Compliance Supervisors at RK PHARMA INC – East Windsor, New Jersey

RK Pharma Inc, a vertically integrated pharmaceutical company headquartered in NJ, is seeking an Compliance Supervisor to work with our growing Quality Assurance 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 Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related technical field.
• 5+ years of experience in pharmaceutical quality, compliance, or regulatory affairs, with at least 2 years in a supervisory role.
• In-depth knowledge of cGMP, GDP, FDA, EMA, and ICH regulations and inspection practices.
• Familiarity with data integrity principles, internal audits, and risk management processes.
• Experience with electronic quality systems (MasterControl).
• Strong analytical, problem-solving, and technical writing skills.
• Excellent communication and leadership abilities to coordinate cross-functional compliance initiatives.

The main expectations and responsibilities for this position are:

• Supervise and ensure the execution and documentation of compliance programs aligned with regulatory and internal quality standards.
• Conduct and support internal audits, self-inspections, and regulatory inspection preparation.
• Monitor and trend quality metrics, deviations, and audit findings, recommending corrective and preventive actions.
• Review and approve quality and compliance documentation, including SOPs, protocols, and validation reports.
• Ensure adherence to data integrity, documentation accuracy, and record retention policies.
• Collaborate with Quality Assurance, Production, and Engineering to resolve compliance gaps and implement continuous improvements.
• Provide training, guidance, and mentorship to QA and operations staff on GMP and compliance best practices.
• Participate in regulatory inspections and coordinate responses to observations or deficiencies.

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.