QA Vendor Specialist

Permanent contract of unlimited duration.

Working within a strongly growing company. 
Attractive salary package with extra-legal benefits.

Questions or interest?

>> lommel@ctrl-f.be

>> 014 33 75 67 

>> WhatsApp: 0477 71 16 88

• You are jointly responsible for qualifying, managing and auditing both internal quality systems and processes, as well as suppliers' quality systems and processes. In doing so, legal frameworks and, in particular, international pharmaceutical guidelines and regulations must be observed.
• Prepare, coordinate and perform the assigned audits in the audit programme.
• Preparing audit reports and following up the actions resulting from the audits.
• In cooperation with Purchase, determine the purchasing strategy, especially with regard to the quality and characteristics of packaging materials and other suppliers.
• Follow-up of new projects related to packaging materials and other services.
• Drafting, reviewing and adjusting contracts with suppliers
• Handling supplier changes
• Carrying out the annual supplier review
• Sending and following up supplier complaints

The company is part of a group and is responsible for the packaging and labelling of medicines. 

• Familiar with performing audits (internal and external) and drafting material specifications
• High standards of quality and integrity
• Good communicator, both verbally and in writing. Able to communicate and convince at any level, from the shop floor to senior management
• Good negotiator, able to maintain professional contacts with both customers and suppliers
• Thinking in processes, positive attitude and thinking in solutions
• Decisiveness and accuracy
• Able to set priorities and secure these priorities
• Known and familiar with the cGMP guidelines, pharmaceutical guidelines
• Experience with quality systems, procedures, training, report writing, etc.
• Good knowledge of MS Office
• Good knowledge of English (written and spoken)