Radiopharmaceutical Production Technician

Somerset, NJ
Full Time
Radiopharma Production
Mid Level

****THIS IS AN OVERNIGHT POSITION - 8pm to 6am four nights a week****
Objective

The Radiopharmaceutical Production Technician II produces radiopharmaceutical products in a just-in-time environment to support clinical and commercial demand. They are responsible for overseeing and executing all tasks associated with formulation, preparation, assembling, and packaging of components, adhering to cGMP Guidelines to meet production demands. S/he serves as a key resource, providing guidance, decision-making authority, and support to junior employees while coordinating work within the standard operating procedures (SOPs).

 Essential Functions

  • Supports all technical aspects related to pharmaceutical production readiness including manually cleaning the classified manufacturing rooms, performing environmental monitoring and performing sterilization of the isolators
  • Performs continuous manufacturing of pharmaceutical products with automated synthesis system
  • Demonstrates advanced proficiency in following quality, safety, regulatory guidance, and written procedures.
  • Performs complex batch record calculations and maintains all documentation according to cGMP guidelines.
  • Performs dispensing of each individual product vial in a highly classified isolator cell while ensuring the sterility of the injectable drug product. This includes dispensing vials, removing those vials using a delivery system and preparing vials for shipment.
  • Prepares all materials while maintaining material identity in accordance with the batch records
  • Maintains and prepares equipment and cleanrooms for use
  • Assists in performing deviation investigations and inspections
  • Participates in assigned qualification and validation activities, as necessary
  • Plays a key role in cross-functional teamwork, collaborating with multiple departments to ensure the operational success of the area
  • Sets up, operates, monitors, and cleans production equipment and processes in accordance with cGMP's and SOP's, and provides troubleshooting expertise
  • Exhibits flexibility in accommodating the changing needs of the department and business.

Education/Experience

  • Associate degree or equivalent experience. College-level coursework with a strong scientific background is highly desired.
  • Minimum of two or more years of relevant work experience in a pharmaceutical or cGMP manufacturing industry.
  • Experience with MS Office Suite.
  • Aseptic processing and technique experience is preferred.

Knowledge/Skill/Ability

  • Proficient in handling and managing radioactive materials, with a comprehensive understanding of safety protocols to minimize exposure levels. Actively participates in and contributes to advanced safety programs aimed at ensuring the utmost protection for all personnel.
  • Capable of handling physically demanding tasks, including lifting loads up to 50 lbs. and performing frequent crawling, stooping, crouching, and kneeling. Maintains a high level of fitness and agility to excel in challenging work environments.
  • Extensive experience and willingness to use a variety of advanced personal protective equipment, ensuring strict adherence to safety guidelines and regulations.
  • Proven ability to thrive in a team-based environment, taking on leadership roles when necessary. Collaborates effectively with colleagues, demonstrating advanced interpersonal and communication skills to foster a cohesive work environment.
  • Flexibility to work varying shifts, including overnight and weekends, exhibiting a commitment to meeting production demands and deadlines.
  • Highly organized with an exceptional attention to detail. Possesses the ability to manage complex tasks and projects, ensuring a commitment to delivering high-quality work consistently.
  • Demonstrates ownership and accountability for the production process, assigned production area, and associated documentation.
  • Proficient in providing front-line troubleshooting of manufacturing equipment and process issues, while effectively escalating concerns and issues to appropriate personnel.

Work Environment

****THIS IS AN OVERNIGHT POSITION - 8pm to 6am four nights a week****

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.


During the course of this job, the employee may encounter exposure to radiation hazards.

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

For information on Perspective Therapeutics, visit our website at: www.perspectivetherapeutics.com.

Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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