Summary

Imunon is seeking to hire a QC Analyst at its Huntsville, AL, site to support the company’s ongoing Drug Product Release and Stability testing activity. The position will play a lead role testing nucleic acid APIs, non-viral gene therapy nanoparticle formulations, and liposomal small molecules.

Duties and responsibilities

• Serve as QC Analyst, reporting to QC Lab Supervisor and QC Lab Manager, performing Release and Stability testing of drug substances and drug products.
• Assist in drafting SOPs, including work instructions, test plans, and validation protocols.
• Troubleshoot, optimize, and improve ongoing testing activity with scientific curiousity.
• Stay abreast of changes to cGMPs, technical advancements, and regulatory requirements.
• Support R&D activity, including testing in-process samples and optimizing analytical methods as-needfed to effectively evaluate pilot-scale process development.
• As-needed, perform basic synthetic organic chemistry reactions.
• Prioritize responsibilities, multi-task, and remain flexible with changing objectives.
• Operate effectively under the pressure of meeting demanding deadlines in a dynamic technical environment.

Experience

The successful candidate will have:

• B.S. or M.S. degree in Biology, Chemistry or related technical area.
• Experience working in a GMP analytical lab preferred, but not required.
• Experience developing analytical methods preferred, but not required.
• Working knowledge of Microsoft Office software, particularly Word and Excel required. Experience with Empower HPLC software is desirable.

Benefits

• Health and Dental insurance, matching 401k, and generous PTO for eligible employees.

To apply, please send your resume to careers@imunon.com