CQV Engineer

Introduction
 My Engineering is a human-sized engineering company specialized in biopharma manufacturing sites and providing flexible qualitative turnkey solutions for the major key players in Belgium and abroad. With the continuously increasing number of projects and in order to support its engineering team My Engineering is currently looking for a CQV engineer. 

The compagny
My Engineering is an engineering office specialized in the field of advanced technologies. 

Clean rooms, controlled environments, air conditioning, aseptic areas finishes or the transport of clean fluids are the daily work environment of two passionate young entrepreneurs. My Engineering offers their customers a complete range of services in line with their requirements. My Engineering is able to support projects from the design stage to the commissioning, qualification and validation of complex technical installations, while respecting the timeline and quality requirement of their customers.

What you will do
As a member of our project team you will: 

• Be supported and learn continuously
• Be integrated in a multidisciplinary team
• Follow trainings and keep updated with the current cGMP, regulatory requirements and industry standards
• Strengthen your engineering and CQV skills
• Coordinate CQV activities and develop your validation strategy
• Collaborate intensively with all project stakeholders
• Maintain a project schedule
• Prepare and execute project CQV deliverables according to the validation strategy
• Support the engineering team during installation and start-up
• Participate in all critical testing activities
• Keep track of all changes and maintain a quality documentation database 

What we are looking for
• You hold a Bachelor or a Master’s degree or equivalent by experience, ideally in biotechnology, industrial, pharma, or relevant other expertise
• You have a first experience in the biopharma industry
• You have good communication skills in English, French and/or Dutch or want to develop on of the develop one of the national languages
• You have a sound knowledge of current Industry Standards and regulatory guidelines (Eudralex, FDA, ASTME2500, PICS, ICH, ISO, …)
• You have a sound knowledge of engineering standards and CQV project deliverables
• You have a first field experience with biopharma equipment (sterilisation equipment, washers, clean utitilies, HVAC, …)
• You are eager to learn and looking forward to be our CQV reference
• You are a structured, conscientious and entrepreneur minded
• You are flexible and ready to travel

What we will offer you
By joining our team you will have the chance to be supported by experienced professionals in a flexible work environment, a unique opportunity to find your place and participate in exciting international projects. 

Additionally you will be offered: 

• A full time contract (40hr/wk + 12 RTT) and a long term collaboration
• The necessary support to develop yourself in line with your ambition
• A personal development plan within a fast-growing company
• A great autonomy, an excellent working atmosphere compatible with a family life
• A competitive salary
• Fringe benefits including a company car, fuel card, lunch vouchers, eco vouchers, DKV health insurance plan, phone subscription 

Are you the colleague we are looking for? 

Contact
We’re looking for enthusiastic individuals ready to take the next step and help us in making the upcoming project a success. Ready for the adventure? Please apply here and address your application, CV and a short motivation text, to: 

Mrs. Delphine Bureau – Executive Assistante
Email : d.bureau@my-engineering.be
Phone : +32 479 / 01.41.00
https://my-engineering.be/