vous pouvez faire glisser l'écran de gauche à droite pour voir les jobsutilisez les flèches de votre clavier ( and ) pour voir les différents jobs
description de la société
IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux. Their offices are located at “Hof ter Loonst” in Kampenhout. Since they are expanding their team we are looking for an experienced Quality Assurance Associate who has the ambition and potential to grow in their organization. All projects within IN2Pharma are worked on in close cooperation with one or more colleagues and for some projects, you also work on site at the clients’ offices for 1 or 2 days per week.
Interested? Apply by sending me your resume and cover letter to firstname.lastname@example.org or call me on 03 369 19 80.
description de la fonction
Are you an experienced Quality Assurance Associate who has the ambition and potential to grow in a motivating organization? Then we are looking for you!
As a QA Associate, you will support the RP in setting up, improving and maintaining quality standards for pharmaceutical and healthcare companies in Benelux.
Establish and maintain a quality system: SOP management, change control, training, CAPAs, etc
Review packaging specifications and technical changes in preparation of administrative batch release
Coordinate and investigate product quality complaints and non-conformances
Perform self-inspections and assist in external audits
Draft, implement and monitor quality agreements
Interact with regulatory department, suppliers and contract manufacturing organizations
Cooperate with the QA department of the clients other EU affiliates
Participate in quality related audits or inspections from health authorities
Stay up-to-date with the latest developments and relevant legislation
What do you need to be successful?
Level of education: Master degree in life sciences
Experience within Quality Assurance: GDP, Quality Management System, Quality Control
Familiar with good documentation practices and project management
Good communication skills in Dutch, French, English (both written and verbal)
Proficient with computer and Microsoft Office
Strong initiative, pragmatic and problem solver
Technical knowledge of GMP, regulatory affairs
Detail oriented: concern for quality, compliance and consistency
Good communicator & team player
Our client offers you:
A permanent full-time position with a competitive package and supplementary benefits
Motivating work environment at an exclusive location
Personal development plan and development opportunities by working closely together on challenging projects in different situations and for several pharmaceutical companies