PRINCIPAL RESPONSIBILITIES:

· Follows quality, safety, regulatory guidance, and written procedures.

· Perform batch record calculations and maintain all documentation according to cGMP guidelines.

· Performs the maintenance and cleanliness of department, premises, and equipment daily.

· Follow detailed instructions and communicate effectively, both written and verbally.

· Performs documentation in accordance with cGMP guidelines.

· Participate and perform effectively in a team environment and interact with multiple departments to ensure the operational success of the area.

· Set up, operate, monitor, and clean production equipment and processes in accordance with cGMP's and SOP's.

· Ensures internal / external customer expectations are met or exceeded.

· Capable of adjusting to changes and dealing effectively with uncertainties in the workplace.

· Takes initiative to achieve work goals and quantifiable business results.

· Collaborative attitude for business success.

· Demonstrates willingness to be flexible to the needs of the department and business.

· Perform other job-related duties as assigned.

QUALIFICATIONS:

· Associate degree or equivalent military experience. College level course work with scientific background is highly desired.

· One or more years of relevant work experience is required, preferably in a pharmaceutical or cGMP manufacturing industry.

· Good interpersonal skills and ability to communicate information in a timely manner.

· Takes ownership and accountability for the production process, assigned production area, and associated documentation.

· Must be capable of providing front line troubleshooting of manufacturing equipment and process issues, properly elevating concerns, and issues to appropriate personnel.

· Aseptic processing and technique experience preferred.

· Willingness to work in a facility handling radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.

· Mechanical aptitude required; manual dexterity for manipulating small items; ability to lift up to 50 lbs. and to handle frequent crawling, stooping, crouching, and kneeling.

· Must be willing to wear a variety of personal protective equipment.

· Willingness to work in a team-based environment.

· May be required to sit or stand for long periods of time while performing duties.

· Must be able to work varying shifts including overnight and weekends.

· Excellent communications, interpersonal and collaboration skills, and ability to interact professionally with a wide range of individuals and organizations, internal and external.

· Ability to work independently with minimal direction, and drive deliverables through to completion by deadlines provided.

· Highly organized with strong attention to detail and commitment to high quality work.

· Ability to work in a collaborative manner; identify challenges and barriers and recommend resolutions.

· Ability to work in a cleanroom and sterile compounding environment, adhering to strict health and hygiene standards to ensure the safety and quality of drug products.

· Must report any health conditions (e.g., rashes, active infections) that could impact product integrity or contamination risks.

· Chronic health conditions that prevent long-term performance of essential job functions may require evaluation and could affect employment status.

· Proper garbing and personal hygiene must be maintained at all times when in the cleanroom or compounding areas.

THE FINE PRINT:

The hourly range in Minnesota is $28.00 to $34.00 per hour. 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 reservesthe 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.