Plaats

Hillegom
Nederland
Nederland

Contract

Vooltijds, Onbepaalde duur

Datum gepubliceerd

2026-10-02

Online tot

2026-12-01
EUR 15.00 HOUR

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QA specialist

Avantor Sciences
Nederland Hillegom
6 uur geleden

pIf you are ready to discover your greatest potential and lift your career to the next level, Avantor's brand new site in Hillegom offers challenging opportunities in a biopharma environment! /ppAvantor®, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education government, and advanced technologies applied materials industries. One of our greatest strengths comes from having a global infrastructure that is strategically located to support the needs of our customers. /ppAt Avantor, we set science in motion to create a better world. To achieve this mission, we are currently looking for a one-of-a-kind Quality Inspector. /ppIn 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). You will be responsible for providing Event and Complaint investigation support to other team members. /pbrBent u klaar om te solliciteren? Zorg ervoor dat u alle verantwoordelijkheden en taken die bij deze functie horen begrijpt voordat u verdergaat.brulliComply with company policies, procedures, work instructions, and training requirements focusing on customer service, production, and quality. /liliKeep customer interests and regulatory requirements in mind, ensure customer needs are met by reviewing order requirements, customer documentation requirements, proper filling and assembly requirements, and, where needed, ensure other technicians understand and follow documented VWR Solon procedures and GMP requirements.ulliEnsure customer requirements are met. /liliVerify adherence to policies, procedures, and work instructions. /liliEnsure documentation and physical product segregation and containment of non-conforming material identified during the production process. /liliReview production documentation for accuracy, completeness, and GDP compliance. /liliAssist in correcting order issues and ensure actions that are taken are appropriate. /liliCommunicate issues / concerns to area owner and direct manager. /liliEnsure that the area is in a state of “audit readiness” at all times. /li /ul /liliPerform inspection tasks by following established work instructions and procedures, by using required tools and methods and, when applicable, equipment, to determine acceptability of product, components, and documentation. /liliPerform pre-fill, in-process, and final inspections with the aid of documented work instructions and inspection information as required. /liliStop production when a non-conformance (NCM) is observed and follow appropriate NCM procedures. /liliDocument non-conformances following applicable VWR Solon procedures and work instructions. /liliDocument and trend any quality production issues discovered during the course of inspection duties. /liliEnsure cleanliness of work areas during the inspection processes. /liliUtilize problem solving tools such as 5M+E, 5 Why's, or other root cause analysis tools / methods to identify and permanently resolve issues. /liliAdhere to VWR Solon's QMS and VWR Policies, where applicable. /liliWalk the floor to observe, train, and facilitate / support change. /liliPerform other duties as assigned. /li /ulbrulliHigh School completion or equivalent (GED) and a minimum of 3 years related experience and/or training in a regulated industry is required; OR /liliBachelor's degree is required /liliExperience in a Quality Assurance role within the medical device, biotech, or pharmaceutical industry is preferred /li /ulpstrongYOUR KNOWLEDGE SKILLS AND ABILITIES /strong /pulliMust be able to balance multiple tasks and prioritize efficiently /liliKnowledge of ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, ISO 17025, or EXCiPACT standard is preferred /liliDemonstrated experience or knowledge in conducting root cause analysis as it relates to non‑conforming material investigations /liliKnowledge and experience utilizing Microsoft Outlook, Word, Excel, and Access, or equivalent software packages /liliGood communication skills /li /ulbrulliA challenging job in a service-minded company within an international working environment. /liliYou can count on an attractive salary package including a bonus and other extra-legal benefits. /liliYou will join a company that values its employees and helps them develop internally. xgiwjmb /liliYou will be working in our new site in Hillegom, where you will have the opportunity to take initiatives and be part of a new journey towards Avantor's success. /li /ulbr

Solliciteren

QA specialist

Plaats

Contract

Datum gepubliceerd

Online tot

QA specialist

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