QA Engineering Specialist

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 is an internationally operating services group. From our offices in The Netherlands and Switzerland, we offer a full range of services for the life sciences industry. We are specialised in the areas of project management, engineering, CQV and compliance.

Key responsibilities:

• Holds all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems
• Approves applicable qualification documents
• Assesses and approves change requests with regard to their relevance to the qualified state condition and ensures this supports and approves quality risk analysis (e.g. GMP-FMEA)
• Ensures that deviations are appropriately investigated and addressed in deviation reports processed in deviation reports
• Informs the Group Manager QA Qualification about relevant developments and trend
• Actively supports the formulation and further development of qualification strategies and continues to training accordingly
• Supports internal audits in accordance with the internal audit plan, at customer audits and official inspections as QA representative (SME)

Job Requirements

• Experience in biotechnology or pharmaceutical environment is a must
• Experience as QA Qualification
• Knowledge on FAT/SAT/IQ/OQ/PQ
• You are proactive, with good communication skills and are able to work in a multidisciplinary team towards a common goal.
• You are fluent in German and English

Job offer

• Challenging position within a dynamic and rapidly growing organisation.
• Inspiring projects within our life sciences network
• Attractive salary, depending on education, knowledge and experience.
• Attractive social contributions scheme (high nett retention)
• General 2nd class abonnement for Swiss public transportation
• Training budget
• Employee benefits program
• Internal knowledge sharing program