Senior QC Analyst (Nuclear Medicine)

Proclinical is seeking a Senior QC Analyst to permanently join a dynamic team. This role focuses on supporting the startup of a new production facility dedicated to manufacturing Ac-225, a critical radiotherapeutic for cancer treatment. You will play a key role in ensuring the quality of Ac-225 through advanced analytical techniques such as gamma spectrometry and ICP-MS, while adhering to current Good Manufacturing Practices (cGMP). This is an exciting opportunity to contribute to cutting-edge innovation in a fast-paced, regulated environment.

Responsibilities:

• Qualify equipment and develop methods for analyzing Ac-225 solutions using specialized techniques (e.g., ICP-MS, gamma spectrometry, endotoxin determination).
• Analyze in-process control samples, starting materials, and Ac-225 batches using advanced analytical methods.
• Ensure all qualified equipment and analytical methods comply with cGMP regulations.
• Report data according to standard protocols.
• Manage quality control of raw materials and incoming goods.
• Perform recalibration and maintenance of laboratory equipment.
• Write and maintain Standard Operating Procedures (SOPs).
• Collaborate with subcontractor analytical laboratories as needed.

Key Skills and Requirements:

• Master's degree in Analytical Chemistry or a related field.
• Proven experience with ICP-MS.
• Experience in radiochemical analysis.
• Familiarity with GMP standards and regulatory environments.
• Willingness to learn new analytical techniques and work with radioactive materials.
• Proficiency in specialized techniques such as ICP-MS and gamma spectrometry.
• Strong analytical skills with attention to detail.
• Ability to work independently and collaboratively within a team.
• Adaptability to a fast-paced and evolving environment.

If you are having difficulty in applying or if you have any questions, please contact Jordan Kiely at j.kiely@proclinical.com.

Apply Now:

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