• Degree or Diploma in a relevant Science discipline such as Chemistry, Biochemistry, Biotechnology, Microbiology, Pharmaceutical Sciences, Life Sciences, or equivalent.
• Quality Control experience within a GMP-regulated pharmaceutical, biotechnology, cell therapy, or life sciences environment.
• Hands-on experience in one or more areas including Product Testing, Raw Material Testing, Microbiology/Environmental Monitoring, or Cell Therapy Quality Control.
• Experience with analytical techniques such as HPLC, ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, spectroscopy, TOC, osmolality, flow cytometry, environmental monitoring, or compendial testing.
• Strong knowledge of cGMP requirements, laboratory investigations, data integrity principles, and quality systems.
• Experience supporting method validation, method transfer, equipment qualification, and technical documentation activities.
• Strong analytical, problem-solving, communication, and stakeholder management skills with the ability to work independently in a fast-paced GMP environment.