At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

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

Area Quality Owner (AQO) Parenterals

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 an 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. Experience with Compounding processes, Filling processes (isolator technology), Aseptic Process Simulations (APS), Equipment Process Validation (EPV), Smoke studies, Utility processes and Environmental monitoring is key 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

Your responsibilitiesProvide Quality and Compliance guidance to assigned departments and corresponding supporting departmentsPerform Quality and Aseptic oversight on the shop floorQualification of aseptic operatorsActively contribute to new concepts and projects as well as suggestions for improvement in assigned departmentsProactive risk mitigationAssess and approve Non-Conformances, CAPA investigations, and Corrections/ CAPAs related to utilities, facility, environment and equipment. Quality investigation lead for major Non-Conformances (CAPA investigations)Review and approve Protocols, Reports, SOPs/WIs, Change requests (COCs) and other applicable documentsReview and approve GMP critical SAP master data (e.g. manufacturing instructions)Support ‚customers‘ (Production, Quality Control, Logistics, MSAT, Engineering, etc.) in terms of GMP ComplianceParticipate as Subject Matter Expert in Health Authority inspections and audits

At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

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

Area Quality Owner (AQO) Parenterals

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 an 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. Experience with Compounding processes, Filling processes (isolator technology), Aseptic Process Simulations (APS), Equipment Process Validation (EPV), Smoke studies, Utility processes and Environmental monitoring is key 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

Your responsibilitiesProvide Quality and Compliance guidance to assigned departments and corresponding supporting departmentsPerform Quality and Aseptic oversight on the shop floorQualification of aseptic operatorsActively contribute to new concepts and projects as well as suggestions for improvement in assigned departmentsProactive risk mitigationAssess and approve Non-Conformances, CAPA investigations, and Corrections/ CAPAs related to utilities, facility, environment and equipment. Quality investigation lead for major Non-Conformances (CAPA investigations)Review and approve Protocols, Reports, SOPs/WIs, Change requests (COCs) and other applicable documentsReview and approve GMP critical SAP master data (e.g. manufacturing instructions)Support ‚customers‘ (Production, Quality Control, Logistics, MSAT, Engineering, etc.) in terms of GMP ComplianceParticipate as Subject Matter Expert in Health Authority inspections and auditsWho are youYou have a Bachelor or Master’s Degree in a microbiological, technical or science fieldYou have proven experience (minimum 3 yrs) in a GMP regulated aseptic Pharma production environment, or experience in a relevant Quality role (minimum 2 yrs)You demonstrate strong technical and process background in parenteral fill/ finish productionExceptional knowledge in aseptic processing is key in this roleYou have experience as team or project leadYou are fluent in German and English

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.

For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson Johnson, we all belongWho are youYou have a Bachelor or Master’s Degree in a microbiological, technical or science fieldYou have proven experience (minimum 3 yrs) in a GMP regulated aseptic Pharma production environment, or experience in a relevant Quality role (minimum 2 yrs)You demonstrate strong technical and process background in parenteral fill/ finish productionExceptional knowledge in aseptic processing is key in this roleYou have experience as team or project leadYou are fluent in German and English

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.

For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson Johnson, we all belong