements and provide guidance to address gaps in supplier capabilities and/or technologies

Basic Qualifications:

  • BS in Chemical or Mechanical Engineering, Life Sciences, Materials Sciences, or related discipline with 4-6 years of relevant experience in the biopharmaceutical industry or MS with 1-3 years of relevant experience
  • Experience with process equipment design, qualification, and implementation, preferably with single-use systems at a biopharmaceutical company or bioprocessing supplier
  • Familiarity with GMP biomanufacturing requirements, preferably direct experience working in a GMP environment
  • Self-motivated individual with demonstrated ability to lead and support highly cross-functional teams
  • Demonstrated ability to analyze technical data and design experiments
  • Excellent communication and interpersonal skills

Preferred Qualifications:

  • Working knowledge of industry best practices and standards for single-use systems used in biopharmaceutical and cell and gene therapy applications including extractables and leachables
  • Familiarity with single-use component and assembly manufacturing methods
  • Experience with generating technical drawings using CAD software
  • Experience with technical diligence and/or quality audits

If you want to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients’ lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to . Visit[Register to View] target="_blank"> [Register to View] to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.