Opportunity Description
Job Title: QC Chemist (cGMP / HPLC / Solid Dose)
Location: Cranbury, NJ (Onsite)
Type: Contract-to-Hire
Schedule: 40 hrs/week
Shift: M-F 8am-5pm
Pay: $36-40/hour depending upon experience
Overview
Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis.
Key Responsibilities
+ Perform batch release and stability testing for pharmaceutical products
+ Conduct assay, dissolution, impurity, and related substances testing
+ Operate, calibrate, and troubleshoot HPLC / UPLC systems
+ Maintain GMP documentation and ensure audit readiness (ALCOA+)
+ Investigate OOS / OOT results and support CAPA activities
+ Manage stability programs, sample pulls, and...
Location: Cranbury, NJ (Onsite)
Type: Contract-to-Hire
Schedule: 40 hrs/week
Shift: M-F 8am-5pm
Pay: $36-40/hour depending upon experience
Overview
Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis.
Key Responsibilities
+ Perform batch release and stability testing for pharmaceutical products
+ Conduct assay, dissolution, impurity, and related substances testing
+ Operate, calibrate, and troubleshoot HPLC / UPLC systems
+ Maintain GMP documentation and ensure audit readiness (ALCOA+)
+ Investigate OOS / OOT results and support CAPA activities
+ Manage stability programs, sample pulls, and...