QA Specialist
il y a 21 heures
Driven to uphold the highest standards in pharmaceutical compliance? Step into this role where your expertise ensures operational integrity and supports the delivery of safe, effective treatments worldwide.R&D Partners is seeking a QA Specialist to support quality assurance activities in a multiproduct manufacturing facility. In this role, you will assist with ensuring compliance, reviewing documentation, and providing expertise for clinical and commercial manufacturing processes. Please note that to be considered for this role you must have the right to work in this location.Responsibilities:Create and review quality-related documents for projects, including notes, plans, and procedures.Review and follow up on project documentation such as risk assessments, validation plans, and batch records.Provide quality support and share knowledge about clinical and commercial manufacturing.Prepare and review documents with a focus on preventing errors and deviations.Ensure compliance with internal procedures, global standards, regulations, and product registration requirements.Offer on-the-floor support to ensure Good Manufacturing Practices (GMP) are followed.Collaborate with other departments to maintain quality standards.Escalate any significant quality issues to supervisors or managers when necessary.Key Skills and Requirements:A degree in a scientific field or equivalent experience.Understanding of current Good Manufacturing Practices (cGMP) in a regulated environment.Familiarity with clinical manufacturing and related regulations is a plus.Experience with quality processes and assurance.Strong attention to detail and ability to work independently.Excellent communication and teamwork skills.Proficient in writing and fluent in English.For more information, please contact Mandi CakweIf you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-dpartners.com/privacy-policy/
-
QA Specialist
il y a 2 jours
Geel, Belgique Jefferson Wells Temps pleinVast contract – Geel Binnen de QA operations afdeling zijn we opzoek naar een QA specialist voor productie plant 1. In deze functie ben je verantwoordelijk voor quality ondersteuning van de operations activiteiten van een multiproduct faciliteit.• Opstellen en reviewen van Quality documentation in kader van project (Project notes, Quality plannen, ) •...
-
QA Specialist
il y a 2 jours
Geel, Belgique Jefferson Wells Temps pleinVast contract – Geel Binnen de QA operations afdeling zijn we opzoek naar een QA specialist voor productie plant 1. In deze functie ben je verantwoordelijk voor quality ondersteuning van de operations activiteiten van een multiproduct faciliteit. • Opstellen en reviewen van Quality documentation in kader van project (Project notes, Quality plannen, ...)...
-
QA Specialist
il y a 3 jours
Geel, Belgique CareerWallet Temps pleinVast contract – Geel Binnen de QA operations afdeling zijn we opzoek naar een QA specialist voor productie plant 1. In deze functie ben je verantwoordelijk voor quality ondersteuning van de operations activiteiten van een multiproduct faciliteit. • Opstellen en reviewen van Quality documentation in kader van project (Project notes, Quality plannen, ...)...
-
QA Specialist
il y a 21 heures
Geel, Belgique Randstad Belgium Temps pleinRandstad Professional Life Sciences in Vlaanderen is op zoek naar een QA Specialist Operations in de regio Antwerpen.JobomschrijvingIn deze rol binnen de QA Operations afdeling word je het kwaliteitsgeweten van 'Productie Plant 1'. Je bent verantwoordelijk voor de integrale ondersteuning van alle operationele activiteiten binnen een dynamische, multiproduct...
-
Quality Assurance Specialist
il y a 1 semaine
Geel, Belgique Panda International Temps pleinQA Specialist – Nuclear & Pharmaceutical ManufacturingAs a QA Associate, you will support day-to-day quality assurance activities within a highly regulated pharmaceutical manufacturing environment. You will be involved in batch record review, handling deviations and CAPAs, release of incoming raw materials, and supporting supplier-related quality...
-
Quality Assurance Specialist
il y a 6 jours
Geel, Belgique Panda International Temps pleinQA Specialist – Nuclear & Pharmaceutical ManufacturingAs a QA Associate, you will support day-to-day quality assurance activities within a highly regulated pharmaceutical manufacturing environment. You will be involved in batch record review, handling deviations and CAPAs, release of incoming raw materials, and supporting supplier-related quality...
-
Quality Assurance Specialist
il y a 21 heures
Geel, Belgique Arcadis Temps pleinWe zijn momenteel op zoek naar een QA specialist voor productie plant 1. In deze functie ben je verantwoordelijk voor quality ondersteuning van de operations activiteiten van een multiproduct faciliteit.VerantwoordelijkhedenOpstellen en reviewen van Quality documentation in kader van project (Project notes, Quality plannen, ...)Opvolgen en reviewen van...
-
Quality Assurance Specialist
il y a 6 jours
Geel, Belgique Panda International Temps pleinQA Specialist – Nuclear & Pharmaceutical Manufacturing As a QA Associate, you will support day-to-day quality assurance activities within a highly regulated pharmaceutical manufacturing environment. You will be involved in batch record review, handling deviations and CAPAs, release of incoming raw materials, and supporting supplier-related quality...
-
Cleaning Specialist
il y a 1 semaine
Geel, Belgique Actalent Temps pleinAn exciting QA Cleaning Validation Contractor opportunity in Geel. This role focuses on supporting the QA Engineering department to ensure compliance with cleaning validation requirements.Involves:Reviewing and approving cleaning validation activities (SOPs, trend reports, protocols, and reports).Participating in change controls and projects related to...
