Expires soon AMARIS SERVICES SARL

QUALITY ASSURANCE CONSULTANT (H/F)

  • V.I.E.
  • Basel (Basel-Stadt)
  • Master, Bac +5

Job description

Entreprise:
Amaris is an independent, international Technologies and Management Consulting Group. Created in 2007, Amaris is already established in over 50 countries and supports 500 clients worldwide throughout their projects’ lifecycle. Our expertise covers 5 areas of innovation: Business and Management, IT/IS, Telecom, Engineering and High Technologies, Biotech and Pharma. With 65 offices across the World, the Group offers proximity support to its clients in all their locations and many opportunities of international careers for employees.
In 2017, Amaris aim to reach a turnover of 180 million euros, 3500 employees and the ability to recruit one new employee every 5 hours. We expect to triple our workforce within the next years and reach an international leader position in independent consulting.
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 management solutions for our clients in pharmaceutical industry. You will be present on client’s plant to work on mid and long term project in Quality Assurance. As a Quality Assurance consultant within Amaris you will be working in a team of consultants who are experts in the specific field of Pharmaceutical industries; within this market they have a specialization in: Quality Assurance and GMP management.
Role
Your role as Quality Assurance consultant within Amaris will be to contribute to projects of our clients such as:
Sterility Assurance
Ensure the Product Quality Review (PQR)
Review and improve Quality Process
Be involved in the creation and validation of major documents like validation plans and reports
Review and Release the batch records
Drive adherence to computer Quality & compliance policies and guidelines
Analyse Deviation and updates CAPA/Corrective Actions
Profil:
You have received an engineering degree or equivalent.
You know the legal requirements for pharmaceutical industry (cGMP)
You have proven experiences in one of those above roles
You are proactive, have good communication skills, and are able to change people mindset in the way of efficient working.
You are proficient in English (written, spoken)! German is a plus

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