Nuclear Pharmacy Manager (Phoenix, AZ)

530d PETNET Solutions, Inc.; Phoenix (AZ); On-site; USD 134,000 - 185,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Life insurance

Disability insurance

Paid parking/public transportation

Paid time off

Paid sick and safe time

Job summary

Siemens Healthineers Radiopharma Solutions in Phoenix, AZ, seeks a Production/Nuclear Pharmacy Manager to lead PET radiopharmaceutical manufacturing and pharmacy operations, ensuring safe, compliant, and efficient production and delivery of critical diagnostic products.

You will build and lead a high‑performing team, drive regulatory readiness, quality, and continuous improvement, and manage overnight shift schedules to support around‑the‑clock operations.

Qualifications

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, Engineering, Health Sciences, or related field.
• Minimum 5 years of experience in pharmaceutical manufacturing, radiopharmaceutical production, biotechnology, healthcare manufacturing, laboratory production, nuclear pharmacy, or another highly regulated environment.
• Minimum 3 years of leadership or supervisory experience managing production, laboratory, pharmacy, manufacturing, or operations teams.
• Demonstrated experience working within a cGMP-regulated environment.
• Experience leading quality, compliance, safety, and continuous improvement initiatives.
• Experience managing employee performance, workforce planning, training, and scheduling.
• Knowledge of regulated manufacturing environments, quality systems, investigations, deviations, and corrective actions.
• Strong analytical, problem‑solving, organizational, and decision‑making skills.
• Excellent communication and interpersonal skills with the ability to effectively interact with customers, regulators, and cross‑functional partners.
• Proficiency with Microsoft Office applications and computerized business or manufacturing systems.
• Ability to work overnight, weekend, holiday, on‑call, and alternative shift schedules as business needs require.
• Ability to obtain and maintain all required site‑specific safety, regulatory, and operational qualifications.
• Ability to lift, push, pull, and move materials weighing up to 100 pounds, with or without reasonable accommodation.

Responsibilities

• Lead daily operations of the PET radiopharmaceutical production facility and pharmacy.
• Oversee radionuclide production, radiopharmaceutical manufacturing, quality control, dispensing, and distribution activities.
• Ensure timely, accurate, and compliant production and delivery of customer orders.
• Manage inventory levels, production planning, and resource allocation.
• Monitor operational performance and implement process improvements to enhance productivity, quality, and efficiency.
• Ensure the facility maintains a clean, organized, and safe work environment.
• Lead site inspection readiness activities and support regulatory inspections and audits.
• Lead, coach, and develop a team of exempt and non-exempt employees.
• Manage recruiting, hiring, onboarding, training, scheduling, performance management, and employee development activities.
• Foster a culture of accountability, collaboration, safety, quality, and continuous improvement.
• Ensure employees maintain required qualifications, certifications, and training requirements.
• Manage site financial performance including operating budgets, resource planning, cost controls, and P&L accountability.
• Establish and monitor site performance metrics and operational goals.
• Support business planning initiatives and continuous improvement efforts.
• Partner with Quality, Regulatory, Operations, Supply Chain, and Commercial teams to ensure customer satisfaction and business continuity.
• Manage or delegate operation and maintenance activities for cyclotrons, synthesis modules, analytical instrumentation, QC equipment, and associated software systems.
• Oversee preparation and shipment of radioactive materials in accordance with applicable regulations and company procedures.

Skills

Leadership

cGMP compliance

Regulatory compliance

Quality improvement

Problem solving

Communication

Education

Bachelor's degree in Pharmacy/related field

PharmD or advanced degree preferred

Tools

Microsoft Office

Quality systems documentation

Job description

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Siemens Healthineers' Radiopharma Solutions is a global leader in PET radiopharmaceutical manufacturing and distribution. For nearly three decades, Radiopharma has been a trusted partner in molecular imaging, delivering routine, reliable access to high-quality radiopharmaceuticals that support critical diagnostic procedures. With more than 47 locations worldwide, Radiopharma is the largest PET radiopharmaceutical network in the industry, supplying more than one million doses annually to over 2,800 imaging centers around the globe. Because we operate the industry's largest network of pharmacies, sites support one another to ensure continuity of supply, resulting in a dose fulfillment rate exceeding 99%. Learn more about Radiopharma Solutions: https://www.siemens-healthineers.com/en-us/molecular-imaging/petnet The Production/Nuclear Pharmacy Manager is responsible for leading all aspects of PET radiopharmaceutical manufacturing and pharmacy operations to ensure the safe, compliant, and efficient production and delivery of critical diagnostic products. This position provides operational, regulatory, financial, quality, and people leadership while maintaining compliance with current Good Manufacturing Practices (cGMP), radiation safety requirements, pharmacy regulations, and Siemens Healthineers quality standards. The successful candidate will build and lead a high-performing team, drive operational excellence, maintain inspection readiness, and ensure patients receive life-changing radiopharmaceutical products every day. Please note: This position primarily supports overnight production operations. Flexibility to work alternate shifts, weekends, holidays, and on-call schedules is required based on business needs.

Key Responsibilities

Operational Leadership

Lead daily operations of the PET radiopharmaceutical production facility and pharmacy. Oversee radionuclide production, radiopharmaceutical manufacturing, quality control, dispensing, and distribution activities. Ensure timely, accurate, and compliant production and delivery of customer orders. Manage inventory levels, production planning, and resource allocation. Monitor operational performance and implement process improvements to enhance productivity, quality, and efficiency. Ensure the facility maintains a clean, organized, and safe work environment.

Quality & Regulatory Compliance

Ensure compliance with all applicable federal, state, and local regulations, including cGMP, radiation safety requirements, pharmacy regulations, licensing commitments, and Siemens Healthineers policies. Lead site inspection readiness activities and support regulatory inspections and audits. Oversee investigations, deviations, CAPAs, change controls, and quality system activities. Maintain compliance with all documentation, recordkeeping, and data integrity requirements. Ensure proper performance of aseptic processing, sterility testing, endotoxin testing, and quality control procedures.

People Leadership

Lead, coach, and develop a team of exempt and non-exempt employees. Manage recruiting, hiring, onboarding, training, scheduling, performance management, and employee development activities. Foster a culture of accountability, collaboration, safety, quality, and continuous improvement. Ensure employees maintain required qualifications, certifications, and training requirements.

Financial & Business Management

Manage site financial performance including operating budgets, resource planning, cost controls, and P&L accountability. Establish and monitor site performance metrics and operational goals. Support business planning initiatives and continuous improvement efforts. Collaborate with regional leadership and cross-functional partners to achieve organizational objectives.

Customer & Stakeholder Management

Provide exceptional customer support through proactive communication and issue resolution. Support customer visits, audits, and relationship management activities. Partner with Quality, Regulatory, Operations, Supply Chain, and Commercial teams to ensure customer satisfaction and business continuity.

Technical Oversight

Manage or delegate operation and maintenance activities for cyclotrons, synthesis modules, analytical instrumentation, QC equipment, and associated software systems. Oversee preparation and shipment of radioactive materials in accordance with applicable regulations and company procedures.

Required Qualifications

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, Engineering, Health Sciences, or a related scientific discipline.
• Minimum 5 years of experience in pharmaceutical manufacturing, radiopharmaceutical production, biotechnology, healthcare manufacturing, laboratory production, nuclear pharmacy, or another highly regulated environment.
• Minimum 3 years of leadership or supervisory experience managing production, laboratory, pharmacy, manufacturing, or operations teams.
• Demonstrated experience working within a cGMP-regulated environment.
• Experience leading quality, compliance, safety, and continuous improvement initiatives.
• Experience managing employee performance, workforce planning, training, and scheduling.
• Knowledge of regulated manufacturing environments, quality systems, investigations, deviations, and corrective actions.
• Strong analytical, problem‑solving, organizational, and decision‑making skills.
• Excellent communication and interpersonal skills with the ability to effectively interact with customers, regulators, and cross‑functional partners.
• Proficiency with Microsoft Office applications and computerized business or manufacturing systems.
• Ability to work overnight, weekend, holiday, on‑call, and alternative shift schedules as business needs require.
• Ability to obtain and maintain all required site‑specific safety, regulatory, and operational qualifications.
• Ability to lift, push, pull, and move materials weighing up to 100 pounds, with or without reasonable accommodation.

Preferred Qualifications

• PharmD, Bachelor of Science in Pharmacy, Master's degree, or other advanced scientific degree.
• Nuclear pharmacy experience.
• PET radiopharmaceutical manufacturing experience.
• Active pharmacist license or eligibility for pharmacist licensure.
• Experience serving as Pharmacist‑in‑Charge (PIC).
• Authorized User (AU) designation and/or experience supporting radioactive materials licensing and radiation safety programs.
• Experience leading FDA, State Board of Pharmacy, NRC, Agreement State, or other regulatory inspections.
• Experience managing multiple exempt and non‑exempt employees across multiple shifts.
• Knowledge of cyclotron operations, radiochemistry, and analytical instrumentation.
• Lean Manufacturing, Six Sigma, or continuous improvement certification and experience.
• Direct responsibility for site P&L, budgeting, and operational performance metrics.

The base pay range for this position is: $134,300 - $184,668 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.

The Company offers the following benefits for this position, subject to applicable eligibility requirements:

• medical insurance
• dental insurance
• vision insurance
• 401(k) retirement plan
• life insurance
• long‑term and short‑term disability insurance
• paid parking/public transportation
• paid time off
• paid sick and safe time

Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and affirmative action employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.

EEO is the Law: Applicants and employees are protected under Federal law from discrimination.

Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations. If you require a reasonable accommodation in completing a job application, interviewing, completing any pre‑employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here.

California Privacy Notice: California residents have the right to receive additional notices about their personal information.

Export Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”

Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open.

#LI-AW1 #PetNet #RPhmgr

Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries.

How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

We are a team of 72,000 highly dedicated Healthineers in more than 70 countries.