Senior Validation Engineer

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/ Summary The Senior Validation Engineer will help support the Radiopharmaceutical facility and GMP operations in Indianapolis.  The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly specialized facility, utility, analytical, and process equipment.  The position will utilize a wide range of engineering disciplines to support the advancement from construction to clinical development and subsequent GMP commercial operations.  Additional responsibilities may include the onboarding of new technologies, process development, GMP operations support, deviation investigation, CAPA management, continuous improvement projects, and future facility expansion projects. Job Responsibilities Essential duties and responsibilities include the following.  Other duties may be assigned. Work with the project team and/or General Contractor as required to support the commissioning and validation of a 60,000 sq. ft. office, warehouse, and GMP Radiopharmaceutical production facility. Develop and implement the CQV strategies for the GMP spaces including but not limited to office, warehouse, development, quality control, sterility/microbiology, and GMP production areas. Work with consultant(s) as required to support the implementation and execution of the CQV program.  Support the engineering, QC, and Operations team as required to improve and implement new processes Provide validation support for day-to-day development and GMP operations Provide engineering and operational support as required Expand expertise in additional areas of validation (process validation, QC assets, CSV, cleaning validation, etc) Own and manage a specific area of validation (i.e. process validation, QC assets, CSV, cleaning validation, etc) Apply technical knowledge and abilities to investigate manufacturing deviations Review data and documentation to support investigations Own and drive projects and continuous improvement efforts Draft GMP documentation including but not limited to SOP’s, Forms, Protocols, Technical Documents, Reports, Deviations, CAPAs, Change Controls and reports. Support Health Authority Inspections Maintain department KPIs related to performance Mentor and cross-train other team members Execute and provide support executing equipment and process validations as necessary. Education and Experience BS or MS in scientific related field or equivalent work experience 4-8 years of experience in Radiopharmaceutical or injectable GMP manufacturing environment 4-8 years of validation experience within a GMP environment Skills and Qualifications Good technical writing skill-set Solid understanding of regulatory guidelines for validation and risk management Must possess an independent mindset and tenacity Highly motivated and organized professional with strong interpersonal and communication skills. Proven experience working with teams in a GMP environment. Multi disciplined engineer with GMP experience Excellent professional ethics, integrity, and ability to maintain confidential information. Uses AI tools to enhance individual productivity and quality of work ​ 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. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision and distance vision.  This is a position that requires working in a GMP cleanroom environment, wearing protective clothing, and handling of radioactive materials. Work Environment The noise level in the work environment is usually moderate. If you come across a role that intrigues you but doesn’t 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. Compensation Overview: Indianapolis - RayzeBio - IN: $107,904 - $130,754 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.  Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: 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,