QA Compliance Manager
Location: SwitzerlandSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Chemicals, Healthcare and Pharmaceutical organization, based in Zürich Switzerland.
Our client is a company focused on SkinCare.
ROLE DESCRIPTION
In this interesting and challenging position you are managing and deciding on all safety aspects for raw
materials and finished products and their technical-legal implementation at our client. Your key
task is to ensure our commercialized products are safe to use and compliant.
RESPONSIBILITIES
Safety evaluation raw materials used by LPG according to Annex I, Regulation (EC) No 1223/2009
- safety assessment and safety release of raw materials
- calculation of the safety margin of all ingredients per formula
- issue and update of raw material “restricted” and “not to use” list
- completion/update of toxicological data of new raw materials
Release of raw materials for development and production
Safety assessment of bulk/finished products mainly for EU, Asian countries and Israel
Management of safety testing (define test design, contact to institutes, organisation of samples send out, invoices, assessment of the tests of the finished products)
Management raw material data in SAP-system (parts Safety, INCI, status) implementation and update of raw material legal use limits (for EU, USA)
Monitor and give update by legislation changes to relevant departments regarding raw material and ingredients
Legal check and release of artwork (esp. warnings)
Support first assessment of a new cosmetic formulas and in answering customers inquiries
Continuing education in cosmetic’s safety/toxicology (i.e. seminars, courses)
REQUIREMENTS
PhD or master in toxicology /chemistry / pharmacy / microbiology or equivalent
Profound and +5 years’ experience in safety assessments of ingredients and cosmetic products marked in EU member states
Proof of safety assessor courses including certificates
~10 years’ experience in the area of quality management or regulatory affairs
Good SAP and MS office knowledge
Very good written and spoken English skills; good German skills are necessary
good analytical, communication and organization skills
entrepreneurial spirit with a good business sense
international mindset and flexible personality with great leadership skills
ability to work independently and to take responsibility for own projects/tasks
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.
