We are seeking a QC Supervisor to lead analytical activities within a dynamic GMP-regulated biopharma environment.
Key Responsibilities
* Lead and oversee all QC/ARD Laboratory activities
* Manage sample testing for in-process & finished products
* Review analytical data & ensure compliance with industry standards
* Coordinate material management & vendor qualification
* Drive training, audits & continuous improvement initiatives
Requirements
* BSc/MSc in Chemistry, Biochemistry, or a related field
* 5+ years of QC experience in a GMP-regulated lab (2+ years in a leadership role)
* Strong expertise in analytical techniques (HPLC, GC, method validation)
* Leadership, problem-solving & excellent communication skills