Description :
The Process Specialist manages the process technology transfer to the company's factories or to contractors
Contribute to improving or optimizing existing processes
Perform upscaling between R&D, pilot plant and commercial manufacturing sites (including transfer ratio)
Support the subcontractors in development and production
Participate in the technical evaluation when buying new products
Participate in investigations and propose experimental designs when required
Participate in the preparation of test protocols
Ensure proper communication and exchange of information between customer and validation services
Participate in activities related to; feasibility and clinical trial batches in order to ensure their successful completion
Coordinate the installation and implementation of innovative equipments
Consolidate fabrication policies and procedures with all related documentation such as; cost sheets, transfer reports, etc.)
Revise the fabrication sections of various regulatory documents to ensure quality standards
Monitor any technological developments and communicate any findings and/or recommendations with the organization
Requirements :
Bachelor of Chemical Engineering, Chemistry or a related science with extensive experience in the pharmaceutical and/or cosmetic industry
Minimum 5 years of experience in fabricating pharmaceutical and/or cosmetic products, mainly creams
Experience in the industrialization of new products and marketing / product transfer
Formulation experience is an asset
Knowledge of GMP and US / Canada Regulation within a pharmaceutical environment
Bilingualism (spoken and written)
Availability to travel 15% of the time
Bachelor of Chemical Engineering, Chemistry or a related science with extensive experience in the pharmaceutical and/or cosmetic industry
Minimum 5 years of experience in fabricating pharmaceutical and/or cosmetic products, mainly creams
Experience in the industrialization of new products and marketing / product transfer
Formulation experience is an asset
Knowledge of GMP and US / Canada Regulation within a pharmaceutical environment
Bilingualism (spoken and written)
Availability to travel 15% of the time
All your information will be kept confidential according to EEO guidelines.