Quality Control (QC) Chemist

We are seeking a detail-oriented and Quality Control (QC) Chemist to join our pharmaceutical manufacturing team. In this role, you will perform critical physical and chemical testing on raw materials, in-process samples, and finished products to ensure compliance with cGMP, cGLP, and regulatory standards.

Key Responsibilities

• Perform assigned sampling, physical, chemical tests, and assays on raw materials, active pharmaceutical ingredients (APIs), in-process samples, finished goods, and stability products.


• Utilize wet chemistry, physical methods, and major instruments including HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto Titrator, and Bulk Density apparatus according to USP, in-house, or compendial monographs.


• Document all work clearly and perform tests with high accuracy. Record data, results, and transcribe information onto report sheets and laboratory notebooks exactly as specified by Standard Operating Procedures (SOPs).


• Comply with safety protocols, manage chemical waste, maintain laboratory housekeeping, and adhere to cGMP/cGLP guidelines at all times.


• Maintain proper laboratory logbooks and actively participate in laboratory investigations regarding deviations and Out-of-Specification (OOS) results.


• Perform other routine laboratory duties and tasks as assigned by management.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Pharmacy or related scientific discipline.


• Minimum 2 years of experience in a pharmaceutical QC laboratory or regulated cGMP environment preferred.


• Hands on experience with Empower-3, a plus.


• Strong documentation, organizational and communication (written & verbal) skills.

Physical Demands/Environmental Conditions:

• Laboratory environment.


• Able to lift about 25 pounds.


• Able to stand and or sit for longer period of time.