R&D Laboratory Analyst

invoX; Diepenbeek; Sur place; EUR 42 000 - 65 000; Plein temps

Résumé du poste

invoX in Diepenbeek is seeking an R&D Laboratory Analyst to join our Analytical Lab team. You will advance formulation development, analytical method development, and product testing while supporting ISO and GxP compliance.

You will work in a multidisciplinary environment, collaborating with cross-functional teams to develop inhalation therapies and ensure robust data generation and regulatory compliance.

Qualifications

• Degree in chemistry, pharmaceuticals, or related field.
• Experience in GxP environments, preferably GMP, and familiarity with ISO 13485 or USFDA medical device guidance.
• Strong skills in data analysis and statistical methods.
• Prior experience with analytical method development and validation (e.g., HPLC, UPLC).
• Collaborative mindset and ability to work across teams.

Responsabilités

• Analytical Test Development: Develop and execute analytical methods (e.g., HPLC/UPLC) to support inhalation formulation activities and SOP updates.
• Formulation Support: Conduct experiments to validate hypotheses and support formulation of solutions and complex drug products.
• Data Management and Reporting: Record, analyse, and report experimental results and present findings to teams.
• Product Testing: Perform tests on inhaler devices, including particle size distribution and active substance quantification.
• Lab Management: Maintain lab equipment and inventory with safety and regulatory compliance.

Connaissances

GxP experience

Data analysis

Analytical method development

HPLC

UPLC

Formation

Bachelor's degree in chemistry, pharmaceuticals, or related field

Outils

HPLC

UPLC

Description du poste

We are currently seeking a skilled R&D Laboratory Analyst to join our Analytical Lab team in Diepenbeek. In this role, you will focus on advancing the development of our SMI device by contributing to formulation development, analytical method development, and product testing while striving to support the laboratory’s compliance to ISO and Good Practice (GxP).

This position offers the opportunity to work on impactful projects within a dynamic, multidisciplinary environment, collaborating with cross-functional teams. You’ll directly contribute to developing therapies that improve patients' lives.

Key Responsibilities

Analytical Test Development: Develop and execute analytical methods (e.g., HPLC/UPLC) to support inhalation formulation activities. Including the drafting and updating of Standard Operating Procedures (SOPs) to ensure consistent and compliant laboratory practices.

Formulation Support: Conduct experiments to validate scientific hypotheses. Providing support on the formulation of solutions and complex drug products.

Data Management and Reporting: Record, analyse, and report experimental results with precision. Present findings to internal and external teams to inform ongoing development.

Product Testing: Perform a variety of tests on inhaler devices, including particle size distribution and quantification of active substances.

Lab Management: Maintain lab equipment and inventory, ensuring compliance with safety and regulatory guidelines.

Skills, Knowledge and Expertise

• A degree in chemistry, pharmaceuticals, or a related field.
• Experience working in GxP environments, preferably GMP, and familiarity with regulatory standards such as ISO 13485 or USFDA medical device guidance.
• Strong skills in data analysis and statistical methods.
• Prior experience with analytical method development and validation (e.g., HPLC, UPLC).
• A collaborative mindset and the ability to work across teams.