Senior Manager, Benchtop IT Systems – Devens Cell Therapy Facility at Bristol-Myers Squibb

Devens, Massachusetts, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

Bachelor’s Degree (or higher) in Computer Science, Engineering, Life Sciences, or related field
7+ years of experience managing laboratory IT systems in a GMP or GxP-regulated pharmaceutical manufacturing or research environment
Deep knowledge of laboratory informatics systems (e.g., LIMS, CDS, SDMS, ELN) and corresponding validation requirements
Demonstrated experience leading complex IT or digital projects, preferably in biologics or cell therapy manufacturing
Strong understanding of CSV (computer system validation), data integrity, and regulatory requirements in laboratory environments
Proven leadership, people management, and cross-functional project management skills
Excellent communication, organizational, and stakeholder management abilities
Advanced Degree (MS, PhD, or MBA) in a relevant discipline (preferred)
Experience delivering IT solutions for advanced therapy manufacturing (preferred)

Responsibilities

Lead and manage the end-to-end lifecycle of benchtop and laboratory IT systems (LIMS, CDS, SDMS, ELN, bespoke instrument software) within the Cell Therapy Facility, including requirements gathering, design, implementation, validation, and ongoing support
Oversee system integration with manufacturing, quality, and enterprise platforms, ensuring seamless data flow and strong information security
Ensure strict adherence to GxP, FDA, and other applicable regulatory standards in system implementation, validation, and operations
Partner with internal stakeholders (lab users, engineers, QA, manufacturing) to clarify user needs, recommend scalable solutions, and drive digital innovation at the bench level
Direct vendor relationships and manage contractors supporting laboratory IT systems, including service level agreements and performance monitoring
Monitor system performance and proactively resolve incidents, collaborating closely with global support teams
Develop and maintain robust documentation, validation plans, SOPs, and change control records for laboratory IT systems
Drive continuous improvement initiatives, including system upgrades, user training, cybersecurity enhancements, and lifecycle planning
Effectively manage operational budgets, resources, and schedules, tracking and reporting progress to site leadership and global IT function
Provide leadership, coaching, and mentorship to direct reports and cross-functional project teams

Skills

Key technologies and capabilities for this role

LIMSCDSSDMSELNGxPSystem IntegrationValidationLaboratory AutomationIT Lifecycle Management

Questions & Answers

Common questions about this position

What benefits does Bristol Myers Squibb offer?

Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Is this position remote or onsite?

This information is not specified in the job description.

What are the key responsibilities for this role?

The role involves leading the lifecycle of benchtop and laboratory IT systems like LIMS, CDS, SDMS, ELN, ensuring GxP compliance, system integration, stakeholder collaboration, vendor management, and driving continuous improvements.

What is the company culture like at Bristol Myers Squibb?

The culture is challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow alongside high-achieving teams, and emphasis on balance and flexibility.

What makes a strong candidate for this Senior Manager position?

Strong candidates will have leadership experience in managing IT systems lifecycles in GxP environments, expertise in laboratory systems like LIMS and ELN, regulatory knowledge, cross-functional collaboration skills, and ability to manage vendors and budgets.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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