Principal Automation Systems Administrator, Manufacturing & Lab Support

Regeneron

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Menands, NY
Salary
$92,200–$176,000 / yr
Posted
43 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $167k
This role $134k
$80k most similar roles pay here $208k

This role pays less than 77% of similar roles. Most pay $137,948–$195,275 — the shaded band above. At the midpoint, this role pays about $134k versus about $167k for comparable roles.

Based on 239 similar postings.

Employer

About Regeneron

Regeneron is a leading science-driven biotechnology company that invents, develops, and commercializes life-transforming medicines for serious diseases.

Regeneron currently has 18 open roles on FindRole.

Listed pay typically runs $141,100–$243,350 across 18 roles with salary data.

Most-posted roles

View all roles at Regeneron

At a glance

TL;DR · Principal Automation Systems Administrator, Manufacturing & Lab Support

The Principal Automation Systems Administrator joins the IOPS team to provide technical leadership in configuring and administering automated systems, servers, and network infrastructure across manufacturing and laboratory operations. This role serves as a technical subject matter expert bridging automation and business needs by driving validation, continuous improvement, and strategic vendor partnerships. Key responsibilities include developing hardware and software specifications, managing SAT/FAT and qualification efforts, and authoring Software Lifecycle Documentation, SOPs, and risk assessments. The position requires advanced experience troubleshooting control systems, monitoring tools, product release testing systems, and network infrastructure. Candidates must possess expertise in GAMP 5 guidelines and cGMP biotech and pharma operations. Essential skills include project management, technical mentoring, and the ability to resolve complex problems within a regulated pharmaceutical manufacturing environment involving specialized equipment and high-standard quality policies.

What you'll do

  • Develop hardware and software specifications, code, and network configurations to meet cGMP requirements.
  • Provide advanced technical troubleshooting and investigations for automated systems following GAMP 5 guidelines.
  • Lead system SAT/FAT, validation, qualification, and improvement projects across multiple departments.
  • Author and review lifecycle documentation including SOPs, Change Controls, risk assessments, and CAPA plans.
  • Act as a technical liaison to identify solutions for complex problems and drive process improvements.
  • Manage strategic vendor relationships and oversee the selection of automation partners.
  • Provide training and mentorship to internal teams and external contractors.

What we're looking for

  • Bachelor's degree in Science, Engineering, or a related field.
  • At least 8 years of relevant experience for the Principal level or 10 years for the Staff level.
  • Advanced experience configuring and troubleshooting control, monitoring, and product release testing systems.
  • Advanced experience troubleshooting network infrastructure and server-based systems.
  • Knowledge of cGMP biotech and pharma operations, including regulatory and quality policies.
  • Experience in a pharmaceutical or biopharmaceutical manufacturing facility is preferred.
  • Strong project management skills to lead multiple workstreams and changing priorities.
  • Ability to perform physical requirements for up to 10 hours in a cleanroom environment, including lifting up to 50lbs.

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