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Aantal uren
Categorieën
Type contract
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Categorieën
Branche
Steden
Regio's
Sollicitatie methode
Reistijd
Taal van de job
Begeerde jobs
11 resultaten voor manufacturing-supervisor vacatures in Schiphol Centrum, Schiphol Zuid binnen een 30 km straal
We hebben je zoekopdracht uitgebreid met 11 gelijkaardige vacatures.
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We are seeking an experienced and people-focused Supervisor, Laboratory Support Services to a team supporting critical laboratory operations within a highly regulated pharmaceutical environment. * Experience within pharmaceutical, biotechnology, CRO, laboratory, or regulated manufacturing environments.
We are seeking an experienced and people-focused Supervisor, Laboratory Support Services to a team supporting critical laboratory operations within a highly regulated pharmaceutical environment. * Experience within pharmaceutical, biotechnology, CRO, laboratory, or regulated manufacturing environments.
At Avantor, we're looking for a Manufacturing Operations Specialist to help us optimize our manufacturing operations in Hillegom. In this role, you will work alongside , , and other stakeholders to ensure our manufacturing processes run smoothly, efficiently, and consistently. * Create and improve manufacturing documentation and work instructions. * Support daily manufacturing operations and help resolve operational challenges. You understand that strong processes are the foundation of successful manufacturing, but you're also motivated to challenge the status quo and find smarter ways of working. * Experience in manufacturing, production, operations, process engineering, or a similar environment. * Experience with technical documentation, work instru
At Avantor, we're looking for a Manufacturing Operations Specialist to help us optimize our manufacturing operations in Hillegom. In this role, you will work alongside , , and other stakeholders to ensure our manufacturing processes run smoothly, efficiently, and consistently. * Create and improve manufacturing documentation and work instructions. * Support daily manufacturing operations and help resolve operational challenges. You understand that strong processes are the foundation of successful manufacturing, but you're also motivated to challenge the status quo and find smarter ways of working. * Experience in manufacturing, production, operations, process engineering, or a similar environment. * Experience with technical documentation, work instru
Create and maintain Bills of Materials (BOMs) and Method of Manufacturing (MOM) documentation within the ERP system. * Support manufacturing and quality teams with engineering-related expertise. * Minimum 3-5 years of experience in design engineering, manufacturing, or technical engineering environment.
Create and maintain Bills of Materials (BOMs) and Method of Manufacturing (MOM) documentation within the ERP system. * Support manufacturing and quality teams with engineering-related expertise. * Minimum 3-5 years of experience in design engineering, manufacturing, or technical engineering environment.
Minimum 3 years of experience in transportation, logistics, or supply chain roles, preferably within a manufacturing or industrial environment.
Minimum 3 years of experience in transportation, logistics, or supply chain roles, preferably within a manufacturing or industrial environment.
In this role, you will ensure customer and regulatory requirements have been met by inspecting product and review of documentation throughout all aspects of the production process (e.g., manufacturing, filling, and labeling / assembly, etc.). You will also ensure compliance with all applicable standards and regulations (e.g., ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, ISO 17025, and EXCiPACT), Good Manufacturing Practices (cGMPs), and Good Documentation Practices (GDPs).
In this role, you will ensure customer and regulatory requirements have been met by inspecting product and review of documentation throughout all aspects of the production process (e.g., manufacturing, filling, and labeling / assembly, etc.). You will also ensure compliance with all applicable standards and regulations (e.g., ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, ISO 17025, and EXCiPACT), Good Manufacturing Practices (cGMPs), and Good Documentation Practices (GDPs).
Promote products and services that support the manufacturing of monoclonal antibodies, vaccines, cell and gene therapies, peptides, and other biologics * Identify and lead the development of new custom manufacturing opportunities * Minimum of 5 years of sales experience within the biopharmaceutical manufacturing industry or a related life sciences sector
Promote products and services that support the manufacturing of monoclonal antibodies, vaccines, cell and gene therapies, peptides, and other biologics * Identify and lead the development of new custom manufacturing opportunities * Minimum of 5 years of sales experience within the biopharmaceutical manufacturing industry or a related life sciences sector
Create and maintain Bills of Materials (BOMs) and Method of Manufacturing (MOM) documentation within the ERP system. * Support manufacturing and quality teams with engineering-related expertise. * Minimum 3-5 years of experience in design engineering, manufacturing, or technical engineering environment.
Create and maintain Bills of Materials (BOMs) and Method of Manufacturing (MOM) documentation within the ERP system. * Support manufacturing and quality teams with engineering-related expertise. * Minimum 3-5 years of experience in design engineering, manufacturing, or technical engineering environment.
Entering/maintaining Bills of Materials (BOM) and Method of Manufacturing (MOM) in ERP system.
Entering/maintaining Bills of Materials (BOM) and Method of Manufacturing (MOM) in ERP system.
Avantor is seeking a Quality professional (QA Engineer / Senior Quality Assurance Officer) to support the expansion of manufacturing capabilities in Hillegom. * Support qualification and validation activities for new equipment and manufacturing processes. * 3-5 years of experience in Quality Assurance, Quality Engineering, Validation, or Manufacturing Quality. * Experience in pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Be part of a strategic manufacturing expansion project. * Gain exposure to validation, manufacturing, and quality improvement initiatives.
Avantor is seeking a Quality professional (QA Engineer / Senior Quality Assurance Officer) to support the expansion of manufacturing capabilities in Hillegom. * Support qualification and validation activities for new equipment and manufacturing processes. * 3-5 years of experience in Quality Assurance, Quality Engineering, Validation, or Manufacturing Quality. * Experience in pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Be part of a strategic manufacturing expansion project. * Gain exposure to validation, manufacturing, and quality improvement initiatives.
Contribute directly to the development of next-generation bioprocess and manufacturing technologies.
Contribute directly to the development of next-generation bioprocess and manufacturing technologies.
Participate and work within ISO 9001:2015 quality standards guidelines in all manufacturing areas in accordance with company quality goals. * Meet internal manufacturing schedules which drive on-time delivery. * Knowledge of Lean manufacturing
Participate and work within ISO 9001:2015 quality standards guidelines in all manufacturing areas in accordance with company quality goals. * Meet internal manufacturing schedules which drive on-time delivery. * Knowledge of Lean manufacturing