QA Specialist

Sentior, Ltd.; Schaffhausen; Híbrido; CHF 100.000 - 140.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work model

Descripción de la vacante

Johnson & Johnson Schaffhausen is seeking a QA Specialist in QA Parenteral Products for the AME project in sterile drug production. Hybrid work with 3 days on-site and 2 days from home; German and English fluency required.

You will assess and approve master data, manufacturing instructions, and process adjustments, support QA workflow, and collaborate with Local Quality Owners, production, and the AME team to ensure GMP compliance.

Formación

• Background in QA within pharmaceutical or medical device industry.
• Aseptic manufacturing and GMP experience.
• Fluency in German and English.

Responsabilidades

• Provide quality support for the AME project in sterile drug production.
• Assess and approve quality-relevant master data, manufacturing instructions, and process adjustments.
• Optimize workflows within the assessment and approval of master data, manufacturing instructions, and process adjustments through project work.
• Provide general administrative support for the QA Workstream Lead.
• Collaborate with Local Quality Owners, production, AME team, and LCM.

Conocimientos

Aseptic manufacturing

GMP experience

MES experience

SAP

MS Office

German language

English language

QA mindset

Project experience

Teamwork

Educación

Vocational training or degree

Herramientas

SAP

MES

Descripción del empleo

# QA SpecialistJohnson & Johnson Schaffhausen 1 maandGepubliceerd 11 uur geleden · Opportunity ID: 1052825Tarief indicatie —Uren 40 u/wStart 31 Oct 2026Duur 1 maandInteresse in deze opdracht?## De opdrachtQA Specialist in QA Parenteral Products MES SupportLocation: Schaffhausen, SwitzerlandLanguages: Very good language skills and fluency in German and EnglishDuration: This project is likely to run 18-24 monthsHours: 40 hours per weekCilag AG is an international development and manufacturing company within the pharmaceutical division of Johnson & Johnson, producing pharmaceutical, medical, and chemical products at its manufacturing site in Schaffhausen, Switzerland. For our Quality Assurance Parenteralia (Sterile Production) department, we are looking for an effective team member, immediately or by agreement.This position is a 2-year temporary contract created due to additional workload and new technology associated with the new MES production project. Working arrangement is hybrid, featuring 3 days on-site and 2 days working from home, with 0% travel.roles and responsibilities- Provide quality support for the AME project in sterile drug production- Assess and approve quality-relevant master data, manufacturing instructions, and process adjustments- Optimize workflows within the assessment and approval of master data, manufacturing instructions, and process adjustments through project work- Provide general administrative support for the QA Workstream Lead- Collaborate closely with Local Quality Owners, production departments, the AME team, and LCMhow to succeed- Completed vocational training or degree- Background and experience in Quality Assurance within the pharmaceutical or medical device industry- Strong QA mindset with aseptic manufacturing and GMP experience- MES experience is required- Project experience- Good IT and computer skills (SAP, MES, MS Office)- Very good language skills and fluency in German and English- Proactive personality with a quick grasp who enjoys working in a team- Careful, independent, accurate, reliable, and team-oriented way of workingbenefitsThis role offers a very competitive hourly rate. This contract will run for 18-24 months.you are welcome hereJohnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.about Johnson & JohnsonCaring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.application processWe are looking to process the first round of applications within the next 2 working days. We do not accept applications via email or LinkedIn InMail - you must apply direct to this advert.Diversity, Equity & InclusionFor more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.