QUALITY ASSURANCE CONSULTANT H/F

Job description

Entreprise:
Amaris
Amaris is an independent and international Management and Technologies Consulting Group created in 2007. Present in more than 45 countries and 60 offices worldwide, it offers proximity support to its clients, wherever their locations. Amaris' added value lies in its teams' quality, in their attention to detail, and in their commitment to always deliver the most innovative solutions.
Poste et missions:
You will join Amaris as a consultant and be part of a team coordinated by your Manager. Together you will design technical and/or management solutions for our clients in pharmaceutical and biotechnology industries. You will be present on client’s plant to work on mid and long term project in Quality Assurance. As a Quality Assurance Consultant you will be working in a team of consultants who are experts in a specific field in the Pharmaceutical Industry: within these markets they have a specialization in: Quality Assurance, Deviation and CAPA management, GMP management.
Your role as a QA consultant will be to contribute to implementation and optimization of the QA policy of the client and to ensure that manufactured product comply to quality, legal and client’s requirements by :
? Technical Documentation, technical writing
? Controlling the application of local procedures and other cGMP requirements
? Performing and facilitating the use of quality processes (CAPA, deviations, change controls, training, sterility assurance, validation, batch release)
? Supporting departments during quality audits and inspections
Profil:
You have received a scientific education: engineer, chemist, biologist and pharmacist or similar. You know the legal requirements for the pharmaceutical industry (cGMP) and have a work experience in such environment. You are proactive, have good communication skills, and are capable of working in a multidisciplinary team towards a common goal. You are proficient in Dutch and English (spoken and written)! Furthermore, you possess 1 to 5 years of experience in a relevant industry and with GMP / GLP.