Senior Process Engineer
Senior Process Engineer
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1 Vacancy
Job Description
Working with Us
Challenging. Meaningful. Lifechanging. Those arent 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. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside highachieving teams. Take your career farther than you thought possible.
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. Read more: 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. Led by a successful and experienced entrepreneurial team RayzeBio aims to be the global leader in radiopharmaceuticals.
Summary
The Senior Process Engineer will manage engineering support activities for production operations including management and execution of maintenance and calibration activities. The Senior Process Engineer will provide technical expertise to support the operation and maintenance of all process equipment. Further the Senior Process Engineer will implement improvement projects to the process equipment including design execution and handover within cost time schedule quality and functionality specification.
Job Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned.
Manage and execute new asset installation and configuration
Manage investigation and troubleshooting efforts in case of equipment issues or failures
Maintain asset inventory within CMMS
Maintain calibration preventive maintenance and corrective maintenance programs
Develop and maintain spare parts requirements for process equipment
Develop revise and maintain technical documents for process equipment and GMP risk assessments.
Interpret P&IDs equipment/system layouts wiring diagrams and specifications and manage revisions.
Own and drive process equipment and procedures deviations root cause analysis investigations and CAPAs.
Reviews equipment and engineering systems to support data collection root cause analysis investigations and trend investigations.
Lead continuous improvement efforts to increase asset reliability including asset modifications.
Coordinate and execute of assigned projects.
Support commissioning qualification and validation activities when applicable
Provide technical support during Startup PQ and validation activities
Support change requests/change control as needed
Support internal and external audits.
Education and Experience
BS in Engineering discipline and 5 years of handson experience leading and executing plant maintenance and calibration activities in a GMP manufacturing facility.
Or AAS in Engineering discipline and 10 years of handson experience leading and executing plant maintenance and calibration activities in a GMP manufacturing facility.
Skills and Qualifications
Experience in the GMP Pharmaceutical or Medical Device industry is required
Experience in pharmaceutical aseptic manufacturing is preferred
Experience with isolators is preferred
Basic knowledge of Environmental Monitoring Building Automation and CMMS systems and architecture is required.
Vendor management experience is preferred
Experience managing projects is preferred
Must be able to adhere to all applicable procedures cGMPs company policies and any other quality or regulatory requirements. (FDA USP OSHA etc.)
Proficiency with MS Office Suite
Working knowledge of electrical automation systems and robotics
Must be willing to work around radioactive materials.
Familiarity with PLC control systems and instrumentation bus technologies.
Must be flexible to work weekends and holidays as required
Physical Demands
Ability to climb ladders and lift up to 50 lbs.
This is a position that requires working in a GMP cleanroom environment wearing protective clothing and handling of radioactive materials.
WorkEnvironment
The noise level in theworkenvironment is usually moderate.
#RayzeBio #LIOnsite
If you come across a role that intrigues you but doesnt 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.
Uniquely Interesting Work Lifechanging Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.
Onsite Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes siteessential sitebydesign fieldbased and remotebydesign jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Siteessential roles require 100% of shifts onsite at your assigned facility. Sitebydesign roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For fieldbased and remotebydesign roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.
BMS cares about your wellbeing and the wellbeing of our staff customers patients and communities. As a result the Company strongly recommends that all employees be fully vaccinated for Covid19 and keep up to date with Covid19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Required Experience:
Senior IC
Employment Type
Full-Time
