Description
I have an immediate opening for a Process Quality Engineer (Labelling) with a leading medical device company based in Cork who are embarking on some exciting projects. This is an initial fixed term contract position.Reporting to the Quality Engineering Section Manager you will provide quality engineering support to the facility with primary responsibility for managing the product labelling process.
On a daily basis you will be required to demonstrate your strong quality engineering expertise, your excellent interpersonal skills, your knowledge of FDA and MDD labelling requirements and strong technical expertise in labelling generation and verification systems.
Key responsibilities include:
- Work with a cross-functional team to develop, approve and implement product labelling elements of key projects.
- Co-ordinate with internal business partners to determine and implement country specific labelling requirements for existing products.
- Maintain internal label approval process to meet internal and external regulatory requirements.
- Lead a cross-functional team to identify and implement process improvements.
- Provide Quality Engineering support to manufacturing process and quality systems, as required.
Candidates should have:
- Degree in a technical discipline.
- At least 4 years quality engineering/technical experience with experience in labelling, either medical device or pharma.
- Demonstrable knowledge of FDA and MDD requirements.
- Excellent communication and skills - written, oral and pc.
If you are interested in hearing more about this excellent opportunity please apply directly to this advert or contact Derek Sheridan on for immediate consideration.