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.
Job Description
SIRE 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.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control / Production Audit
