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Theranostics Manufacturing Associate

PHARMALOGIC HOLDINGS
Posted 4 days ago, valid for 22 days
Location

New York, NY 10008, US

Salary

$36 - $42 per hour

Contract type

Full Time

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Sonic Summary

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  • The Theranostics Manufacturing Associate position at PharmaLogic involves producing and validating radiopharmaceutical treatments for patients, requiring hands-on experience in radiochemistry synthesis and quality control.
  • Candidates must hold a bachelor's degree in chemistry or a related field and have a minimum of two years of laboratory experience, preferably in a GMP manufacturing environment.
  • Key responsibilities include synthesizing radiopharmaceuticals, performing analytical testing, and maintaining safety protocols while ensuring compliance with cGMP regulations.
  • The role demands strong teamwork, communication, and problem-solving skills, along with proficiency in analytical equipment and laboratory safety practices.
  • The position offers a competitive salary, with variable hours expected at 40 hours per week.

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: 

1. 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. 

2. Operate and maintain automated radiochemistry synthesis units. 

3. Operate and maintain onsite analytical equipment. 

4. Assist with improvement of current cGMP and non-GMP processes. 

5. Follow all SOP guidelines for manufacturing and QC release testing of radiopharmaceutical product, raw material, finished and semi-finished product, environment and facilities. 

6. Maintain clean and safe work environment, performing radiation safety duties in compliance with safety and pharmaceutical regulations. 

7. Maintain accurate production and test/validation results. 

8. A passion for continuous learning and curiosity to find innovative ways to improve our ways of working. 

9. Perform other job-related duties as assigned.

Job Requirements │ Skills │ Education:

 • 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.

Ability to work varying shifts both independently and as part of a team.

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.



Variable hours
40 hours/week



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