Sr Engineer Computer Systems Validation

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: careers.bms.com/working-with-us.

Position Summary

The Senior Engineer, IT Compliance and CSV, supports computerized system validation, IT compliance, and change/deviation management for regulated computerized systems across the Devens Campus, including the Cell Therapy Facility (CTF). This role executes System Life Cycle deliverables, serves as a CSV subject matter expert for computerized system changes, and supports the IT Deviation Management, Computer System Audit, Change Management, and Risk Management programs. The Senior Engineer works collaboratively with Quality, Validation, Manufacturing, Engineering, and enterprise teams, and interfaces with global compliance and validation initiatives, serving as a site delegate as needed.

Duties/Responsibilities

· Execute assigned computer system validation (CSV) and IT compliance activities, including in support of the Devens Cell Therapy Facility (CTF), in alignment with team and site objectives.

· Serve as a Computer System Validation (CSV) subject matter expert (SME) for computerized system changes and associated IT/Automation projects, advising operations on CSV matters.

· Support the IT Deviation Management, Computer System Audit, Change Management, and Risk Management programs at the site.

· Provide guidance to Digital Plant and site functional groups on CSV process implementation; participate in analyzing and addressing process deficiencies.

· Support the BMS Data Integrity and Quality Risk Management programs.

· Provide IT quality support through review and approval of investigations and change controls, deviation ownership of computerized system events, and CSV activities.

· Enter and support deviations, associated actions, root cause analysis, corrective/preventative actions (CAPA), and effectiveness reviews within the Quality Management System, as needed.

· Participate in regulatory and internal audits/inspections as a Digital Plant representative and help generate timely responses to audit observations.

· Support the implementation and tracking of Service Level Agreements (SLA) for supported business-critical activities.

· Develop and maintain procedures, guidance documents, and other GxP-related documents in a high state of compliance and audit readiness.

· Execute validation, implementation, and change management activities for regulated IT systems in compliance with applicable regulatory requirements.

· Track assigned project progress to meet schedules, maximize productivity, reduce costs, and increase efficiencies; provide updates to management through established tools and dashboards.

· Identify opportunities to improve the efficiency and quality of CSV documentation and processes, and evaluate new technologies, tools, and process improvements.

Qualifications

· Bachelor’s degree in Engineering, Science, Information Technology, or a related IT/OT discipline, with a minimum of 3–5 years of relevant experience in Compliance and Computer System Validation (CSV), preferably including Cell Therapy, Biologics Manufacturing, or related life sciences experience.

· Solid knowledge of regulatory computer system validation requirements, including FDA, EMA, and applicable global requirements (e.g., ICH Q7, Q8, Q9), particularly as applied to Cell & Gene Therapy or Biologics manufacturing.

· Working knowledge of 21 CFR Part 11, 21 CFR Parts 210/211, GAMP, for validation of automated systems (working knowledge of and ISO 9001 standard is a plus).

· Working knowledge of health authority requirements and regulatory issues pertaining to digital assets, including Data Integrity.

· Experience implementing and supporting quality systems, risk management, audit readiness, deviation management, and change management within a fully automated, regulated manufacturing environment.

· Demonstrated ability to represent the department before stakeholders, external regulatory agencies, and management.

· Ability to support interactions with US FDA and other regulatory agencies, as needed.

· Strong project management, communication, and technical writing skills.

· Past experience in developing training materials and conducting training

· Working understanding of Lean Six Sigma and OPEX principles.

· Ability to develop and apply innovative approaches to projects and processes.

· Ability to understand business needs and synthesize solutions across functions.

· Strong collaboration and cross-functional skills to support continuous improvement, promote knowledge sharing, and implement best practices across the network.

· Communicates effectively across different levels of the business; exercises sound judgment within established practices and procedures, escalating to management when necessary.

· Ability to work in a dynamic work environment and manage multiple priorities.

· Experience/training in performing internal audits/inspections is not mandatory, but would be an advantage

· Willingness to mentor junior team members and contribute to knowledge-sharing within the team.

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:

Devens - MA - US: $99,480 - $120,551

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

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, 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.

*Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work, Life-changing 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.

On-site Protocol

BMS 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.

Supporting People with Disabilities

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 View email address on us.fitly.work. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

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:

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If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at View email address on us.fitly.work. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1605360 : Sr Engineer Computer Systems Validation