Job Description

Cilag AG is an international production company of the pharmaceutical division Janssen of the Johnson & Johnson Group and manufactures pharmaceutical and medical products as well as chemical agents (APIs) for the 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.
Within the Quality Control (QC) department, we seek a dedicated personality - entry immediately or as agreed on.

Main Tasks

• Deputy of the laboratory lead in administrative and professional management of the laboratory for Combination products.
• 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.
• Processing and review of Lab Events, Lab Deviations and CAPAs.
• Support implementation of New products introduction
• Change Control-Ownership, Action-Owner & Assessor in the Change Control system for the subordinate 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.

The offered job in the QC FF SM Combo 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 production departments) as well as the work for new equipment introduction on site make the daily activities extremely interesting and varied.Qualifications

Your Profile

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 very good organizational and communication skills, a customer-oriented approach and "can do" mentality.
• You have very good knowledge of analytical/physical methods.
• You have first experience 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.