Fulltime Vacatures in America

Over de vacature

Vacaturebeschrijving Introductie

Een tuin vanaf de basis opbouwen tot een complete buitenruimte waar de klant jarenlang van geniet: dat is jouw werk als vakbekwaam hovenier aanleg in America. Je realiseert particuliere tuinen waarin beplanting, straatwerk, houtwerk, vijvers en verlichting goed op elkaar aansluiten. Daarbij krijg je ruimte voor eigen inbreng en zie je aan het einde van ieder project precies wat jouw vakmanschap heeft opgeleverd.

Waar ga je werken

Je werkt bij een professioneel hoveniersbedrijf in America dat particuliere tuinen aanlegt. De projecten verschillen in stijl en omvang, maar vragen steeds om een zorgvuldige uitvoering en nette afwerking. Je werkt met een compact team dat tuinontwerpen vertaalt naar complete buitenruimtes. Dankzij het regionale werk, de verschillende projecten en het directe contact met klanten blijft je werk persoonlijk en afwisselend.

Wij bieden

• Een voorgestelde salarisrange van € 2.900 tot € 3.900 bruto per maand, gebaseerd op 40 uur.
• De mogelijkheid om 32 tot 40 uur per week te werken.
• 25 verlofdagen bij een fulltime dienstverband en 8% vakantiegeld.
• Pensioenopbouw vanaf je eerste werkdag.
• Een reiskostenvergoeding volgens de geldende regeling.
• Arbeidsvoorwaarden volgens de Cao Hoveniersbedrijf.
• Jaarrond werk met passende ontwikkel- en doorgroeimogelijkheden.
• Regionale tuinprojecten met ruimte voor jouw vakkennis en praktische ideeën.

Functie-eisen

• Je hebt ervaring met het aanleggen van particuliere tuinen of beschikt over vergelijkbare praktijkkennis.
• Je kunt zelfstandig onderdelen van een compleet tuinproject uitvoeren.
• Je hebt technisch inzicht en werkt nauwkeurig met maten, materialen en afwerking.
• Je bent in het bezit van rijbewijs B.
• Je hebt rijbewijs BE of bent bereid dit via de werkgever te behalen.
• Je communiceert prettig en duidelijk met particuliere klanten en collega's.
• Je werkt collegiaal, proactief en zorgvuldig.
• Je kunt uren en gebruikte materialen correct registreren.

Werkzaamheden

• Bespreek met collega's de planning, het tuinontwerp en de benodigde materialen.
• Bereid particuliere tuinen voor op de aanlegwerkzaamheden.
• Breng beplanting en andere groene onderdelen van de tuin aan.
• Leg terrassen, paden en ander straatwerk nauwkeurig aan.
• Maak en plaats houten onderdelen die binnen het tuinontwerp passen.
• Werk mee aan de aanleg van vijvers en tuinverlichting.
• Stem praktische keuzes en bijzonderheden duidelijk af met de klant.
• Controleer de afwerking en laat iedere tuin netjes achter.
• Registreer de gewerkte uren en gebruikte materialen.

Sollicitaties

Reageer met je contactgegevens en stuur bij voorkeur je cv mee. Een uitgebreide motivatiebrief is niet nodig. Proflex bekijkt je aanlegervaring en neemt contact met je op om de functie en een passende vervolgstap te bespreken. Heb je veel praktijkervaring, maar niet het gevraagde diploma of nog geen rijbewijs BE? Solliciteer dan gerust, zodat we samen kunnen beoordelen of jouw vakkennis aansluit.

Salarisomschrijving

2900.00

Over de vacature

Ben jij een ervaren elektrotechnicus die graag zelfstandig werkt én energie krijgt van afwisselende technische uitdagingen? Wil jij werken in een unieke omgeving waar geen dag hetzelfde is? Dan zijn wij op zoek naar jou!

Jouw werkdag

Als Technisch Specialist ben jij dé specialist op het gebied van elektrotechnische installaties binnen Center Parcs Het Meerdal. Met je elektrische e-car rijd je door het park om storingen te verhelpen, onderhoud uit te voeren en technische vraagstukken op te lossen.

Je werkt in uiteenlopende technische omgevingen, zoals:

• Aqua Mundo
• Market Dome
• Cottages
• Technische gebouwen en installaties
• Infrastructuur en openbare voorzieningen op het park

Samen met je collega's van de Technische Dienst zorg je ervoor dat onze gasten onbezorgd kunnen genieten van hun vakantie.

Wat ga je doen?

• Uitvoeren van preventief en correctief onderhoud aan elektrotechnische installaties.
• Lokaliseren en oplossen van storingen aan elektrische systemen en installaties.
• Verrichten van onderhoudswerkzaamheden aan gebouwen, cottages en recreatieve voorzieningen.
• Uitvoeren van werkzaamheden aan zwembadinstallaties, watervoorzieningen en technische infrastructuur.
• Signaleren van verbeteringen en meedenken over verduurzaming en energiebesparing.

Wat bieden wij jou?

Een contract van +- 38 uur per week (32 of 36 uur is bespreekbaar);

Een superleuke baan;

Een salaris conform de cao Recreatie schaal 6 (min. €2843,46 en max. €3579,71);

Consignatietoeslag;

Een contract van 12 maanden, met uitzicht op een vast contract;

Reiskostenvergoeding vanaf 5,5 km enkele reis;

Een voordeelpas voor jezelf en het hele gezin met flinke kortingen en activiteiten, zoals gratis bowlen en zwemmen;

Een jubileum-bon, na iedere 5 dienstjaren, voor een park naar keuze in Nederland, België of Duitsland;

Een goed inwerktraject en deelname aan diverse trainingen waardoor je jouw talenten blijft ontwikkelen;

Een jaarlijks personeelsfeest, sportdag en kerstborrel;

Een tof team! Gezelligheid verzekerd!

Profiel

• Een afgeronde mbo-opleiding niveau 3 of 4 in de richting van Elektrotechniek;
• Ervaring als onderhoudsmonteur, storingsmonteur of technisch specialist;
• Kennis van elektrotechnische installaties, besturingstechniek en storingsdiagnose;
• Bereidheid om mee te draaien in storingsdiensten;
• Zelfstandigheid, verantwoordelijkheidsgevoel en een gastgerichte instelling;
• Rijbewijs B.

Werken midden in de natuur, zonder files en met elke dag nieuwe technische uitdagingen.

Over de vacature

In onze parken komen mensen samen voor rust, natuur, activiteiten en vakantieplezier. Met het team van Guest Service zijn we er voor hun veiligheid. Overal waar veel mensen bij elkaar zijn, gebeurt wel eens wat. Een kleine diefstal, onenigheid in het zwembad, een reanimatie, een brandmelding. Als beveiliger treed je op met rust en overwicht. Binnen het team helpt iedereen elkaar. Je bent alert tijdens surveillancerondes, begeleidt aankomst en vertrek van gasten, je treedt op bij verstoring van de openbare orde, je verleent EHBO en calamiteiten handel je af als dat kan. Wanneer nodig schakel je politie, ambulance of brandweer in.

Bij Center Parcs heb je meer dan een standaard baan in beveiliging. Je bent ook gastheer/-vrouw en hulpverlener. Gasten kunnen jou dag en nacht aanspreken, bijvoorbeeld als er iets is gebeurd of als er een klacht is. Je staat ze vriendelijk te woord en doet wat er nodig is. Ook heb je veel contact met andere afdelingen op ons park. Goed kunnen communiceren is dus heel belangrijk.

Wat bieden wij:
• Veel plezier, enthousiaste collega's en leuke gasten;
• Salaris conform cao Recreatie functiegroep 6, tussen de 2843 en 3579 Bruto per maand.
• Reiskostentegemoetkoming, vanaf 5.5 kilometer enkele reis;
• Een contract voor fulltime;
• Collectieve zorgverzekering CZ en pensioenregeling.
• Voordeelpas voor jezelf en het hele gezin met flinke kortingen en activiteiten, zoals gratis bowlen en zwemmen;
• Een jubileumbon, na iedere 5 dienstjaren, voor een park naar keuze in Nederland, België of Duitsland;
• Een goed inwerktraject en deelname aan diverse trainingen waardoor je jouw talenten blijft ontwikkelen.

Profiel

• Je hebt minimaal het diploma algemeen beveiligingsbeambte mbo-niveau 2 en bij voorkeur enige ervaring in een soortgelijke functie;
• Je kunt je redelijk uitdrukken in het Engels en Duits en hebt een groot verantwoordelijkheidsgevoel;
• Ook heb je een EHBO- en/of reanimatiediploma of ben je bereid deze te behalen bij ons op het park;
• Je bent in te plannen op alle weekdagen Maandag tot en met Zondag voor dag- en nachtdiensten;
• Bij goed functioneren een contract omzetting naar onbepaalde tijd.

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis

Over de vacature

Overview

In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting. You translate complex regulatory rules into actionable guidance for executives and product teams, helping balance compliance with innovation. You will contribute to a mission-driven environment focused on expanding access to genomic technology and improving health outcomes.

Arbeidsvoorwaarden / Benefits

• bonus or variable compensation
• equity eligibility
• flexible time off
• private medical insurance (UK)
• pension contribution (UK, 10%)
• life moments support and family-friendly policies

Verantwoordelijkheden

• Provide regulatory legal advisory and strategy across EMEA and Latin America for medical devices, diagnostics, and life science products
• Interpret EU and UK medical device and IVD frameworks, country-specific requirements, and horizontal regulations
• Assess regulatory risk and support informed business decisions
• Support product lifecycle activities, submissions, market access strategies, and post-market obligations with Regulatory Affairs and Quality
• Advise on regulatory considerations for hardware, software, services, digital solutions, and AI-related requirements
• Support global and regional product lifecycle management
• Review product labeling, promotions, and external communications for regulatory compliance
• Collaborate with Commercial Legal, Compliance, Procurement, IT, and others to assess regulatory aspects in contracts and tenders
• Assist with inspection readiness, regulatory audits, recalls, field actions, and post-market responses
• Monitor regulatory developments and contribute to internal policies, training materials, and governance
• Coordinate external counsel across jurisdictions as needed

Belangrijkste vereisten

• Qualified lawyer in the UK, the United States, or an EU Member State

• Significant regulatory advisory experience in medical devices, med tech, biotechnology, or life sciences

• Prior in-house and/or law firm experience advising regulatory clients (preferred)

• Full professional fluency in English; additional languages a plus

• Experience supporting business clients in regulated, international environments

• Experience advising on EU and UK medical device and diagnostics frameworks, including IVDR (preferred)

• Experience with post-market vigilance, inspections, and regulatory authority interactions (preferred)

• Experience collaborating with commercial teams on regulated products

• Ability to work across time zones in a global organization

• Clear, confident communication

• Cross-functional collaboration

• Proactive and adaptable mindset

• Regulatory expertise for medical devices, diagnostics, and life sciences

• EU/UK medical device and IVD frameworks (IVDR)

• Regulatory intelligence and trend analysis