C&Q Engineer

This vacancy is for a specific location, but we have C&Q positions available throughout Belgium. Interested? Apply now 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.

• You keep an overview of the commissioning and qualification activities and you coordinate them. You look at them with an helicopter view and you ensure structure.
• You are responsible for the review and approval of commissioning and qualification documents (risk assessments, FAT, SAT, qualification protocols and reports, change control documents).
• You work with equipment used for pharmaceutical formulation, production and filling.
• You offer support during system/installation initiation in function of CQV testing activities.
• You coordinate the implementation of the validation guideline and the SOPfor the processes and the equipment (validation life-cycle process, qualifications).
• You coordinate the review process of CQV deliverables with stakeholders.
• You escalate quality issues after CQV testing and maintenance of project KPI related to CQV activities.
• You are the bridge between project engineers and QA stakeholders to handle blocking points.
• You coordinate change controls for GMP systems.
• You coordinate the transfer process with the users.

• You will build strong relationships with both internal and external stakeholders.

• You will become part of a dynamic team in full growth.

• You will fully develop yourself in our flat company structure with a no-nonsense culture and where there is room for own initiative.
• Fun colleagues andteam activities for free: Saint Nicholas and staff parties and team buildings.
• We work together, keep each other sharp and inspire each other: brainstorm sessions and focus groups.
• Challenges, trainings, career opportunities and the chance to shape your job.
• You can count on a competitive and flexible salary package.
• Extensive offer of fringe benefits including insurances and bonuses.
• Financial growth based on your performances.
• Bonuses like profit sharing bonusses and the referral program.

• Work regimetailored to your needs: part-time or full-time.

• You have over 3 years of experience within engineering and within a GMP environment.

• Activities concerning validation and qualification do not have any secrets for you, as well as handling according to this mindset.
• You have strong communicational and organisational skills.
• Because of previous experiences you have a broad knowledge about technical installations, P&ID and materials.
• You feel at home within a pharmaceutical production environment and you are a fast learner about technical features of production equipment and processes.
• For solving problems you use a risk-based approach.
• You are fluent in speaking and writing in Dutch and English.

Established in 2016, Normec is an ambitious, independent, and rapidly growing organisation with a Buy-&-Build strategy focused on testing, inspection, certification, and compliance (TICC). Its specialisation enables organisations to innovate safely, efficiently, and cost-effectively. With significant growth over the years, Normec has become one of Europe's leading quality and safety specialists, employing over 5,500 people across 50 locations. To date, the company has completed more than 75 acquisitions in 9 countries and operates across 4 divisions.

Dedicated to both organic growth and strategic acquisitions, Normec builds partnerships that go beyond conventional approaches, ensuring that every project contributes to a shared, sustainable future. The organisation offers its team members the opportunity to contribute to its mission while developing their careers in a dynamic, fast-paced environment, creating impactful solutions for clients and a sustainable tomorrow.

Contact Joke Vanthienen for more informatie

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