Associate Director, Site Automation OT Equipment

Regeneron Pharmaceuticals • Town of Colonie, NY

5d • $147,800 - $241,200 • Onsite

About The Position

Regeneron is seeking an Associate Director, Site Automation to provide technical and automation leadership across manufacturing, testing laboratories, and facilities operations. The role supports either the Red Mill (Bulk Manufacturing) or Temple Lane (Internal Fill Finish) site in Menands, New York, and supervises a team responsible for small-equipment operation technology. The position drives accountability for cGMP automation quality systems, software change control, corrective actions, and equipment procurement and qualification, working with Manufacturing, Quality Control, Engineering, and vendor partners.

The schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m., onsite, with 5–10% travel within the U.S. and internationally. The annual salary range is $147,800–$241,200. The role includes oversight of software administration and periodic evaluation programs, investigation support, project delivery, budget and headcount forecasting, vendor relationships, and equipment commissioning and qualification.

Requirements

• BS/BA in Science, Engineering, or Software Programming, or equivalent years of direct experience with automated control systems or equipment in lieu of a degree.
• 10 or more years of experience with automated equipment in the pharmaceutical or biopharmaceutical industry or a related regulated industry.
• At least 5 years of direct experience in the design, installation, maintenance, and/or troubleshooting of automated control systems.
• Demonstrated experience leading or managing automation teams in a cGMP-regulated environment.
• Strong working knowledge of cGMP quality systems, software change control processes, and regulatory standards applicable to automated systems.

Nice To Haves

• MBA, MS, or another advanced degree.
• Experience with vendor management and approved supplier compliance programs.

Responsibilities

• Lead the automation team by setting clear expectations, modeling compliance, and ensuring adherence to departmental policies and procedures.
• Oversee the cGMP software administration program and automated system periodic evaluation program.
• Ensure SOPs and Software Lifecycle Documentation remain aligned with current regulatory standards and guidelines.
• Oversee investigation support for manufacturing deviations, laboratory testing anomalies, and automation-, software-, or hardware-related issues.
• Lead corrective-action and equipment-performance-improvement projects.
• Ensure timely completion of departmental projects, work orders, and quality management items.
• Maintain the direct team's budget forecast and compliance, and provide headcount forecasts for department growth to senior management.
• Support vendor relationships and compliance with approved suppliers.
• Oversee equipment procurement, commissioning, and equipment and software qualification activities.

Benefits

• Annual bonuses or other incentive plans may be included, depending on country and role.
• Equity awards may be included, depending on country and role.
• Pension or retirement benefits may be included, depending on country and role.
• 401(k) company match may be included, depending on country and role.
• Health and wellness programs may be included, depending on country and role.
• Fitness centers may be available, depending on country and role.
• Insurance benefits may include medical, dental, vision, life, and disability coverage.
• Paid time off may be included, depending on country and role.
• Family support benefits may be included, depending on country and role.

What This Job Offers

• Job Type: Full-time
• Career Level: Director