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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BASEL
- SWITZERLAND
No
openings
SOUTH
SAN FRANCISCO - USA
No openings