This role pays less than
63%
of similar roles. Most pay
$186,737–$256,000
— the shaded band above.
At the midpoint, this role pays about
$206k
versus about
$221k
for comparable roles.
Based on 240 similar postings.
Employer
About Bristol Myers Squibb
Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing and delivering innovative medicines to patients.
Bristol Myers Squibb currently has
33 open roles
on FindRole.
Listed pay typically runs
$125,480–$152,049
across 33 roles with salary data.
Associate Director, Campus Laboratory and Benchtop Systems serves as the campus-wide lead for laboratory informatics and benchtop instrument software and related IT hardware. This role provides strategic leadership for the deployment, validation, integration, and lifecycle management of laboratory software and automation solutions supporting GxP and non-GxP research and quality operations. The individual will manage a dedicated team, oversee informatics activities, and ensure all systems comply with regulatory, data integrity, and cybersecurity requirements. Key responsibilities include defining requirements, managing service providers, and acting as a subject matter expert during audits. The role requires expertise in LIMS, ELN, CDS, and SDMS platforms, alongside proficiency in 21 CFR Part 11, USP, GAMP 5, and ICH guidelines. The position solves critical challenges regarding instrument connectivity, data acquisition, and the maintenance of validated states for complex laboratory environments.
Lead the campus-wide Laboratory and Benchtop Systems team by managing personnel, setting goals, and driving productivity.
Oversee the deployment, validation, and lifecycle management of laboratory software and benchtop instrument systems.
Ensure all laboratory informatics and automation solutions comply with GxP, data integrity, and cybersecurity requirements.
Act as the primary subject matter expert for laboratory systems during internal audits and regulatory inspections.
Manage service providers and ensure alignment with contractual Service Level Agreements (SLAs) for critical activities.
Provide technical guidance to scientists and quality teams on instrument software qualification (IQ/OQ/PQ).
Identify and implement innovative solutions to improve laboratory workflows and system reliability across the site.
Monitor industry trends to evaluate and integrate new technologies that meet evolving business needs.
What we're looking for
Bachelor's degree in Life Sciences, Chemistry, Engineering, Information Technology, or a related field.
Minimum of 10 years of experience in pharmaceutical laboratory operations, informatics, instrument qualification, analytical systems, or IT roles supporting lab environments.
Proven leadership and track record in managing laboratory informatics programs and benchtop systems across a multi-functional campus.
Expertise in 21 CFR Part 11, USP <1058>, GAMP 5 Category 3/4/5 systems, and ICH Q2/Q7 guidelines.
Required hands-on experience with LIMS (e.g., LabWare, SampleManager), ELN, CDS (e.g., Empower, Chromeleon), and SDMS platforms.
Experience with IT oversight and integration of laboratory instruments and electronic systems supporting GMP and R&D operations.
Substantial knowledge of QSR, GMP, FDA, GAMP, ISO, ICH, and other applicable standards and guidance regimes.
Experienced in documentation, technical writing, and troubleshooting for laboratory informatics and benchtop system lifecycle management.
Electrical Power Systems
Liquid Cooling
Data Acquisition
Automation and Controls
Reliability Engineering
Validation Methodologies
AI/HPC Platforms
Instrumentation
Certification Testing
Lab Automation
Digital Instrumentation
Power Infrastructure
Product Development
Remote (Wilmington, DE)10 days ago
$142,400–$224,100
cGMP
Computer System Validation
CSV
IQ
OQ
FAT
SAT
Commissioning
Qualification
Cleaning Validation
VHP
Six Sigma
FMEA
Process Performance Qualification
Tech Transfer
Aseptic Process Simulation
Lyophilization
Chromatography
high-potency manufacturing
Lab Automation
Computer System Validation
GAMP 5
21 CFR Part 11
GMP
IQ
OQ
Data Integrity
Cyber Security
Hamilton Venus
HighRes BioSolutions
Cellario
Laboratory Informatics
Asset Management
Configuration Management
System Integration
ISO
ICH