Senior Analyst QC NPI

Senior Analyst QC NPI

Vollzeit Kein Homeoffice möglich
8

ppAt Johnson Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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. /ppJob Function: Quality Job Sub Function: Quality Control Job Category: Professional All Job Posting Locations: Schaffhausen, Switzerland /ppJob 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. Learn more at The QC New Product Introduction (QC NPI) team is responsible for the successful introduction of new products, devices and technologies into Quality Control. We ensure that the QC laboratories are fully prepared for testing by coordinating analytical method implementation, GMP documentation, training and laboratory readiness activities. Working closely with local and global partners from Development, Manufacturing, Quality and other QC functions, we represent QC in cross-functional project teams and support product launches from development through commercialization. Our work offers a dynamic project environment with broad interfaces and a direct contribution to bringing innovative products to patients. /ph3Main Tasks /h3ulliCoordinate and plan the introduction of new products and devices into QC. /liliParticipation in local and global core teams in relation to the product/device launch. /liliReview and implementation of test methods for new products. /liliCreate and review GMP documents for new products. /liliCoordinate and plan the introduction of new technologies. /liliCoordinate non-conformances, corrective actions (CAPAs) and changes (change control management) related to the introduction of new products. /liliSupport documentation for new product registration. /liliInterfaces 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. /li /ulh3Your Profile /h3ulliIn 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. /liliIn addition to your assertiveness, you are ready to take responsibility and enjoy driving projects forward. /liliYou also have the following 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, or several years of experience in the pharma industry. /liliYou have very good project management and communication skills. /liliYou have a customer-oriented approach and «can do» mentality. /liliYou are interested and have a flair for technological processes. /liliYour structured, pragmatic and goal-oriented approach supports you in developing solutions. /liliYou have experience in the review of analytical data and GMP documents. /liliYou are fluent in German and English. /li /ulpRequired Skills: Preferred Skills: At Johnson Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 /ppDo Not Sell or Share My Personal Information Limit the Use of My Personal Information /p /p #J-18808-Ljbffr

Senior Analyst QC NPI Arbeitgeber: 8562-Cilag AG Legal Entity

Cilag AG in Schaffhausen bietet eine herausragende Arbeitsumgebung, die auf Qualität und Compliance fokussiert ist. Unsere Unternehmenskultur fördert Teamarbeit und kontinuierliche Weiterbildung, sodass Mitarbeiter in ihrer Karriere wachsen können. Zudem profitieren Sie von einem attraktiven Standort in der malerischen Schweiz, der sowohl berufliche als auch persönliche Lebensqualität vereint.

8

Kontaktdaten:

8562-Cilag AG Legal Entity Recruiting-Team