Ervaren 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

Met onze comfortabele cottages, Aqua Mundo, Market Dome en vele activiteiten zorgen we dagelijks voor een onvergetelijke vakantiebeleving. Daar hoort natuurlijk een compleet en verzorgd vakantiehuisje bij. Daarom zijn wij op zoek naar hulpkrachten Logistiek Housekeeping die ons team komen versterken.

Wat ga je concreet doen?

Als hulpkracht Logistiek Housekeeping ondersteun je het logistieke housekeeping team. Jij zorgt er samen met je collega's voor dat onze gasten niets tekortkomen in hun cottage. Je werkzaamheden bestaan onder andere uit:

• Aanvullen, vervangen en verplaatsen van inventaris in de cottages (zoals matrassen, bankkussens, tafels, bestek en pannen);
• Brengen en ophalen van schoon en vuil linnen;
• Ondersteunen van de wasserette (o.a. wassen van gordijnen, kussenhoezen en poetsdoekjes);
• Helpen bij het oplossen van kleine inventaris- en schoonmaakmeldingen.

Wat bieden wij?

• Salaris conform de cao Recreatie, salaris afhankelijk van leeftijd;
  • 21 jaar en ouder: €18,05 per uur (€16,71 excl. vakantiegeld);
  • 20 jaar: €14,44 per uur (€13,37 excl. vakantiegeld);
  • 19 jaar: €10,83 per uur (€10,03 excl. vakantiegeld);
  • 18 jaar: €9,03 per uur (€8,36 excl. vakantiegeld);
  • 17 jaar: €7,13 per uur (€6,60 excl. vakantiegeld);
  • 16 jaar: €6,23 per uur (€5,77 excl. vakantiegeld);
• Een jaarcontract met uitzicht op een vast contract en het gehele jaar door mogelijkheden om in de weekenden en vakanties te werken;
• Reiskostenvergoeding, vanaf 5,5 kilometer enkele reis;
• Een jaarlijks personeelsfeest en kerstborrel en een actieve personeelsvereniging;
• Een enthousiast team van collega's in een gastvrije werkomgeving.

Profiel

• Heb je MBO werk en denk niveau en aantoonbare werkervaring in een vergelijkbare functie;
• Ben je servicegericht en heb je oog voor orde en netheid;
• Ben je in het bezit van eigen vervoer en in het zijn van een rijbewijs B is een pré;
• Ben je flexibel inzetbaar in de ochtenden, middagen en avonden zowel doordeweeks als in het weekend.

Over de vacature

Jouw rol in ons team

Wil jij werken in de ultieme vakantieomgeving en ben jij een geboren zanger(es)? Voor onze live zang avonden zijn wij op zoek naar een entertainer met een goede zangstem.

Jij bent het stralende middelpunt van de vakantie van onze gasten. Als zanger(es) ben jij het gezicht van de avond en neem je de gasten mee in een spetterend optreden.

Wat ga je doen?

• Live muziek: Je zingt tijdens onze live muziek avonden.

Wat bieden wij jou?

• Een contract van minstens 19.5 uur per maand;
• Salaris in schaal 4 van de CAO Recreatie o.b.v. 38 uur (min. €2468,35 en max. €2951,17)
• Reiskostenvergoeding vanaf 5,5 km enkele reis;
• Een gezellig team en veel contact met mensen op het park;
• Een goed inwerktraject met een goede begeleiding van onze praktijkbegeleiders;
• Personeelskorting voor verschillende activiteiten op het park;
• 20% korting bij het boeken van een verblijf bij Center Parcs;
• Een jubileum bon, na iedere 5 dienstjaren, voor een park naar keuze in Nederland, België of Duitsland.

Profiel

• Je barst van de energie, bent spontaan en stapt makkelijk op mensen af (jong én oud);
• Je voelt je als een vis in het water met een microfoon in je hand of op een podium;
• Je hebt ervaring met zang en kunt hiermee aansluiten bij de behoeften van de gasten;
• Uiteindelijk is jouw ongekende enthousiasme en uitstraling voor ons het allerbelangrijkste;
• Je bent flexibel. Omdat we in de vrijetijdssector werken, ben je ook bereid om (in overleg) in de weekenden, tijdens schoolvakanties en op feestdagen te werken;
• Het aanvragen van een VOG vormt geen probleem voor jou.

Enthousiast geworden? Laat deze kans niet schieten en kom ons entertainmentteam op Het Meerdal versterken! Solliciteer direct en wie weet sta jij binnenkort bij ons in de spotlights.

Let op: een casting is onderdeel van de sollicitatieprocedure.

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