Trainee Quality Control NPI (m/w/d)

jj· 8562-Cilag AG Legal Entity
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Full timeHybrid Work8562-Cilag AG Legal Entity

About this role

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 jnj.com.

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.

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 New Product Introduction 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:

  • Recently 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.

  • 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!

#JnJTrainee #JnJEMEAStudentCareers

 

 

Required Skills:

 

 

Preferred Skills:

Frequently Asked Questions

Is the salary disclosed for the Trainee Quality Control NPI (m/w/d) position at jj?
The salary for this Trainee Quality Control NPI (m/w/d) role at jj is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Trainee Quality Control NPI (m/w/d) position at jj located?
This Trainee Quality Control NPI (m/w/d) role at jj is based in Schaffhausen, Switzerland. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Trainee Quality Control NPI (m/w/d) role at jj full-time or part-time?
This is listed as a Full time position. It is posted as a Trainee Quality Control NPI (m/w/d) role in the 8562-Cilag AG Legal Entity department at jj.
Which team or department does the Trainee Quality Control NPI (m/w/d) at jj belong to?
This Trainee Quality Control NPI (m/w/d) position is part of the 8562-Cilag AG Legal Entity department at jj. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Trainee Quality Control NPI (m/w/d) position at jj?
Click the "Apply Now" button on this page. You will be redirected to jj's official application portal hosted on workday where you can submit your application directly.
Trainee Quality Control NPI (m/w/d)
jj
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