Johnson & Johnson Careers

SENIOR QA SPECIALIST

Schaffhausen, Switzerland
Quality (Generalist)


Job Description

Requisition ID: 1905744992W

"Caring for the world… one person at a time” inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo.
 

Cilag AG in Schaffhausen belongs to the group of Johnson & Johnson pharmaceutical companies operating under the “Janssen Pharmaceutical Companies of Johnson & Johnson” trademark and manufactures high quality pharmaceutical products, active pharmaceutical ingredients (APIs) and medical devices. 
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.

 

Cilag AG in Schaffhausen, Switzerland is part of the Janssen Supply Chain organization, within Johnson & Johnson and is currently recruiting for a


Senior QA Specialist Sterile Fill&Finish

 

The function holder is responsible for QA oversight for equipment and premises used for parenteral products manufacturing at the JSC Schaffhausen site. This includes quality oversight for all relevant activities in sterile fill and finish, assembly and packaging of the respective combination products.


Main responsibilities

  • Quality and aseptic oversight for sterile fill and finish manufacturing departments
  • Quality System Matter Expert on aseptic processing
  • Proactive risk mitigation
  • Investigation lead for major non-conformances (deviations)
  • Review and approval of non-conformances (deviations) records and change control requests
  • Review and approval of GMP critical SAP master data (e. g. bill of material, manufacturing instructions etc.)
  • Review and approval of work instructions and standard operating procedures
  • Support of projects
  • Support of ‚customers‘ (production, logistics, engineering, etc.) in terms of  GMP Compliance

Qualifications
  • Bachelor or Master Degree in a technical or science discipline
  • Five years of experience in a GMP regulated aseptic Pharma production environment or three years of experience in a relevant quality role
  • Strong technical and process background in sterile fill and finish production
  • Strong knowledge in aseptic processing preferred
  • Experience as team or project lead preferred
  • Advanced communication skills in German and English (oral and written)
You are a team-oriented, dynamic and highly motivated person with strong communication skills. 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.
 
We are offering you a multifaceted challenge in a dynamic, international environment with attractive terms and an excellent infrastructure.
 
If you feel attracted by this challenge and want to be part of a successful and growing organization, then please send us your online application (CV, Motivation Letter, Working References etc.) by clicking here.
 
Internal: Please be aware: internal employees have to inform their line manager about the application before their first interview.
 



Primary Location
Switzerland-Schaffhausen-Schaffhausen-
Organization
Cilag AG (8562)
Job Function
Quality (Generalist)
Requisition ID
1905744992W