Trainee QC NPI

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

Job Function:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

All Job Posting Locations:
Schaffhausen, Switzerland

Job Description:

Johnson & Johnson is currently seeking a Trainee to join our QC NPI team located in Schaffhausen.

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.

Join us to advance the future of human health and take the first steps toward building a career with a purpose.

Position Overview - Tasks & Responsibilities:



* Assist in ensuring adherence to project schedules for the launch of new products in the Quality Control (QC) department.


* Support the coordination and planning of new product introductions into QC.


* Contribute to resource planning activities for new product launches.


* Participate in AD Subteam and TLI meetings to gain insight into project workflows.


* Support data collection, evaluation, and handling related to new product testing.


* Help organize meetings with QC representatives during new product implementation.


* Assist in reviewing and implementing test methods for new products.


* Contribute to the creation and review of GMP documentation such as Protocols, Reports, Work Instructions, SOPs, and training materials.


* Support the planning and coordination of new technologies, materials, and software applications in QC.


* Assist in training activities and testing for new test methods.


* Support data verification in eLIMS and review raw data under supervision.


* Assist in preparing documentation for inspections related to new product launches.


* Support the management of non-conformances, CAPAs, and change control activities.


* Contribute to process improvement initiatives.


* Support documentation activities for new product registration.


* Interfaces to numerous local and global departments (such as the development department, various QC departments and production) as well as the work with new products on site mak...