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Senior Associate Engineer, Device Development

Company: E.R. Squibb & Sons
Location: New Brunswick
Posted on: May 16, 2022

Job Description:

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.The Device Development team within the Global Product Development and Supply organization supports the BMS pipeline to create new drug/device combination products which bring hope to patients. The team achieves these objectives by a mixture of sourcing and developing third party device technologies, and in-house innovation driven by market needs or opportunity. We now have a vacancy for a Senior Associate Engineer to join our team and contribute to our success in meeting the needs of our business and our patients.The Senior Associate Engineer role will be accountable for the following:Performance of Design Control and device development activities including but not limited to creation of Design History File records, e.g. test protocols, test reports, test method development, test method qualification, risk management, design verification studies, design validation studies (including Human Factors studies).Execution of design and development activities, such as concept generation, CAD design, prototyping and testing.Compliance with basic company processes and procedures including Procedural Documents, EHS and training.QUALIFICATIONS:Bachelor's degree or equivalent in a relevant scientific or engineering discipline is required.Minimum of 2 years of device development experience in the Medical Device, Pharmaceutical or Biotechnology industry for combination products.Prior work experience within disciplined product development and design control processesTechnical aptitude for product development such as concept development, test method development, test method qualification, design verification, human factors engineering, design transfer, validations, and regulatory submission process.Able to work semi-autonomously under the guidance of DD leadership across a majority of DD activities.Able to engage and collaborate with cross-functional team members as part of a matrix project team, which may include Quality, Regulatory, Clinical, Medical, Legal, Procurement, Operations and/or Market Research.Strong written and verbal communication skills, with special emphasis on technical writing to support regulatory filings.Desire to develop skills required to support DD goals and objectives to meet patient needs and excel in competitive landscape, industry trends, and regulatory environment for combination products.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 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.

Keywords: E.R. Squibb & Sons, New Brunswick , Senior Associate Engineer, Device Development, Engineering , New Brunswick, New Jersey

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