20 jobs voor quality assurance specialist gevonden

Quality assurance:..

Documentatie bijhouden volgens ISO 9001 normen;.De QA Manager ondersteunen bij het beheren van belangrijke documenten en rapporten;.Kwaliteitscontroleurs begeleiden en hun werk evalueren;.Ondersteunen bij externe audits en interne controles;.

Procedures, risk assessments) opmaken en reviewen met oog op DPP (deviation prevention) and HEP (human error prevention)..Compliance met SOP's, globale standaarden, regulations en productregistratie (filing) m.b.t.

Onze klant is gespecialiseerd in de outsourcing van verschillende technische bedienden op lange of flexibele termijn, eveneens voor freelancers.Gedreven, ambitieus, steeds met de focus op de mentaliteit en visie van uw bedrijf; dit zowel in INDUSTRIE ( Technisch tekenaars, project engineers, automation engineers,.) als BOUW (Facility engineers, HVAC engineers, werfleiders, projectleiders, …) Voor hun klant te Brugge/Zottegem, een Europese producent van rijst & maïs, zijn we op zoek naar versterking voor onderstaande: Functieomschrijving:Quality Assurance Specialist food (audits) mét zin voor verantwoordelijkheid.

Trefwoorden: life sciences, quality, kwaliteit, pharma, farma, project engineering, consultancy, hvac, cleanrooms, gmp, gxp .

Vast Contract – Regio Roeselare.#quality #assurance #control #food.

Dit alles gebeurt volgens de normen van ISO 9001, FSSC 22000, ISO 13485 en GMP+...

Allowing them to independently monitor, prevent and remediate emerging critical data quality issues.Evaluate data from data sources to identify and interpret trends.Identify data quality issues, determine business impact, find out the root cause, collaborate to resolve, and make recommendations for long term solutions.Gather data from data sources to identify and interpret trends, optimize its efficiency and quality by analyzing and cleansing it, as well as resolving data quality issues.Run data queries to identify coding issues and data exceptions.Support clients in their journey towards becoming data driven by bridging the gap between business and technology and advising them on best practices, tooling, implementation processes,Implement data quality principles, processes, and standards and embed them into the clients’ daily operating rhythm to improve trust in both business and technical data domains.Collaborate with business and database/application developers to improve processes, system and database designs.Follow up on the latest developments and trends in data quality analysis and tooling. 

De opslag en archivering van GMP (= good manufacturing practice) documenten & batchgerelateerde records..Nakijken van GMP logboeken en controleren en goedkeuren van SOP's (= standard operating procedures)..

Within a test team, you will be responsible for testing activities over multiple projects.Beside that you will also advise the product teams with an eye for improvement of quality.

Waarborgen van de stroom van documenten, gerelateerd aan het productieplan..De opslag en archivering van GMP (= good manufacturing practice) documenten & batchgerelateerde records..

Vast Contract – Regio Langemark.#quality #assurance #specialist #food.

Cert.Plast (soon ISO 9001).HSE responsibilities: You are responsible for the practical, executive part of our HSE governance such as issuing work permits, keeping track of incident reports, carrying out job observations, risk analyses, etc.

.Provide testing/ quality advice on product level and report about test results..Execute other automation processes and going beyond your own expertise.

Ervaring met datakwaliteitstools zoals Collibra DQ, Soda, Great Expectations, Informatica CDQ, etc..Kennis van data landschappen binnen een organisatie, begrip van end to end dataflows (van bron tot consument), data architectuur en principes van data engineering/ science..

.Managing batch related documents (issue, review, release and reconciliation)..You perform everything in a manner consistent with safety policies, quality systems and GMP requirements..

Managing batch related documents (issue, review, release and reconciliation)..Issuing and periodically reviewing existing procedures..

GMP cleanroom environment.Job duties are performed within a team according to an assigned, production shift schedule.Reviews documentation for all manufacturing activity execution in accordance with good documentation practices.Independently executes paper/electronic batch record review associated with commercial; development; and engineering production.Performs duties under limited supervision and according to standard operating and manufacturing procedures.Contributes to process improvement of batch records and turnaround times to ensure turnaround times and QA batch disposition deadlines.Collaborates within Manufacturing to resolve batch record discrepancies or errors as it relates to Good Documentation Practices or Manufacturing Execution System (MES) inventory.Implements appropriate corrective and preventive actions by investigating non conformances in a timely manner.Strive to reduce non conformances in supported areas by dedicatedly driving compliance.Perform tasks in a manner consistent with the safety policies; quality systems and c.

Provide exceptional customer service to clients, ensuring their inquiries and concerns are addressed promptly and accurately..Collaborate with cross functional teams, including Sales, Logistics, and Quality Assurance, to ensure seamless order fulfilment..

Nieuwe projecten, en supply chains te verbeteren met focus op.kosten, kwaliteit, logistiek, product en procesontwikkeling,.