SUPERVISOR CLEANING VALIDATION.
View: 235
Update day: 21-03-2024
Location: Schaffhausen Schaffhausen SH
Category: Executive management Production / Operation
Industry: Medical Equipment Manufacturing Hospitals Health Care Pharmaceutical Manufacturing
Job type: Full-time
Job content
Caring for the world ... starting with the individual. This guiding principle inspires and unites the people at Johnson & Johnson. The culture of caring is at the heart of our corporate philosophy, which is anchored in the Credo.Cilag AG is an international manufacturing company of the pharmaceutical division of the Johnson & Johnson Group and produces pharmaceutical and medical device products as well as active pharmaceutical ingredients (APIs) for global markets at its production site in Schaffhausen. Thanks to our innovative products, processes and technologies, Cilag AG is today one of the leading pharmaceutical companies in Switzerland and at the same time a strategic launch and growth site and competence center for sterile production.
We Are Looking For a Highly Committed
SUPERVISOR CLEANING VALIDATION based in Schaffhausen
(Permanent)
Overview
The offered job in the QC Cleaning validation laboratory team offers a responsible GMP position in the pharmaceutical industry. Interfaces to numerous local and global departments (such as the development department, various QC departments, Quality assurance and pharmaceutical and chemical production departments) as well as the work for new equipment introduction on site make the daily activities extremely interesting and varied.
Further Responsibilities And Duties Are
- Administrative, professional and personnel management of the laboratory for cleaning validation.
- Responsible for meeting deadlines and correct execution of analysis orders and method transfers, processing of investigational testing and maintenance activities in the laboratory.
- Authorised for raw data review and verification of results in eLIMS as well as QC releases in the SAP system.
- Processing and review of Lab Events, Lab Deviations and CAPAs.
- Change Control-Ownership, Action-Owner & Assessor in ETS for the subordinate laboratory.
- Supervision of inspections and customer audits in the laboratory.
- Responsible for cleanliness, orderliness as well as compliance with GMP, safety and work regulations in the laboratory.
- Preparation of control regulations, work instructions and SOPs.
In addition to an analytical thinking and structured way of working and strong team and communication skills, you can tackle challenges in a solution-oriented and systematic way, you can solve complex and multi-layered tasks and set your priorities in a correct manner. In addition to your assertiveness, you are ready to take responsibility and enjoy driving projects forward.
You Also Have The Following Qualifications
- You successfully completed your science or technology studies, preferably with a focus on the pharmaceutical, (bio-)medical engineering or life science fields, or you have several years of experience as a laboratory assistant in quality control, preferably in a GMP-environment.
- You have first leadership experience.
- You have very good organizational and communication skills, a customer-oriented approach and «can do» mentality.
- You have very good knowledge of analytical methods.
- You are experienced in project management.
- You have experience in the review of analytical data and GMP documents. Experience in dealing with eLIMS are beneficial.
- You have very good knowledge in the application of Microsoft Office programs.
- You are fluent in German and English.
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 in Switzerland are 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.
Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”!
If you want to be a change agent in a challenging environment and shape the future quality organization, please send us your online application (CV, Motivation Letter, Working References etc.).
Primary Location
Switzerland-Schaffhausen-Schaffhausen-
Organization
Cilag AG (8562)
Job Function
Quality
Requisition ID
2205999518W
Deadline: 05-05-2024
Click to apply for free candidate
Report job
SIMILAR JOBS
-
⏰ 15-05-2024🌏 Schaffhausen, Schaffhausen SH
-
⏰ 15-05-2024🌏 Schaffhausen, Schaffhausen SH
-
⏰ 30-04-2024🌏 Stein am Rhein, Schaffhausen SH
-
⏰ 15-05-2024🌏 Schaffhausen, Schaffhausen SH
-
⏰ 15-05-2024🌏 Schaffhausen, Schaffhausen SH
-
⏰ 30-04-2024🌏 Stein am Rhein, Schaffhausen SH