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/.
For our QC department in Schaffhausen, we are looking for an open-minded, goal driven, motivated Specialist QC Services.
Trainee QC NPI (f/m/d), fixed-term 12 months, Location: Schaffhausen

Main Tasks

• Coordinate and plan the introduction of new products into QC
• Review and implementation of test methods for new products.
• Create and review GMP documents for new products.
• Coordinate and plan the introduction of new technologies and the implementation of software applications (e.g. Empower Master projects).
• Review of analytical data.
• Coordinate non-conformances, corrective actions (CAPAs) and changes (change control management) related to the introduction of new products.
• Support documentation for new product registration.

The offered job as a trainee in the QC NPI team offers university graduates an ideal entry opportunity for a responsible GMP position in the pharmaceutical industry. 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.
In addition to an analytical thinking and structured way of working and strong team and communication skills, you can tackle challenges in a solution-oriented and systematic way, you can solve complex and multi-layered tasks and set your priorities in a correct manner. In addition to your assertiveness, you are ready to take responsibility and enjoy driving projects forward.

QUALIFICATIONS

• You successfully completed your science or technology studies, preferably with a focus on the pharmaceutical, (bio-)chemical or biotechnological fields, or you have several years of experience as a chemical or biological laboratory assistant in quality control, preferably in a GMP-environment.
• You have very good project management skills (good communication skills, pro-active).
• You have very good organizational and communication skills, a customer-oriented approach and «can do» mentality.
• You have very good knowledge of analytical methods.
• You have experience in the review of analytical data and GMP documents. Experience in dealing with eLIMS and the Empower laboratory system are beneficial.
• You have very good knowledge in the application of Microsoft Office programs.
• You are fluent in German and English
  For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
  We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
  At Johnson & Johnson, we all belong.
  

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• Coordinate and plan the introduction of new products into QC
• Review and implementation of test methods for new products.
• Create and review GMP documents for new products.
• Coordinate and plan the introduction of new technologies and the implementation of software applications (e.g. Empower Master projects).
• Review of analytical data.
• Coordinate non-conformances, corrective actions (CAPAs) and changes (change control management) related to the introduction of new products.
• Support documentation for new product registration