Synerfac
Quality Control Chemist III
Synerfac, Miami, Florida, us, 33222
About Us:
We are a leader in manufacturing, packaging, and distributing over-the-counter pharmaceuticals. We're committed to quality, innovation, and excellence, and we're seeking a Senior QC Chemist to ensure our products meet the highest standards.
Job Overview:
As a Senior QC Chemist, you"ll oversee testing of raw materials, in-process samples, and finished products. You"ll use HPLC, GC, and other techniques to lead impurity profiling, API quantification, and stability testing while adhering to ICH Guidelines (Q8, Q9, Q10).
Key Responsibilities:
**Perform advanced quality control testing
**Validate/troubleshoot analytical methods
**Operate HPLC, GC, UV, and more
**Lead batch release and stability studies
**Mentor junior chemists
**Drive efficiency and risk management
**Maintain cGMP/SOP lab records
**Resolve OOS results
**Ensure compliance with USP/NF, EP, BP, JP standards
Job Requirements
Qualifications:
**Bachelor's in Chemistry (Advanced preferred)
**15+ years of cGMP-regulated QC Chemist experience in Pharmaceutical manufacturing
**Expertise with HPLC, GC, and validation methods
**Strong leadership and organizational skills
Preferred Experience:
**UV-Vis Spectroscopy, Dissolution Testing, Karl Fischer Titrations, FTIR, LC-MS, Potentiometric Titrations, Thermal Analysis/DSC, ICP-MS, NIR, TOC, Particle Size Analysis, X-Ray Powder Diffraction (XRPD)
We are a leader in manufacturing, packaging, and distributing over-the-counter pharmaceuticals. We're committed to quality, innovation, and excellence, and we're seeking a Senior QC Chemist to ensure our products meet the highest standards.
Job Overview:
As a Senior QC Chemist, you"ll oversee testing of raw materials, in-process samples, and finished products. You"ll use HPLC, GC, and other techniques to lead impurity profiling, API quantification, and stability testing while adhering to ICH Guidelines (Q8, Q9, Q10).
Key Responsibilities:
**Perform advanced quality control testing
**Validate/troubleshoot analytical methods
**Operate HPLC, GC, UV, and more
**Lead batch release and stability studies
**Mentor junior chemists
**Drive efficiency and risk management
**Maintain cGMP/SOP lab records
**Resolve OOS results
**Ensure compliance with USP/NF, EP, BP, JP standards
Job Requirements
Qualifications:
**Bachelor's in Chemistry (Advanced preferred)
**15+ years of cGMP-regulated QC Chemist experience in Pharmaceutical manufacturing
**Expertise with HPLC, GC, and validation methods
**Strong leadership and organizational skills
Preferred Experience:
**UV-Vis Spectroscopy, Dissolution Testing, Karl Fischer Titrations, FTIR, LC-MS, Potentiometric Titrations, Thermal Analysis/DSC, ICP-MS, NIR, TOC, Particle Size Analysis, X-Ray Powder Diffraction (XRPD)