For our Abbott Laboratories site in Zwolle we are looking for a:

QA Engineer Abbott Laboratories Zwolle

Are you analytical qualitydriven and motivated by improving and standardizing processes At Abbott in Zwolle we are looking for a QA Engineer who strengthens our quality systems by designing implementing and optimizing quality workflows. You will play a key role in ensuring that our manufacturing processes remain controlled compliant and consistently executed across the organization.

What will you do

Process Design & Quality Workflow Implementation

• Design and implement review processes for productrelated documentation and quality evaluations (approval flows data review steps).

• Develop templates procedures and process flows that support consistent GMP and quality standards.

• Collaborate with document owners supervisors and SMEs to embed quality checks into documentation workflows (GMP documents batch records technical instructions).

• Ensure process designs are efficient compliant and well understood by all involved functions.

Quality System & Documentation Improvements

• Lead projects to update optimize or streamline quality system documentation including SOPs work instructions and QA processes.

• Coordinate crossfunctional input when updating batch records forms or templates to meet regulatory expectations.

• Assess documentation gaps and implement corrective and preventive improvements.

Compliance & Change Management

• Participate in assessments by translating quality requirements into clear process steps.

• Drive QA elements of compliance projects ensuring new regulatory requirements are integrated into daily workflows.

• Support the organization in understanding how procedural or regulatory changes impact documentation responsibilities and approval flows.

Audit Support & CAPA Governance

• Coordinate CAPA workflows ensuring actions are clear assigned and completed on time.

• Ensure recurring issues lead to sustainable process improvements rather than oneoff fixes.

• Support audit preparation and followup when required.

CrossFunctional Collaboration & Training

• Work with Operations QA/QC Engineering and other departments to align expectations and standardize qualityrelated tasks.

• Provide guidance on applying GMP and documentation standards in practice.

• Support teams in adopting new processes to ensure smooth and sustainable implementation.

What do you bring

• Bachelors/HBO in Life Sciences Food Technology Chemistry Microbiology Pharmacy or a related field.

• 35 years of QA experience in food pharma nutrition or another manufacturing environment.

• Strong understanding of GMP documentation control and quality management systems.

• Experience with designing or improving process flows review processes or documentation workflows.

• Proven ability to coordinate and implement crossfunctional QA projects.

• Analytical structured with strong communication skills and attention to detail.

• Comfortable collaborating with diverse stakeholders and driving alignment without direct authority.

Will you be our new QA Engineer Apply today and contribute to the development of highquality products that make a worldwide impact! What do we offer

We offer a competitive salary and an Individual Choice Budget (IKB) that includes holiday allowance 13th month special leave and additional vacation days.

How to apply

We look forward to receiving your application if you are interested in this position in working at Abbott and if you recognize yourself in the profile above.
You can apply with your CV and motivation through our website. Or contact Meltem Cakir at . We look forward to hearing from you as soon as possible.