Your new company

Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.
The company focusses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, They have grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

Your new role

As Senior Associate QA, you will have a number of objectives within the department. Firstly, you will provide QA guidance and support in the production area at ABR. Secondly, you will perform batch record review of batches assembled, packaged and labelled at ABR and finally, you will establish working relationships with Production, Warehouse, Maintenance and Engineering, QA management and the QP. Within these objectives you will be involved in the following activities:

• Providing daily guidance and support to production staff.
• Act as point of contact in case of production enquiries (quality related).
• Performing finished product checks during production runs.
• Compile and review batch records for lots assembled, packaged and labelled at ABR in preparation for the QP.
• Perform GMP compliance checks and review and approve deviation records.
• Initiate and own QA deviations as required.
• Author and review operational SOPs & Work Instructions as needed.
• Contribute in the development and delivery of GMP training activities for QA and Production.

What you'll need to succeed

You have an MBO or BSc degree in Pharmaceutical / Life Sciences or related field with around 3 years of Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in investigations and batch records reviews. You are experienced in GMP, GDP AND GCP with the ability to interpret and apply in mainly routine cases. You also have experience with Manufacturing and/or Quality analytical processes and operations with good communication skills in English (Dutch is not required but it can be a bonus).

What you'll get in return

Hays Detachering | This is a project that will start with a contract for 1 year through Hays. Extension to stay within the department is anticipated. In this position, you will get a competitive salary and your travel expenses are covered.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.