
Analytical Chemist
10h10 hours agoSyqe Medical
Tel Aviv, IL · Full-time · ILS 180,000 – ILS 280,000
About this role
Syqe Medical develops breakthrough technologies for precise delivery of therapeutic molecules via inhalation. The mission is to enhance patients’ quality of life with accessible and effective treatments. We seek an Analytical Chemist to join as a temporary maternity leave replacement.
As part of the CMC team, you will play a central role in chemical characterization of products. This involves developing and implementing analytical methods to identify and quantify known and novel plant-derived compounds. You will operate instruments including GC/MS, UPLC, and Karl Fischer titrators.
You will work closely with multidisciplinary teams including QA/QC, Regulatory Affairs, Tech, and Clinical. These collaborations support drug development activities and regulatory submissions. The work contributes to FDA approval of Syqe’s inhalation technology.
This position offers the opportunity to contribute to ongoing research and development initiatives. You will write protocols for method development and validation while preparing regulatory documentation. The role demands strong analytical thinking in a dynamic startup environment.
Requirements
- B.Sc. in Chemistry, Biotechnology, or a related field - Mandatory.
- Minimum of 3 years of experience in an analytical or R&D role within the pharmaceutical industry.
- Hands-on experience with analytical instrumentation, particularly GC/MS - Mandatory.
- Proven experience in analytical method development and validation - Mandatory.
- Strong technical writing skills and familiarity with regulatory submission requirements - Mandatory.
- Experience with HPLC – Advantage.
- Familiarity with MassHunter software – Strong Advantage.
Responsibilities
- Operate, maintain, and troubleshoot analytical instruments such as GC/MS, UPLC, and Karl Fischer titrators.
- Perform routine and non-routine chemical analyses.
- Develop, optimize, and validate analytical methods.
- Write and execute protocols related to method development and validation.
- Contribute to the preparation of regulatory documentation for drug development submissions.
- Support ongoing and future research and development initiatives.
- Collaborate effectively with cross-functional teams to advance project goals.
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