Quality Assurance Manager
CQV professionals play a vital role in ensuring the safety and reliability of pharmaceutical equipment, systems, and processes. As a Technical Unit Manager with expertise in Commissioning, Qualification, and Validation (CQV), you will be responsible for leading projects from inception to completion, guaranteeing that all deliverables meet regulatory and client expectations.
About this Role:
* Project Leadership: Lead CQV projects, overseeing commissioning, qualification, and validation activities to ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
* Bid Management: Analyze technical requests, identify risks, and develop tailored proposals to meet client needs.
* Technical Expertise: Oversee commissioning, qualification, and validation activities to ensure seamless project execution.
* Risk Assessment: Identify and mitigate risks associated with equipment, processes, and systems.
* Stakeholder Engagement: Collaborate with clients, project teams, and stakeholders to ensure alignment and satisfaction.
Key Requirements:
* Minimum 5 years of experience in CQV within the pharmaceutical or life sciences sector.
* Proven expertise in managing commissioning, qualification, and validation projects independently.
* Strong analytical skills to understand technical requests, identify risks, and define project assumptions.
* Deep understanding of regulatory requirements and validation standards.
* Exceptional communication and interpersonal skills.
* Bachelor's or Master's degree in engineering, life sciences, or a related field.
* Native level of Italian and fluency in English is required.
What We Offer:
* Competitive salary based on experience.
* Opportunities for career development in a dynamic and growing international company.
* A collaborative and inclusive work environment.