Quality Control Associate

RK Pharma Inc, a vertically integrated pharmaceutical company headquartered in NJ, is seeking an Quality Control Associate 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. 

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

• Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, or a related field. 
• 1–3 years of experience in a pharmaceutical or regulated laboratory environment. 
• Working knowledge of cGMP, GLP, and FDA regulations. 
• Experience performing raw material, in-process, and finished product testing using techniques such as HPLC, GC, UV-Vis, FTIR, or titration. 
• Familiarity with laboratory documentation systems, data entry, and electronic records (LIMS or Empower preferred). 
• Understanding of OOS/OOT, deviation reporting, and sample management procedures. 
• Strong analytical, organizational, and documentation skills with high attention to detail. 
• Ability to work collaboratively in a fast-paced, quality-focused environment. 

The main expectations and responsibilities for this position are:

• Conduct testing of raw materials, intermediates, and finished products in accordance with approved methods and specifications. 
• Accurately document results and ensure data integrity in compliance with cGMP and company standards. 
• Prepare, label, and maintain samples, reagents, and test solutions according to SOPs. 
• Operate and maintain laboratory instruments, ensuring calibrations and maintenance logs are up to date. 
• Support investigations for OOS, deviations, and CAPAs as directed by QC management. 
• Participate in stability testing, environmental monitoring, and method validation activities as assigned. 
• Maintain clean, organized, and audit-ready laboratory conditions at all times. 
• Collaborate with Quality Assurance and Production teams to ensure timely release of materials and products.  

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.