PRINCIPAL RESPONSIBILITIES:

• Manage the day-to-day operations of the maintenance team to ensure reliable and compliant facility and equipment operations

• Provide technical guidance and act as Subject Matter Expert (SME) for equipment, maintenance, and commissioning/qualification/validation (CQV) activities

• Lead department initiatives in continuous improvement to optimize performance, reduce downtime, and deliver cost-saving outcomes

• Participate in the preparation and execution of documentation activities in accordance with CGMP requirements.

• Collaborate with Quality, Operations, and Regulatory functions to support project activities and issue resolution

• Maintain compliance with safety, quality, and regulatory standards during equipment maintenance and troubleshooting

• Mentor, develop, and evaluate maintenance staff with varying skill sets, fostering a high-performing and accountable team culture

• Perform staff planning to maintain adequate coverage and ensure 24/7 support of manufacturing operations.

• Support the establishment and execution of preventive and predictive maintenance programs

• Work extended hours, weekends, or travel as required to meet production needs

• Perform other duties as assigned

QUALIFICATIONS AND REQUIREMENTS:

• Bachelor’s degree in Mechanical, Electrical, Mechatronic Engineering, or related discipline required.

• Minimum 3 years of experience managing a maintenance team in a regulated manufacturing environment required.

• Proven experience in managing teams within a cGMP-regulated environment. Radiopharmaceutical experience preferred but not required.

• Strong knowledge of equipment maintenance, reliability engineering, and CQV documentation practices.

• Demonstrated ability to lead and develop multidisciplinary teams effectively

• Skilled in problem-solving and troubleshooting in high-compliance environments

• Ability to work both independently and as part of a team

• Comfortable working for extended periods in cleanroom environments and able to lift up to 70 lbs.

• Excellent organizational and communication skills

• Proficiency with Microsoft Office and familiarity with CMMS and project management tools.

• Highly detail-oriented with a strong commitment to quality

• Willingness to work weekends, evenings, and travel as needed to support production schedules.

THE FINE PRINT:

The salary range for this position is $110,000 - $130,000 per year. Please note that compensation may vary outside of this range depending on several factors, including but not limited to a candidate’s qualifications, skills, competencies, experience, and location.

Benefit packages for this role include medical, dental, and vision insurance, as well as a Health Savings Account or Flexible Spending Account options (depending on the plan chosen), and 401k retirement account access with employer matching. Team members in this role are also entitled to paid sick leave and/or other paid time off in compliance with applicable law. Relocation is available to qualified team members.

This job description is a summary of the typical functions of the position, not necessarily an exhaustive or comprehensive list of all possible position responsibilities, tasks, and duties. The company reserves the right to assign or reassign duties and responsibilities to this job at any time. This job does not constitute a written or implied contract of employment; employment remains “at-will”.

Nucleus RadioPharma is an equal opportunity employer and believes everyone deserves respect, dignity, and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.