Site Name: Belgium-Wavre Posted Date: Jun 21 2024 The Specialist for Reagent Qualification for Testing is a vital role in our organization, ensuring the integrity of our testing procedures and results. If you have a strong background in reagent qualification and a passion for quality control, we would love to hear from you. Your key responsibilities: Management of the qualification and validation of all reagents used in testing procedures. Develop and implement qualification protocols for new reagents. Work closely with the Quality Assurance team to ensure all reagents meet regulatory and company standards. Troubleshoot and resolve issues related to reagent performance. Collaborate with cross-functional teams to improve testing procedures and outcomes. Coordination with other departments the change implementation (reagent change) in respect of timing Establishment of strategy for reagent to validate in collaboration with supervisor in charge of the method Translation of strategy into validation protocol and experimental plan and communicate with supervisor and lab technicians in charge of the analytical method Follow-up of experiments related to validations with laboratories and collect data Redaction and approval of validation reports Harmonise practices at laboratory and documentation level Ensure adequate management / validation of analytical reagent using appropriate planning tools, statistical tools, in line with projects timelines Act as eCC coordinator for the reagent implementation approve eCC Play a supportive role during internal and external inspections Lead the respect of the cGMP/QA rules application in the team (SOP, documentation, training, audits) Participate in governance meetings Reagents and Standards Escalade risks and defend QC points during TCLT and/or CEI meetings Ensure the adequate treatment of all deviations in his/her team Why you? Basic qualifications: Bachelor's degree in Chemistry, Biology, or a related field with the relevant experience Previous relevant experience in a laboratory setting, with a focus on reagent qualification Strong knowledge of regulatory standards and quality control procedures Excellent problem-solving skills and attention to detail Strong communication and team collaboration skills Proficiency in data analysis and reporting Fluent in French and good knowledge of English Preferred qualifications: Master's degree or Ph.D. #Li-GSK #GSKVaccines If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.