QA-officer Job in Olen 2250, Antwerp Belgium

For a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products,we are currently looking for a QA-officer for a 4-5 month contract. (replacement of colleague on maternity leave).

 

Job description

 

•              Take ownership of assigned processes and follow up on all required activities including follow up on actions assigned by QA manager and Supervisor. This includes but is not limited to Hold management, Sterilization releases, IRR releases, Documentation management and Retour management;

•              Ensure delivery against QA department goals and objectives, i.e. meeting commitments and coordinating overall quality assurance schedule;

•              Maintain and improve the documentation management system, hold management process, Quality Control processes such as Receiving inspection, BAS relabeling, Split e.g.);

•              Implement ongoing quality improvement processes working with interdepartmental teams like Distribution, Supply Chain, Customer Service and Facilities;

•              Maintain product consistency throughout product cycle by following the Quality Manual instructions, through EDC supply chain storage and handling phases through Distribution cycle by quality check points and testing and other QA activities such as hold, release, rework;

•              Support  in the development and support in managing quality assurance metrics for performance improvement;

•              Support QA management by managing and responding to software quality assurance issues with related groups such as development, database, integration, and customer support;

•              Anticipate (release) problems and takes corrective action, escalating as needed, to resolve and achieve commitments as defined in the QA functional goals;

•              Provide effective communication regarding issues, objectives, initiatives and performance to plan;

•              Responsible and accountable of flagging the timing of inter-departmental deliverables and the quality of their output.

 

Profile

 

Languages:

Dutch and English are required.  French is an asset.

 

Education:

Science background, Administration, Logistics or business background. 

 

Experience:

Minimum of 3 years of Quality Assurance experience either with Medical Device or Pharmaceutical organisation.

 

Qualification level:

Engineer level would be a plus, administrator with experience will be considered.

 

Additional comment:

Temporary replacement for maternity leave.

 

 

- we offer a 4-5 month contract.