Radiopharmaceutical Manufacturing Specialist

Nucleus-Radiopharma; Rochester (MN); On-site; USD 75,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k retirement account with employer匹

Relocation assistance

Job summary

Nucleus RadioPharma in Minnesota is seeking a Manufacturing Specialist to support radiopharmaceutical production, including cleaning, reagent prep, assembly, formulation, dispensing, and packaging under CGMP. The role requires independent decision making and coordination of production runs with training responsibilities.

The candidate must have a STEM degree or equivalent experience, 2+ years in FDA CGMP, aseptic processing, and ability to work 24/7 with overtime.

Qualifications

• Bachelor’s degree in STEM or equivalent experience.
• Minimum 2 years FDA CGMP regulated experience (21 CFR Parts 210 and 211).
• Experience in aseptic processing.
• Experience in radiopharmaceuticals, pharmaceuticals, biologics, or cell/gene therapy.
• Ability to work nights/weekends/overtime as needed.

Responsibilities

• Lead and support team in fast-paced manufacturing to meet goals.
• Adhere to quality, safety, regulatory guidance and procedures.
• Perform routine cleaning of manufacturing areas and equipment setup.
• Operate equipment and perform manual chemistry for radiopharmaceuticals.
• Develop and update SOPs with cross-functional teams.
• Coordinate production schedules and staffing for 24/7 operations.

Skills

Strong mechanical aptitude

Independent work

Attention to detail

Communication skills

Teamwork

Problem solving

Microsoft Office

Manual dexterity

Cleanroom experience

Education

Bachelor’s degree in STEM

Tools

Hot cells

Automated processing equipment

Aseptic processing

Job description

Nucleus RadioPharma in Minnesota is seeking a Manufacturing Specialist to support radiopharmaceutical production, including cleaning, reagent prep, assembly, formulation, dispensing, and packaging under CGMP. The role requires independent decision making and coordination of production runs with training responsibilities.

The candidate must have a STEM degree or equivalent experience, 2+ years in FDA CGMP, aseptic processing, and ability to work 24/7 with overtime.