Job Description

• Conduct analytical development, support formulation development and coordinate all analytical activities of pharmaceutical product development
• Implements testing instructions and Standard Operating Procedures relating to the Raw Material / Finished Products in GR&D Analytical Laboratory and in compliance with requirements of Good Manufacturing Practice (cGMP)
• Performs tests, documents and reports in a professional, correct, reliable and accurate manner
• Prepares and sign analytical reports and analytical documents for regulatory submissions
• Performs tests, documents and reports in a professional, correct, reliable and accurate manner
• Develops all analytical methods related to the product under his responsibility and validate them
• Prepares and sign analytical reports and analytical documents for regulatory submissions
• Serves as "analytical center of knowledge" of a given project
• Participates in product development strategy and characterization tests determining. Executes tests accurately and efficiently. Performs data analysis, interprets and communicates test results
• Perform the tasks according to safety instructions and regulations
• Ensures that all samples are tested in a timely manner, according to work plan
• Supervises the analytical performance, reviews the raw data, approves and signs the test records for work performed by other researchers for the product under his/her responsibility. Ensures that project goal and deadline are met
• Responsible for transfer of analytical methods to Teva's quality control laboratories / sub-contractor laboratories / other Teva's R&D outside Israel for the product under his/her responsibility

Qualifications

• B.Sc. in chemistry or equivalent;
• M.Sc or PhD an advantage
• Experience in analytical pharmaceutical field not less than 5 year – obligatory
• Experience in LC-MS technic and Peptide analysis – significant advantage

Apply here: https://bit.ly/2FiKsWL