Director, IT Automated Manufacturing Suite

Not Interested
Bookmark
Report This Job

profile Job Location:

Devens, MA - USA

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Working with Us
Challenging. Meaningful. Life-changing. 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 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: Summary:

The Director AMS IT provides strategic technical and hands on leadership for the Automated Manufacturing Suite supporting GoSolos digital manufacturing transformation. This role is accountable for building strategic roadmaps architecting building and integrating the technology systems that enable scalable reliable manufacturing operationsincluding MES platform modernization recipe execution environments DeltaV automation integration and manufacturing scheduler capabilities.

The Director AMS IT leads a team of technical architects engineers and integration specialists by balancing workload resolving technical conflicts and achieving operational excellence through hands-on execution and accountability. This leader partners closely with cross-functional teams including Manufacturing MS&T Quality IT PMO GxP and vendor organizations to anticipate requirements manage integration risks allocate resources and ensure alignment with manufacturing priorities.

This role also serves as a key contributor to digital manufacturing innovation leveraging AI-enabled automation data analytics and modern DevOps practices to strengthen system reliability reduce operational risk and accelerate time-to-therapy for patients. This role also supports the development of future-ready technical talent within the manufacturing systems domain.

Key Responsibilities:

The Director IT Automated Manufacturing Suite (AMS) serves as the primary technology leader partnering with the AMS Business Lead to deliver an integrated digital manufacturing foundation supporting GoSolo. This role connects MES platform modernization DeltaV integrations MES recipe lifecycle and manufacturing scheduling into a unified execution stack that enables scalable compliant and reliable manufacturing operations. The Director translates manufacturing priorities into technology strategy and coordinated delivery ensuring systems integrations and data flows operate cohesively to support execution today and scale for the future.

Key Responsibilities:

  • Serve as the primary IT partner to the AMS Business Lead translating manufacturing needs into technology strategy roadmap and delivery alignment.

  • Build the strategic 3 year roadmap and own development for the build out of AMS through partnership within the IT and the business teams.

  • Lead through a matrix organization on the integration of MES DeltaV recipes and manufacturing scheduling into a cohesive execution platform.

  • Provide technology leadership across MES platform scaling DevOps validation and system architecture.

  • Establish MES as the central execution environment connecting automation recipes and scheduling.

  • Drive integration between DeltaV automation systems and enterprise manufacturing platforms including process data and equipment signals.

  • Define and standardize recipe lifecycle data models and configuration patterns across sites.

  • Enable end-to-end execution by embedding the manufacturing scheduler into MES and connecting it to DeltaV.

  • Coordinate priorities dependencies and technical decisions across AMS workstreams.

  • Partner with Manufacturing MS&T Quality and enterprise IT teams to align delivery and operational outcomes.

  • Ensure compliance with GxP validation and data integrity requirements across all systems and integrations.

  • Lead continuous improvement through adoption of modern DevOps automation and AI-enabled capabilities.

  • Manage technical escalations delivery risks and cross-program dependencies within the AMS portfolio.

  • Develop and support technical talent through coaching hiring and capability-building across the AMS IT team.

  • Establish performance metrics and operating rhythms that ensure consistent high-quality delivery aligned to CT Manufacturing Automation goals.

Education & Experience:

  • Bachelors degree in Computer Science Engineering Information Systems or related technical field; advanced degree (MS MBA) preferred but not required.

  • 1215 years of experience in the pharmaceutical or life sciences industry with solid expertise in digital manufacturing manufacturing systems and/or manufacturing IT.

  • 5 years in technical leadership roles including hands-on architecture platform engineering and cross-functional team coordination.

  • Strong working knowledge of MES platforms manufacturing execution systems automation integration and manufacturing IT best practices; experience in biologics or cell therapy manufacturing is a plus.

  • Proven ability to architect build and deliver complex technical systems within regulated environments meeting timelines and budgets.

  • Deep hands-on experience with MES platforms (e.g. Syncade and manufacturing execution systems.

  • Proven ability to architect and build integrations with DeltaV or comparable automation platforms

  • Strong technical skills in manufacturing system architecture data modeling API design and integration patterns.

  • Experience designing and implementing scheduling and execution integrations in manufacturing environments.

  • Track record of building and delivering large-scale platform modernizations in GxP-regulated environments.

  • Hands-on experience implementing systems under GxP compliance and computer system validation (CSV) requirements.

  • Experience leading technical teams and coordinating with vendors across complex multi-initiative programs.

  • Excellent problem-solving written/verbal communication and interpersonal skills.

  • Familiarity with cloud platforms (AWS Azure) DevOps practices and modern software delivery approaches.

  • Demonstrated ability to drive technical process improvements and operational efficiency.

  • Technical architect who designs and builds cohesive solutions across disparate initiatives.

  • Hands-on leader who drives execution while coordinating across IT and business partners.

  • Strategic thinker with strong implementation skills and attention to technical detail.

  • Comfortable leading teams through complexity ambiguity and evolving technical requirements.

  • An equivalent combination of education and experience may be considered.

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.

Compensation Overview:

Devens - MA - US: $208880 - $253112

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 employees 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 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: The 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 . Visit 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: Protection

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . 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.

R: Director IT - Automated Manufacturing Suite

Required Experience:

Director

Working with UsChallenging. Meaningful. Life-changing. 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 breakthrou...
View more view more

Key Skills

  • Computer
  • Fitness
  • Facilities Management
  • Account Development
  • Maintenance Engineering
  • Asic

About Company

Company Logo

Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more

View Profile View Profile