Chemist

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. About 3,000 employees work for Glatt at more than 15 companies and offices all over the world.

Responsible for supporting multiple projects under limited supervision. Provide scientific expertise and ability to independently investigate and resolve analytical problems/issues. Write analytical method validation, verification, transfer and stability protocols and reports. Provide training and mentoring to chemists. May supervise chemists on project basis. Must maintain a high degree of flexibility to accommodate fluctuating priorities in a fast‑paced environment.

• Supervise a small staff of chemists on project basis.
• Train laboratory personnel in the use of equipment and analytical techniques.
• Write, review and revise SOP’s, method validation, verification, transfer and stability protocols and reports as required.
• Develop/transfer and validate/verify analytical methods as necessary.
• 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.

• 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.
• Master’s or Ph.D. in a relevant scientific field with 5–7 years of experience in a GMP environment.
• Advanced chromatography skills.
• Strong hands‑on experience with HPLC (High‑Performance Liquid Chromatography) and GC (Gas Chromatography) equipment, including maintenance and troubleshooting.
• Strong knowledge and experience in dissolution techniques.
• Proficient with Microsoft Office and data acquisition software.
• In‑depth understanding of analytical methods, product specifications, and historical data. Ability to independently investigate and resolve analytical issues.
• Skilled in writing validation, verification, transfer, and stability protocols and reports.
• Strong analytical and problem‑solving abilities.
• High attention to detail and accuracy.
• Ability to prioritize, multitask, and meet deadlines with minimal supervision.
• Excellent communication, interpersonal, and presentation skills.

Salary Range:

$70,000-$90,000

You have the opportunity to perform an interesting and responsible job in a successful, renowned company. 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.

Glatt Air Techniques Inc., Human Resources, 20 Spear Road, Ramsey, NJ 07446, USA