Associate Director, BI&T Compliance & CSV

Bristol Myers Squibb

Quick summary

Work type
On-site
Location
Devens, MA
Salary
$176,720–$214,137 / yr
Posted
4 days ago
Closes
Aug 28, 2026
Nearby
99+ roles within 25 mi

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $196k
This role $195k
$135k most similar roles pay here $249k

This role pays more than 55% of similar roles. Most pay $153,925–$238,381 — the shaded band above. At the midpoint, this role pays about $195k versus about $196k 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 36 open roles on FindRole.

Listed pay typically runs $137,530–$165,315 across 36 roles with salary data.

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View all roles at Bristol Myers Squibb

At a glance

TL;DR · Associate Director, BI&T Compliance & CSV

Role Posting Log in to save

As an Associate Director of Biotechnology and Information Technology (BI&T) Compliance and Computer System Validation (CSV), you will lead the Devens Campus IT Compliance and CSV team, ensuring a safe and compliant environment while driving continuous improvement in productivity and KPIs. Your daily responsibilities include managing service providers, fostering business partnerships, and representing Digital Plant during audits. You will also act as the CSV process owner, providing guidance on implementation and supporting data integrity programs. Key technologies involve ServiceNow and other regulated IT systems used across the site. Essential skills include expertise in 21 CFR 210, 211, and 11, GAMP standards, and experience with FDA regulations. This role demands a bachelor’s degree in Engineering or related fields, along with extensive experience in pharmaceutical quality operations and computer system validation.

Skills

ServiceNow GAMP ISO 9001 21 CFR 210 21 CFR 211 21 CFR 11 QSR GMP FDA ICH Technical Writing Documentation Troubleshooting Problem Solving Project Management

What you'll do

  • Lead and manage the Devens Campus IT Compliance and CSV team to ensure compliance and productivity.
  • Set goals and objectives for the team, driving continuous improvement in KPIs and project delivery.
  • Act as the Computer System Validation process owner, providing guidance on implementation and addressing deficiencies.
  • Ensure GxP business operations support across the Devens campus by defining and tracking SLAs.
  • Manage service providers to ensure alignment with contractual SLAs and maintain business continuity.
  • Represent Digital Plant during internal audits and regulatory inspections to uphold compliance standards.

What we're looking for

  • Bachelor’s degree in Engineering, IT, Computer Science or related field with 12+ years of experience.
  • Proven leadership in managing regulated IT compliance and validation initiatives.
  • Expertise in 21 CFR 210, 211, 11, GAMP standards, and computer system validation principles.
  • Experience with IT oversight of electronic systems supporting GMP operations.
  • Demonstrated ability to work effectively with US FDA and other regulatory agencies.
  • Strong collaboration and cross-functional leadership skills for continuous improvement.

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