Lead Engineer, IT Quality and Compliance

Bristol Myers Squibb

Quick summary

Work type
On-site
Location
Summit West, NJMadison Giralda, NJ
Salary
$107,530–$130,295 / yr
Posted
4 days ago
Closes
Aug 28, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $186k
This role $119k
$94k most similar roles pay here $232k

This role pays less than 98% of similar roles. Most pay $161,187–$211,200 — the shaded band above. At the midpoint, this role pays about $119k versus about $186k 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.

Most-posted roles

View all roles at Bristol Myers Squibb

At a glance

TL;DR · Lead Engineer, IT Quality and Compliance

As a Lead Engineer in IT Quality and Compliance at Summit West, you will join a dedicated team responsible for ensuring the highest standards of quality and compliance across Manufacturing and Laboratory IT systems. Your daily responsibilities include overseeing site-level quality oversight, managing change control processes, acting as a Validation Lead, maintaining ongoing compliance accountability, and leading periodic monitoring programs to mitigate risks. You will also serve as a key liaison with training teams to develop robust curricula for inspection readiness and support Health Authority inspections. This role requires expertise in IT Quality & Compliance applications within biotech manufacturing environments, familiarity with cGMP, GXP, GAMP, SDLC regulations, and strong technical problem-solving skills. Knowledge of pharmaceutical systems and equipment supporting Biologics and clinical manufacturing is essential, as well as the ability to communicate effectively across all levels of the organization.

What you'll do

  • Own site-level quality oversight for Manufacturing and Laboratory IT systems.
  • Manage IT Change Management governance and act as primary authority for change control.
  • Serve as Validation Lead for Manufacturing IT and OT systems, ensuring compliance.
  • Maintain ongoing compliance for IT systems supporting CAR-T manufacturing operations.
  • Lead the Site IT System Periodic Monitoring program to ensure inspection readiness.

What we're looking for

  • Bachelor's degree in a STEM discipline required.
  • 5+ years of hands-on experience in biotech manufacturing and supply chain.
  • Expertise in cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11.
  • Proven ability to lead complex IT quality and compliance projects.
  • Strong technical skills with knowledge of pharmaceutical systems and equipment.

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