Cqv Director

Hobson Prior ae currently looking for a CQV Director for a pharmaceutical organisation on a permanent basis located in Geneva with the ability to work remotely from home. Our client is focused on offering a broad range of cGMP biologics manufacturing services to biopharmaceutical companies worldwide.

Please note that to be considered for this role you must have the right to work in this location.

**Key Responsibilities**:

- For this role, you will need to be able to travel to client sites for business needs.
- To Guarantee project success, you will efficiently manage project teams handling scope, budget and schedule.
- Constant knowledge of the local pharma market.
- You will be responsible for handling business development which involves recognising possible growth areas and development of CQV suggestions.
- Manage and/or support with project implementation.
- Cultivating relationships with clients, business development.
- Accountable for hiring CQV staff.

**Requirements**:

- Educated to a degree level in an engineering discipline such a chemical engineering which would be ideal or in another applicable life science discipline. However, educational needs for the role may be lenient if prior experience is fitting.
- At least 12 years of experience in engineering, commissioning, qualification, and validation largely in pharmaceuticals.
- General experience in commissioning/qualification/validation and an exhaustive comprehension of cGMPs.
- Former experience ideally as an Engineering/CQV service supplier.
- In-depth knowledge in cGMPs, commissioning, qualification, validation, and CQV project management.
- Capable of managing a team, scheduling, as well as classifying and forming client relationships.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.