QC Chemist- IMMEDIATE NEED
$70k - $90kGlatt Ingenieurtechnik GmbH
Chemist
Work experience
Medicine, Pharmacy, Laboratory
We are a leading world supplier of integrated processing solutions for customers in the area of pharmaceuticals, food processing, feeds and fine chemicals. Our products and services stand for reliability and quality worldwide. For our site in Ramsey, NJ (USA) we have an immediate opening for a
Chemist / Senior Chemist
Responsible for supporting multiple projects under limited supervision. Provide scientific expertise and ability to independently investigate and resolve analytical problems/issues. Provide training and mentoring to chemists. May supervise chemists on project basis. Supervise a small staff of chemists on project basis.
Train laboratory personnel in the use of equipment and analytical techniques.
Conduct analytical testing in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines.
Maintain laboratory records per CGMPs regulations and in compliance with applicable SOP's.
Peer review data and reports in accordance with applicable Test Monographs, Protocols and SOP's.
Recognize deviations from normal results and inform VP, Quality Control & Development of any out of specification (OOS) results and/or deviations that may affect the integrity of the data and drive corrective action of problems.
Review and revise laboratory systems on an ongoing basis.
Other responsibilities as assigned by the VP, Quality Control & Development
Qualifications: Bachelor's degree in Chemistry, Physical Chemistry, Chemical Engineering, Biology, or related sciences with 7-10 years of experience in a GMP-compliant pharmaceutical environment
D. in a relevant scientific field with 5-7 years of experience in a GMP environment.
Strong hands-on experience with HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography) equipment, including maintenance and troubleshooting
Proficient with Microsoft Office and data acquisition software
In-depth understanding of analytical methods, product specifications, and historical data
Skilled in writing validation, verification, transfer, and stability protocols and reports
Ability to prioritize, multitask, and meet deadlines with minimal supervision
If this interesting position appeals to you, we look forward to receiving your online application.Applications that do not reach us personally via the online portal can unfortunately not be considered.
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