Laure Devy Email & Phone Number

Rheinfelden, Ch

Release of finished products to the European Economic Area (EEA) market for sale by certification Ensure that the products are in accordance with the product registration and the current EU législation covering Medicinzl Products for Human Use and Médical Devices, GMP as well as GDPSupport Tillotts Pharma GmbH in setting up and maintaining a Quality Management System (QMS)Support all relevant QA processus performed in Rheinfelden Tlillotts AG accordibg to Swiss and European regulationsSupport and supervise contract manufacturers

Cambridge, Ma, Us

Perform EU QP certification for IMPs Certify all manufacturing steps up to the finished product.Ensuring that each finished medicinal product batch has been manufactured in accordance with GMP, the terms of MIA (Manufacturing and Import Authorization) and the IMPD.Issue QP Declarations equivalence to EU GMP for IMPs manufactured in third countries

Courroux, Ch

Head of QA: quality system management, secure the compliance of the manufacturing of sterile liquids and freeze-dried products with GMP, internal policies/procedures and client requirements, hire and lead a 17 members team in a customer focused approach and with entrepreneurial spiritResponsible Person: batch release, establish/approve quality agreements with international clients, manage swiss and foreign health authorities inspections

Courroux, Ch

lab creation, implement specifications and procedures to be appropriate for Quality Control of sterile products, oversee qualification of QC equipments, hire and train full team from lab technician to deputy manager, coordinate the activities of Quality Control in line with reception of raw materials and manufacturing.

Nazareth, Be, Be

Ensure quality systems and SOPs are designed to be appropriate for the manufacture, testing and timely release and distribution of liquids and tablets commercial products, prepare and run Health Authorities inspection, hire and train quality deputy, collaborate and interact with production team to ensure the handling of deviations and definition of supportive CAPAs

Arlesheim, Ch

Manage 40 people in production in two sub units (Pharma production and cosmetics) in different galenic forms (sterile ampoules, creams, liquids, powders).Coordinate daily production operations in cooperation with the quality department to ensure time and quality customer's satisfactionPlan and budget production operationsReview and approve manufacturing instructions

Manage a QC team, coordinate analysis of raw materials and commercial products (liquids and tablets) for QC release, data analysis on raw materials and finished products analytical results.

Doctor In Pharmacy

Master In Industrial Pharmacy (D.E.S.S. De Pharmacie Industrielle Montpellier), Pharmacie