Quality Specialist

BioTalent; Turnhout; Sur place; EUR 42 000 - 56 000; Plein temps

Résumé du poste

BioTalent, partnered with SciPharm (AOP Health Group), is expanding and seeks a brand new QC specialist—the first Quality Control hire in the team. You will own inspection of components and raw materials, and drive procurement activities to ensure supply quality.

Ideal candidates have at least 2 years in Quality Control, experience with EU suppliers, and exposure to class 2b/3 devices, Doc Control, QMS or audits. English is required; Dutch is a plus.

Qualifications

• Minimum of 2 years of experience within Quality Control.
• Experience working with EU suppliers is preferred.
• Experience with class 2b/3 devices and exposure to Doc Control, QMS or audits.

Responsabilités

• Own inspection of components and raw materials.
• Procure parts and manage supplier relationships.
• Support QMS, CAPAs, audits and supplier activities.
• Help shape company quality culture as an early hire.

Connaissances

Quality Control

Supplier management

QMS

CAPAs

Audits

Outils

Document Control

Quality Management System

Description du poste

BioTalent is currently partnered exclusively with SciPharm part of AOP Health Group. SciPharm specialize in implantable infusion products, one of only 5 businesses currently in development/use in the world.

As part of their current rapid expansion they are looking for a brand new QC specialist - their first Quality Control hire into the team.

The role with give you:

• A chance to own all inspection of components/raw materials into the business
• Conduct procurement of these parts
• Support other quality activities including QMS, CAPAs, supplier and audit support
• Shape the culture of the business as one of their first hires

You will need to bring in:

• Minimum of 2 years of experience within Quality Control
• Demonstrate ability to work with suppliers within EU. Benefits to working with other markets
• Ideal candidates will have worked with class 2b/3 devices and have exposure to supporting other quality activities such as Doc Control, QMS or audits
• Must be able to speak English with Dutch being an advantage

If this role sounds interesting please apply or reach out on [e-mail] or call [phone]