Associate Director, Equipment Engineering

Bristol Myers Squibb • Indianapolis, IN

8d • $164,838 - $199,745 • Onsite

About The Position

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/ Job Description The Associate Director, Equipment Engineering is an integral part of bringing RayzeBio’s innovative drug products to patients in need. In this role, you will report directly to the Director, Engineering Innovation and be primarily responsible for leading a team of Engineers to achieve clinical and commercial manufacturing objectives at the Indianapolis site(s). The Associate Director, Equipment Engineering will manage a team of Engineers to successfully design, implement, maintain and improve process equipment with novel Radiopharmaceutical technologies including but not limited to custom Hot Cells, robotics, automation and digitization. Additional responsibilities will include managing budgets and working with architectural and engineering firms and specialty equipment manufacturers to achieve our technology and commercialization goals.

Requirements

• 10+ years’ engineering experience on manufacturing equipment in a cGMP Biopharmaceutical or Radiopharmaceutical environment is strongly preferred.
• Proven engineering leadership and management experience.
• Demonstrated experience implementing automation and digitization projects.
• BS/MS Engineering degree.
• Strong GMP manufacturing equipment engineering experiences on at least one of the disciplines: automation, process, mechanical
• Deep understanding of GMP, validation, regulatory standards, and industry best practices.
• Strong track record managing budgets and engineering projects.
• Proven leadership and personnel management experience.
• Strong knowledge of injectable and/or radiopharmaceutical drug product manufacturing.
• Strong knowledge of Automation software platforms and GMP and data integrity controls in automation equipment.
• Commitment to continuous improvement and operational excellence.
• Excellent professional ethics, integrity, and ability to maintain confidential information.
• Organized and detail oriented.
• Strong time management and organizational skills.
• Strong interpersonal communication skills.
• Motivated, adaptable, and able to work under pressure.

Responsibilities

• Accountable for continuous operation and maintenance of process equipment and automation systems for Radiopharmaceutical Clinical and Commercial manufacturing.
• Manage or support engineering capital and facility expansion projects specific to innovative isotope and drug product radiopharmaceutical manufacturing.
• Build and manage a team of highly talented engineers responsible for a wide range of engineering disciplines including automation, process and mechanical.
• Develop and maintain departmental procedures and processes related to equipment engineering activities.
• Support routine GMP manufacturing related activities including but not limited to, Deviation investigation, CAPA and change control.
• Design and implement engineering and related functional systems in alignment with BMS and RayzeBio objectives.
• Work with Production, Quality, Digital IT, Validation and Facility Engineering counterparts to successfully develop and implement novel radiopharmaceutical technologies.
• Coordinate and manage external vendors, partners and service providers as required for the design and implementation of novel radiopharmaceutical isotope and drug product equipment technologies.
• Ensure Engineering personnel comply with site EHS and Radiation Safety programs and promote a culture of safety.
• Review, author and/or revise technical documents (SOPs, URS’s, forms, reports, etc.) as needed.
• Ability to travel as required to support job role.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level