MECHELEN - BELGIUM

Scientist Cellular Pharmacology (m/f full time) MEC-077

Job description
You will be part of a team that develops target-specific cellular assays for screening and pharmacological characterization of small synthetic molecules from our drug discovery programs.
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QUALITY and SAFETY MANAGER in Drug Discovery (m/f full time) MEC-075

Job description
The Quality and Safety Manager is responsible to ensure that Galapagos’ Drug Discovery activities at the Mechelen, Romainville and Leiden sites are quality driven and operating in a safe working environment.
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ROMAINVILLE - FRANCE

Technician Bioanalysis / DMPK (m/f temporary 12 months) RMV-039

Job description
You will join an experienced team that is dedicated to bring bioanalytical support to research projects in bone and joint diseases...
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LIMS Data Manager/Software Developer (m/f full time) RMV-038

Job description
The Discovery Informatics team at Galapagos has developed a Laboratory Information Management System (LIMS) to support scientific data management and decision taking within the Drug Discovery division of the company. You are responsible for an efficient use of this LIMS by end users in the drug discovery teams (chemistry, biology and compound logistics), by providing support, training and writing user documentation…
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LEIDEN - THE NETHERLANDS

Laboratory Technician, (m/f full time) LEI-014

Job description
This position offers a unique experience to work in an exciting and dynamic environment of a well-known international biotech company. You will be performing top-level target discovery research through collaborations with our international partners (Nat Biotech 20:1154, Genome Res 13:2325, Drug Discov. Today 10:1385). All this is done in a team-oriented, result-driven, international research environment that provides an excellent career opportunity for motivated scientists.
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HARLOW - UNITED KINGDOM

Temporary Medicinal and Synthetic Chemists, (m/f full time) HAR-395

Job description
We have a number of temporary contract vacancies for self-motivated, experienced medicinal chemists with previous relevant industrial experience.
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HR Manager, (m/f part time) HAR-100

Job description
This is a front-line position, responsible for all aspects of HR at Argenta’s site in Harlow. You will report to the Group VP Human Resources, who is based in Saffron Walden, and work closely with the BioFocus HR Manager at Saffron Walden. The role includes all aspects of resourcing and employee relations at this busy site, where optimum use of IT is fundamental to the success of the role.
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SAFFRON WALDEN - UNITED KINGDOM

Associate Scientist (Analytical & Purification), (Maternity Contract) CRP-386

Job description
This contract will be for up to 9 months, depending on when the employee returns to work from maternity leave.
The position is predominantly a lab based role and involves provision of purification support for the various internal and external projects being undertaken by our chemists within medicinal chemistry department.Teamwork is the key to our success and you will work closely with other analysts and chemists to ensure that compounds are purified to the required purity and returned within the set timeframe.
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Electrophysiologist, CRP-400

Job description
We are looking for an experienced electrophysiologist to join our ion channel team in Saffron Walden, near Cambridge. The ideal candidate will be a skilled conventional electrophysiologist with either expertise in the use of automated electrophysiology assay platforms or a willingness to expand their practical skills in this area.
You will have recently completed your PhD or be a graduate with several years’ practical work experience in ion channel research. As you will be handling multiple projects in parallel, you will need excellent communication, organization and time management skills, and an ability to work independently within a multidisciplinary team.
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Temporary ADME/PK Bioanalytical Scientist, CRP-380.2

Job description
As part of our continued success we are looking for a temporary ADME/PK Bioanalyst to support both multidisciplinary and stand alone ADME/PK programs. You will support a diversity of global organizations in most therapeutic areas. As you will be handling multiple projects in parallel, you will need excellent communication, organization and time management skills, and an ability to work independently within a multidisciplinary team. The contract will be for the period of up to 12 months.
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Temporary in vitro ADME Scientists, CRP-380.1

Job description
As part of our continued success we are looking for two temporary ADME Experimental Scientists to support both multidisciplinary and stand alone ADME/PK programs. You will support a diversity of global organizations in most therapeutic areas. As you will be handling multiple projects in parallel, you will need excellent communication, organization and time management skills, and an ability to work independently within a multidisciplinary team. The contract will be for the period of up to 12 months.
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Molecular Biologist/ Protein scientist, (m/f full time) CRP-300

Job description
As part of our structural biology team, you will be dealing with molecular cloning of target proteins, expression in either E-coli or Sf9 insect cells using baculovirus, protein purification using the ÄKTA purification platform and protein crystallization.
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Group Leader, Medicinal Chemistry, (m/f full time) CRP-306

Job description
As a key member of our Medicinal Chemistry department, you will be involved in running multiple drug discovery programs and arranging resources to best fit the needs of our partners and the business. You will take a leading role in client interactions, both with existing projects and in seeking out new business.
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Computational Chemistry Team Leader (m/f full time) CRP-231

Job description
You will provide innovative solutions to continuingly evolving problems on both multidisciplinary and stand alone computational chemistry projects. You must have the ability to multitask and deliver to tight deadlines.

Clear and compelling communication skills, both written and oral, are vital and applicants must be confident presenters with the ability to think on their feet.

Technical competences must include a strong scientific background with at least 5 years’ exposure in the pharmaceutical industry. A broad skill set including structure-, ligand- and fragment-based methodologies with experience in hit finding, hit to lead, lead optimisation through to preclinical is paramount. Familiarity with software such as Moe, Cresset, Discovery Studio, Pipeline Pilot and the Schrödinger suite is an advantage along with an understanding of computational biology and its application in the design of therapeutics.
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