Technical Project Manager
This challenging role requires a seasoned professional to lead CQV projects from inception to completion, ensuring all deliverables meet regulatory and client expectations.
* Project Leadership
* Bid Management
* Technical Expertise
* Risk Assessment
* Stakeholder Engagement
* Continuous Improvement
The ideal candidate will have a strong background in CQV, excellent analytical skills, and the ability to manage bids autonomously.
Key Responsibilities:
Lead CQV projects from inception to completion
Manage complex projects and client interactions, especially during the bidding process
Oversee commissioning, qualification, and validation activities, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations
Requirements:
* Minimum of 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, including presales and client presentations
* Excellent analytical skills to understand technical requests, identify risks, and define project assumptions
* Deep understanding of regulatory requirements (e.g., GMP, FDA, EMA) and validation standards
* Exceptional communication and interpersonal skills to effectively engage with clients and stakeholders
* Bachelor's or Master's degree in engineering, life sciences, or a related field
* Native level of Italian and fluency in English is required
We Offer:
* Competitive salary based on experience
* Company car as part of the benefits package
* Opportunities for career development in a dynamic and growing international company
* A collaborative and inclusive work environment
This is an exciting opportunity for a skilled professional to make a significant impact in a fast-paced industry.
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