Quality Control Supervisor

Description

RK Pharma Inc, a vertically integrated pharmaceutical company headquartered in NJ, is seeking an Quality Control Supervisor to work with our growing Quality Control Team  as we scale towards commercial manufacturing in the next upcoming months. As a company focused on the development, manufacturing and sale of high quality and affordable generic pharmaceutical products worldwide we are looking for sharp, driven, self-directed individuals to help us grow our mid-stage start-up team.
 

This position is located in East Windsor, NJ and is required to be onsite. 

Requirements

If this sounds interesting to you, it’s probably because up to this point you have:

• Bachelor’s degree in Chemistry, Microbiology, Pharmaceutical Sciences, or a related field (Master’s preferred). 
• 5+ years of experience in pharmaceutical Quality Control, with at least 2 years in a supervisory or lead role. 
• Strong understanding of cGMP, GLP, FDA, and USP requirements in a regulated manufacturing environment. 
• Hands-on experience with analytical techniques such as HPLC, GC, FTIR, UV-Vis, dissolution, and wet chemistry. 
• Working knowledge of laboratory investigations, OOS/OOT management, and stability programs. 
• Proficiency with LIMS, Empower, and other QC documentation systems. 
• Demonstrated ability to manage teams, coordinate testing schedules, and ensure timely release of materials and products. 
• Excellent analytical, organizational, and written communication skills.  

The main expectations and responsibilities for this position are:

• Supervise daily QC laboratory operations, ensuring all testing is performed in compliance with cGMP and company standards. 
• Review and approve analytical data, test results, and laboratory documentation for accuracy and completeness. 
• Oversee raw material, in-process, and finished product testing, ensuring adherence to specifications and timelines. 
• Lead or support OOS/OOT investigations, CAPA activities, and deviation reports in collaboration with QA. 
• Ensure instrument calibration, maintenance, and qualification are performed and documented as required. 
• Train, mentor, and evaluate QC analysts to maintain a high-performing and compliant laboratory team. 
• Participate in internal and external audits, providing documentation and responses as needed. 
• Support continuous improvement initiatives to enhance lab efficiency, data integrity, and compliance. 

WE ARE SLATING THESE HIRES FOR START DATES IN OCTOBER OF 2026 BUT ARE COLLECTING APPLICATIONS NOW,

NEXT STEPS WILL BE SENT TO YOU IN EARLY AUGUST 2026

ONSITE INTERVIEWS WILL BE SCHEDULED IN SEPTEMBER 2026

START DATES IN OCTOBER 2026

If this sounds like something that is of interest to you, please don’t hesitate to apply to start a conversation.

We look forward to getting to know more about you and the skills you can bring to a company like RK Pharma Inc.