. Project management
•    Assisting in all aspects of batch manufacturing activities, in accordance with SOPs and batch record instruction for multiple products
•    Working and handling BoNT, a toxin for compounding activities and manufacturing batches as required per procedures
•    Updating / generation of SOPs/ Risk Assessments and manufacturing documentation
•    Supporting installation of new equipment as required
•    Completion of quality records in QMS
•    Implementation of product dedicated controls for the Core 1 area.
•    Performing sterile filtration and filter integrity testing.
•    Supporting regulatory inspections as required

. MSc with 3 years’ experience or Bachelor’s degree with 3-5 years’ experience preferred
•    Minimum 3-5 years in a relevant environment with applicable experience preferred
•    Understanding requirements of cross contamination controls in multi-product facility
•    Knowledge and experience with GMP regulatory inspections
•    Excellent report / procedure writing skill set required
•    Working knowledge of Quality Management System (QMS)
•    Flexibility of working hours may be required, and shift work may be required upon request