Behind every presentation of each product sold by Roche is the involvement of Pharma Global Technical Operations (PT). Starting with Phase I of the development process and continuing through to product maturity, PT makes medicines at sites around the world and includes more than 10'000 employees worldwide.
As a Lab Expert, you will be working in the Small Molecules Technical Development organization within Global Technical Development .
Global Technical Development" (PTD) actively collaborates and develops innovative technical solutions to efficiently transform scientific ideas into products.
The mandate of the group is, to reliably deliver the pipeline and supply quality products to patients. The group excels in its work through innovation, collaboration, dedication, and mutual respect and makes valuable contributions every single day, continuously improving what it does.
Small Molecules Technical Development (PTDC) brings a broad range of experience across drug substance (DS), drug product (DP), analytical sciences and manufacturing S&T, and collaborates closely with key partners in the departments Research and Early Development (pRED / gRED), Small Molecules (PTC) and PTD.
PTDC is responsible for late stage technical development of our small molecule pipeline, manufacture of DS and DP for clinical studies.
As a Lab Expert in the Lab Support & Compliance team of Operations Support & Compliance (PTDC-T) you serve as a key contact and partner to provide PTDC specific services and support in the area of GMP compliance for analytical labs.
You are an expert for phase appropriate implementation of local and global requirements in the field of IMP QC analytics and analytical development.
This role is key to enabling smooth operations for colleagues in Small Molecules Technical Development and aligns business requirements with several partners and stakeholders.
As a Lab Expert in Operations Support & Compliance your key contribution is : Management and improvement of stability, reference- and sample management processes for IMP large and small molecules including medical devicesCoordination and improvement of lab equipment qualification and lifecycle processesCoordination and improvement of stability related LIMS activitiesRepresent GMP related topics during health authority inspections and internal auditsEnsuring compliance of Small Molecules Technical Development labs with Roche PQS and health authority requirements for IMP analytics and analytical development Collaborating with all leaders and employees to build and grow relationships with customers and partners across functional boundaries.
Your Profile : You have a Master or equivalent and / or higher degree in chemistry or pharmaceutical sciences and at least 5 years operational experience in a GMP environment within the pharmaceutical / biopharmaceutical business environment.
For this position, you bring the following qualifications : Strong technical background and solid understanding of health authority requirements and a deep understanding of health authority expectations for IMP analyticsCollaboration and interpersonal skills with proven influencing and negotiation skills as well as excellent skills at building and maintaining constructive and effective relationships with team members as well as internal and external partners and stakeholdersStrong ability to make decisions, inspire, lead changes and assess risksGood verbal and written communication skills in German and EnglishIf you have questions then please check our FAQs and videos on careers.
roche.ch / faqRoche is an equal opportunity employer.Quality, Quality >
Quality ValidationFull time