QA Qualification Specialist — GMP & Compliance Expert

Adryan; Zürich; On-site; CHF 90,000 - 130,000; Full time

Benefits offered by this job

Training budget

Employee benefits program

Internal knowledge sharing program

Public transport subsidy (2nd class)

Job summary

Adryan, an internationally operating services group with offices in Switzerland, invites a QA Qualification professional to join our life sciences team in Zürich. You will oversee daily qualification activities for facilities, equipment and systems, ensuring compliance with GMP and quality standards.

The role requires hands-on experience in biopharma, knowledge of FAT/SAT/IQ/OQ/PQ, and the ability to work in a multidisciplinary team. Fluent German and English are essential.

Qualifications

• Experience in biotechnology or pharmaceutical environment is required.
• Experience as QA Qualification.
• Knowledge of FAT/SAT/IQ/OQ/PQ.
• Proactive with good communication and able to work in a multidisciplinary team.
• Fluent in German and English.

Responsibilities

• Holds all quality related responsibilities for daily qualification activities on facilities, equipment and systems.
• Approves applicable qualification documents.
• Assesses and approves change requests with regard to the qualified state condition and supports quality risk analysis (GMP-FMEA).
• Ensures deviations are investigated and addressed in deviation reports.
• Informs the Group Manager QA Qualification about relevant developments and trends.
• Formulates and develops qualification strategies and pursues training accordingly.
• Supports internal audits in accordance with the internal audit plan, at customer audits and official inspections as QA representative (SME).

Skills

Biotech/Pharma exp

QA Qualification

FAT/SAT/IQ/OQ/PQ

Multidisciplinary teamwork

German & English

Job description

Adryan, an internationally operating services group with offices in Switzerland, invites a QA Qualification professional to join our life sciences team in Zürich. You will oversee daily qualification activities for facilities, equipment and systems, ensuring compliance with GMP and quality standards.

The role requires hands-on experience in biopharma, knowledge of FAT/SAT/IQ/OQ/PQ, and the ability to work in a multidisciplinary team. Fluent German and English are essential.