Job Description - Trainee in Quality Control and New Product Introduction, fixed-term 12 months (2406221476W)
Description
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.
For our QC department in Schaffhausen, we are looking for an open-minded, goal-driven, motivated Specialist QC Services.
Main Tasks
1. Coordinate and plan the introduction of new products into QC.
2. Review and implement test methods for new products.
3. Create and review GMP documents for new products.
4. Coordinate and plan the introduction of new technologies and the implementation of software applications (e.g. Empower Master projects).
5. Review analytical data.
6. Coordinate non-conformances, corrective actions (CAPAs), and changes (change control management) related to the introduction of new products.
7. 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 analytical thinking and a structured way of working, strong team and communication skills are essential. You should be able to tackle challenges in a solution-oriented and systematic way, solve complex and multi-layered tasks, and set your priorities correctly. Assertiveness and a readiness to take responsibility while enjoying driving projects forward are also key attributes.
Qualifications
* You have 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 possess very good project management skills (good communication skills, pro-active).
* You have excellent organizational and communication skills, a customer-oriented approach, and a “can do” mentality.
* You have strong knowledge of analytical methods.
* You have experience in reviewing analytical data and GMP documents. Experience with eLIMS and the Empower laboratory system is beneficial.
* You are proficient in Microsoft Office programs.
* You are fluent in German and English.
Primary Location
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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