DPS

DPS is a leading Project Management and Engineering Company serving industry around the world for 40 years. Our reputation is based on forming successful partnerships with our clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.
We provide Full Service Engineering for our clients including Project and Programme Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification and Start-up on numerous projects across a range of market sectors. Our Main market sectors are; Pharmaceutical and Biotechnology, Medical Technologies, Oil & Gas, Advanced Technology, Science & Education, Food & Beverage, and Energy.

Responsibilities

The Fill & Finish Process team (FFP) is responsible for the external manufacturing of drug product. The manufacturing GMP specialist is involved in all GMP-related activities for the preparation, execution and follow-up actions of aseptic drug product manufacturing at our external DP manufacturing sites. You will work with the different members of the project teams and your main responsibilities will be:

• ensuring and maintaining the quality level of the group
• inspection readiness, facilitating audits and inspections
• being key user in the documentation system, supporting in the creation of documents
• being key user of the quality system (TrackWise), responsible for creation and on-time closure of change controls, quality investigations and other quality records
• maintaining the training strategy and program for the department
• requesting purchase orders and facilitate the invoicing process
• aligning with key stakeholders from clinical supply chain, logistics, FFP specialist and QA
• driving continuous improvement in our processes

Required Level of Expertise

• We are looking for a person who is pro-active, has a strong quality mindset and works accurately. We are a global company and you will be part of a truly global and international organiz932429.186145ation. You can have MSc/BSc in pharmaceutical sciences or other relevant disciplines (i.e., pharmacy, (bio)chemistry). At least 4 years of experience in QA or aseptic drug product manufacturing is required, experience in (bio-) pharma industry is desirable. Our highly dynamic environment requires you to be flexible, creative and result oriented.
• Your development is key and our day-to-day responsibility. We believe we can make a difference together and take your career seriously. We are looking forward to receiving your application!

Available and interested?

If you’re interested in this role and if you want to be part of growing organisation within engineering projects in the pharma industry or if you would like to discuss this vacancy further and to discuss your career options in confidence, please telephone Ralf Huisman on +31 6 11408791 or send your CV to ralf.huisman@dpsgroupglobal.com