Senior Quality Engineer

Title: Quality Engineer, New Product Development (Contract)
Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements.

Location: Hybrid, Flemish Region, Belgium, c. 2-3 days/week.

Contract: Interim, c. 6 months with potential to extend.

Start ASAP (urgent replacement).

Contact:

The Company:

A science-led manufacturer of high-precision components for the medical device and pharmaceutical packaging sector, including combination products. With a major customer development already live and moving at pace, they need hands-on quality engineering support to step straight in alongside the team, not at arm's length, and keep the programme and its customer-facing documentation on track.

The Opportunity

This is hands-on, embedded quality work on a live combination-product development at a pivotal moment, not an oversight role. You'll own the quality engineering that keeps the programme moving, working shoulder to shoulder with the project team on-site and acting as the day-to-day quality point of contact for a key OEM customer.

Key responsibilities:

• Own the quality engineering on a combination-product development
• Review and adapt development documentation to meet customer quality requirements, including PPAP-equivalent expectations
• Apply design control and stage-gate rigour across the development lifecycle
• Act as the embedded quality contact, working hands-on with the team rather than remotely
• Ensure documentation supports ISO 13485 and combination-product / medical device requirements

Requirements

Role:

• Hands-on quality engineer who embeds as part of the team for the duration, not an outside consultant looking in.
• English-speaking environment. xlxgzvr

Experience:

• Medical device or combination-product new product development background, with a solid command of design control and stage-gate processes and strong working knowledge of ISO 13485.
• Comfortable adapting technical documentation to meet customer quality expectations (PPAP or equivalent).
• Advantageous: Direct OEM / pharma customer interface; familiarity with ISO 15378.

#Quality #NewProductDevelopment #MedicalDevices #DesignControl #CombinationProducts #ISO13485 #Consulting