Our client, a leading contract development and manufacturing organization (CDMO) based in the US, is seeking a QC Technician to join their growing team. This is a great opportunity to contribute to the development and commercialization efforts.

Position Summary: The QC Technician will perform quality control tests on radioactive drug products, operate and maintain analytical instrumentation, and ensure compliance with GMP and safety standards. Responsibilities include stability testing, method validation, and maintaining lab cleanliness.
 

Key Responsibilities:

• Conduct QC stability and chemical tests.
• Operate and calibrate analytical equipment (e.g., HPLC, rTLC).
• Develop and validate analytical procedures.
• Maintain lab safety and cleanliness and ensure radiation safety.
• Prepare chemical reagents and manage QC supplies.

Qualifications:

• Bachelor’s degree in chemistry, Biology, or related field.
• Minimum of 1 year of pharmaceutical lab experience.
• Experience with HPLC, rTLC, and GMP.
• Strong communication, organizational, and problem-solving skills.
• Proficiency in Microsoft Word and adaptability to new software.