Accessibility Links

Research Scientist, Small Molecule

Expired
  • Salary: Negotiable
  • Job type: Permanent
  • Location: Leinster
  • Sector: Science
  • Date posted: 17/01/2018
  • Job reference: J376629A

We're really sorry, but it looks like this job has already been filled.

Register your CV with us, see our latest jobs or use the search below.

Research Scientist, Small Molecules

My clients GMP laboratory offers fully integrated solutions for product development and analytical development, including analytical testing services in method development and secondary packaging, labelling and storage. Thier highly qualified GMP lab staff work with large and small molecules, including active pharmaceutical ingredients (API), drug products, inhaled products and other medical devices.

Due to further expansion of their site, they have a new opening for a Research Scientist in our Small Molecule team.

About the Research Scientist position

The role of Research Scientist is to provide full analytical testing support in accordance with cGMP practices, including analytical method development and validation. This is an exciting opportunity to join a Lab that focuses on method development and validation, stability and quality control testing for all phases of drug development, with particular emphasis on inhalation, small molecule and biopharmaceutical products.

Responsibilities include:

  • Co-ordinate all aspects of managing method development and validation
  • Supervise and assist senior technical staff in laboratory operations
  • Interface with clients on scientific issues, study design and project technical requirements
  • Plan, direct and implement improvements in systems and processes in order to enhance efficiency and quality
  • Assist with strategic planning, business development and new technology implementation

Qualifications

  • The successful candidate will possess a degree (or equivalent) in Chemistry.
  • Significant experience within an analytical testing laboratory and cGMP environment is essential, as well as solid scientific supervisory experience in the pharmaceutical or analytical contract laboratory industry (to include R&D project and program management, direct supervision of technical staff, and direction of laboratory operations).

Other requirements also include:

  • Expertise in cGMP regulated environment in the areas of analytical method development and validation for trace level analysis and for a variety of dosage forms, using a variety of instrumentation which may include the following: GC, HPLC, IC, AA, ICP and other applicable analytical instruments.
  • Knowledge with GC/MS and LC/MS/ instrumentation detection techniques for the purposes of impurity structural elucidation / unknown identification and quantitative assays for impurities in pharmaceutical products.
  • Excellent analytical expertise in method development and validation
  • Excellent communication and presentation skills
  • Strong mentoring and training skills
  • Ability to build and develop client relationships
  • Understanding of budgeting and revenue projection
  • Ability to plan, organize and work to deadlines

For Additional information on this and other opportunities please contact Kathryn on or call 01 6455244/0873555378

Similar jobs
View more similar jobs