Our client is a leading project management and engineering company for industry around the world.
Our client is a leading project management and engineering company for industry around the world. Their reputation is based on forming successful partnerships with their customers, offering them innovative designs and cost-effective solutions in the context of sound judgment, strong management and technical excellence. They offer Full Service Engineering for their customers, including project and program management, purchasing, design, construction management, health and safety management, commissioning, qualification and start-up for numerous projects in various market sectors.
At least 5-7 years of relevant work experience, preferably in medical device/pharmaceutical industry with some level of supervisory experience.
A working knowledge of relevant GMP, QSR CFR 820 , ISO 13485, ISO 14971.
Ability to operate and maintain relationships at different levels within the organization.
Effective communication skills and ability to work across the organization
Decisive and with the ability to set the correct priorities.
Ability to use own initiative and make the difficult decisions.
Excellent command of the English language (verbal and written)
Knowledge of MS Office
What do you get?
Pension entitlement as from day one
Collective WGA / WIA insurance
NBBU / ABU collective labor agreement
25 holidays days
8,33% holiday allowance
100% payment in case of illness after one waiting day
Maintain documentation management / change control system and documentation archive.
Corrective and preventive actions (CAPA) program
Quality assurance support of operations, research projects and process development projects.
Execution and review of internal and supplier audits, support external audits.
The generation and review of qualification and validation protocols and reports.
Ensure that quality awareness is improved in the organization.
Generation of QA engineering input for site QA planning and site business planning.