Our client, a
major multinational pharmaceutical company
in
Westport, Co. Mayo
, is seeking to recruit a
Senior Scientist
to join their team on a
12-month contract.
Responsibilities:
* Lead the development and testing of lab methods (mainly HPLC and ELISA) for new products, making sure everything is done to high quality and meets regulations.
* Manage the handover of these lab methods from the research team to the manufacturing team, making the process as smooth as possible.
* Plan and track projects related to testing methods to make sure all deadlines and goals are met.
* Ensure all testing methods follow strict industry and safety rules.
* Work closely with teams in research, quality, manufacturing, and regulatory areas to solve problems and improve processes.
* Spot potential technical issues early and fix them before they become bigger problems.
* Write, review, and maintain important lab documents, including instructions, reports, and procedures.
* Train and guide junior staff on how to develop and use testing methods properly; help with training the quality control team when methods are handed over.
* Keep up to date with new technologies and trends and bring useful innovations into the work.
* Clearly communicate progress and key updates to everyone involved in the project.
Requirements:
* B.Sc. in a relevant science subject with a minimum of 10 years' experience / or a M.Sc. with at least 8 years / or a PhD with at least 3 years' relevant industry experience.
* Preferred experience in analytical method development, transfer, and validation.
* Proficiency with chromatographic (e.g., HPLC) and bioassay (e.g., ELISA) techniques.
* In-depth knowledge of GMP, ICH guidelines, and regulatory standards for analytical methods.
* Understanding of the drug development process and regulatory submissions (e.g., IND, NDA).
For a confidential discussion on the Senior Scientist role, please contact Emma Barry today.