Associate Director of Facilities Engineering

Description

We are seeking an experienced Director of Facilities Engineering to lead the facilities and utilities
engineering organization for a high-compliance pharmaceutical manufacturing/CDMO site. This strategic
leadership role is accountable for developing and executing a robust facilities engineering strategy
that ensures compliant, reliable, safe, and cost-effective infrastructure supporting manufacturing,
labs, utilities, and corporate facilities.

Essential Job Functions:

·       Define and implement long-term facilities engineering strategy aligned with corporate goals.

·       Lead and develop multi-disciplinary teams including engineering, maintenance, calibration, and contractors.

·       Ensure full compliance with cGMP, FDA/EMA, OSHA, and environmental regulations.

·       Oversee preventative and corrective maintenance programs for critical utilities and infrastructure.

·       Lead capital projects including expansions, upgrades, and infrastructure improvements.

·       Manage facilities budgets, forecasting, and cost-control initiatives.

·       Serve as site representative during regulatory inspections and audits.

·       Partner cross-functionally with Quality, Manufacturing, EHS, and Supply Chain.

Special Job Requirements:

·       Bachelor’s degree in Engineering or related field (Master’s preferred).

·       10+ years of progressive leadership experience in pharmaceutical/CDMO or regulated manufacturing.

·       Strong expertise in GMP-compliant facility operations and utilities systems (HVAC, WFI, clean steam, power).

·       Demonstrated success leading capital projects and reliability programs.

·       Experience supporting regulatory inspections and audit readiness.

·       Strong leadership, communication, and organizational skills.

Additional Preferences:

·       Advanced degree (MS/MBA) or professional certifications (PE, PMP, Six Sigma).

·       Experience with CMMS, BMS, and digital facilities management tools.

·       Multi-site or global pharmaceutical experience.

Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.

If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.

INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.  All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.

By submitting your resume and details, you are declaring that the information is correct and accurate.