technological or engineering field of relevance to eco- and bio-biotechnologies An MBA is considered as an asset Competencies At least 10 years of experience in the broader sector of eco- and bio-technologies, among which at least 5 years direct experience in partnership and business development Documented
regulatory variations: - Writing IMPDs as far as CMC is required - Registration of files and variations for EU - Writing Module 2 of regulatory files that can are to be submitted through eCTD Modules Report to RA Director REQUIREMENTS MSc. in life science with relevant
across multi-site locations in the UK and EU within the regulated pharmaceutical industry. If you are currently working in the life sciences / pharmaceutical sector, with either consulting or in-house experience and want to work in a dynamic, entrepreneurial, agile, fast paced environment, leading
You will be responsible for overall QA activities related to the products life cycle like new product lounges, reviewing and approving artwork. You will work close together with the QP also for releasing for example unlabelled products after going through the quality inspection. It is your ambition
ideal. - Fluent professional knowledge in Dutch and English. - Preferably living in or near Brussels, else in triangle Gent-Leuven-Brussels. - Experience with molecular biology technologies PCR, qPCR and NGS are mandatory. Are you interested
biology - Experience with molecular biology technologies PCR, qPCR and NGS are mandatory - Willing and able to travel frequently within Belgium - Ability to manage multiple tasks in a result-oriented business environment - Fluent in Dutch and English
THE COMPANY Our client is a professional Biotechnology and Medical Devices organization, based in Belgium. The company is a worldwide known organisation that specialises in molecular sample and assay technologies, They provide testing kits which
THE COMPANY Our client is a professional Medical Devices organization, based in Noord-Brabant Netherlands. The company is part of an large multinational holding with over 1000 employees in 100 countries. Using advanced technologies, they strive for
ROLE DESCRIPTION As artwork coordinator you will provide high quality and reliable products for people in need of healthcare, by continuously exploring innovative technologies that positively impact patient care and care for the environment. RESPONSIBILITIES
- Implement and improve quality procedures - Support and manage internal and external audits - Develop and improve existing food safety systems REQUIREMENTS - BSc, In Food Technologies - > 7 years of experience in the food industry - Knowledge of HACCP, GMP ...
THE COMPANY Our client is a professional Medical Devices organization, based in Zuid-Holland Netherlands. The company is part of an large multinational holding with over 1000 employees in 100 countries. Using advanced technologies, they strive for
find a balance between career development opportunities and personal life planning. We offer our employees a wide range of excellent career prospects around the world, a modern working environment and competitive compensation. We strive to hire the best, most talented people from around the world, and
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
implementation and post-implementation REQUIREMENTS - Degree in Life Sciences and relevant Sales Experience - > 4 years of Sales in a consultative environment - Willingness to continuously increase and sharpen therapy and technical knowledge as your selling skills ...
candidate will be responsible for the developing of packaging technologies for a new line as a member of a larger project team RESPONSIBILITIES - Working together with the manufacturer to lead the design, to ensure that the Packaging Equipment is delivered on time, is