ABOUT US

We are dedicated to the

research, development, manufacture and distribution of allergen immunotherapy products , contributing to improving the quality of life of patients worldwide through innovative healthcare solutions.

Our

Technical, R&D; and Clinical Trials headquarters

are located in Zamudio, where our manufacturing site is also based. As part of our growth and expansion plans, we are looking for talented professionals committed to quality, innovation and continuous improvement.

Our values:

PEOPLE-CENTRIC:

We put people at the centre of everything we do. SELF-DEMANDING PEOPLE:

We encourage individual accountability and high standards in pursuit of shared success. CURIOUS PEOPLE:

We continuously learn and innovate, valuing the unique experience and perspectives that each person brings to the organisation.

ABOUT THE JOB

We are looking for a

Quality Assurance Technician with a strong specialisation in Quality Control

to join our team and continue developing professionally with us.

The successful candidate will report to the

Head of the Quality Assurance Unit , within the Technical Directorate.

Mission

To ensure compliance with

Roxall’s Quality Management System (QMS)

and with applicable

GMP, GDP, regulatory and legal requirements , with a particular focus on

Quality Control activities, analytical results and analytical method validation .

The position will also contribute to the implementation of the actions required to maintain a continuous improvement approach in accordance with the company’s guidelines and objectives.

Main Tasks and Responsibilities

Prepare, review or supervise

Quality Management System (QMS) procedures and documentation , particularly documentation related to Quality Control activities. Review analytical results

and participate in the investigation of





Out-of-Specification (OOS) results, deviations and other quality events , as well as in the definition and follow-up of

Corrective and Preventive Actions (CAPAs) . Participate in the preparation and review of

Product Quality Reviews (PQRs) . Collaborate in the evaluation and follow-up of

Change Controls . Participate in the

GMP qualification of equipment and facilities . Provide Quality Assurance oversight of

analytical method validation activities , including the review of validation plans, protocols and reports. Collaborate in the review of validation activities related to

manufacturing processes and cleaning procedures , where applicable. Review

manufacturing batch records and Quality Control documentation . Train company personnel in

Quality Management and GMP requirements . Collaborate with the Head of the Quality Assurance Unit to promote GMP compliance and propose improvements to the Quality Management System. Support different organisational units in the implementation and maintenance of approved procedures, promoting

continuous improvement, quality risk management, contamination prevention and compliance with applicable regulatory requirements . Collaborate in the

supplier qualification process , managing the information received and supporting supplier classification according to established approval levels. Collaborate with the IT/UI department to ensure compliance with

21 CFR Part 11 and EU GMP Annex 11 ,



including computerised system validation and support in the selection of new equipment or systems. Ensure

Data Integrity

principles are applied to data used for decision-making in GxP and business environments.

REQUIREMENTS

University degree in

Biochemistry, Biotechnology, Pharmacy, Chemistry or a related scientific discipline . At least

2 years of professional experience in a GMP-regulated pharmaceutical laboratory , preferably in

Quality Assurance/Quality Control or Analytical Development . Practical experience in the

review of analytical results and investigation of OOS and/or deviations . Experience in

analytical method validation . Experience working under

EU GMP requirements . Knowledge of

Quality Systems and applicable ICH Guidelines . User-level computer skills. Fluent English, both written and spoken, minimum C1 level or equivalent.

Desirable

Additional training in

Pharmaceutical Quality Control, Analytical Validation and/or Quality Assurance . Experience with

biological products, allergen immunotherapy products and/or sterile products . Experience with

CAPAs, Change Controls, PQRs and GMP documentation . Knowledge of

21 CFR Part 11, EU GMP Annex 11 and Data Integrity principles .

REMUNERATION

According to the

Company Agreement (Category 6 of the Chemical Industry Collective Agreement) .

PROFILE

We are looking for an

analytical, rigorous and results-oriented professional

who is comfortable working cross-functionally with Quality Assurance, Quality Control, R&D; and other technical areas.

The adecuado candidate will combine a strong

scientific and analytical background

with a clear commitment to

GMP compliance, analytical quality, robust documentation, investigation of quality events and continuous improvement .

📌 Quality Assurance Technician – QC Analytical Validation (Madrid)
🏢 Roxall Medicina España
📍 Madrid