QA Officer

• Location:
  Braine l’Alleud
Type:
Contracting

#17141

Walloon Brabant – Contracting

#QA #qualityassurance #GMP #supplychain #quality #pharmaceutical

Our client is looking for a QA Officer to reinforce its teams. Our client is a well-known pharmaceutical industry.

What are your responsibilities?

As a QA Officer, you will work in an environment where you can:

• Assist the Supply QA team in establishing, implementing, maintaining, and continuously improving, an effective Level of Quality linked to the supply chain activities, including Purchasing and warehouse activities
• Evaluate constantly changing cGMP requirements and their impact on our client’s activities
• Adjust the Level of Quality and associated procedures based on changing regulatory requirements, technical and scientific knowledge
• Monitor and adjust local supply chain and warehousing operations in order to assure they comply with applicable national and/or international regulations and guidelines, relevant our client’s Quality Policies and Level of Quality requirements
• Continuously assess the Level of Quality of procedures and practices to identify gaps and opportunities for improvements and simplification (strive for quality and operational excellence)
• Support QA and BTO Management to ensure requested Level of Quality within the Supply Chain, Purchasing, Warehousing areas and SAP aspects
• Pro-actively help operations, identify, develop and implement quality and operation excellence improvements in response to business requirements, technical changes and regulatory requirements in the relevant scope

As a QA Officer, you will also contribute by:

• Assisting in drawing up, reviewing and approving the procedures and instructions related to the Supply Chain, Purchasing and Warehousing activities
• Being one of the QA representatives for those activities and departments on the site in case of alignment and level of quality related issues
• Treating alignment and level of quality related issues and follow up on the related corrective and preventive actions
• Performing continuous GAP analysis between new expectations and Quality Management System documentation and between documentation and actual practice
• Ensuring that suppliers and contract services organizations comply with all regulatory expectations
• Ensuring the cold chain and controlled temperature process in order to maintain / improve the GDP practice
• Identifying, managing and communicating to QA and the entire department management the possible issue of non-compliance within the Quality Management System and providing expertise, interpretation and direction in order to create a framework of operational excellence enabling implementation of continuous improvements.
• As SAP user, providing cGMP and QA expertise, interpretation and direction on SAP system enabling implementation of continuous improvement regarding specific domain of knowledge

Who are you?

You hold a master’s degree (or equivalent by experience). You have a relevant experience in the pharmaceutical industry, and you have an in-depth knowledge of cGMP. You speak fluently French and English. You are a real team player, stress-resistant and you are quality oriented.

What can you expect?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.