Quality Control Supervisor
Company: Careers at RK Pharma Inc.
Location: Hightstown
Posted on: February 23, 2026
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Job Description:
Job Description Job Description 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.
Keywords: Careers at RK Pharma Inc., Hackensack , Quality Control Supervisor, Science, Research & Development , Hightstown, New Jersey
