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Cilag AG in Schaffhausen, Switzerland, is part of the Johnson & Johnson Innovative Medicine (J&J IM) organization, and is currently recruiting for two

2x Junior Area Quality Owner (Jr AQO) Parenterals, 80-100% (f/m/d)

We manufacture high quality pharmaceutical products and active pharmaceutical ingredients (APIs). Today Cilag AG is one of the largest pharmaceutical manufacturers in Switzerland supplying all the major global markets. The Schaffhausen facility is a Johnson & Johnson strategic launch and growth site for parenteral products, and we have an impressive pipeline of new and innovative products!

Position summary

As a junior AQO in QA Process Parenterals you will join a dynamic team which is responsible for Quality and Compliance guidance, as well as Quality and Aseptic oversight of equipment and premises used for manufacturing in the Business Units Parenterals (compounding and subsequently filling of syringes and vials), Optical Inspection & Device Assembly Packaging and Warehouse departments at the JSC Schaffhausen site.

The focus for our future colleague will be on processes, equipment and projects in the Parenteral departments. Basic experience with Compounding processes, Filling processes (isolator technology), Aseptic Process Simulations (APS), Equipment Process Validation (EPV), Smoke studies, Utility processes or Environmental monitoring is an advantage in this role!

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting opportunity!

Qualifications

• Provide Quality and Compliance guidance to assigned departments and corresponding supporting departments

• Perform Quality and Aseptic oversight on the shop floor

• Qualification of aseptic operators

• Proactive Risk Mitigation

• Assess and approve Non-Conformances, CAPA investigations, and Corrections/ CAPAs related to utilities, facility, environment and equipment.

• Review and approve SOPs/WIs, Change requests (COCs) and other applicable documents

• Review and approve GMP critical SAP master data (e.g. manufacturing instructions)

• Support‚ customers (Operations, Quality Control, Logistics, MSAT, Engineering, etc.) in terms of GMP Compliance

Who are you

• You have a Bachelor’s or similar Degree in a microbiological, technical or science field

• You have proven experience (minimum 2 yrs) in a GMP regulated aseptic Pharma production environment, or experience in a relevant Quality role (minimum 2 yrs)

• Knowledge in aseptic processing is of advantage in this role

• You are fluent in German

If you are a team-oriented, open-minded dynamic and highly motivated person with strong interpersonal skills you might be the one we are looking for. For collaboration with different departments, you will need flexibility, social competence, and a reasonable degree of authority. You will take decisions independently and provide advice as needed.

If you are a team-oriented, open-minded dynamic and highly motivated person with strong interpersonal skills you might be the one we are looking for. For collaboration with different departments, you will need flexibility, social competence, and a reasonable degree of authority. You will take decisions independently and provide advice as needed.

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