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

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 make the daily activities extremely interesting and varied.

Qualifications
In addition to analytical thinking and structured way of working and strong team and communication skills, you can address challenges in a solution-oriented and systematic way, you can solve complex and multi-layered tasks and set your priorities in an accurate manner. In addition to your assertiveness, you are ready to take responsibility and enjoy driving projects forward.

You Also Have The Following Qualifications

• Recent graduated with a University/PhD/master's degree in chemistry, Pharmacy, Life sciences or a related field.
• Basic understanding of analytical methods (e.g., HPLC, cIEF, cSDS, Bioassays) is desirable.
• Eagerness to learn and develop skills within a complex, global matrix organization.
• Knowledge of Quality Assurance, GMP, and EH&S principles is a plus.
• Strong communication skills in English and fluent in German.
• Good IT skills and applications of Microsoft Office
• Motivated, flexible, and eager to chip in as part of a team.