The position is a full-time job and appeals to both men and women
JOB DESCRIPTION
• Suggest, design, develop and implement biological QC assays for various projects according to relevant regulatory guidelines.
• Building and guiding the team to develop R&D assays into QC tests.
• Leading qualification and validation projects.
• Perform data analysis, interpretation, and presenting the data for appropriate decision making.
• Writing & reviewing protocols, reports, and formal working documents.
• Work on multiple projects with multiple teams.
• Hands-on lab work.
• Managing a growing team with multiple disciplines.
JOB REQUIREMENTS
• Master’s in engineering or Ph.D. degree in Biology, Biochemistry and Biotechnology; and relevant experience in a similar position in the sector of biotech/pharma/cell therapy – mandatory
• Experience as a team leader
• Hands-on experience with cell-based bioassays, FACS, ELISA, and qPCR.
• Experience with Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
• Experienced with cellular assay development including qualification and validation process.
• Adaptability to changing work assignments and priorities
• Excellent teamwork
• Excellent interpersonal and communication skills
• Able to prioritize different activities
• Able to identify opportunities for continuous improvements and enable implementation
• Well organized, methodologic, quick learner, team player, motivated and responsible
• Assertive and working well under pressure
• Fluent English: oral and written, experience with scientific writing
• This position may include occasionally traveling abroad
