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(U)HPLC and/or Electrophoresis laboratory professional

Technoparc de Thudinie 2, 6536 Donstiennes, Belgium

With which degree can I apply for this position?

  • Academic bachelor
  • Preparatory programme
  • Academic master
  • PhD
  • Professional bachelor

Which programmes can apply for this position?

  • Biology
  • Biomedical Sciences
  • Chemistry
  • Computer Science
  • Pharmacy
  • Physics

Note that companies can often be very flexible in whom they hire for which positions, depending on choices during your education, prior experience, or personal interest. If your profile is not listed here, this does not necessarily mean that you cannot apply for this position. The best way to find out is to go and talk to the recruiters!

Who should I contact?

Isabelle Lebrun
recrutement@quality-assistance.be

About this position

More information: https://www.quality-assistance.com/jobs/laboratory-professional-uhplc-andor-electrophoresis

SCOPE

We are currently actively looking for an (U)HPLC and/or Electrophoresis laboratory professional.

You will be part of a team involved in projects outsourced by our clients.

Those projects are related to the development, validation and/or application of analytical methods based on a protocol for the characterisation and quality control of biomolecules.

YOUR MISSION
You will be part of a team of 5/6 people and report to the Technical Leader Chromatography.

You will work on the bench and you will perform daily laboratory activities. 

Depending on your level of expertise, you will work on projects related to either application, development and/ or validation of analytical methods.

This implies:
• Analysing samples according to specifications and ensuring traceability of every analysis.
• Processing data.
• Writing reports and associated supporting documents.
• Presenting/discussing results.

Depending on your level of autonomy, you will be requested to ensure the following tasks:
• Validating raw data.
• Training team members and others on technical skills .
• Taking part in the writing/preparation of protocols.
• Supporting audits and investigations.

PROFILE
You have a scientific background ideally with knowledge of biologics (Antibodies, peptides, proteins, ADCs…).

You have hands-on technical expertise in either:
• HPLC / (U)HPLC 
• Capillary and/or gel Electrophoresis (cGE, cIEF, SDS-Page)

You have work experience experience working in a regulated environment ideally in the pharmaceutical industry.

You are experienced working with software such as Empower, iICE3, 32 KARAT., Quantity one is a plus.
You are fluent in French and have a good command of English (spoken and written).

Work @ Quality Assistance s.a.
We are a true career partner.
We accelerate people’s access to new medicines.
We offer an inspiring work-life balance in a human scale environment.
We care about mutual respect, assistance and communication.
We listen to your needs and your suggestions.
We offer a market-competitive and package including numerous fringe benefits.

About Quality Assistance s.a.
Quality Assistance is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products.

We assist our clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences.  

For each customer and each project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs. 

The company holds a unique position on the market with all its laboratories on one site, 190 highly qualified professionals and over 35 years’ expertise at the forefront of analytical sciences.

The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant.
Visit https://www.quality-assistance.com/quality-assistance/leading-analytical-cro to learn more

How can you apply ?
Send your application (reference JOB186.2) now to Mrs Isabelle Lebrun, Talent Acquisition Manager, to recrutement@quality-assistance.be or consult the Careers page on our website http://www.quality-assistance.com/careers/jobs.