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QC Supervisor

Garonit Pharmaceutical

Fairfield3w ago

About the role

<p><strong>QC&nbsp;Supervisor</strong></p> <p>Onsite&nbsp;in<strong>&nbsp;Fairfield,&nbsp;NJ</strong></p> <p>We’re looking for a QC Supervisor who’s both a hands-on technical expert and a strong leader. This role manages the daily operations of our QC Laboratory - leading testing, method development, and data review while ensuring full cGMP compliance.</p> <p><strong>&nbsp;What&nbsp;You’ll&nbsp;Do</strong></p> <ul> <li>Supervise&nbsp;and&nbsp;lead&nbsp;a&nbsp;team&nbsp;of&nbsp;QC&nbsp;chemists&nbsp;and&nbsp;analysts.</li> <li>Oversee&nbsp;all&nbsp;analytical&nbsp;testing&nbsp;for&nbsp;manufacturing,&nbsp;release,&nbsp;and&nbsp;stability.</li> <li>Review&nbsp;and&nbsp;interpret&nbsp;HPLC,&nbsp;GC,&nbsp;and&nbsp;wet&nbsp;chemistry&nbsp;data&nbsp;in&nbsp;compliance&nbsp;with&nbsp;cGMP.</li> <li>Author&nbsp;and&nbsp;review&nbsp;SOPs,&nbsp;analytical&nbsp;methods,&nbsp;and&nbsp;validation&nbsp;protocols.</li> <li>Conduct&nbsp;and&nbsp;support&nbsp;laboratory&nbsp;investigations,&nbsp;CAPA,&nbsp;and&nbsp;change&nbsp;controls.</li> <li>Manage&nbsp;and&nbsp;schedule&nbsp;lab&nbsp;workloads&nbsp;to&nbsp;meet&nbsp;production&nbsp;timelines.</li> <li>Ensure&nbsp;lab&nbsp;safety,&nbsp;data&nbsp;integrity,&nbsp;and&nbsp;adherence&nbsp;to&nbsp;FDA&nbsp;and&nbsp;ICH&nbsp;guidelines.</li> <li>Collaborate&nbsp;cross-functionally&nbsp;to&nbsp;resolve&nbsp;quality-related&nbsp;issues&nbsp;quickly.</li> <li>Develop&nbsp;and&nbsp;mentor&nbsp;QC&nbsp;staff&nbsp;through&nbsp;training&nbsp;and&nbsp;performance&nbsp;development.</li> <li>Support&nbsp;continuous&nbsp;improvement&nbsp;initiatives&nbsp;to&nbsp;enhance&nbsp;compliance&nbsp;and&nbsp;efficiency.</li> </ul> <p><strong>&nbsp;What&nbsp;You’ll&nbsp;Bring</strong></p> <ul> <li>Bachelor’s&nbsp;degree&nbsp;in&nbsp;Chemistry&nbsp;or&nbsp;a&nbsp;related&nbsp;scientific&nbsp;field.</li> <li>2+&nbsp;years&nbsp;in&nbsp;a&nbsp;supervisory&nbsp;or&nbsp;management&nbsp;role&nbsp;in&nbsp;a&nbsp;pharmaceutical&nbsp;QC&nbsp;lab.</li> <li>Strong&nbsp;experience&nbsp;with&nbsp;Empower&nbsp;3,&nbsp;HPLC,&nbsp;GC,&nbsp;and&nbsp;wet&nbsp;chemistry.</li> <li>Deep&nbsp;understanding&nbsp;of&nbsp;cGMP,&nbsp;ICH,&nbsp;CFR,&nbsp;and&nbsp;USP&nbsp;testing&nbsp;requirements.</li> <li>Experience&nbsp;in&nbsp;method&nbsp;development,&nbsp;validation,&nbsp;and&nbsp;stability&nbsp;testing.</li> <li>Proven&nbsp;leadership,&nbsp;training,&nbsp;and&nbsp;coaching&nbsp;skills.</li> <li>Excellent&nbsp;problem-solving,&nbsp;documentation,&nbsp;and&nbsp;communication&nbsp;abilities.</li> <li>High&nbsp;attention&nbsp;to&nbsp;detail,&nbsp;strong&nbsp;work&nbsp;ethic,&nbsp;and&nbsp;commitment&nbsp;to&nbsp;quality.</li> </ul> <p><strong>&nbsp;Why&nbsp;Garonit&nbsp;Pharma</strong></p> <ul> <li>Work&nbsp;with&nbsp;cutting-edge&nbsp;equipment&nbsp;in&nbsp;a&nbsp;collaborative,&nbsp;growth-oriented&nbsp;environment.</li> <li>Play&nbsp;a&nbsp;key&nbsp;role&nbsp;in&nbsp;ensuring&nbsp;product&nbsp;quality&nbsp;and&nbsp;regulatory&nbsp;success.</li> <li>Competitive&nbsp;compensation&nbsp;and&nbsp;career&nbsp;growth&nbsp;opportunities.</li> </ul>

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