Description
• Participate in method development, validation and technology transfer: execute experiments to develop biological assays (such as RT-PCR, ELISA, and cell-based assay).
• Perform Validation and transfer of biological assays to QC Department.
• New technology development.
• Perform tests to support process development
• Review relevant technical documents, procedures, protocols and reports.
• Collect and analyze data, present information and data in both written and verbal form.
Requirements
• BSc or MS in biotechnology, molecular biology, life sciences or a related field.
• 3+ years of biopharmaceutical industry experience with strong experience in Biological assays
• Experience in pharma and Working under GMP regulation is an advantage
• Strong ability in execution and driving for results independently and in collaboration.
• Detail oriented with good organizational skills and ability to work in a high paced group environment to meet deadlines and prioritize work on multiple projects.
• Excellent communication skills, and the ability to build and maintain relationships with group members, partners, customers, and collaborators.