Laboratory Projects Specialist
Il y a 2 heures
Thuin, Walloon Region, Belgique
Jobbydoo
Temps plein
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Your next challenge
Ready to make a difference? Here's what awaits you.
As a Laboratory Projects Specialist, you will be at the heart of analytical projects that support the development of new medicines. Acting as the link between internal laboratory teams and project requirements, you will coordinate analytical activities, ensure high-quality deliverables and contribute to keeping projects on track. Through your work, you will help accelerate access to innovative therapies for patients around the world.
Your
key responsibilities
Here's what you'll take ownership of:
- Coordinate project implementation with laboratory teams while ensuring timelines, protocols and contractual requirements are respected
- Monitor the availability of samples and reference standards throughout project execution
- Communicate analytical progress to internal stakeholders
- Ensure the review of analysis reports and certificates of analysis
- Maintain quality documentation in collaboration with laboratory and compliance teams Who we are And why it matters Quality Assistance is a leading European CRO focused on analytical sciences for innovative drug development. Based in Belgium and GxP-certified, the company provides EMA
- and FDA-compliant services from a fully integrated, single-site facility equipped with a comprehensive suite of state-of-the-art technologies. With over 40 years of experience and 280 professionals, it supports the development of complex modalities such as biologics, oligonucleotides, peptides, cell and gene therapies, vaccines and nanomedicines. Having contributed to more than 2,000 drug candidates, we are now more than doubling our capacity with a new facility and investing in the development of our people through an internal Pharma Academy. At the same time, we continue to expand internationally while remaining anchored in scientific excellence, regulatory reliability, and operational rigor.
key responsibilities
Here's what you'll take ownership of:
- Coordinate project implementation with laboratory teams while ensuring timelines, protocols and contractual requirements are respected
- Monitor the availability of samples and reference standards throughout project execution
- Communicate analytical progress to internal stakeholders
- Ensure the review of analysis reports and certificates of analysis
- Maintain quality documentation in collaboration with laboratory and compliance teams Who we are And why it matters Quality Assistance is a leading European CRO focused on analytical sciences for innovative drug development. Based in Belgium and GxP-certified, the company provides EMA
- and FDA-compliant services from a fully integrated, single-site facility equipped with a comprehensive suite of state-of-the-art technologies. With over 40 years of experience and 280 professionals, it supports the development of complex modalities such as biologics, oligonucleotides, peptides, cell and gene therapies, vaccines and nanomedicines. Having contributed to more than 2,000 drug candidates, we are now more than doubling our capacity with a new facility and investing in the development of our people through an internal Pharma Academy. At the same time, we continue to expand internationally while remaining anchored in scientific excellence, regulatory reliability, and operational rigor.