Analytical Method Validation Specialist — Flexible Hours

SmartRecruiters, Inc.; Sint-Katelijne-Waver; À distance; EUR 45 000 - 65 000; Plein temps

Avantages offerts par ce poste

40 hours / week

Permanent contract with flexible hours

Wavre, Belgium

Eco-Cheques 250€ / year

12 ADV days

Well-being program

Payflip access

Team lunches and teambuilding

Professional development

Résumé du poste

Eurofins PSS Insourcing Solutions® seeks an experienced Analytical Method Validation Specialist to support QC Operations in a pharmaceutical manufacturing setting. You will coordinate validation activities, author validation documentation, and ensure GMP compliance while driving improvement projects.

You'll collaborate with laboratory teams, statisticians, and project stakeholders, providing quality systems support and ensuring ongoing validated state of analytical methods in a dynamic,

Qualifications

• Master’s degree in chemistry, biochemistry, pharmaceutical sciences, biotechnology or related field.
• Minimum 1.5 years of experience in pharmaceutical Quality Control, Analytical Development, Validation, or Quality Assurance.
• Strong experience with analytical method validation in a GMP-regulated environment.
• Experience authoring technical and validation documentation.
• Experience with Change control, Deviation Management and CAPA management.
• Fluent English; French is a plus.

Responsabilités

• Author and maintain validation-related documentation (protocols, reports, amendments, risk assessments, etc.).
• Coordinate validation activities across multiple stakeholders.
• Support quality events linked to validation activities (deviations, CC, CAPA).
• Participate in peer review and quality review of validation documentation.
• Contribute to maintaining validated state of analytical methods and support continuous improvement.

Connaissances

English fluency

Formation

Master’s degree in chemistry / Biochemistry / Pharmaceutical Sciences / Biotechnology (or related)

Description du poste

Eurofins PSS Insourcing Solutions® seeks an experienced Analytical Method Validation Specialist to support QC Operations in a pharmaceutical manufacturing setting. You will coordinate validation activities, author validation documentation, and ensure GMP compliance while driving improvement projects.

You'll collaborate with laboratory teams, statisticians, and project stakeholders, providing quality systems support and ensuring ongoing validated state of analytical methods in a dynamic,