For our client we are looking for a

Tasks & Responsibilities:

• Responsible for planning and conducting qualification and validation activities
• Creating and reviewing qualification and validation documents
• Producing SOPs and providing support in the creation of manufacturing specifications
• Responsible for maintaining the qualified and validated status of rooms, infrastructure and equipment
• Ensuring compliance with internal and external regulatory requirements with regard to qualification and validation
• Collaborating closely and communicating intensively with other departments
• Providing assistance in the processing of deviations, changes and CAPAs

Must Haves:

The perfect candidate is an experienced qualification expert with several years of hands-on experience in qualification within a GMP environment, preferably the pharmaceutical industry.

• Technical degree or relevant work experience in qualification with GMP (***)
• Further training and hands-on experience in the area of GMP (*****)
• Min. 3-5 years of experience in the qualification and validation of machines and processes, preferably in the pharmaceutical industry (*****
• Several years hands on work experience in qualification is a MUST(*****)
• Experience with Siemens COMOS, EVAL and VIVA is a plus (**)
• Very independent and structured way of working with a self-image of self and to continuously improve the processes
• High degree of initiative, flexibility and quick comprehension skills
• Enthusiasm for working together in self-organised teams and for your own areas of responsibility areas of responsibility with a focus on the big picture
• Fluency in German spoken and written needed, English fluency written and reading comprehension

General Information:

• Start date: ASAP 
• End date: 1 year (extension possible)
• Work location: Kaiseraugst
• Remote/Home Office: 20% possible
• Workload: 100%

Your Application:

Please apply online. For further information about the position, please contact your Gi Group Recruiter, Fatbardha Igrishta (fatbardha.igrishta[a]gigroup.com).

Branche: Pharma-Industrie

Funktion: Qualitätsprüfung

Führungsperson: Nein

Anstellungsart: Temporäre Arbeit

Karrierestufe: Angestellte/r