qp

Serve as the primary QP contact point for operational issues in a defined manufacturing area.Provide QP-related guidance to QA engineers during early involvement meetings and identify deviations or changes requiring escalation to the QP Governance meeting.Perform detailed review and approval of batch release dossiers and Certificates of Analysis...

DescriptionInterested in this role You can find all the relevant information in the description below.The QP Delegate serves as a key quality assurance representative, supporting the Qualified Person (QP) in ensuring compliance with regulatory requirements and internal quality standards for the release of commercial and clinical batches. While the QP...

About the Role QP Delegate Locatie: Geel Level: L2-2 Hiring manager: Gunter Aerts Key Responsibilities Quality & Batch Release Acts as the first QP contact point for quality-related issues Performs detailed review and approval of batch release dossiers Reviews and approves Certificates of Analysis / Certificates of Conformity Changes the Usage Decision in...

The QP Delegate serves as a key quality assurance representative, supporting the Qualified Person (QP) in ensuring compliance with regulatory requirements and internal quality standards for the release of commercial and clinical batches. While the QP delegate has the responsibility for approving the batch release dossier based on a detailed review of the...

h3QP Delegate /h3pLocatie: Geel /ppLevel: L2-2 /ppHiring manager: Gunter Aerts /ph3About the Role /h3pThe QP Delegate serves as a key quality assurance representative, supporting the Qualified Person (QP) in ensuring compliance with regulatory requirements and internal quality standards for the release of commercial and clinical batches. While the QP...

FUNCTIEOMSCHRIJVING The QP Delegate serves as a key quality assurance representative, supporting the Qualified Person (QP) in ensuring compliance with regulatory requirements and internal quality standards for the release of commercial and clinical batches. While the QP delegate has the responsibility for approving the batch release dossier based on a...

Sanofi heeft meer dan 110.000 medewerkers, is gevestigd in meer dan 100 landen en is daarmee één van de grootste farmaceutische ondernemingen ter wereld. Sanofi’s sterktes zijn diabetesoplossingen, vaccins, innovatieve geneesmiddelen, consumer health care, opkomende markten en diergeneesmiddelen.Door de overname van Genzyme in 2011 heeft Sanofi haar...

Cenexi is a contract development and manufacturing organization (CDMO) that has quickly built a reputation for excellence based on its sterile expertise, innovation and high quality products. The Braine-l'Alleud site is located 20 km south of Brussels and employs 300 people. The site is specialized in the manufacture of highly active sterile injectables,...

Importante azienda farmaceutica operante a livello internazionale, attiva nello sviluppo e nella produzione per il mercato globale e caratterizzata da elevati standard qualitativi e regolatori, è alla ricerca di una figura di:La risorsa, con riporto diretto al Quality Unit Director, avrà la responsabilità di guidare e coordinare un team di professionisti...

pSanofi Geel is seeking a QP Delegate (Location: Geel) to oversee quality and batch release activities. You will act as the primary QP contact for quality issues, review and approve batch release dossiers, and manage certificates of analysis/conformity. /ppKey responsibilities include QP governance, deviations/change controls with regulatory impact, and...

Randstad Belgium seeks a Qualified Person (QP) for a direct replacement role in a defined manufacturing area. You will serve as the primary QP contact for operational issues, guiding QA engineers and escalating deviations as needed.You will review and approve batch release dossiers and CoAs, execute releases of commercial and clinical lots in the ERP system,...

Sanofi Geel seeks a QP Delegate to support the Qualified Person in batch release for clinical and commercial products. You will review dossiers, approve COA/CoC, and ensure compliance within the site quality system. Requirements include a Master of Industrial Pharmacy, a valid QP number, 8–10 years in pharma, and fluency in Dutch and English. Based in...

Scheldezoom Farmacie is een veelzijdige en innovatieve farmaceutische organisatie met locaties in Terneuzen, Goes en de centrale apotheek in ’s-Gravenpolder. Hier worden farmaceutische patiëntenzorg, productie, laboratoriumactiviteiten, instellingszorg en ondersteunende diensten gecombineerd binnen één organisatie. De dynamiek tussen deze disciplines...

ALTEN Group Life Sciences zoekt een Qualified Person (met QP nummer) die verantwoordelijk is voor het releasen van batches op de IPT Specialties. De functie is volledig onsite bij de klant en vereist een industriële apotheker met QP erkenningsnummer, plus 1–2 jaar relevante farmaceutische ervaring.Je werkt nauw samen met de quality afdeling en andere...

Cenexi is seeking a QA/QP Director to lead all quality-related activities at its Braine-l'Alleud site south of Brussels. You will oversee QA, QC, release activities and validation, ensuring GMP compliance and effective interaction with health authorities and customers.The role demands strong leadership, strategic budgeting, and a passion for continuous...

Sanofi Genzyme Geel seeks a QP Delegate to support the Qualified Person in ensuring regulatory and quality standards for the release of commercial and clinical batches. The role relies on the site pharmaceutical quality system and involves detailed review of batch release dossiers.You will collaborate with QA, manufacturing and governance to maintain...

Anotech Energy, a leading healthcare and pharmaceutical organization, seeks a Quality Control Manager/QP for its Belgium pharmaceutical manufacturing site. The role combines operational quality leadership, batch release, and project management with GMP compliance.Reporting to the Pharmaceutical Affairs Director, you will act as the primary quality...

Johnson & Johnson is seeking a Quality Assurance Associate – Delegate Qualified Person in Belgium to develop quality expertise across global clinical supply chains for ATMPs and related products. You will review clinical batch documentation, support investigations, and contribute to continuous improvements under experienced guidance.This role offers...

QA Director role at Johnson & Johnson Innovative Medicine in Belgium, overseeing quality management for pharmaceutical drug product release. Requires Master's degree, QP certification, 10+ years experience, and Dutch/English fluency.

QA Director role at Johnson & Johnson Innovative Medicine in Belgium, overseeing quality management for pharmaceutical drug product release. Requires Master's degree, QP certification, 10+ years experience, and Dutch/English fluency.