Quality Assurance (Barcelona)

Quality Assurance (Barcelona)

17 oct
|
Pqe Group
|
Barcelona

17 oct

Pqe Group

Barcelona

Are you ready to join a
world leader
in the exciting and dynamic fields of the
Pharmaceutical and Medical Device industries
?
PQE Group
has been at the forefront of these industries
since 1998
, with
40 subsidiaries
and more than
2000 employees in Europe, Asia and the Americas
.

We are looking for an experienced
Quality Assurance & Regulatory Affairs (QARA) professional
to support a Medical Device organization. In this role, you will act as an extension of the manufacturer's Quality and Regulatory team, helping to maintain compliance with applicable regulatory and quality standards, including
EU MDR 2017/745
,
ISO 13485
,
ISO 9001
, and
ISO 14001
.

This is an excellent opportunity for a hands-on quality and regulatory expert who enjoys working in a dynamic MedTech environment and collaborating across multiple stakeholders.

Responsibilities include:
- Maintain and continuously improve the Quality Management System (QMS).
- Update quality documentation, procedures, forms, and records.
- Manage non-conformities, CAPAs, deviations, and change controls.
- Plan,



coordinate, and conduct internal audits.
- Support external audits and inspections, including ISO 13485, ISO 9001, ISO 14001, Competent Authorities, and customers.
- Follow up on audit findings and corrective actions.
- Support Management Reviews and quality performance monitoring.
- Assist with supplier quality management.
- Support complaint handling, vigilance, and post-market surveillance.
- Maintain regulatory documentation for distributed medical devices and support product launches.
- Support the Technical Responsible Person for Distribution with technical documentation and AEMPS/RECOPS registrations.

Requirements:
- Degree in Life Sciences, Engineering, Pharmacy, Quality, or a related field.
- Minimum 3 years of experience in Quality Assurance and/or Regulatory Affairs within the medical device industry.
- Good knowledge of EU MDR 2017/745 and ISO 13485, ISO 9001, and ISO 14001.
- Experience in QMS mai

📌 Quality Assurance (Barcelona)
🏢 Pqe Group
📍 Barcelona

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