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33,000+ live jobsLab Analyst I - HPLC, KF, Dissolution (QC laboratory, Assen)
On-site in Assen·Added 8 days ago (last checked 6 Nov)
Our summary
- Work mode
- On-site, Assen
- Contract
- Permanent
- Languages
- Dutch
This job advert was originally written in Dutch.
Requirements
What we're looking for
- Knowledge of laboratory processes. Knowledge of GMP is a plus.
- A completed MBO-4 or HBO laboratory education.
- You can perform analyses independently.
- You have good problem-solving skills and work accurately and flexibly.
- You are available 32 to 40 hours per week.
The role
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
At ICON, you are not merely witnessing the future of clinical drug development, you are part of it!
ICON plc is a leading clinical research organization in the field of drug research. We are proud to create an inclusive environment where innovation and excellence are central. We warmly welcome you to shape the future of clinical development together with us.
What you'll do
The Quality Control (QC) laboratory is part of the CMC department (Chemistry, Manufacturing and Control) and is located in Assen. The QC laboratory analyzes various types of new medication before it is used in clinical drug trials.
The QC laboratory supports the development of drug formulations, the setting up and validation of new analytical methods, and the analysis of new medication before it is administered to humans.
We have a great opportunity for a Lab Analyst I to come and strengthen our QC laboratory in Assen.
What will you do?
- Performing Quality Control analyses on new medication intended for human administration in clinical drug trials. The release of new medication depends in part on the data generated by the QC laboratory.
- You will perform various analytical techniques in a GMP environment, including: HPLC/UPLC analysis, Endotoxin determination, Osmolality, Particle analysis, Density, pH, Dissolution, Disintegration, Water content (Karl Fischer), Compendial testing according to international standards.
- Interpreting and processing data, reporting results, and approving or rejecting analyses.
- Independently planning analyses within projects.
- Independently performing analyses as part of a project team.
- Performing data reviews for quality control.
- Contributing to research when analyses show unexpected results.
- You will start with a one-year contract with a view to permanent employment.
What do you bring?
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
About ICON plc
ICON is a clinical research organisation (CRO) providing outsourced clinical development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company describes itself as the world's leading clinical research organisation and operates at global scale, with employees in 119 locations across 53 countries.
Its services span clinical and scientific operations, decentralised clinical trials, early clinical and laboratory services, medical imaging, regulatory affairs, consulting, commercialisation, medical writing, biometrics and outcome measures. ICON works across sectors including pharmaceuticals, biotech, medical devices and government and public health, and across therapeutic areas such as oncology, cardiovascular, central nervous system, vaccines and rare and orphan diseases.
- Industry
- Clinical research
- Headquarters
- Dublin, Ireland
€3k
€3k