Job Details

Company: PPD
Location: Europe, Middle East & Africa-Ireland-Westmeath-Ath
Reference: 143954
Closing Date: 20 Jul 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Due to continued success and growth, PPD are looking for experienced Scientists/Stability Analysts to be based in our Biopharm department of our GMP Lab in Athlone, Ireland. The role of Scientist is to perform a variety of complex sample preparation and analysis procedures to quantitatively measure small and large biomolecules such as proteins, peptides, nucleotides/oligonucleotides, DNA, carbohydrates/polysaccharides and liposomes using a wide range of analytical instrumentation. ...

Requirements:

Due to continued success and growth, PPD are looking for experienced Scientists/Stability Analysts to be based in our Biopharm department of our GMP Lab in Athlone, Ireland. The role of Scientist is to perform a variety of complex sample preparation and analysis procedures to quantitatively measure small and large biomolecules such as proteins, peptides, nucleotides/oligonucleotides, DNA, carbohydrates/polysaccharides and liposomes using a wide range of analytical instrumentation. This role will work with minimal supervision, interpret analytical data in regards to acceptability and consistency and set up and maintain analytical instrumentation.

Duties & Responsibilities: 

• Perform a variety of complex sample preparations
• Analysis procedures to quantitatively measure pharmaceutical compounds in a variety of formations for stability testing and other studies for analytical testing support
• Review and compilation of results
• Performing work assignments accurately, timely and in a safe manner
• Training on routine operation, maintenance and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines.
  

Qualifications

• Education to a Bachelors or higher level in Biochemistry or related subjects
• 4 years’ work experience within a GMP laboratory
• 4 years industry experience with Lab techniques relevant to Biopharm: ELISA, SDS-Page, Western Blot, HPLC. Capillary electrophoresis would be an advantage.
• Detailed knowledge of method validation; method development would be an advantage.
• The ability to plan, schedule and carry out work for successful project completion
• A positive attitude and ability to work well with others
• The ability to write protocols and reports with minimum supervision
• Excellent attention to detail
• Be able to communicate effectively and follow detailed written and verbal instruction

We look forward to receiving your application.

IndeedPPDGBIE