Senior QC/ Analytical Development Consultant
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 Biotechnology and Pharmaceutical organization, based in Basel-Stadt Switzerland.
- Biopharmaceutical company with a very promising portfolio
- The team is approximately 25-30 people
- The Business Unit is responsible for 5 commercial products and +30 products in different development phases
ROLE DESCRIPTION
The QC/ Analytical Development Consultant will be responsible for the supervision and coordination of the CMOs and suppliers of drug substances and products.
He/ she will provide strong Quality, Regulatory and Validation expertise.
This role involves Project Management responsibilities (budget, staff, deadlines).
Additional information
- Starting date: asap
- Availability: 50-80% (negotiable)
- Duration: 12 months
RESPONSIBILITIES
- The QC/ Analytical Development Consultant will coordinate the CMOs and suppliers of drug substances/products
- Development and Validation of Analytical methods
- Performing stability studies
- Project Management (budget, deadlines, staff)
- Close interaction with the Quality, Regulatory and Manufacturing departments
- Ensure GMP compliance
- Analytical transfer
- Preparation of specifications from API's to commercial product
REQUIREMENTS
- Scientific background
- +8 years of experience managing external partners (more is preferred)
- Strong Project Management skills
- Previous work with drug substances and drug products
- Good knowledge of Validation, GMP compliance, regulatory
- Language: English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
