Quality Officer

hace 1 semana

Barcelona, España Qualifyze GmbH A tiempo completo

At Qualifyze, each person has the ability to make a difference. We all have a mission-critical role in transforming supplier qualification in pharma. With the support of other teams, the goal of the Quality Officer is to ensure that our services meet all the requirements and they are high-quality before they reach the consumers.

**As a Quality Officer at Qualifyze, you will**:

- Support the auditor during audit preparation (gathering information from auditees and customers, preparing the audit agenda, discussing the audit best approach and potential critical points, etc.)
- Review audit reports to identify deviations from quality standards, and to ensure the audit has been conducted in compliance with legal standards and meeting customers' expectations.
- Conduct and/or participate in GxP audits (API, excipients, and packaging materials manufacturers & distributors, etc.).
- Follow-up on CAPA derived from audits.
- Participate in the development of _Qualifyze common voice_ (templates, internal guidance, internal training sessions, auditor webinars, and forums).
**Why Qualifyze?**
- Be part of a hyper-growth startup redefining how supplier qualification in pharma will be carried out.
- Professional development through direct contact with GxP audits and top-level auditors around the world.
- Dynamic team who attaches great importance to reliability, stakeholder-oriented thinking, creativity, pragmatism, and open communication.
- Modern co-working space in the heart of Barcelona.
- Flexible working hours and the ability to work from home, when it suits you.
- Innovative company with a strong emphasis on a positive intercultural environment and diversity culture.
- An international working environment characterized by flat hierarchies, a great company spirit, and an open feedback culture.
- Steep learning curve that is supported by training and development sessions.
- Employee Benefits (Flexible working hours and home office, Regular company events, Training and mentoring, Travel stipend, Additional equipment).
- Academic background in life sciences (pharmacy, chemistry, biology, biotechnology, biomedicine)
- At least 2 years of experience in pharmaceutical industry or GxP audit service providers
- Knowledge of GxP standards/guidance (GMP, GDP, ISO15378, ISO 13485, Pharmacovigilance “GVP”)
- English language proficiency on a business level
- Strong speaking and written communication skills
- Strong tech-savvy skills.
- You place a high value on attention to detail
- You are empowered to try out new things take ownership

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