Senior Automation Systems Administrator, Manufacturing & Lab Support

Regeneron

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Menands, NY
Salary
$67,400–$128,700 / yr
Employment
Full-time
Posted
31 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $164k
This role $98k
$52k most similar roles pay here $211k

This role pays less than 96% of similar roles. Most pay $131,800–$195,550 — the shaded band above. At the midpoint, this role pays about $98k versus about $164k for comparable roles.

Based on 240 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 42 open roles on FindRole.

Listed pay typically runs $128,600–$219,200 across 32 roles with salary data.

Most-posted roles

View all roles at Regeneron

At a glance

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

Senior Automation Systems Administrator, Manufacturing & Lab Support joins the IOPS team to provide expertise in configuring and administering automated and computerized system software and firmware across manufacturing and laboratory operations. This role involves maintaining cGMP software for process control, monitoring, and testing while managing user access, security, and recipe management to meet regulatory requirements. The individual will lead projects involving change control, risk assessments, and root cause analyses, while also performing SAT/FAT, validation, and qualification efforts for automated equipment. Key responsibilities include designing data backup processes and integrating systems with platforms like LIMS and Historian. Required skills include experience with GAMP 5 guidelines, Software Lifecycle Documentation, and technical evaluations. The role addresses the critical need to maintain a compliant and validated state within a pharmaceutical manufacturing environment through advanced troubleshooting and continuous improvement of infrastructure.

What you'll do

  • Configure and maintain cGMP software for process control, monitoring, and testing systems.
  • Manage user access, system security, configuration management, and recipe/method management to meet regulatory requirements.
  • Determine data backup and archive configurations while designing and maintaining recovery processes.
  • Process change control requests including requirement specifications, test plans, and quality risk assessments.
  • Lead SAT/FAT efforts and execute testing protocols for automated process and monitoring equipment.
  • Author and review technical documentation such as Change Controls, risk assessments, and corrective action plans.
  • Provide advanced technical troubleshooting for manufacturing, quality control, and facility systems.
  • Integrate systems with platforms like LIMS and Historian while drafting relevant software SOPs.

What we're looking for

  • Bachelor's degree in Science, Engineering, or a related field.
  • At least 2 years of experience as an Automation System Administrator.
  • At least 5 years of experience as a Senior System Administrator.
  • Experience in pharmaceutical or biopharmaceutical manufacturing facilities (preferred).
  • Advanced experience configuring and troubleshooting process control, monitoring, and product release testing systems.
  • Expertise in developing Software Lifecycle Documentation and test plans for cGMP equipment following GAMP 5 guidelines.
  • Knowledge of cGMP biotech and pharma operations, regulatory policies, and documentation methods.
  • Ability to perform physical requirements including lifting up to 50lbs and working in a cleanroom environment.

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