Head of Engineering, Florida; AD level

Play a defining role in launching a new Radioligand Therapy manufacturing site, shaping the engineering foundation that enables safe, compliant, and reliable operations from day one.

As the Head of Engineering, you will lead engineering and facilities for a new U.S. site, guiding activities from design through commissioning, qualification, and start‑up. As a member of the site leadership team, you will shape the site master plan, oversee major capital investments, and build a high‑performing engineering organization that ensures inspection‑ready operations at launch.

Location:

Winter Park, Florida, USA

• Provide leadership for engineering and facilities operations to enable successful launch of a new RLT manufacturing site
• Develop and execute the site engineering strategy and five‑year Site Master Plan, including capacity, capital investment, and resource planning
• Build, lead, and develop a high‑performing engineering and facilities organization, including succession planning and talent development
• Ensure facilities, utilities, and equipment are designed, commissioned, qualified, and maintained to meet regulatory and business requirements
• Lead capital project planning and execution, ensuring delivery on time, within budget, and aligned with site launch milestones
• Establish and maintain a state of continuous compliance with regulatory requirements, quality standards, and internal policies
• Partner closely with Quality, Production, Supply Chain, and Health, Safety & Environment leaders to support inspection readiness and operational excellence
• Drive a strong culture of safety, quality, accountability, and continuous improvement across engineering and facilities operations

• Bachelor’s degree in engineering or a related discipline, or an equivalent combination of education and relevant experience
• Minimum of 10 years of progressive engineering experience in U.S. cGMP environments
• At least 5 years of leadership experience of engineering and maintenance in cGMP plant, including facility design aligned to Lean concepts for materials, people, and waste flows
• Strong expertise in pharmaceutical engineering systems, including facilities, utilities, equipment, commissioning, qualification, and lifecycle maintenance
• Direct involvement with quality regulatory inspections of facilities from major agencies such as FDA or EMA
• Excellent knowledge of engineering standards for buildings, facilities, and equipment in the pharmaceutical industry along with management of construction projects
• Significant Environment Health and Safety, and GxP/QA experience building an injury and error‑free culture with knowledge of multiple compliance areas (corporate governance, financial, quality, environment, safety, etc.)

• Experience supporting radiopharmaceutical, radiochemistry, or sterile drug product manufacturing operations
• Prior involvement in new site start‑up and launch projects, including design through commissioning and qualification

The salary for this position is expected to range between $138,600 and $257,400 per year. The final salary offered is determined based on factors such as relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time‑off package including vacation, personal days, holidays and other leaves.