· Responsible for planning and implementation of process andcleaning validation activities according to cGMP Guidelines and related SOPs
· Ensures that GMP requirements defined by MOH, Novartis Quality Manual and policies are met
· Supports equipment process qualification for new technologies
· Prepares the validation protocols, supervise and follow-up the validation activities according to related SOPs and prepare the validation reports on time
· Participates in improvement and remediation of products
· Participates in transfers and launches, liaise with technical development for new products and align on the product validation approach
Qualifications:
· University degree in Pharmaceutics, Chemical Engineering or Chemistry
· Master degree in Chemistry, Chemical Engineering or Pharmaceutics is an asset
· Excellent command of verbal and written English
· Excellent knowledge of MS Office applications
· Minimum 3 years of related experience in a pharmaceutical company
· Team working and customer oriented mindset