QA Validation Manager

Panda International; Oberwallis; Vor Ort; CHF 120.000 - 150.000; Vollzeit

Zusammenfassung

Panda International in Visp, Switzerland, is seeking an experienced QA Validation Manager to provide QA oversight across validation activities in a pharmaceutical/biotechnology environment.

The role focuses on ensuring GMP processes meet product requirements and regulatory standards, with emphasis on Process Validation, Cleaning Validation and qualification of equipment and systems. Strong English is required, German a plus.

Qualifikationen

• Bachelor’s degree in Science, Biotechnology or a related field.
• 5–7+ years of experience in a pharmaceutical GMP environment.
• Strong experience in Process Validation and Cleaning Validation.
• Fluent English; German is a plus.

Aufgaben

• Lead and oversee Process Validation and Cleaning Validation activities
• Provide QA oversight for equipment and system qualification
• Support Continuous Process Verification (CPV) and validation strategies
• Review and approve GMP documentation, including protocols, reports, SOPs and validation records
• Manage and assess change controls, deviations and non-conformities
• Support product transfer and validation projects
• Participate in audits, inspections and risk assessments
• Support Data Integrity and continuous improvement initiatives
• Work closely with MSAT, Manufacturing and other stakeholders

Kenntnisse

Fluent English

Process Validation

Cleaning Validation

Equipment Qualification

GMP Knowledge

Change Controls & Deviations

Ausbildung

Bachelor’s degree in Science/ Biotechnology or related field

Tools

Qualification Equipment

GxP Regulations

Jobbeschreibung

QA Validation Manager – Visp, Switzerland

Contract: Until the end of 2026

Extension: Option to renew

The Role

We are looking for an experienced QA Validation Manager to join a pharmaceutical/biotechnology environment in Visp.

The successful candidate will provide QA oversight across validation activities, ensuring critical GMP processes remain compliant with product requirements and global regulatory standards.

Key Responsibilities

• Lead and oversee Process Validation and Cleaning Validation activities
• Provide QA oversight for equipment and system qualification
• Support Continuous Process Verification (CPV) and validation strategies
• Review and approve GMP documentation, including protocols, reports, SOPs and validation records
• Manage and assess change controls, deviations and non-conformities
• Support product transfer and validation projects
• Participate in audits, inspections and risk assessments
• Support Data Integrity and continuous improvement initiatives
• Work closely with MSAT, Manufacturing and other stakeholders

Requirements

• Bachelor’s degree in Science, Biotechnology or a related field
• 5–7+ years of experience in a pharmaceutical GMP environment
• Strong experience in Process Validation and Cleaning Validation
• Experience with equipment/system qualification
• Knowledge of change controls, deviations and GMP investigationsExperience in biotechnology, cell & gene manufacturing or low-bioburden environments
• Strong understanding of GMP and regulatory requirements
• Fluent English; German is a plus