Job Description

We are seeking a highly motivated Scientist to join our Biopharmaceutical Analysis team. This role, reporting to the Department Manager, focuses on validation of Small Molecules products in a GMP-regulated environment.


Key responsibilities:


  • Design, supervision and execution of validations studies of Small Molecules Products.

  • Hands-on experience with techniques such as chromatography and HPLC.

  • Lead and manage assigned the assigned projects keeping the deadlines and establishing a direct communication with the client

  • Draft, review, and manage technical documentation associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.)

  • Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.


Requirements


  • Bachelor's or higher...

Apply for this Position

Ready to join Kymos Group? Click the button below to submit your application.

Submit Application