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5 years of experience in Pharmaceutical Industry associate with a GMP background * Good knowledge of the pharmaceutical current best practice in analytical and manufacturing technologies, validation and GMP compliance
The job holder participates in the necessary training defined for his job, e.g. SOP training sessions, GMP training sessions, projects management, technical/scientific trainings, conferences, etc - Operational GMP or quality experience would be a distinct advantage
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Operational experience in GMP in Quality, Manufacturing, or Quality Control would be an asset. * Experience in GMP audits and inspections
Assurer le respect strict des procédures établies et des normes de qualité telles que GMP et ISO 17025. * Vous maîtrisez les standards de qualité tels que GMP, ISO 17025, avec une connaissance approfondie des pharmacopées.
Knowledge of GMP regulations and best qualification practices
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Kennis GMP omgeving nice to have
Perform all activities in compliance with GMP/HSE rules and regulatory requirements for each development phase of the product. * A good knowledge of GLP/GMP rules is a plus.
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Thorough knowledge of both GMP and safety standards are critical * Good knowledge of occupational safety, food safety and quality standards (GMP, ISO, ...)
Oversee the CPLO GMP activities and ensure all employees understand and follow all standard operating procedures. * Assist in ensuring inspection readiness, as well as participate in maintaining facility GMP compliance. * Assist management and in the writing of quality items such as Deviations, CAPA, Change Control, as well as writing of GMP documents relative to CPLO documentation to ensure compliance with all policies and procedures. * Excellent understanding in GMP related environment : at least 5 years of experience in the pharmaceutical industry in the field of Manufacturing or Quality. * Proven and recognized expert in the field of GMP Compliance.
Maintain Quality System elements associated with the ISO, MDR and GMP activities in a compliant manner * Maintain GMP compliance and inspection/audit readiness at all times. Operational GMP experience or clinical activities experience would be a distinct advantage.
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Easy Apply
Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP.
Strong knowledge of Good Manufacturing Practices (GMP).
Knowledge of Good Manufacturing Practices (GMP) in a laboratory setting.
Experience: Preferably in CAPEX projects within a commercial GMP facility.
Ensure compliance with all relevant regulatory regulations, analytical methods and specifications, GMP and safety.
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Easy Apply
Diepgaande kennis van HACCP, GMP, en ISO 22000.
Easy Apply
Sterke kennis van HACCP, GMP, FSSC22000, IFS, ACS en andere voedselveiligheidsnormen
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Ontwikkelen, implementeren, borgen en evalueren van kwaliteits- en voedselveiligheidsbeleid (HACCP, GMP).
Good knowledge qualification and validation process, IT compliance, GMP knowledge, data Integrity principles
Barry Callebaut * Halle * Contract duration unspecified * Full Time - Introduction - At Barry Callebaut, we are on a journey to transform the cocoa and chocolate industry. As the world's leading manufacturer of high-quality chocolate and cocoa products, our actions truly shape the future of our industry. We are a business-to-business company, serving the entire food sector, from the cocoa bean to the finest chocolate product. We are a company with a purpose, we believe in doing well by doing good and reinvesting in the communities we operate. We have a long-standing commitment to sustainability and our goal is to shape a sustainable cocoa and chocolate future. We are headquartered in Zurich, and have more than 12,000 passionate Employees working in more than 40 countries worldwide. We are very proud of who we are and what we do.
The GMP oversight of different laboratories and production pilots, including packaging, and outsourcing * The GSP oversight (non- GMP activities) of different development entities, located on the Braine site (BE), the Slough site (UK) and the Monheim site (DE). * Provide guidance and expert advice to development scientists, particularly with regard to the appropriate interpretation of national and international GMP regulations and guidelines * Lead the GMP refresher project for CSC and Lab entities
Diepgaande kennis van procestechniek, validatiemethoden, risicobeoordeling en regelgeving (GMP-compliance).
Sterke kennis van HACCP, GMP en andere voedselveiligheidsnormen.
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Je waakt over de correcte toepassing van de GMP, HACCP en BRC procedures
Vadigran * LENNIK * Vast contract, onbepaalde tijd * Voltijds - Introductie - Vadipro produceert hoogwaardige graan- en zadenmengelingen voor vogels, kleine dieren en honden – altijd met natuurlijke ingrediënten en een scherp oog voor kwaliteit. Naast het produceren van alle mengelingen voor de merken van Vadigran, biedt Vadipro ook dezelfde soort producten aan andere spelers in de dierenvoeding sector onder private label. Wij, bij Vadipro, zijn op zoek naar een Productiemanager om ons productieteam te leiden. Jouw verantwoordelijkheden - In deze rol ben je verantwoordelijk voor een gestroomlijnde productie, het doorvoeren van verbeteringen en het garanderen van topkwaliteit in de dierenvoeding sector. Dit alles binnen een hands-on omgeving waar je echt impact kunt maken. Als onze Productiemanager leid je het volledige productieproces – waarbij je efficiëntie stimulee