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 ation for drug development submissions.
Support ongoing and future research and development initiatives.
Collaborate effectively with cross-functional teams to advance project goals.
דרישות:
B.Sc. in Chemistry, Biotechnology, or a related field (M.Sc. – advantage).
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 Empower software – advantage.
Strong analytical thinking and problem-solving abilities.
Ability to work effectively in a multidisciplinary team environment.
Self-motivated, curious, and detail-oriented
ניסיון נדרש: 1-2 שנים