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QA Raw Material Compliance Specialist m/w/d (DE)
[17497]
QA, Compliance, Supplier
The Raw Materials Support Specialist provides essential support to the Lonza Visp site as part of the QA Supplier Management Team. In this role, you will support the management of Vendor Change Notifications (VCNs), ensuring that any changes from suppliers are thoroughly assessed, documented, and implemented in a controlled and compliant manner. The Specialist will work across multiple systems, including SAP, TrackWise, and the Document Management System. Zu besetzendes Projekt: QA Raw Material Compliance Specialist m/w/d Art der Beschäftigung: Payroll Branche: Biotech Fähigkeiten: QA,Compliance,Supplier Projektstart: asap Projektdauer: 6 Monate Einsatzort: 3930 Visp, Schweiz What you will do: ·Review, assess, and coordinate the evaluation of VCNs from suppliers. ·Ensure appropriate impact assessments are conducted with relevant departments. ·Track and document VCNs in compliance with internal procedures and regulatory expectations. ·Ensure timely implementation of required actions and updates to documentation. What we're looking for: ·Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Chemistry, or related field. ·Ideally, you have already gained initial experience in a similar position. ·Strong understanding of GMP regulations and change control processes. ·Detail-oriented, organized, and able to manage multiple priorities. ·Familiarity with supply chains, raw materials, equipment, facilities and logistics is a plus. ·Excellent communication and teamwork skills (oral and written), with the ability to work independently and as part of a team. • Fluent in English, German is a plus Additional Information: ·Hybrid: Two days on site ·5+ years of experience in relevant position and extensive experience with Trackwise
- Review, assess, and coordinate the evaluation of VCNs from suppliers.
- Ensure appropriate impact assessments are conducted with relevant departments.
- Track and document VCNs in compliance with internal procedures and regulatory expectations.
- Ensure timely implementation of required actions and updates to documentation.
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Chemistry, or related field.
- Ideally, you have already gained initial experience in a similar position.
- Strong understanding of GMP regulations and change control processes.
- Detail-oriented, organized, and able to manage multiple priorities.
- Familiarity with supply chains, raw materials, equipment, facilities and logistics is a plus.
- Excellent communication and teamwork skills (oral and written), with the ability to work independently and as part of a team. • Fluent in English, German is a plus
- Hybrid: Two days on site
- 5+ years of experience in relevant position and extensive experience with Trackwise
Luca Furler