Intern Data Integrity / CSV (m/w/d, 80-100%)

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/ .

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, treatments are smarter and less invasive, and solutions are personal.

The Cilag AG is an international manufacturing company of the Johnson & Johnson Group's Janssen pharmaceutical division and manufactures pharmaceutical products and medical devices as well as active pharmaceutical ingredients (APIs) for global markets at its production site in Schaffhausen.

With its innovative products, processes, and technologies, Cilag AG is one of the leading pharmaceutical companies in Switzerland and at the same time a strategic location for product launches.

Within the Quality Control (QC) department, we are looking for a dedicated personality as

Intern Data Integrity / CSV (m/w/d, 80-100%)

in Schaffhausen (Switzerland) to commence immediately or by agreement.

As an intern in laboratory equipment and software qualification, you will be joining a team which is passionate about introducing new laboratory equipment, laboratory automation and improved software solutions.

You will be part of the Lab Services department of Site Quality Control and as such responsible for the lifecycle management of the laboratory equipment.

As part of the newly founded Data Governance & Lab Automation team it will be your task to qualify laboratory equipment and software solutions.

In addition, you will be supporting the investigation of instrument and software related deviations and to implement corresponding corrective and preventive actions.

If you are also enthusiastic to ensure patient safety by implementing new laboratory equipment, improve lab automation and develop new strategies to ensure data integrity, we would like to meet you.


* Key Responsibilities:

- Planning and coordinating qualification activities for laboratory equipment in compliance with current GMP and regulatory requirements

- Preparation and execution of change control records related to equipment lifecycle management

- Creation of detailed, comprehensive, and well-structured qualification lifecycle documents (e.g., Impact & Risk Assessments, URS, IOPQ protocols and decommissioning documents)

- Drafting of procedures (WIs, SOPs) related to equipment lifecycle management

- Installation, configuration, testing and maintenance of application software and sy...