Overview
Engineer Manufacturing Material/Johnson & Johnson Jobs in Bern – Switzerland at Randstad (Schweiz) AG
Title: Engineer Manufacturing Material/Johnson & Johnson
Company: Randstad (Schweiz) AG
Location: Bern – Switzerland
Category: Pharmaceutical, Quality Assurance – QA/QC
Position: Engineer Manufacturing Material / Johnson & Johnson
Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. We embrace research and science – bringing
innovative
ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world.
We have more than 265 operating companies in more than 60 countries employing approximately 120,000 people.
Johnson & Johnson
Innovative
Medicine is a global pharmaceutical company dedicated to bringing meaningful
innovation
to global health. We do this by discovering, developing, manufacturing and marketing products that combat major threats to the health of people worldwide. The Bern site, with its approx. 600 people of over 25 nationalities, acts as a center of expertise for development and manufacturing of
innovative
cell based viral- and bacterial vaccines and bacterial based therapeutic products.
Main
Responsibilities
Manage projects and activities related to materials compliance (Material assessment for new product introduction)
Serve as liaison between Suppliers, Material science and Supplier Quality and the users from early stages of Development for introduction of new Materials intended to use for GMP processes
Act/serve as a liaison between all functions including suppliers, materials science, supplier quality, and end-users from the early stages of development for the introduction of new materials intended for use in GMP processes
Ensure materials compliance with user requirements
Understanding biotechnology processes to ensure materials comply with GMP production user requirements
Change Control owner for Material Qualification
Coordinate and lead the introduction and changes of non-GxP and GxP raw materials and ancillary supplies throughout the life cycle of products produced at the Bern site
New Material and application scouting and point of contact for selected suppliers, and global functions (Material Science and Supplier Quality)
Coordinate material Leachable & Extractable evaluation
Coordinate the implementation of alternative/back up materials, dual sourcing strategy in close
collaboration
with Business operations, Material Science, Supplier Quality, Operations and Development
Support the site during audits/inspection for Material topics
Qualifikationen
Who we are looking for
A minimum of a bachelor’s degree or equivalent pharma discipline
2+ years of experience in a GMP environment, in a pharmaceutical, or similar regulated industry with detailed knowledge of relevant regulations and standards
Understanding of contamination control for manufacturing processes, aseptic manufacturing, and sterility assurance
Thorough knowledge in clean rooms environments is a major plus
Experience with
the requirements for material qualification from R&D to Commercial
Demonstrated
collaborative
nature and proactive
communication skills
to work efficiently and effectively in a
diverse community
on cross-functional project teams
Excellent organizational and time management skills
This job based in Bern, Switzerland will initially be limited to approx. 12 months. If you are int…
