Job Description
Job title: Project Engineer – Capital Projects in Devens, MA at Bristol-Myers Squibb
Company: Bristol-Myers Squibb
Job description: Working with Us
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. 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: .Project Engineer – Capital Projects (Ref:7660), Bristol-Myers Squibb Company, Devens, MA. Execute various capital projects, including modification and improvement of upstream or downstream biological process systems (e.g. Bioreactor, Harvest, Ultrafiltration and Diafiltration, Chromatography, Liquid handling skid) and Clean/plant utilities (e.g. WFI, Clean steam, clean compressed air, glycol system). Execute different phases of projects, beginning with requirement gathering, and continuing through feasibility, cost estimation, conceptual and detail design, procurement, execution, commissioning and validation, and project closeout. Oversee procurement and installation of new biotechnologies in the areas of biologics production equipment, utilities, and facilities enhancements. Replace aging bioprocess and Quality Control equipment. Manage cross-functional teams of internal and external stakeholders throughout project execution for timely completion of the project. Internal stakeholders/departments include manufacturing engineering, manufacturing/scheduler, Environmental Health & Safety, maintenance, asset management, automation, validation, and quality assurance. External stakeholders include vendors, mechanical, electrical, piping, construction management, quality, and other contractors. Review and redline Piping & Instrumentation Diagrams, isometric drawings, and construction documents. Review and approve submittals of biological process equipment, valves, instruments, and other components. Review and approve commissioning and qualification documents. Develop, maintain, and update Engineering Tum Over Package (ETOP). Administrate construction activities, including reviewing technical drawings, answering RFls, performing on-site inspections and pre-startup safety reviews (PSSR), and maintaining and closing punch list. Execute projects in highly regulated GMP cleanrooms that require cleanroom and equipment shutdowns. Implement projects keeping regulatory and safety standards. Follow Maximo service request process to execute coordinated project activities.40 hrs/week, Mon-Fri, 8:30 a.m. - 5:30 p.m. Salary: $142,475/yr. to $149,240/yr.MINIMUM REQUIREMENTS:Bachelor’s degree or foreign equivalent degree in Biological Engineering, Biotechnology, Chemical Engineering, or related field, and six (6) years of related work experience.Must have experience with/in:
- Project management with Engineering/Capital projects in biologics including procurement, installation, commissioning/start-up, review installation compliance to design documents, Qualification and project closeout;
- Regulatory and safety requirements - Working in GMP cleanrooms and with Process & clean/plant Utility Equipment;
- Engineering principles;
- Construction techniques including Mechanical, Electrical, and Plumbing;
- Supporting manufacturing operations;
- Creating a full project scope including requirement gathering, cost estimation, schedule, risk register, define project goals/milestones and project necessity;
- Administrate construction activities including review of technical drawings, review submittals, answering RFls, performing on-site inspections.
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.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design 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 field-based and remote-by-design 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 well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 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:Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Expected salary: $142475 - 149240 per year
Location: Devens, MA
Job date: Sat, 26 Apr 2025 04:59:13 GMT
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