Senior Microbiologist

Nucleus RadioPharma; Rochester (MN); On-site; USD 80,000 - 120,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k with employer matching

Relocation assistance

Job summary

Nucleus RadioPharma in Rochester, MN is seeking a Senior Microbiologist to provide technical leadership in microbiology quality control for sterile radiopharmaceuticals in a cGMP environment.

You will mentor technicians, manage environmental monitoring, investigations, and ensure regulatory compliance, collaborating across Manufacturing, QA, Engineering, Validation, and Technical Operations.

Qualifications

• Bachelor’s degree in Biology, Microbiology, or a related scientific discipline.
• Minimum 5 years of experience in a cGMP microbiology laboratory supporting sterile pharmaceutical manufacturing.
• Demonstrated experience writing microbiological QC SOPs, test methods, protocols, and reports.
• Experience with aseptic techniques while performing Sterility, Endotoxin, Particulate Matter, and Bioburden testing of drug products, intermediates, and raw materials per USP and SOPs.

Responsibilities

• Lead microbiological methods for radioactive drug products in a GxP environment, including Sterility and Bioburden testing.
• Review FDA/EU regulations and guidelines on sterilization and contamination control.
• Perform Growth Promotion testing per USP and prepare Biological Indicators for validation/qualification.
• Oversee microbiology and Environmental Monitoring programs, including sampling strategy, EM data review, and trend analysis.
• Analyze microbial samples, support environmental monitoring activities, and assist with EM excursions.

Skills

Communication

Problem solving

Interpersonal skills

Team collaboration

Education

Bachelor degree in Biology/Microbiology

Master’s degree preferred

Job description

Job Title: SENIOR MICROBIOLOGIST

Reports to: Sr. Manager, Sterility Assurance

Classification: Full Time, Exempt

Work Location: Rochester, MN – On‑Site

About Nucleus Radiopharma

Nucleus RadioPharma is an end-to-end CDMO accelerating radiopharmaceutical therapies through isotope‑flexible manufacturing, breakthrough partnerships, and end-to-end innovation that brings complex medicines to patients. We are driven by a vision of a world where every patient with cancer has access to the right therapeutic, at the right time.

Position Summary

The Senior Microbiologist provides technical leadership and independently executes microbiological quality control activities that support the manufacture of sterile radiopharmaceuticals in a cGMP environment. This role serves as the subject matter expert for microbiological testing, environmental monitoring, contamination control, aseptic processing support, investigations, and data trending, partnering cross‑functionally with Manufacturing, Quality Assurance, Engineering, Validation, and Technical Operations. Working with minimal supervision, the Senior Microbiologist mentors laboratory personnel and drives scientific excellence to ensure the highest standards of product quality, regulatory compliance, and patient safety.

Principal Responsibilities

• Lead the execution of microbiological methods for radioactive drug products in a GxP environment, including Sterility and Bioburden testing of drug products, intermediates, and raw materials per USP and Standard Operating Procedures (SOP).
• Review and interpret FDA, EU, and other international regulations, standards, and guidelines covering sterilization and microbial contamination control in the manufacture of aseptic radiopharmaceutical products.
• Perform Growth Promotion testing per USP methods for various microbiological media, and prepare and analyze Biological Indicators in support of validation and qualification activities.
• Lead and support the site’s microbiology and Environmental Monitoring (EM) program, including sampling strategy, cleanroom monitoring, data review, trending, and evaluation of alert and action level excursions to ensure compliance with cGMP and contamination control requirements.
• Analyze microbial samples to quantify growth and subculture pure isolates as required, providing support and assistance with environmental monitoring activities.
• Lead microbiological investigations involving environmental monitoring excursions, contamination events, out-of-specification (OOS) results, deviations, and CAPAs, using scientific, risk-based decision making to identify root causes and implement effective corrective actions.
• Provide microbiological support for sterile radiopharmaceutical manufacturing operations, including aseptic processing, cleanroom and classified area activities, hot cell or isolator operations, line clearance, and campaign-based production activities.
• Support contamination control strategy execution by identifying microbial risks, evaluating trends, and partnering with Manufacturing, Quality Assurance, Engineering, Facilities, MSAT, and Validation to drive effective corrective actions.
• Author, revise, and review SOPs, validation protocols, validation reports, technical assessments, and investigation documentation in accordance with cGMP, USP, FDA, and applicable regulatory expectations.
• Support aseptic process simulations, media fills, cleaning and disinfection effectiveness studies, cleanroom qualification, smoke studies, and process performance activities, as applicable.
• Provide day‑to‑day technical guidance, mentoring, and training to Microbiology Technicians and other laboratory personnel, serving as a technical resource in support of the Manager, Sterility Assurance.
• Develop and deliver technical training on microbiological methods, aseptic practices, and cGMP requirements for laboratory personnel.
• Manage inventory of laboratory supplies and provide technical input regarding laboratory resource needs and equipment to support efficient laboratory operations.
• Ensure a safe and quality‑minded working environment through conformance with training, general awareness, and compliance with safety, quality, and radiation protection guidelines and SOPs.
• Perform other general duties as assigned or directed by supervisors.

Qualifications & Requirements

Required

• Bachelor’s degree in Biology, Microbiology, or a related scientific discipline.
• Minimum 5 years of experience in a cGMP microbiology laboratory supporting sterile pharmaceutical manufacturing.
• Demonstrated experience writing microbiological QC SOPs, test methods, protocols, and reports.
• Experience with aseptic techniques while performing Sterility, Endotoxin, Particulate Matter, and Bioburden testing of drug products, intermediates, and raw materials per USP and Standard Operating Procedures.
• Working knowledge of regulations applicable to drugs and devices (21 CFR Parts 210, 211, and 212, ICH Q7, USP , and FDA guidances) and the ability to apply them based on the phase of the project.
• Good verbal and written communication skills.
• Demonstrated problem‑solving and interpersonal skills, utilizing resourceful thinking and strong empathy.
• Ability to foster an inclusive and cooperative work environment.
• Ability to work sitting and standing for extended periods, with grasping/gripping and fine motor control, and to lift, move, transport, and position equipment and work items weighing up to 30 pounds on a frequent basis.

Preferred

• Master’s degree in Biology, Microbiology, or a related scientific discipline.
• Experience testing radioactive drug products.
• Experience handling radioactive materials (gamma, beta, and/or alpha emitters) in radiological facilities, including shielded glove boxes and hot cells.
• Experience supporting contamination control programs, environmental monitoring trending, and microbiological investigations.

Ideal

• Demonstrated ability to provide technical leadership, mentoring, and training to laboratory personnel without formal supervisory responsibility.
• Demonstrated ability to independently manage microbiology projects and laboratory priorities while supporting multiple manufacturing programs.
• Strong collaboration and communication skills, with demonstrated ability to influence technical decisions and work effectively across Quality, Manufacturing, Engineering, MSAT, and Regulatory functions.

Compensation & Benefits

The salary range for this role in Minnesota is $80,000–$120,000 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, and experience.

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 assistance 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.