Production Quality Assurance Specialist
3 days ago
PharmaRelations ApS
Copenhagen, Denmark
We are seeking a talented Quality Engineer Consultant to ensure the site Quality Policy is understood, implemented, and maintained at all levels of the site organization.
The position is a temporary 6-month assignment with the possibility for extension.
The successful candidate will be responsible for key assignments such as CAPA process, validation, documentation, and case handling. This includes batch release and complaint handling.
Key Responsibilities- Develop and mature QA processes with a focus on Complaint handling, Deviation/CAPA, and batch release.
- Excel in communication and thrive as a Quality ambassador in the organization.
- Bring know-how and expertise to the full end-to-end process with experience from production within ISO-certified or regulated industries.
- A degree in engineering or life sciences.
- Working knowledge as QA for production and/or engineering.
- Understanding of industry standards such as GMP or ISO.
- Experience in working in the device or pharmaceutical industry.
- Flair for various technical aspects in production and quality documentation systems.
- Good communication capabilities.
- Ability to work cross-functionally in an international setting.
- QMS systems skills.
- Fluent in Danish and English.
- Case handling.
- Complaint handling.
- Deviation/CAPA.
- Batch release.
This is a unique and challenging job in a global market-leading company where you will have opportunities to excel and expand your competencies together with highly skilled and committed colleagues.
You become part of an ambitious company with strong core values also regarding its workforce.
Opportunities for growth and development
Collaborative and dynamic work environment
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