QA Specialist

QA Specialist
We are looking for you who has thorough understanding of quality systems and has a few years of work experience working in Quality Assurance to support the manufacturing of drugs, biologics or devices. Our client is responsible for QP sign off of pharmaceuticals manufactured in the US and then packaged in EU and they are now looking to strengthen their group with a QA specialist.

You will be working alongside the QP´s helping them with reviewing batch documentation, supporting batch disposition and European Union Audits, leading deviation and CAPA investigations to resolve, change control etc.

Business: Dfind Science & Engineer

City: Lund

Application deadline: 2014-08-31 We will have ongoing interviews and we recommend you to apply as soon as possible thru www.dfind.se.

Qualifications:

It is essential that you have an academic education and a few years of experience working in Quality Assurance to support the manufacturing of drugs, biologics, or devices. You have a thorough understanding of quality systems and cGMPs. If you also have experience in conducting audits and working alongside a QP this is a favorable. Interpersonal skills are important for both internal end external contacts and its essential that you read, speak and write English. The job requires that you are able to travel approximately 20% and to work during routine business hours but be flexible to cover US business hours when needed.

As a person you preferably are/have the following traits: flexible, organized, able to prioritize, able to critical thinking, able to multi-task and able to work independently.

Further information: Please contact Camilla Wern, +46(0)733 436098