C&Q Engineer

At Advipro, as a C&Q Engineer you will be responsible for coordinating and reviewing CQV deliverables (commissioning, qualification & validation) in line with project specifications in collaboration with the engineering project team. Does that excite you? Read on quickly, because then we are looking for you as C&Q Engineer! 

This is Advipro

Advipro supports its clients in the pharmaceutical, biopharmaceutical, medical and high-tech sectors to realize, optimize and sustain high quality projects and processes. When looking for a project, we always look at how we can match the experience and ambition of colleagues with project requests from our customers. Advipro delivers the Complete GxPerience!

Your challenge at Advipro

As a C&Q Engineer, you have a helicopter view and you are the one who keeps an overview of the commissioning and qualification activities and coordinates these independently and in a structured way.

One of your tasks is to review and approve commissioning and qualification documents. This includes risk assessment, FAT, SAT, change control documents and qualification protocols and reports.

In addition, as a C&Q Engineer you will also take on the following tasks:

• You will work with equipment used for pharmaceutical formulation, production and filling;
• You provide support during system/installation startup in the area of CQV testing activities;
• You coordinate the implementation of the validation guideline and SOP for the processes and equipment (validation life-cycle process, qualifications); 
• You coordinate the review process of CQV deliverables with stakeholders;
• Quality issues after CQV testing and maintain project KPI related to CQV activities;
• You are the liaison between project engineers and QA stakeholder to address blocking issues;
• You coordinate Change controls for GMP systems;
• You coordinate the handover process with users;
• And last but not least, you build strong relationships with both internal and external stakeholders.

Are you...

A person with a helicopter view, structure and the one who always keeps the overview? Do you also have:

• At least 3 years of experience in engineering as well as in a GMP environment;
• Experience with various activities concerning validation and qualification. This holds no secrets for you;
• Communicative and organizational skills, you speak and write Dutch and English fluently;
• Experience and a good knowledge of technical installations, P&ID and materials;
• A quick understanding of the technical characteristics of production equipment and processes. You feel at home in a pharmaceutical production environment;
• You use a risk-based approach to problem solving;
• Finally, if you possess a dose of humor, enthusiasm, commitment and passion, you will have an edge over the rest!

What can you expect from Advipro?

• A competitive salary and good working conditions;
• A dynamic company in full growth with a no-nonsense culture and where there is a lot of room for own initiative;
• An enthusiastic and fun team full of team activities: Sinterklaas and staff party, team building, ... 
• At Advipro we work together, keep each other sharp and inspire each other: think tanks, focus groups, brainstorms, ... . 
• We offer you challenges, training, career opportunities and the chance to shape your own job.
• Extensive range of fringe benefits. Count on financial growth based on performance and bonuses such as profit-sharing bonus and referral program.