Combine Pharma/ Med devices in one, Senior Research Associate

仕事内容

Brilliantly located in the city of Leuven it would be easy to reach from various areas in Belgium. The beauty of the role is that you will be part of an international company so don’t really have to speak any other language but English.
The company specialises on Medical Devices manufacturing and boasts an advanced technology that makes their products leaders in their field. It’s very specialised and you will be able to combine Medical devices and Chemical/ Pharma experience so lots of room to learn and develop.
You will be supporting development of new products as well as life cycle management of existing ones; support QMS activities, complaint, internal audits and pharmacovigilance reporting; product/ process change control, risk management activities as well as many other relevant tasks.
You will design the experiments to solve technical problems and lower the project risks; provide technical leadership in the areas of CMC development and review, formulation development, analytical methods development and validation, preclinical activities, manufacturing process validations; set up studies to test ideas for new pharmaceutical and devices solution, review experimental data and validate the results. You will also develop, validate and perform chemical analysis methods on a variety of samples, perform critical review of data obtained and issue reports. You will also lead the project teams for the development of new products, effectively managing milestones and schedules as well as life cycle management activities, including process change control, risk management, QMS activities.
Like what you hear? Then please check that you meet the necessary below criteria and get in touch:
S. with 4+ years or Ph.D. without industrial experience (degree in Biochemistry, Biology, Chemistry, Industrial Engineering or similar)
Strong experience in analytical chemistry
Experience designing and implementing technical studies
good knowledge of pharmaceutical and Med Devices requirements ( ICH guidelines, EN ISO 13485, MDD 93/42/EEC, GMP)
Fluent English
If you like what you see, please forward me your CV in a Word to Oksana at [email protected] or via linked in.
This role is in Belgium, in Leuven area so please apply only if you are eligible to live and work here as sponsorship will not be provided.
If you do not hear from me you might not have the exact skills required for the position, however, I will make sure to keep your profile for any other possible opportunities.
The job market changes very quickly so do not forget to connect with me on Linked in, check other roles that I am hiring for at the moment and follow for any future relevant roles.
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