Director, Production Job at Bristol Myers Squibb in Indianapolis

Bristol Myers Squibb Director, Production Indianapolis, Indiana Apply Now

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 rich in diversity.

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.

RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors.

The Director, Production 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, Operations and be primarily responsible for directing the day-to-day production activities to achieve corporate objectives at the site. The Director, Production will oversee and lead a team of production personnel to successfully deliver quality finished radiopharmaceutical products, on time, and in accordance with the production schedule. Additional responsibilities will include working with the Director, Operations in readying the site for scalability, as we work towards commercialization goals and expanded pipeline products.

Job Responsibilities

1. Provide leadership and direction to members of the production team including manager(s), supervisor(s), operator(s), and associate(s).
2. Collaborate with other functional areas for the triage of deviations, investigations, and CAPAs.
3. Represent production for the internal and external technical transfer of future projects.
4. Collaborate with the Project Management team to assure production schedule adherence.
5. Assist the Director, Operations in mentoring and development of key members of the production team.
6. Align with leadership on the Isotope Production team to ensure GMP compliance and synergy across all operations at the site.
7. Work with Quality, Validation, Engineer Services and Facility Engineering counterparts to successfully develop and implement novel radiopharmaceutical technologies.
8. Work with EM/Microbiology team to ensure contamination control strategies are followed and any OOT or OOS issues are addressed in a timely manner.
9. Develop and manage production related performance metrics.
10. Assist the Director, Operations with production-related budgeting.
11. Ensure production personnel comply with site EHS and Radiation Safety programs and promote a culture of safety.
12. Review, author and/or revise technical documents (SOPs, forms, deviations, etc.) as needed.
13. Up to 15% of travel required.

Education and Experience:

1. 10+ years' manufacturing experience in a cGMP injectable or Radiopharmaceutical environment is required.
2. Proven production leadership and management experience.
3. Demonstrated experience creating and managing production related metrics.
4. Working knowledge of industry related electronic systems (ERP, EQMS, etc.)
5. BS or MS Degree in a related technical field.

Skills and Qualifications:

1. Proven leadership and personnel management experience.
2. Strong knowledge of injectable and/or radiopharmaceutical drug product manufacturing.
3. Excellent professional ethics, integrity, and ability to maintain confidential information.
4. Organized and detail oriented.
5. Strong time management and organizational skills.
6. Strong interpersonal communication skills.
7. Motivated, adaptable, and able to work under pressure.

Physical Demands:

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear and climb stairs with or without accommodation. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and distance vision.

This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials.

Company: Bristol-Myers Squibb

Location: Indianapolis-IN

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.