Job Description
QA CQV Expert - Vevey, Switzerland
Are you a seasoned Quality Assurance and Commissioning, Qualification, Validation (CQV) specialist ready to make a significant impact in the pharmaceutical industry? Join our dynamic team in the scenic locale of Vevey, Switzerland, where your expertise will drive critical quality projects and ensure regulatory excellence. This is an exciting opportunity to leverage your skills in a fast-paced, innovative environment with a renowned organization committed to life-changing solutions.
Overview
We are seeking a highly skilled QA CQV Expert to lead and support validation activities within a cutting-edge pharmaceutical setting in Vevey. In this pivotal role, you will ensure that all quality and validation standards are meticulously met, adhering to global compliance requirements. Your expertise will be crucial in the successful execution of Qualification programs, supporting product launches, and maintaining the highest quality standards across facilities. If you thrive in detail-oriented environments and excel in cross-functional collaboration, this is your chance to advance your career while working on impactful projects in Switzerland.
Required Skills
* Extensive experience in QA and CQV within the pharmaceutical or biotech industries
* Strong understanding of validation lifecycle, commissioning, qualification, and validation protocols
* Proven ability to develop and review validation master plans, protocols, and reports
* Excellent problem-solving skills with a detail-oriented mindset
* Fluency in both French and English, with excellent communication skills
* Solid knowledge of GMP regulations and compliance standards
* Ability to coordinate with cross-functional teams and manage multiple projects concurrently
Nice To Have Skills
* Experience working in multinational or regulated environments
* Certification in CQV or related fields (e.g., ASQ Certified Pharmaceutical GMP Professional)
* Knowledge of risk assessment methodologies and deviation management
* Familiarity with computer systems validation (CSV)
* Prior experience in a similar on-site role in Switzerland
Preferred Education And Experience
* Bachelor's or Master's degree in Life Sciences, Engineering, or related field
* Minimum of 5 years of relevant validation and QA experience in pharmaceutical manufacturing
* Proven track record of successful validation project leadership
Other Requirements
* Must be willing to work on-site in Vevey, Switzerland, with flexibility for occasional travel if required
* Excellent written and oral communication skills in French and English are essential
* Ability to work independently and collaboratively within a fast-paced environment
If you're ready to bring your expertise to a leadership role that shapes the future of pharmaceutical quality, we want to hear from you. Apply now and contribute your skills to a company dedicated to excellence and innovation
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.