Quality Assurance Professional
A high-level quality assurance professional is sought after to oversee commissioning, qualification, and validation activities for pharmaceutical equipment, systems, and processes. This role involves ensuring compliance with regulatory requirements such as Good Manufacturing Practices (GMP) and other relevant regulations.
Key Responsibilities:
* Project Leadership: Lead projects from inception to completion, guaranteeing all deliverables meet client expectations.
* Bid Management: Analyze technical requests, identify risks, define assumptions, develop tailored approaches, estimate workload, and manage the bidding process autonomously.
* Technical Expertise: Oversee commissioning, qualification, and validation activities.
* 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.
* Continuous Improvement: Stay updated on industry trends, regulatory requirements, and best practices.
Qualifications:
* 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 ability to manage bids autonomously.
* Excellent analytical skills.
* 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 required.
Benefits:
* Competitive salary based on experience.
* Company car as part of the benefits package.
* Opportunities for career development in a dynamic international company.
* A collaborative and inclusive work environment.