Scientific Associate

Scientific Associate

Eurofins

Rixensart, Belgium

Job Description

• Drafting and reviewing scientific documentation, including method validation protocols, standard operating procedures (SOPs), and other technical reports.
• Collaborate and interact with Quality Assurance (QA) and Regulatory Affairs (RA) departments.
• Managing critical quality system elements such as deviations, Corrective and Preventive Actions (CAPAs), and Change Controls.
• Perform hands-on laboratory work involving sophisticated analytical instrumentation (LC-MS).

Qualifications

• A master’s degree or equivalent in a scientific discipline such as Chemistry or Biology is preferred.
• Proven expertise in mass spectrometry of biomolecules (peptides, proteins, lipids and/or oligonucleotides) as well as in chromatography (LC‑MS).
• At least 2 years of experience within quality control working within a GMP Environment.
• Proficiency in drafting and reviewing scientific documentation, including method validation protocols, standard operating procedures (SOPs), and other technical reports.
• Proven ability to effectively collaborate and interact with Quality Assurance (QA) and Regulatory Affairs (RA) departments.
• Experience in managing critical quality system elements such as deviations, Corrective and Preventive Actions (CAPAs), and Change Controls.
• Highly motivated to perform hands-on laboratory work involving sophisticated analytical instrumentation.
• Excellent interpersonal and communication skills, with the ability to collaborate effectively within a small, dedicated team.
• Proficiency in English communication, both written and spoken, is essential.