Bristol Myers Squibb · 5 months ago
Engineer, IT Compliance, Lab and Quality Systems
Devens - MA - US
Full-time
Onsite
Entry, Mid Level
$89K/yr - $108K/yr
2+ years expBristol Myers Squibb is a leading biopharmaceutical company focused on transforming patients' lives through science. The role involves providing support for laboratory and manufacturing instrument systems, ensuring compliance with regulations, and collaborating with teams to implement technology improvements.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Execute, update, and support staff on documentation for the support of benchtop equipment and lab and quality systems to ensure assets are reliable, accessible, and secure
Utilize BMS systems to support changes, incidents, problems, and asset management activities for the support of benchtop equipment and lab and quality systems with limited guidance and provide ownership of assets
Executes and/or leads multiple projects and technical work assignments as a point of contact for project stakeholders
Provides digital plant subject matter expertise (SME), to multi-function teams, advises operations on application configurations, data integrity, cyber security, and defends their work before regulatory agencies
Ensures alignment with BMS directives and industry guidelines for applications
Execute on technology improvements and efficiencies opportunities to improve business and compliance
Providing on-call support, as needed, for 24/7 commercial operations
Support Quality and Manufacturing areas during audit and inspections from internal and external organizations
Work both independently and in a team environment at all levels of the organization, in particular Quality, Quality Control, and Manufacturing Operations
Work within all Site Facilities, which requires one to give a high attention to detail and on occasion to properly use Personal Protective Equipment (PPE). May work on cross-site initiatives to drive policy
Qualification
Required
BS degree in life sciences, engineering or computer field or equivalent experience
Minimum of 2+ years of experience working in regulated industries such as Biotech, Pharmaceutical, and Medical Devices familiarity supporting benchtop instruments and applications within a GxP compliant manufacturing or laboratory setting
Comprehensive knowledge of Data Integrity guidance, GxP compliance, Software Development Life Cycle, and Good Documentation Practices
Comprehensive knowledge of SOPs, cGMPs and other compliance requirements and regulatory guidelines (FDA, EU) and the know how to work and manage within a regulatory environment
Demonstrated leadership skills and the ability to negotiate in a complex environment
Demonstrated track record of IT Support in a fast-paced regulated environment supporting benchtop instruments, quality and lab applications
Excellent verbal and written communication skills
The ability to plan and lead small and medium size projects and enhancements
Self-driven and capable of prioritizing
Expanding understanding of network, databases, servers, and PCs
Understanding of usage and administration of Waters NuGenesis
Familiarity with Empower and one or more LIMS, LES/ELN and Document Management Systems
Developed system and business analysis skills
Ability to apply lean and OpEx principles
Project management, communication, and technical writing skills are required
The successful candidate will possess the professionalism and technical competency required to represent the department before our stakeholders, regulatory agencies, and management
Ability to sense, understand, and react to others emotions and recognize the impact of their emotions on your and other's performance and behaviors
Benefits
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.
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.
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
10001+ employees
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
Recent News
2026-01-23
Company data provided by crunchbase