What are the responsibilities and job description for the Theranostics Manufacturing Associate position at PharmaLogic?
Division │ Department: PharmaLogic
Position Title: Theranostics Manufacturing Associate
Reports To: Theranostics Laboratory Manager
Role Summary:
Join our team at the forefront of precision medicine. As a Theranostics Manufacturing Associate, you’ll be part of a team bringing innovative radiopharmaceutical treatments from the lab to patients who need them most. You’ll gain hands-on experience in producing and validating cutting-edge life-changing therapies. This hands-on position involves radiochemistry synthesis, aseptic processing, and quality control — ensuring every dose meets the highest standards of safety and innovation, in a collaborative, purpose-driven environment.
Job Responsibilities and Duties:
Physical and Intellectual Requirements: Required are a mechanical aptitude; manual dexterity for manipulating small items; ability to lift between 16 to 50 lbs. and to handle frequent crawling, stooping, crouching and kneeling; ability to analyze situations, set priorities and meet deadlines.
Position Title: Theranostics Manufacturing Associate
Reports To: Theranostics Laboratory Manager
Role Summary:
Join our team at the forefront of precision medicine. As a Theranostics Manufacturing Associate, you’ll be part of a team bringing innovative radiopharmaceutical treatments from the lab to patients who need them most. You’ll gain hands-on experience in producing and validating cutting-edge life-changing therapies. This hands-on position involves radiochemistry synthesis, aseptic processing, and quality control — ensuring every dose meets the highest standards of safety and innovation, in a collaborative, purpose-driven environment.
Job Responsibilities and Duties:
- Responsible for production of radiopharmaceuticals:
- Synthesis of diagnostic and therapeutic radiopharmaceuticals.
- Analytical testing using HPLC, GC, TLC and other techniques.
- Aseptic processing and fill/finish operations.
- Completion of associated cGMP documentation.
- Operate and maintain automated radiochemistry synthesis units.
- Operate and maintain onsite analytical equipment.
- Assist with improvement of current cGMP and non-GMP processes.
- Follow all SOP guidelines for manufacturing and QC release testing of radiopharmaceutical product, raw material, finished and semi-finished product, environment and facilities.
- Maintain clean and safe work environment, performing radiation safety duties in compliance with safety and pharmaceutical regulations.
- Maintain accurate production and test/validation results.
- A passion for continuous learning and curiosity to find innovative ways to improve our ways of working.
- Perform other job-related duties as assigned.
- Requires a bachelor's degree in chemistry or related field.
- Two or more years of laboratory experience are preferred.
- Familiarity with a GMP manufacturing environment and working with FDA and FDA cGMP regulations required. Knowledge of molecular imaging techniques and pharmaceutical study design and execution desired.
- Experience with laboratory procedures and analytical equipment (HPLC, GC, TLC, ICP, Radiation measurement) strongly preferred.
- Experience with radiation protection techniques and laboratory safety strongly preferred.
- Superior teamwork, multi-tasking and time/project management skills.
- Excellent communication, analytical, problem solving, presentation and computer/pc skills (including proficiency in Microsoft Suit and related software).
- Superior attention to detail in a fast-paced and dynamic environment.
Physical and Intellectual Requirements: Required are a mechanical aptitude; manual dexterity for manipulating small items; ability to lift between 16 to 50 lbs. and to handle frequent crawling, stooping, crouching and kneeling; ability to analyze situations, set priorities and meet deadlines.
Salary : $30 - $42