Quality Assurance Associate

PANTERA; Molise; In loco; EUR 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

Ein innovatives Unternehmen sucht einen erfahrenen QA Associate, der sich auf Qualifikation und Validierung spezialisiert hat. In dieser Schlüsselrolle tragen Sie zur Sicherstellung der höchsten Qualitätsstandards bei, indem Sie Qualifikations- und Validierungsdokumente erstellen und überprüfen. Sie arbeiten eng mit verschiedenen Teams zusammen, um die Einhaltung regulatorischer Anforderungen zu gewährleisten und die Produktqualität zu sichern. Dies ist eine einzigartige Gelegenheit, in einem dynamischen Start-up-Umfeld zu arbeiten, das sich der Verbesserung der Lebensqualität von Patienten widmet und einen bedeutenden Beitrag zur Gesundheitsbranche leistet.

Servizi

Einzigartige Möglichkeit zur Arbeit in einem innovativen Umfeld

Zusammenarbeit mit unterstützenden Kollegen

Dynamische Unternehmenskultur

Engagement für die Verbesserung der Lebensqualität von Patienten

Competenze

• Mindestens 5 Jahre Erfahrung in Qualitätssicherung und Validierung in der Pharmaindustrie.
• Starkes Verständnis der Validierungsprinzipien und regulatorischen Anforderungen.

Mansioni

• Unterstützung bei der Erstellung und Dokumentation von Qualifikations- und Validierungsdokumenten.
• Zusammenarbeit mit Ingenieur-, Fertigungs- und F&E-Teams zur Sicherstellung der ordnungsgemäßen Qualifikation.

Conoscenze

Qualitätskontrolle

Validierung

Analytische Fähigkeiten

Dokumentation

Kommunikationsfähigkeiten

Microsoft Office

Formazione

Bachelor in Lebenswissenschaften

Bachelor in Chemie

Bachelor in Ingenieurwesen

Strumenti

Risikomanagement-Tools (z.B. FMEA)

Softwarevalidierung (CSV)

Descrizione del lavoro

Context

Nuclear medicine has evolved considerably over recent years with the emergence of radiotherapeutics used in the treatment of cancers. The principle is based on the fact that radiotherapeutics can bring radioisotopes to the cancer cells which when they disintegrate, emit radiation that destroys selectively the tumour. Among this therapeutic isotopes, one of the most promising is the alpha-emitting Actinium-225 which is used in the development of new radiotherapeutics by many pharmaceutical companies.

One of the main challenges is to make this radioisotope available in high quality in large quantities. By joining their unique expertise and resources SCK-CEN and IBA have launched the company PanTera which aims at enabling the production of Actinium-225 and make it available for the pharmaceutical industry.

Job Summary

We are seeking an experienced QA Associate specializing in Qualification and Validation to join our quality team. The ideal candidate will have a strong background in quality assurance, a keen eye for detail, and a deep understanding of industry regulations. This role is crucial in ensuring our products meet the highest standards of quality and compliance, thereby maintaining customer satisfaction and regulatory adherence.

The QA Associate (Qualification & Validation) ensures that equipment, systems, processes and facilities comply with regulatory standards and internal quality requirements. This role mainly supports validation activities, documents qualification efforts, and collaborates with cross-functional teams to maintain product quality and regulatory compliance.

The ideal candidate will have a strong background in quality assurance within a manufacturing environment, excellent analytical skills, and the ability to communicate effectively with both internal teams and external suppliers.

Key Responsibilities

Qualification and Validation :

• Support creation and document qualification and validation documents including protocols, master plans, …
• Support validation lifecycle activities, including risk assessments, test plan creation, execution, and summary reporting
• Review and approve validation protocols and reports to ensure completeness and accuracy

Compliance and Documentation :

• Develop and maintain SOPs related to qualification and validation activities
• Assist in audit preparation and participate in internal audits as needed.

Cross-Functional collaboration

• Work closely with engineering, manufacturing, and R&D teams to ensure proper qualification of equipment
• Provide QA oversight for validation activities conducted by third party vendors or contractors
• Train and guide team members on validation processes

Team Support and Backup :

• Act as a backup for other QA team members, providing support during absences or peak workload periods
• Stay familiar with broader QA functions to ensure smooth operations across the Quality department.

Profile

• Bachelor degree in Life Sciences, Chemistry, Engineering, or a related field
• Minimum 5 years of experience in a quality assurance and validation role in the pharmaceutical, industry.
• Strong understanding of validation principles, regulatory requirements, and quality systems.
• Experience with software validation (CSV) is a plus
• Knowledge of risk management tools and methodologies (e.g. FMEA)

Skills and Competencies:

• Excellent organizational skills
• Excellent attention to detail and analytical skills.
• Strong written and verbal communication skills.
• Ability to work independently in a collaborative team environment.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Quick learner and able to work in a fast-changing environment
• Willingness to work in a controlled environment with adherence to strict safety and regulatory protocols.

Our offer

• Unique opportunity to work in a cutting-edge environment, contributing to the production of critical products used in the fight against cancer
• Collaborative work environment with supportive colleagues who prioritize teamwork
• Thriving start-up company with a dynamic entrepreneurial culture
• Company dedicated to enhancing the quality of life for patients and making a difference in the healthcare industry.