Uitdagende en veelzijdige kwaliteitsfunctie...

Onze opdrachtgever produceert en exporteert een breed assortiment geneesmiddelen voor patiënten over de hele wereld. Vanuit de ‘state of the art’ productielocaties in Amsterdam en Brussel bereiden zij een breed scala aan geneesmiddelen uit bloedplasma. De productie vindt plaats onder de hoogste veiligheidseisen. Deze medicijnen worden gebruikt voor een groot aantal aandoeningen, waarvan vele levensbedreigend zijn. Daarnaast stellen zij kennis en infrastructuur ter beschikking van diverse partner...

In de rol van QA Project Specialist ben je direct verantwoordelijk voor het uitvoeren van change control projecten. Je draagt zorg voor het borgen van Master Data door het beheren van het data management kwaliteitssysteem. Je participeert in projecten en change controle trajecten, daarbij vertegenwoordig je de afdeling op het gebied van validatie vereisten. Ook zorg je dat de strategieën en vereisten adequaat zijn vertaald in aanpassingen in documenten voor processen en systemen en begeleidt de ...

• afgeronde hbo- of wo-opleiding; • minimaal 2 jaar werkervaring in een QA functie binnen een cGMP werkomgeving; • aantoonbare kennis en ervaring met validatie en testmethoden; • zelfstandig, communicatief vaardig en sociaal; • goede beheersing van de Engelse taal in woord en geschrift; • kwaliteitsbewust, stressbestendig en secuur. ...

Challenging Management Team role within an international and fast growing organization....

Or client, Pivot Park Screening Centre, is an organization specialized in the scientific research. They provide highly regarded screening assessments and research programs. Their long-standing experience in an early drug discovery and state-of-art High Troughput Screening infrastructure provides their partners with the best confirmed leads. The High Troughput Screening (HTS) is a widely applied approach to find starting points for the development of new medicines. The organization are continuous...

The purpose of this position is to develop and implement an international growth strategy for the organization. Based on facts, data and analyses, you formulate a strategic plan in which you are not only responsible for the drafting, but also for implementation. The Global Business Development Director will also segment the market and focus in particular on the opportunities offered by Asia (Japan) and United States. The Global Business Development Director is responsible for managing and develo...

• university degree or higher with a preference for a Phd, Pharmacy, biology or chemical background • a minimum of 7 years of experience within an international sales position • knowledge off, affinity with and understanding of the pharmaceutical R&D field • a network in the Asian or American pharmaceutical market is recommended • demonstratable acquisition results, excellent negotiation skills, data-driven and market-oriented • strong conceptual capacity to translate organizational develop...

Challenging position within an inspiring, inclusive and respectful working environment...

The organization produces and exports a broad range of pharmaceuticals for patients throughout the world. At their production sites in Amsterdam and Brussels, they prepare a broad range of medicines derived from blood plasma. These products are used for a large number of disorders, many of which life-threatening. This position will be part of the QC Support team which is one of the two QC departments within the organization. These teams support QC operations with validation, maintenance and ca...

Our client is looking for an experienced QC Senior Systems Officer with knowledge about laboratory Information Management Systems (LIMS) to support the QC Support Equipment, Facility and Systems team in the build and introduction of the new LIMS system. You will build different parts of the LIMS system and will be involved in building different systems- and instrument interfaces. Furthermore, you are responsible for gathering the systems requirements and you will review required validation docum...

• preferably HBO with at least 5 years of experience in a Pharmaceutical laboratory and cGMP environment • familiar with Pharmaceutical QC testing • broad knowledge in LIMS-, ELN, SDMS Systems • experience with Business Analyses, Infrastructure, Software, Database, Software Systems Architecture • broad experience with equipment validation guidelines and rules • good communication and negotiation skills to operate in multidisciplinary teams • stress resistant, flexible, independent, pro-act...

Challenging role within the Market Access & Corporate Affairs Department ...

Our client is a leading biotech organisation that discovers, develops and delivers therapies to improve the lives of patients. They offer therapies for neurological diseases, globally, through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. The atmosphere is very open and accessible. This is also reflected in the mutual cooperation, along with their key focus on professionalism and a drive to accomplish the best results for the so...

As Sr. Manager Market Access you will lead the payer related activities for the organizationals Neuroscience (Alzheimer and a larger scope within their neuroscience pipeline) products in the Netherlands. You will be working in close collaboration with the local medical team in addition to global Value & Access teams to develop and execute the local market access strategy. Your key responsibilities in this role encompass leading the preparation of the market to enable a successful launch of new p...

• M.Sc. with a strong preference for the field of Health Economics or Pharmacy • +5 years or relevant experience required (in market access, governmental affairs management, public affairs) • experience in direct interaction with the external stakeholders (Zorginstituut etc.) and proven track record of access succession is a must have • experience in a cross-functional position • knowledge of NL healthcare legislation • used to travelling, working independently and planning of own time and ...

Project Manager QA Food (hbo/wo)...

Normec Quality Assurance is onderdeel van Normec Foodcare, een allround dienstverlener en nummer één kennispartner op het gebied van kwaliteit en voedselveiligheid. Normec Quality Assurance begeleidt klanten bij vraagstukken over voedsel- en productveiligheid, kwaliteitsmanagement en duurzaamheid.

Normec kenmerkt zich in een open en informele sfeer waar jij van toegevoegde waarde bent. Er is veel kennis en expertise binnen handbereik, waardoor jij de mogelijkheid krijgt om veel kenni...

Jij werkt voor de klant die je optimaal ondersteunt, begeleidt en ontzorgt bij allerlei vraagstukken omtrent kwaliteit en voedselveiligheid. Jouw klanten zijn verschillende levensmiddelenproducenten, handelsbedrijven en transporteurs in jouw regio.

Samen met de klant bepaal je de kwaliteits- en voedselveiligheidsdoelstellingen en voer je deze uit. De opdrachten en klanten zijn elke keer weer anders, net als je eigen functie binnen een bedrijf. Zo kan het zijn dat je de ene dag bij ee...

Wij zoeken voor Normec Quality Assurance een Project Manager QA die voor de klant waarde creëert door de beste en persoonlijke zorg te regelen in kwaliteit en voedselveiligheid.

Verder van belang voor deze vacature:

• Je bent in het bezit van een HBO/WO Voedingsmiddelentechnologie, Food & Business of vergelijkbare opleiding
• Je beschikt over QA-werkervaring als QA medewerker/manager of kwaliteitsmedewerker binnen de levensmiddelenproductie. Hierdoor heb je ervaring in het...

Diverse position for an experienced technician in the field of development and transfer of cellular assays and binding assays within a growing biotech company. ...

This job is at a fast growing biotech company with strong focus on research and development. There is a high level of expertise, and everyone is very motivated to contribute to creating the best products available on the market. The environment is driven and challenging and therefore very motivating.

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You will join a team that works on development and execution of bioassays. The team works on several projects simultaneously and therefore your job will also be varied. The main focus of this job we be on several laboratory tasks, including culturing of mammalian cells, binding assays (ELISA a.o.) and functional cell assays. Depending on your experience your focus will be either on execution of the assays or development and transfer of the assays. Additional tasks will be the writing of proto...

We are looking for candidates who can check the following boxes:

• MSc or HLO degree in the life science or biotech field
• Several years of laboratory experience, preferably within a company or CRO
• At least 2 years of experience with cell culture, binding assays (f.i. ELISA) and functional cell assays
• Assay development experience is a plus
• GLP and/or GMP experience is a plus
• Ambition to develop yourself and grow into a specialist rol...

Voor een organisatie in de voedingsmiddelenindustrie, in de omgeving van Geldermalsen, is Morgan Green op zoek naar een QA Officer. Ben jij ijzersterk in communicatie, en denk jij graag mee over verbeterprocessen binnen de organisatie? Dan kom ik graag in contact om de functie verder te bespreken!

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Voor een organisatie in de voedingsmiddelenindustrie, in de omgeving van Geldermalsen, is Morgan Green op zoek naar een QA Officer. Ben jij ijzersterk in communicatie, en denk jij graag mee over verbeterprocessen binnen de organisatie? Dan kom ik graag in contact om de functie verder te bespreken! ...

QA...

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Heb je interesse in de functie of wil je andere mogelijkheden bespreken? Neem dan contact op met Carlos da Silva via 020-7979825 of druk op de sollicitatieknop hieronder

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Werken bij Cargill is een kans om te ontwikkelen en te groeien—een plek om uw carrière optimaal te ontwikkelen terwijl u zich bezighoudt met zinvol werk dat een positief effect heeft over de hele wereld....

U zult er trots op zijn om voor een bedrijf te werken dat bekend staat om zijn ethische waarden en zich inzet voor het voeden van mensen. We bieden een afwisselende, ondersteunende omgeving waar u zowel persoonlijk als professioneel zult groeien terwijl u leert van een aantal van de meest getalenteerde mensen in uw vakgebied. Cargill heeft meer dan 150 jaar ervaring met het leveren van voedings-, landbouw-, financiële en industriële producten en diensten aan de wereld. We hebben 160.00 werknemer...

Omschrijving Primary job location: Minneapolis, USA Other location(s): Schiphol, Netherlands; Mechelen, Belgium Description Are you motivated by providing expert consultation on how to best utilize service delivery enabling technologies and always keep the end client in mind when proposing solutions? Are you interested to join a dynamic global team who focuses on modernizing HR service delivery and is eager to continue to increase utilization of our direct access technologies? We aim...

Kwalificaties Bachelor’s Degree in related field 5+ years of consulting experience in the request management or customer relationship management space Strong technical, HR, and consulting skills as well as ability to translate HR needs to technical capabilities Demonstrated application of request management/ ticket management principles and practices Experience answering product feature and technical questions from clients and designing and managing global processes ...

Our Culture of Ownership, Meritocracy and Collaboration We’re not afraid to think differently. Embrace new ideas. Dream big. It all comes down to the way we empower our people to own their work. It’s true Our employees are our competitive advantage. As part of the Kraft Heinz family you’re supported to grow and achieve. You’re recognized and rewarded for outstanding performance at every level. You’re given the opportunity to leave your mark and build legacies. But you won’t do it alone. T...

As one of the world’s largest food and beverage companies, we are proud to spark joy around mealtimes with a global portfolio of more than 200 brands. Some are iconic brands like Philadelphia Cream Cheese, Kraft Peanut Butter, Kraft Dinner and Heinz Ketchup. Others are fast growing new sensations that defy status quo like CRAVE. No matter the brand, we are united under one vision To Be the Best Food Company, Growing a Better World. Bringing this vision to life are our 36,000+ teammates around t...

As HR Business Partner Central Operations (HRBP) at the Kraft Heinz Company you will partner with the International Operations department to drive the talent agenda. You will advise and partner with dynamic and high performing leaders to help attract, engage and grow people. All our decisions are based on data analytics. Therefor a data-driven mindset will be key to your success. You'll be reporting into the Head of People & Performance Central Operations International. What you will do in sh...

Qualifications “Please kindly note that you need to have an EU Working Permit (Orientation Year Visa not included) in order to proceed for this position.” Bachelor or Master degree; 5 - 7 years of 360 degree HR working experience and/or background in consultancy; Fluency in English; Proven track record of delivering consistent results; Professional Attributes We're looking for someone who is a functional leader to the team and is able to build and maintain close relationships with d...

The Director, Clinical Project Scientist develops and drives the goals and activities of Clinical Research department such as designing, planning, developing and monitoring of clinical evaluation projects. ...

(geen informatie)

nterprets research results and evaluates the safety, marketability and medical usefulness of drug and product candidates. Responsible for the compliance of department, company and regulatory standards and procedures. Primary Responsibilities: Executes clinical research strategies and contributes to the development and execution of clinical research programs. Directs study design, protocol development and implementation of clinical studies. Defines clinical study paramet...

REQUIREMENTS Bachelor’s degree required. An advanced degree (MS, MSN, RN, PharmD, PhD) preferred. A minimum of 6 years of progressively responsible experience in clinical research and development, or related experience within the industry (pharmaceutical, biotech, CRO, etc.) is required. Experience in oncology therapeutic area is required. Significant experience with clinical trials including development of protocols, case report forms, informed consent, study initiation, p...