IT Lead, Manufacturing GxP
Company: Regeneron Pharmaceuticals, Inc.
Location: Cambridge
Posted on: March 26, 2026
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Job Description:
We are seeking a skilled IT professional to serve as the IT Lead
for Regeneron's Cell Medicines (RCM) Manufacturing operation to
support and maintain all Clinical Manufacturing Equipment and data
acquisition/monitoring systems. This role will require strong
management skills to effectively manage the support needed from
multiple Regeneron Corporate IT services groups and external
support vendors as needed, in addition to strong technical skills
as the primary On-Site IT SME for the Clinical Manufacturing area.
This individual will ensure seamless communication, service
delivery, and networking of points of contact across multiple IT
groups and the business. The ideal candidate will have leadership
and communication skills, experience in a GMP (Good Manufacturing
Practices) environment, and the ability to troubleshoot on-site IT
issues related to all Manufacturing and QC equipment and facilities
IT systems. As an IT GxP Manufacturing Lead, a typical day may
include: Serve as the primary point of contact between RCM and
Corporate IT, coordinating support across internal groups and
external vendors. Align IT services with RCMs needs by facilitating
clear stakeholder communication on requirements, timelines, and
deliverables. Lead planning and execution of IT projects and
initiatives within a GMP environment, ensuring effective cross-team
coordination. Provide regular operational and project status
updates, metrics, and risk/issue reports to leadership. Manage and
direct contracted IT personnel and oversee vendor performance for
service delivery. Troubleshoot and resolve on-site IT issues for
manufacturing, QC equipment, and facilities systems
(hardware/software), ensuring rapid restoration. Ensure high
availability and resilience of critical systems through monitoring,
preventive maintenance, backups/archiving, and recovery readiness.
Develop and maintain GxP documentation, including specifications,
test protocols, validation/CSV records, and system administration
SOPs. Support integration of equipment and systems with LIMS and
other enterprise platforms in coordination with Corporate IT;
supervise EMS for compliance and reliability. Ensure GMP/regulatory
compliance by partnering with QA, managing IT tasks in CMMS,
maintaining audit readiness, and driving continuous improvement of
workflows and support processes. This role could be for you if you:
Strong management and leadership abilities. Excellent written and
verbal communication skills. Ability to collaborate effectively
with cross-functional teams. Proven track record of collaborating
with corporate IT teams. Ability to adapt to a fast-paced,
multifaceted work environment. To be considered for this role, you
must meet the following: Bachelors degree in information
technology, Computer Science, or a related field. 5 10 years'
demonstrated ability in an IT role, preferably within a
GMP-regulated environment. Proficiency in troubleshooting all IT
aspects of manufacturing/QC equipment and other data
collection/monitoring systems (e.g. EMS) Familiarity with GMP
requirements and IT compliance standards. Does this sound like you?
Apply now to take your first step towards living the Regeneron Way!
We have an inclusive culture that provides comprehensive benefits,
which vary by location. In the U.S., benefits may include health
and wellness programs (including medical, dental, vision, life, and
disability insurance), fitness centers, 401(k) company match,
family support benefits, equity awards, annual bonuses, paid time
off, and paid leaves (e.g., military and parental leave) for
eligible employees at all levels! For additional information about
Regeneron benefits in the US, please visit
https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.
For other countries specific benefits, please speak to your
recruiter. Please be advised that at Regeneron, we believe we are
most successful and work best when we are together. For that
reason, many of Regenerons roles are required to be performed
on-site. Please speak with your recruiter and hiring manager for
more information about Regenerons on-site policy and expectations
for your role and your location. Regeneron is an equal opportunity
employer and all qualified applicants will receive consideration
for employment without regard to race, color, religion or belief
(or lack thereof), sex, nationality, national or ethnic origin,
civil status, age, citizenship status, membership of the Traveler
community, sexual orientation, disability, genetic information,
familial status, marital or registered civil partnership status,
pregnancy or parental status, gender identity, gender reassignment,
military or veteran status, or any other protected characteristic
in accordance with applicable laws and regulations. The Company
will also provide reasonable accommodation to the known
disabilities or chronic illnesses of an otherwise qualified
applicant for employment, unless the accommodation would impose
undue hardship on the operation of the Company's business. For
roles in which the hired candidate will be working in the U.S., the
salary ranges provided are shown in accordance with U.S. law and
apply to U.S.-based positions. For roles which will be based in
Japan and/or Canada, the salary ranges are shown in accordance with
the applicable local law and currency. If you are outside the U.S,
Japan or Canada, please speak with your recruiter about salaries
and benefits in your location. Please note that certain background
checks will form part of the recruitment process. Background checks
will be conducted in accordance with the law of the country where
the position is based, including the type of background checks
conducted. The purpose of carrying out such checks is for Regeneron
to verify certain information regarding a candidate prior to the
commencement of employment such as identity, right to work,
educational qualifications etc. Salary Range (annually) $80,300.00
- $131,100.00
Keywords: Regeneron Pharmaceuticals, Inc., Waltham , IT Lead, Manufacturing GxP, IT / Software / Systems , Cambridge, Massachusetts