Quality Officer

Há 7 dias


Lisboa, Portugal CordenPharma Tempo inteiro

CordenPharma ist ein führender Anbieter für die Entwicklung und Herstellung von pharmazeutischen Wirkstoffen (APIs), Hilfsstoffen, Fertigarzneimitteln und Verpackungsaktivitäten mit mehr als 2.600 Mitarbeitenden weltweit. Mit unseren Dienstleistungen unterstützen wir Pharma
- und Biotech-Unternehmen bei der Herstellung von Medikamenten mit dem vorrangigen Ziel, das Leben der Menschen zu verbessern.

Unser Netzwerk in Europa und den USA bietet flexible und spezialisierte Lösungen auf fünf Technologieplattformen: Peptides, Lipids & Carbohydrates, Injectable, Highly Potent & Oncology; and Small Molecules. Wir sind bestrebt in all diesen Bereichen höchste Qualität zum Wohl der Patienten zu liefern.

Am Standort Plankstadt sind wir mit rund 350 Mitarbeitenden spezialisiert auf die Entwicklung und Herstellung von Arzneimitteln mit hochwirksamen Wirkstoffen (Highly-potent APIs) als feste Darreichungsformen sowie auf die Verpackung von Arzneimitteln und die Herstellung klinischer Prüfpräparate.

**Quality Officer**
**Refª 02.2025_Quality Officer**:

- Lissabon
- 01/04/2025
- Vollzeit
- Begriff

**Ihre Aufgaben**:

- Provide on-the-floor support and oversight of manufacturing processes to ensure compliance with GMP and company quality standards.
- Reinforce Right First Time (RFT) principles by monitoring and guiding production activities.
- Overview, when applicable/necessary, line clearance activities to ensure the production area is prepared for the next batch or product changeover.
- Overview, when applicable/necessary, batch records, logbooks, and other documentation to ensure accuracy and completeness.
- Identify and address quality issues promptly, working with cross-functional teams to implement corrective and preventive actions (CAPAs).
- Participate in internal audits and inspections to ensure continuous compliance with regulatory requirements.
- Provide, when applicable/necessary, training and guidance to production staff on quality-related procedures and best practices.
- Maintain accurate and detailed records of all performed activities.
- Support the implementation and maintenance of quality management systems (QMS).
- Stay current with industry trends, regulatory changes, and advancements in quality assurance practices.
- Support the areas of Quality Assurance in what refers to the shopfloor activities.

**Ihr Profil**:

- Degree in a scientific discipline (e.g., Pharmaceutical Sciences, Chemistry, Biology,) or equivalent experience.
- Minimum of 2-3 years of experience in Quality (Quality Assurance or other Quality areas) within the pharmaceutical or related industry.
- Strong knowledge of GMP and regulatory requirements (e.g., FDA, EMA).
- Excellent attention to detail and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to work independently and collaboratively in a fast-paced environment.
- Experience with Quality Management Systems (QMS) and electronic documentation systems is a plus.
- Good level of English.

**Was wir Ihnen bieten**:
**Free Parking***:
**Positive working atmosphere and open management culture with focus on continuous improvement of processes to stay innovative***:
**Das könnte passen?**:
Wenn Sie gerne im Team arbeiten und an einem vielseitigen Verantwortungsbereich interessiert sind, es für Sie selbstverständlich ist, über Ihren eigenen Bereich hinaus zu denken und zu handeln, dann sind Sie bei uns richtig

**Sie haben noch Fragen?**

Sie haben noch Fragen zu Ihrer Bewerbung, dem Job oder anderen Dingen? Ich beantworte sie gerne.

**Rita Salvador**
- Zurück Bewerben


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