Director, Engineering

Catalent Pharma Solutions; Greendale (IN); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Paid time off

Day one benefits

Global opportunities

Job summary

Catalent Pharma Solutions' Greendale gummy facility is a 100% on-site operation focused on traditional gelatin and plant-based gummies for nutraceuticals. The Director, Engineering leads maintenance, facilities, utilities, and capital projects, ensuring compliant, efficient operations and continuous improvement across packaging and process engineering.

The role builds a high-performing engineering team, owns the site Master Plan and capital strategy, and partners with site leadership to align

Qualifications

• Bachelor’s degree in engineering; MS or MBA preferred.
• 10+ years engineering, continuous improvement, manufacturing technology, validation.
• 5+ years management experience in a regulated industry.
• Certified Lean Six Sigma Green Belt or Black Belt preferred.

Responsibilities

• Provide direct and indirect leadership to maintenance and facilities teams; ensure safe, compliant execution.
• Oversee facilities, utilities, and infrastructure for readiness and compliance.
• Lead Process Engineering to improve robustness, yield, and throughput.
• Lead Packaging Engineering for line performance, transfer, and optimization.
• Own and execute the capital project portfolio from concept to validation.
• Prioritize capital allocation to maximize ROI and capacity expansion.
• Develop engineering leaders, engineers, and technicians; build bench strength.
• Own engineering performance metrics and budget execution; ensure site strategy alignment.

Skills

Leadership

Analytical thinking

Problem solving

Strategic thinking

Communication

Education

Bachelor's degree in engineering

MS or MBA preferred

Tools

Lean Six Sigma

OSHA 10

Job description

Director, Engineering Position Summary: 100% on-site Greendale is one of two gummy technology development and manufacturing facilities in North America. The site has the capability to manufacture traditional gelatin gummies as well as 100% plant-based pectin gummies for nutritional supplements and nutraceuticals. With extensive development and manufacturing expertise and a wide range of flavors, shapes, sizes, and colors available, we can work with complex ingredients to help create engaging new products consumers will love.

The Director, Engineering will provide strategic leadership and oversight for all site engineering functions, including maintenance, facilities, utilities, capital projects, packaging engineering, and process engineering. This role is responsible for ensuring reliable, compliant, and efficient operations across manufacturing and packaging through disciplined asset management, engineering excellence, and execution of both minor and major capital projects.

The Director will lead, develop, and coach a multi-disciplinary engineering organization to deliver maximum asset reliability, operational performance, and continuous improvement. Own the Site Master Plan, and capital strategy to align infrastructure, technology, and capacity with current and future business needs. Accountable for ensuring all engineering, maintenance, and facilities activities fully comply with site, corporate, and regulatory requirements, including cGMP, safety, and environmental standards, while supporting audit readiness and inspection success.

The Role:

Provide direct and indirect leadership to maintenance and facilities teams, ensuring safe, compliant, and efficient execution of all activities. Oversee facilities, utilities, and infrastructure to ensure operational readiness, environmental compliance, regulatory adherence, and long-term facility integrity. Lead Process Engineering to improve manufacturing robustness, yield, and throughput through data-driven process optimization and problem solving. Lead Packaging Engineering to ensure packaging line performance, technical transfer, equipment capability, and continuous improvement of packaging operations. Own and execute the capital project portfolio, including both minor and major engineering projects from concept through commissioning, qualification, and validation. Prioritize and manage capital allocation to maximize ROI, capacity expansion, compliance, and operational efficiency. Lead, coach, and develop a team of engineering leaders, engineers, and technicians; build organizational capability and technical depth while continuously assessing talent, building bench strength, and ensuring succession readiness across critical roles in a complex, fast-paced environment. Own engineering performance metrics, including asset reliability, OEE, project execution, and compliance indicators, and lead disciplined execution against CAPEX and R&M budgets to deliver both short- and long-term business outcomes. Contribute as a key member of the site leadership team, shaping site strategy, operational priorities, and resource allocation to enable delivery of business objectives in a complex, dynamic environment. Drive proactive identification and mitigation of compliance risks related to equipment, utilities, facilities, and engineering processes. Other duties as assigned.

The Candidate:

Bachelor’s degree in engineering; advanced degree (MS or MBA) preferred MBA a plus. 10+ years engineering, continuous improvement, manufacturing technology, validation. 5+ years management experience and in a regulated industry. Strong analytical/problem solving/process improvement skills. Certified Lean Six Sigma Green Belt or Black Belt preferred.

Knowledge/Skills Requirements:

• Combustible Dust and Wastewater Management experience preferred.
• Understanding of mechanical, electrical, pneumatic, hydraulic, and utility systems.
• Strong leadership skills, with an ability to partner, build trust, provide direction, and execute with excellence.
• Ability to prioritize and follow-through to achieve results and meet deadlines.
• Strong foundation interpersonal communication concepts, specifically, written, oral, presentation, listening, and facilitation skills.
• Bilingual English/Spanish is a plus.
• OSHA 10 or equivalent training.
• Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Why you should Join Catalent:

• Potential for career growth on an expanding team
• Abundance of cross-functional exposure to other areas within the organization
• Opportunity to work globally
• 152 hours of paid time off annually + 8 paid holidays
• Day one benefits! Medical, dental, vision and 401K benefits effective on your first day
• Catalent offers rewarding opportunities to further your career!
• Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
• Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
• Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
• Join us in making a difference.
• personal initiative.
• dynamic pace.
• meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [e-mail] for us to investigate with local authorities.

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Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis. Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacturing, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.