Associate Director Quality/Regulatory Project Management
Location: United KingdomSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Surrey United Kingdom.
- Responsible for regulatory affairs for drug products
- Responsible for scale-up tech transfers
- Responsible for project management from R&D/clinical to commercial manufacturing
- Significant experience in Pharmaceutical RA & QA
- Project management/leadership skills in a matrix environment
- Good communication skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
The Company
We are looking for multiple Associate Directors Quality/Regulatory Project Management in the Surrey area for different clients in the Pharmaceutical and Biotech.Role Description
Associate Director Quality/Regulatory Project ManagementResponsibilities
- Responsible for quality assurance in your product group- Responsible for regulatory affairs for drug products
- Responsible for scale-up tech transfers
- Responsible for project management from R&D/clinical to commercial manufacturing
Requirements
- Master/Bachelor/PhD in Chemistry/Biology or related field- Significant experience in Pharmaceutical RA & QA
- Project management/leadership skills in a matrix environment
- Good communication skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.