CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Mentor Medical Systems (Leiden, Nederland), we are searching for a Validation Engineer - New Equipment.


Keywords

• B.Sc./M.Sc.
• Validation
• Medical Devices
• New equipment

Profile
Do you have experience with the validation of new equipment in a pharma or medical devices environment? Then this is a great opportunity for you!
As Validation Engineer - New Equipment your daily job consists of:

• Being both behind laptop / on the shop floor as well;
• Current process improvements - new processes;
• Writing protocols for validation;
• Connecting with Production and Engineers, part of projects most of time;
• Day to day supporting CAPAS: non-conformances;
• Technical investigation process and equipment;
• Stake holder & relationship management, aligned on ways of working being efficient;
• Focus on patient, risk assessment, work safely and efficient (prioritise).

Who we're looking for
The ideal candidate has a B.Sc. or M.Sc. in a relevant area with 3 to 6 years of Equipment Validation experience preferably in the field of Medical Devices or Pharmaceutical/Healthcare industry. We are looking for someone who takes ownership, is a fast learner and not afraid of jumping in new things getting the information.

Company profile
A Global Leader in Aesthetic Medicine Founded in 1969, Mentor World-wide LLC is a leading supplier of medical products for the global aesthetic medicine market. The Company develops, manufactures, and markets innovative, science-based products for aesthetics markets around the world. Headquartered in Santa Barbara, California, Mentor has manufacturing and research operations in the United States, Mauritius, and the Netherlands. Mentor has made breast implant devices for more than 20 years. Mentor's breast implants are for use in both breast augmentation and breast reconstruction and are of the highest quality, and made under strict standards of design and testing.


Additional vacancy information

Reference	:	A2100025
Contract	:	Temporary contract with CLS Services
Education	:	HBO/BSc. WO/MSc.
Employment terms	:	Project for at least 6 months with intention to extend. Partially onsite, 1 - 2 days per week onsite now rest remote, but after Covid-19 restrictions this role is 100% onsite. Days of leave: 25 + 11 See here our other employment terms for this vacancy
Publication date	:	11-2-2021
Location	:	View location with Google Maps
Contactperson	:	René Kemps
		+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100025). You can also check our other vacancies. You can also follow us on Twitter.

CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for an Analytical Project Manager.


Keywords

• Communication skills
• Immunological assays
• GxP
• Clinical development of vaccines
• Team player

Profile
Do you want to be involved in the immunological evaluation of new vaccines? Do you have experience in immunological assays but you do not want to be in the lab anymore? Then this is a nice opportunity for you!
As Analytical Project Manager, you will assist in the timely and correct sample analysis of clinical samples, either in house or out sourced to CRO’s or partners. For out sourcing, you are responsible for monitoring the sample analysis in out sourced activities. For in house activities, you are responsible for co-ordination of the clinical sample analysis. The required activities must be executed, documented and reported according to Good Clinical Laboratory Practice (GCLP) quality requirements. Additionally, you will be responsible for organising the clinical samples in the Biobank system and will assist in shipments and co-ordination of sample analysis of the clinical studies.


Who we're looking for
The ideal candidate has a B.Sc. (HLO) in biological/medical sciences with some experience in the immunological assays that are performed. Preferably, you have experience with the clinical development of vaccines and/or GxP experience. We are looking for someone who has excellent communication skills and is quality minded. Are you not afraid to show initiative and a great team player? Then we are looking for you!

Company profile
Janssen Vaccines & Prevention B.V. is part of Johnson & Johnson, one of the biggest and most respected health care companies in the world. They are dedicated to bringing meaningful innovation to global health. Their teams focus on the discovery, development, manufacturing, and marketing of novel vaccines to prevent some of the most devastating and complex infectious diseases. These range from respiratory infections like respiratory syncytial virus (RSV) to human immunodeficiency virus (HIV) and pathogens of global concern, such as Ebola and COVID-19.
In this organisation, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are of crucial importance. They are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen. The offices of Janssen Vaccines & Prevention are located in Leiden, The Netherlands.


Department
The Clinical Immunology department is responsible for the immunological evaluation of vaccine candidates in clinical trials. Hereto, the department executes the immunological strategy supporting the clinical development, and ensures the development, and validation of the required immunological assays, as well as the clinical sample analysis. Typical assays to determine the immunogenicity of vaccines are antibody ELISA, T cell ELISpot, Intracellular Cytokine Staining, and virus neutralisation assays.

Additional vacancy information

Reference	:	A2100044
Contract	:	Temporary contract with CLS Services
Education	:	HBO/BSc.
Employment terms	:	Salary: >3085 Days of leave: 25 + 11 Project for at least 1 year See here our other employment terms for this vacancy
Publication date	:	2-3-2021
Location	:	View location with Google Maps
Contactperson	:	Claudia Erwich-Faaij
		+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100044). You can also check our other vacancies. You can also follow us on Twitter.

CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for a Scientist Immunology/Bacteriology.


Keywords

• PhD
• Immunogenicity testing
• Bacterial vaccines
• Assay development
• Certified to work with animal models

Profile
Within the Bacterial Vaccine department, the Immunology group evaluates the immunogenicity and efficacy of potential vaccine candidates against several bacterial diseases in animal models. Assays to examine humoral and cellular immune responses will be developed and used to generate appropriate scientific data to show proof of concept and thereby enabling vaccine candidates to progress towards clinical phase evaluation.
We are looking for a motivated scientist, who loves challenges, to evaluate the immunogenicity and efficacy of potential vaccine candidates. The role requires knowledge of immunological techniques such as ELISA, killing assays, Electrochemiluminescence assays (ECL), B- and T-cell ELISPOT, proliferation assays, cytokine release assays, intracellular cytokine staining, FACS analysis and cell culturing. You will be responsible for the development and implementation of new assays to measure immune responses of various bacterial vaccine candidates. In addition, it is important to have experience with designing and evaluation of pre-clinical in vivo models. You will work in close collaboration with other scientists and technicians in evaluating vaccine candidates. Also some supervision of the work of technicians is anticipated.

Who we're looking for
For this role we are looking for candidates with a Ph.D in biological/medical sciences with a strong immunology/bacteriology background. You are certified to perform Animal experiments (art. 9 or comparable) and you have experience with developing immunological assays like ELISA, FACS and other assays.
You will actively contribute to the discovery and development of bacterial vaccines therefore we are looking for a flexible, motivated team-player with problem solving capabilities. You maintain accurate written records, and organize your data efficiently (e.g. databases).



Company profile
Janssen Vaccines & Prevention B.V. is part of Johnson & Johnson, one of the biggest and most respected health care companies in the world. They are dedicated to bringing meaningful innovation to global health. Their teams focus on the discovery, development, manufacturing, and marketing of novel vaccines to prevent some of the most devastating and complex infectious diseases. These range from respiratory infections like respiratory syncytial virus (RSV) to human immunodeficiency virus (HIV) and pathogens of global concern, such as Ebola and COVID-19.
In this organization, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are of crucial importance. They are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen. The offices of Janssen Vaccines & Prevention are located in Leiden, The Netherlands.


Department
The Bacterial Vaccine department (BacVac) at Janssen Vaccines & Prevention is working on the discovery and early development of novel vaccines for bacterial infectious diseases. This working process includes ‘state of the art’ vaccine discovery, with subsequent in vivo evaluation of vaccine candidates in animal models for immunogenicity and/or efficacy. In addition, manufacturing processes are established and optimized, and the resulting clinical trial material is evaluated in human clinical studies.

Additional vacancy information

Reference	:	A2100030
Contract	:	Temporary contract with CLS Services
Education	:	PhD.
Employment terms	:	Contract for at least one year Salary: > 4200 Days of leave: 25 + 11 See here our other employment terms for this vacancy
Publication date	:	12-2-2021
Location	:	View location with Google Maps
Contactperson	:	Claudia Erwich-Faaij
		+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100030). You can also check our other vacancies. You can also follow us on Twitter.

CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Astellas Pharma Europe B.V. (Leiden, Nederland), we are searching for a Quality Systems Document Control Associate .


Keywords

• Quality Documents
• SOP's
• Excel experience
• Independant worker
• Contact with customers

Profile
In your role as Quality Systems Document Control Associate you are responsible for the development and maintenance of the Quality Management System (QMS) Document Control system supporting Regulatory Affairs, Pharmacovigilance, Development, Medical Affairs, and other functions that utilize the Medical and Development QMS. You will contribute to the development, implementation, and successful execution of the CRQA mission, objectives and 3-5 year strategic plan.
Responsibilities:

• Function as the Quality Document (QD) Administrator responsible for reviewing new or revised Quality Documents for compliance to established standards;
• Ensure all Quality Documents meet required standards before processing documents in the Astellas Document Management System - Quality Document (ADMS QD) workflows;
• Ensure impacted stakeholders are involved in the review of new and revised Quality Documents;
• Deliver effective communication of requirements and standards to Authors of Quality Documents as well as to the Users of the Astellas Document Management System - Quality Document (ADMS QD);
• Support the development, review and delivery of training materials to provide to new users of the ADMS QD system;
• Provide guidance on proper methods for writing SOPs and other Quality Documents to meet standards;
• Support Document Control initiatives that lead to process improvements;
• Respond to email inquiries and user support questions;
• Support ADMS QD users on document retrieval for superseded and obsolete documents as well as completing requests for uploading documents into the ADMS QD Repository.

Who we're looking for
We are looking for an enthusiastic candidate with a Bachelor degree with some experience in the pharmaceutical industry. Preferable, you have experience within Quality Assurance and/or within SOP writing, Process Improvement or similar discipline. You are proficient in working with Microsoft Microsoft Office tools (e.g., Word, Excel, PowerPoint) and PDF editor software (e.g., Adobe Professional, Foxit).
Because of the intercontinetal team, it is important that you are a self-starter and that you can work independantly. Excellent communication skills are a must. You can multitask and shift workload according to the department/team priorities and you have strong planning and organizational skills.

Company profile
Astellas is a Japanese multinational pharmaceutical company employing over 17,000 people worldwide with global sales exceeding 11 billion euro. The group’s EMEA headquarters are based in London, with affiliates throughout Europe engaged in research & development (R&D), manufacturing and sales & marketing. With over 4,500 employees, EMEA is an important and growing Astellas region, having key strengths in the therapy areas of Urology, Transplantation, Anti Infectives, Pain Management and Oncology. The global annual R&D investment of 15% to 20% of sales is evidence of the group’s commitment to improving the health of people worldwide through the provision of innovative and reliable products. Astellas employs around 950 persons in the Netherlands, in Leiden and Meppel.


Additional vacancy information

Reference	:	A2100040
Contract	:	Temporary contract with CLS Services
Education	:	HBO/BSc.
Employment terms	:	Salary: max 2700 Days of leave: 25 + 13 See here our other employment terms for this vacancy
Publication date	:	24-2-2021
Location	:	View location with Google Maps
Contactperson	:	Aniek Vugts
		+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100040). You can also check our other vacancies. You can also follow us on Twitter.

NofaGroup maakt deel uit van de Cotecna Group, een internationale organisatie die diensten levert op het gebied van analyse, inspecties en certificering.

Het netwerk van Cotecna bestaat uit meer dan 100 kantoren in meer dan 60 landen, met een personeelsbestand van bijna 4.000 werknemers. Als een lang bestaande speler van wereldklasse combineert Cotecna professionaliteit, betrouwbaarheid, infrastructuur en expertise met de flexibiliteit en nabijheid van een kleiner bedrijf.

 

NofaGroup is holdingmaatschappij van een aantal toonaangevende entiteiten op het gebied van inspecties, controlewerkzaamheden, bemonstering en analyses in zowel food, feed en environmental safety.

Doelgerichtheid en deskundigheid in combinatie met een grote betrokkenheid van alle medewerkers kenmerken het bedrijf. Binnen ons bedrijf zijn de lijnen kort en er is volop ruimte om flexibel en slagvaardig te werken. Om de gerealiseerde groei te continueren is er binnen het team ruimte voor een Manager QESH (Quality, Environment, Safety and Health).

 

Als Manager QESH rapporteer je direct aan de CEO en maak je deel uit van het operationeel managementteam. Je bent samen met jouw team verantwoordelijk voor een de implementatie en werking van het QESH-managementsysteem binnen NofaGroup.

Je bent nauw betrokken bij de werkzaamheden van het laboratorium en je werkt samen met collega’s en klanten om het kwaliteitsniveau continu te verbeteren.

 

Jouw hoofdtaken bestaan uit:

• Leiding geven aan jouw team met medewerkers;
• Ontwikkelen, implementeren en evalueren van het QESH-beleid, conform wettelijke verplichtingen, normeisen en interne doelstellingen;
• Zorg voor een goede werking van het QESH-managementsysteem, het evalueren en herzien van bestaande procedures en documenten en het ontwikkelen en implementeren van nieuwe procedures en documenten;
• Formuleren van verbeteracties ten aanzien van kwaliteit en/of veiligheid;
• Het interpreteren en verwerken van resultaten uit controles;
• Het plannen, organiseren en uitvoeren van interne audits;
• Eerste aanspreekpunt voor alle accreditatie- en certificatie-instellingen voor het hele bedrijf;
• Het ondersteunen en begeleiden van externe audits en beoordelingen van klanten en accreditatie-instellingen;
• Interne communicatie ten aanzien van relevante QESH-onderwerpen in de gehele organisatie;
• Externe communicatie aan stakeholders;
• Het adviseren van het management met betrekking tot de door het bedrijf gestelde normen; het bijhouden van relevante wetgeving en de interpretatie daarvan;

 

Functie-eisen

• Hogere opleiding in het chemisch-analytisch vakgebied (HLO) of daaraan gelijkgestelde opleiding(en);
• Opleiding(en) op het gebied van kwaliteitsmanagement;
• Minimaal 3 jaar relevante werkervaring bij voorkeur in een commerciële laboratoriumomgeving;
• Ervaring met normeisen (NEN-EN-ISO 17025, 9001, GMP+ etc.) is een pré;
• Goede mondelinge en schriftelijke taalbeheersing in de Nederlandse en Engelse taal;
• Goede kennis van MS-Office en andere functiegerichte applicaties;
• Hands-on en service verlenende mind set aan zowel derden als collega’s.

 

Competenties

• Je beschikt over goede communicatieve en administratieve vaardigheden
• Je denkt in oplossingen met een positieve mind-set
• Je kunt snel schakelen en behoudt daarbij het overzicht
• Je hebt leidinggevende capaciteiten

Aanbod

NofaGroup biedt een uitdagende functie binnen een organisatie met ambitie. Je maakt deel uit van een klein, gemotiveerd en slagvaardig team, waarbij je de ruimte krijgt voor het inbrengen van ideeën en je ambities waar te maken. In overleg behoort doorgroeien binnen de organisatie tot de mogelijkheden. Wij bieden arbeidsvoorwaarden passend bij de inhoud van de functie.

 

Reageren

Ben je nieuwsgierig naar de functie en wil je aanvullende informatie of solliciteren? Mail dan je sollicitatiebrief met een actueel CV naar

saskia.dahlhaus@cotecna.com

.

CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Janssen Vaccines & Prevention (Leiden, Nederland), we are searching for a Scientist Analytical Development - Biophysics and Process Analytics.


Keywords

• Ph.D.
• Biochemistry/Biophysics/Protein Chemistry
• Bioanalytics
• Outside the box

Profile
We are looking for a motivated person who enjoys working in a multidisciplinary team. You will be managing, designing and executing biochemistry and biophysics experiments and analysing biochemical and biophysical data as well as communicating actively with stake holders. Further responsibilities include instrument maintenance, troubleshooting, written reporting and oral presentations in various settings.

Who we're looking for
The ideal candidate has a Ph.D. in Biochemistry, Biophysics and/or Protein chemistry with a proven track record in biophysical and biochemical analytics and/or process analytics technologies.
You are science minded, flexible and dynamic in approaches and have a proven and robust theoretical and experimental track record in the field of bioanalytics with comprehensive hands-on experience with techniques such as: UV-VIS, fluorescence and circular dichroism and/or FTIR spectroscopy, multi-angle and dynamic light scattering (DLS), capillary isoelectric focusing, electrophoresis, isothermal and differential scanning calorimetry, biomolecular interactions (ex. Octet, ELISA, MSD, AlphaLISA and/or others), mass spectrometry, atomic force and/or electron microscopy. Experience in early analytical development and/or process analytics technologies is a plus.
We are looking for someone who is flexible and likes to think outside the box. You are keen to explore new technologies and to share your own experience and knowledge. Are you the team player with excellent communication skills we are looking for?

Company profile
Janssen Vaccines & Prevention B.V. is part of Johnson & Johnson, one of the biggest and most respected health care companies in the world. They are dedicated to bringing meaningful innovation to global health. Their teams focus on the discovery, development, manufacturing, and marketing of novel vaccines to prevent some of the most devastating and complex infectious diseases. These range from respiratory infections like respiratory syncytial virus (RSV) to human immunodeficiency virus (HIV) and pathogens of global concern, such as Ebola and COVID-19.
In this organisation, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are of crucial importance. They are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen. The offices of Janssen Vaccines & Prevention are located in Leiden, The Netherlands.


Department
The Biophysics and Process Analytics (BPA) team is a young and dynamic group (35 team members), which is part of Analytical Development (AD), responsible for a range of activities focused on biophysical and analytical vaccine characterisation. Their responsibilities include project bridging and transfer from late discovery to development, analytical support for process development, scouting exploration and implementation of novel analytical technologies.

Additional vacancy information

Reference	:	A2100046
Contract	:	Temporary contract with CLS Services
Education	:	PhD.
Employment terms	:	Salary: >4243 Days of leave: 25 + 11 Project for at least 1 year See here our other employment terms for this vacancy
Publication date	:	2-3-2021
Location	:	View location with Google Maps
Contactperson	:	Claudia Erwich-Faaij
		+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100046). You can also check our other vacancies. You can also follow us on Twitter.

CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Astellas Pharma Europe B.V. (Leiden, Nederland), we are searching for a RA Coordinator.


Keywords

• Regulatory Affairs
• Pharmaceutical experience
• International market
• Strategy development

Profile
As part of a Global Project, you will act as a Regulatory Affairs Project Coordinator. Driven by Commercial having an impact on the registered portfolio in Astellas International Markets. The markets include 47 countries across Latin America, Middle-East Africa, Russia-CIS, and Asia
Main Tasks:

• Develop the regulatory strategy and planning to support the commercial strategy in the selected countries, which may imply MA discontinuation and/or implementation of alternative access models when applicable;
• Coordinate its execution in collaboration with other functions (incl. Commercial, Supply Chain, QA, PV, Medical Affairs, Legal) and in line with Astellas SOPs.

Who we're looking for
The ideal candidate has at least a bachelor’s degree in scientific discipline and at least 5-8 years previous experience with regulatory affairs in the pharmaceutical industry, preferably with International Markets. You have strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to internal stakeholders and others in the department as needed. Project leader experience is required.
Other requirements:

• Excellent communication and writing skills (advise, convince, negotiate, listen, present and edit);
• Ability to communicate effectively with cultural awareness and sensitivity and maintain effective working relationships;
• Experience in working in multidisciplinary teams;
• High integrity with respect to maintenance of proprietary, confidential information;
• Fluent in English, both spoken and written.

Company profile
Astellas is a Japanese multinational pharmaceutical company employing over 17,000 people worldwide with global sales exceeding 11 billion euro. The group’s EMEA headquarters are based in London, with affiliates throughout Europe engaged in research & development (R&D), manufacturing and sales & marketing. With over 4,500 employees, EMEA is an important and growing Astellas region, having key strengths in the therapy areas of Urology, Transplantation, Anti Infectives, Pain Management and Oncology. The global annual R&D investment of 15% to 20% of sales is evidence of the group’s commitment to improving the health of people worldwide through the provision of innovative and reliable products. Astellas employs around 950 persons in the Netherlands, in Leiden and Meppel.


Additional vacancy information

Reference	:	A2100043
Contract	:	Temporary contract with CLS Services
Education	:	HBO/BSc.
Employment terms	:	Contract for 3 - 4 days per week Salary: >5500 Days of leave: 25 + 13 See here our other employment terms for this vacancy
Publication date	:	1-3-2021
Location	:	View location with Google Maps
Contactperson	:	Aniek Vugts
		+31 (0)31 (0)88 22 77 555

Apply
Please apply online here for this job (Job Ref: A2100043). You can also check our other vacancies. You can also follow us on Twitter.

Sales Executive Health/ Beauty wereld
Wat ga je doen?
Als Sales Executive/Accountmanager in de beauty wereld vertegenwoordig je biologische health care producten van hoge kwaliteit. Het zuid/westen van Nederland neem jij volledig tot je regio en ga je retailers (drogisterijen, natuurwinkels etc. ) bezoeken en benaderen om jouw product voor te stellen en te adviseren. Daarbij ben je als zelfstandige Sales Executive volledig verantwoordelijk voor het hele proces van A tot Z. Je bent creatief en ambitieus met als doel, het verkopen van je producten via allerlei kanalen. Met deze job krijg jij veel vrijheid om je sales skills volledig in te zetten en daarbij trainingen te volgen op het hoofdkantoor, waar je vervolgens ook regelmatig gaat sparren/rapporteren met je sales team. Ben jij een duizendpoot en ondernemend ingesteld? Waar wacht je dan nog op!
Wat wordt jou geboden?
* Een aantrekkelijk salaris tussen de €45K - €55K
* Geweldige kortingen op producten voor eigen gebruik
* Een leuk team met veel vrijheid en ruimte voor creativiteit
* Auto, Home-office
* 25 Vakantiedagen met pensioenopbouw
Wat wordt er van jou verwacht?
* 5+ jaar werkervaring in de beauty/ health sector
* HBO werk/ denk niveau
* Je spreekt vloeiend Nederlands
* Je bent woonachtig in de regio Den-Haag/ Rotterdam
* Je hebt een representatief voorkomen en daarbij ben je gedreven in het behalen van je targets
Waar ga je werken?
Je gaat werken voor een leuk familiebedrijf die al jarenlang in de business zit van de health en beauty sector in het zuiden van Nederland. Het bedrijf is gespecialiseerd in biologische homeopathische producten. Zelf zijn ze distributeur van verschillende merken nationaal/ internationaal en hebben daarbij ook een eigen healthcare lijn ontwikkeld. Je gaat werken in een sales team van ongeveer 10 man. De familiare sfeer is erg belangrijk in het bedrijf, dus worden er ook regelmatig leuke uitjes georganiseerd voor de juiste teamspirit!
Meer informatie of direct solliciteren?
Klik op de knop "Solliciteer op deze vacature'' om direct te solliciteren. Mocht je informatie over de vacature of werkzaamheden hebben, voel je dan vrij om contact met mij op te nemen via barbara.doganay@samrecruitment.nl. Mocht je zelf niet geïnteresseerd zijn, maar je kent wel dé persoon voor deze functie laat ons dan wat weten want wij stellen hier bijzondere beloningen tegenover. Kijk op onze website bij "Recommend a friend'' voor meer informatie.
Locatie:
Standplaats; Rotterdam. Buitendienst.
Contactpersoon:
Barbara Doganay
Recruitment Consultant
Gespecialiseerd in Sales FMCG Professionals
+31 20570 8120
barbara.doganay@samrecruitment.nl

Zoek jij een nieuwe uitdaging als Health & Safety Engineer? Voor onze opdrachtgever in Den Haag zijn wij op zoek naar een Health & Safety Engineer voor 40 uur in de week. Als H&S Engineer ga jij aan de slag om de veiligheid binnen de bedrijfsprocessen te waarborgen. Je wordt ingezet voor twee projecten waarbij je heen en weer beweegt tussen Den Haag, Amsterdam en Nieuwegein. Wat ga je doen? Bieden van ondersteuning in de implementatie van het Health & Safety beleid en procedures Opleiden en aansturen van medewerkers op het gebied van nieuwe werkmethoden, procedures en instructies Zorgen dat de organisatie voldoet aan de Nederlandse wettelijke vereisten voor de Health & Safety Rapporteren en afhandelen van mogelijke ongevallen die optreden Voorbereiden van de veiligheidsrapporten en het regelmatig uitvoeren van geplande inspecties op de werkplek Zorg ervoor dat alle medewerkers en stakeholders werken via de H&S standaarden Bezoeken van depots waarbij je ervoor zorgt dat de H&S procedures worden nageleefd Assisteren in het ontwikkelen van de bedrijfsdoelstellingen a.d.h.v. trend analyses Periodiek rapporteren aan het hoofdkantoor in Spanje Jouw profiel Je beschikt over een HBO opleiding Engineering Je hebt minimaal 3 jaar ervaring als Health & Safety Engineer in een technische omgeving. Je spreekt vloeiend Nederlands én Engels, zowel in woord als geschrift. Bij voorkeur heb je kennis over de Franse en/of Spaanse taal Je hebt ervaring met OHSAS 18001 Je bent in staat prioriteiten te stellen en georganiseerd te werk te gaan Je kunt communiceren binnen een multinational waar veel cultuur diversiteit is Je hebt kennis van Health & Safety management systemen en wettelijke reguleringen in Nederland Je bent standvastig, kritisch, analytisch en stressbestendig Je bent bereid te werken op verschillende locaties Als Health & Safety Engineer kom je te werken bij een grote speler in het ontwerp, productie en onderhoud van rollend materiaal. Onze opdrachtgever is producent van 118 nieuwe Sprinters en zo’n 100 nieuwe trams in Nederland. Wereldwijd werken 8000 mensen verspreid over 33 landen. Wat jij kunt verwachten: Dynamische werkomgeving Marktconform salaris met 27 vakantiedagen en 13 roostervrije dagen Een laptop en telefoon Eventuele bedrijfsbezoeken in het buitenland Flinke dosis uitdaging binnen jouw functie! Word jij enthousiast van deze functie als Health & Safety Engineer? Mail dan je CV in het Engels met motivatie naar werken@werktech.nl Heb je vragen of opmerkingen over deze vacature? Laat het ons weten