Trainee Quality Control NPI (mwd)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

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Johnson & Johnson is currently seeking a Trainee to join our QC New Product Introduction team located in Schaffhausen!

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 addition to your assertiveness you are ready to take responsibility and enjoy driving projects forward.

You also have the following qualifications:

• Recently graduated with a University/PhD/Masters degree in chemistry Pharmacy Life sciences or a related field.

• Basic understanding of analytical methods (e.g. HPLC cIEF cSDS Bioassays) is desirable.

• Strong communication skills in English and German.

• Eagerness to learn and develop skills within a complex global matrix organization.

• Knowledge of Quality Assurance GMP and EH&S principles is a plus.

• Good IT skills and applications of Microsoft Office

• Motivated flexible and eager to chip in as part of a team.

We look forward to receiving your application!

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