Quality Assurance Specialist (m/f)

Grupo Azevedos; Lisboa; Vor Ort; EUR 30.000 - 40.000; Vollzeit

Zusammenfassung

A leading pharmaceutical group in Lisbon is seeking a detail-oriented Quality Assurance Specialist. The ideal candidate will support quality-related activities to ensure compliance with GMP regulations and internal procedures. Key responsibilities include ensuring compliance with quality standards, reviewing documentation, and collaborating with cross-functional teams. The position requires a degree in Pharmaceutical Sciences, Chemistry, or a related field, along with good communication skills and attention to detail.

Qualifikationen

• Previous experience in Quality Assurance within the pharmaceutical industry is preferred.
• Intermediate to advanced English proficiency is required.

Aufgaben

• Ensure compliance with GMP and company quality standards.
• Review batch records, SOPs, deviation reports, CAPAs, and change controls.
• Monitor quality metrics and contribute to continuous improvement initiatives.
• Participate in training activities and promote a strong quality culture.
• Support internal and external audits, including regulatory inspections.
• Collaborate with cross-functional teams such as Production, QC, Regulatory Affairs, and Engineering.

Kenntnisse

Attention to detail

Good communication

Teamwork

Ausbildung

Degree in Pharmaceutical Sciences, Chemistry or related field

Jobbeschreibung

Azevedos Group, a brand with more than two centuries of service to medicine, always at the forefront of pharmaceutical development.

We are one of the most solid national pharmaceutical groups, responsible for the development of the first medicinal product in Portugal and, since then, we have continued to produce pharmaceutical products you can trust.

Besides the trust that distinguishes us from the beggining, it is also our expertise in the control of the complete medicinal product chain, from the development and manufacturing to marketing and distribution, that make us a solid and competitive pharmaceutical group.

Currently, we are looking for a highly motivated and detail-oriented Quality Assurance Specialist to join our team. The ideal candidate will support quality-related activities to ensure compliance with GMP regulations, internal procedures, and industry standards. This role plays a key part in guaranteeing product quality, patient safety, and regulatory compliance.

Key Responsibilities:

• Ensure compliance with GMP and company quality standards;
• Review batch records, SOPs, deviation reports, CAPAs, and change controls;
• Monitor quality metrics and contribute to continuous improvement initiatives;
• Participate in training activities and promote a strong quality culture;
• Support internal and external audits, including regulatory inspections;
• Collaborate with cross-functional teams such as Production, QC, Regulatory Affairs, and Engineering.

Requirements:

• Degree in Pharmaceutical Sciences, Chemistry or related field;
• Previous experience in Quality Assurance within the pharmaceutical industry (preferential);
• Good communication and teamwork abilities;
• Attention to detail and the ability to work independently;
• Intermediate to advanced English proficiency.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Quality Assurance, Science, and Production

Industries

• Pharmaceutical Manufacturing

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