First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Validation

Location: Switzerland

Join our client and play a key role in maintaining top-tier quality standards! If you have a keen eye for detail and a passion for compliance, this could be your perfect opportunity.

̽��ϼ� is seeking a QA Validation Manager to oversee and ensure compliance of critical GMP processes with product requirements, process parameters, and global regulatory guidelines. This role involves close collaboration with cross-functional teams, Manufacturing, and clients, to provide scientifically sound evidence supporting sustainable product quality. You will act as a key QA point of contact for validation projects, product transfers, and validation strategies while supporting compliance throughout the product lifecycle.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

Ensure critical GMP processes are validated and maintained in compliance with regulatory guidelines and product requirements.
Oversee validation activities for biotechnological manufacturing processes in low bioburden environments.
Support validation of manual and automated cleaning and sanitization processes.
Manage qualification requirements for related equipment and systems.
Lead continuous process verification (CPV) and process validation activities.
Act as a QA point of contact for product transfer activities and validation strategies.
Perform change control and deviation impact assessments.
Support investigations of non-conformities and ensure resolution.
Review and approve SOPs, protocols, reports, change controls, deviations, and other GMP records.
Participate in audits and inspections to demonstrate compliance with European and US FDA regulations.
Contribute to continuous improvement initiatives.
Serve as a subject matter expert (SME) for Process Validation and Cleaning Validation SOPs.
Review and approve validation documentation, including Process Validation, Cleaning Validation, and Computer System Validation (CSV).
Participate in risk assessments and support the Data Integrity Program.

Key Skills and Requirements:

Degree in Science, Biotechnology, or a related field.
Strong knowledge of process validation, cleaning validation, and equipment/system qualification.
Experience with change controls, deviation management, and non-conformity investigations.
Understanding of cell and gene manufacturing processes and low bioburden environments.
Proficiency in English; German language skills are a plus.

If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at o.worch@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

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

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy.