Senior Scientist

Collins McNicholas Recruitment; Connacht; On-site; EUR 70,000 - 90,000; Full time

Job summary

A major multinational pharmaceutical company in Westport is seeking an experienced Senior Scientist. The role involves leading the development of lab methods, ensuring high quality and adherence to regulations, and training junior staff. The ideal candidate will possess a relevant degree and significant industry experience, particularly in analytical method development. This position offers a 12-month contract with competitive compensation.

Qualifications

• Minimum of 10 years' experience with B.Sc. or 8 years with M.Sc. or 3 years with PhD.
• Preferred experience in analytical method development and validation.
• In-depth knowledge of GMP and ICH guidelines.

Responsibilities

• Lead the development and testing of lab methods for new products.
• Manage handover of lab methods from research to manufacturing.
• Write, review, and maintain important lab documents.

Skills

Analytical method development

Chromatographic techniques

Bioassay techniques

Problem-solving

Education

B.Sc. in relevant science subject

M.Sc. in relevant science subject

PhD in relevant science subject

Job description

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.

[e-mail]

091 706719