11.04.24 | Vollzeit | Schaffhausen | Johnson & JohnsonQuality Control, Logistics, MSAT, Engineering, etc.) in terms of GMP ComplianceParticipate as Subject Matter Expert in Health Authority inspections and auditsSupport and guide more junior AQOs and QA specialists in the teamQualificationsWho are youYou have a Bachelor or Master’s Degree
Später ansehen09.04.24 | Vollzeit | Lachen (SZ) | Estée Lauder AG LachenWill be assigned programs and/or buildings of focus as a member of a campus EHS team. You will also be responsible for collaborating with the operations teams to support current and future business objectives while ensuring compliance with applicable a member of a campus team, the EHS Lead will work
Später ansehen03.04.24 | Vollzeit | Zürich | SWITCHThat applications from candidates and recruiters will only be accepted through our job portal. Unfortunately, applications submitted via email cannot be considered. We appreciate your understanding and thank you for your ere Stellenangebote findest Du /jobsJetzt bewerben
Später ansehen27.03.24 | Vollzeit | Fribourg | JobLeads GmbH | CHF 150’000 - CHF 200’000 To the EMEA FRA function - Strive for excellence in quality, timeliness and compliance of all implemented solutions, ensuring all requirements are met WHAT YOU’LL BRING TO ALCON Education (minimum/desirable) Certified specialist (i.e. Chartered Accountant, CPA) for Finance and Accounting or similar
Später ansehen02.05.24 | Vollzeit | Michael Page InternationalOf CE marking About Our Client Our client is a reference in the medical technology sector Job Description - Directs the preparation and coordination of comprehensive regulatory submissions for Medical Devices, ensuring compliance with local and international regulations and achieving company objectives
Später ansehen02.05.24 | Vollzeit | Vaud | Michael Page InternationalIn QMS improvements and audits - - Ensure regulatory compliance and process optimization - - Cross-functional collaboration and advice to internal teams. The Successful Applicant - Academic background in engineering; - Minimum 3 years of experience within a medical devices company - - Experience
Später ansehen02.05.24 | Vollzeit | Michael Page InternationalOf regulatory submissions (such as IDE, original PMA and supplements)in the context of new product and product changes in accordance with FDA requirements - Coordinate the responses to questions raised by FDA - Review of product labelling - Participate in audits and inspections, ensuring compliance with FDA
Später ansehen02.05.24 | Vollzeit | Michael Page InternationalTo provide change control & documentation control guidance to the European sites - Collaborate in the elaboration of in classroom training materials related to compliance topics (CAPA, audit readiness) - Supports Quality Management system activities, such as CAPA, quality plans and audits - Participates
Später ansehen02.05.24 | Vollzeit | Zürich | Michael Page InternationalFor the firm and its Special Purpose Vehicles (SPVs). - Verify and reconcile accounts, ensuring accuracy and compliance with regulatory standards. - Oversee the preparation and maintenance of legal documentation related to investment activities. - Conduct thorough data collection and analysis to support
Später ansehen02.05.24 | Teilzeit, Vollzeit | Thun, Baar, Fribourg, Sion, Zü | Michael Page InternationalWill be a versatile professional with expertise in various domains including commercial, negotiation, finance, legal and compliance. Your responsibilities will encompass participation in and oversight of third-party commercial activities - International environment - Evolution perspectives Save Job - Zürich Permanent
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