Key Responsibilities
Operates and maintains various analytical instruments, including UPLC, spectrophotometers, Karl Fischer titrators, GC/MS, and GC/TCD.
Conduct both routine and non-routine chemical analyses.
Develop and validate new analytical methods.
Write and execute protocols and reports for method development and validation.
Investigate and resolve analytical issues.
Contribute to the preparation of regulatory documentation for drug development submissions.
Support ongoing and future research initiatives.
Collaborate effectively with cross-functional teams to drive project success.
Option 1:
B.Sc. in Chemistry, Biotechnology, or a related field
Minimum of 3 years of experience in an analytical lab within the pharmaceutical industry
Option 2:
M.Sc. or Ph.D. in Chemistry or a related field
Industry experience is an advantage but not required
In addition (for both profiles):
Hands-on experience with analytical instruments, especially HPLC required
Proven expertise in analytical method development required
Proficiency with EMPOWER software required
Experience with Karl Fischer, GC/MS, or GC/TCD an advantage
Strong scientific writing skills required
Strong problem-solving skills and the ability to work collaboratively in a multidisciplinary team environment
Self-motivated, curious, and detail-oriented
***Note: This is a temporary position as a maternity leave replacement.***
