Uitdagende baan waarin je je innovatieve en baanbrekende visie op de gezondheidszorg in Nederland los mag laten en veranderprocessen bij Zilveren Kruis mag aansturen. ...

Zilveren Kruis bouwt aan de toekomst van de gezondheidszorg in Nederland. Zij zetten veranderingen in gang om de zorg in ons land op hoog niveau te houden. De collega’s van Visie & Innovatie bij Zorginkoop werken bevlogen en vanuit overtuiging aan deze (regionale) zorgtransformatie. Als manager geef je deze verandering mede vorm. De uitdagingen om zorg betaalbaar en kwalitatief te houden zijn groot. We worden met z’n allen steeds ouder waardoor de zorgvraag stijgt. Tegelijk is er een blijvend pe...

In deze functie geef je leiding aan een team van 16 medisch en zorginhoudelijk adviseurs, innovatie adviseurs, analisten en beleidsadviseurs. Het team ontwikkelt visie en strategie voor uiteenlopende onderwerpen. Onderwerpen die breder zijn dan een zorgsoort of die nieuw zijn. Zoals een landelijke strategie voor het strategisch thema Zorg Veilig Thuis. Een speerpunt waarmee Zilveren Kruis en haar klanten online zorg en telemonitoring opschalen. Ook ontwikkelt het team inkoopstrategieën voor vers...

• wo werk- en denkniveau ; • minimaal 8 jaar managementervaring; • conceptueel sterke verbinder met coachende vaardigheden; • ervaring met het succesvol aansturen van veranderprocessen; • ervaring met innovatieve projecten op het vlak van E-health en digitalisering; • ervaring met Lean en/of Agile werken. ...

Challenging position in a hardworking pharmaceutical packaging organization(Etten-Leur, the Netherlands)...

Our client is a pharmaceutical packaging organization, that is dedicated to shaping the future of the pharmaceutical Supply Chain to be safer and more reliable for their customers and patients. They have over 30 years of experience that they use to offer flexible packaging and Supply Chain services. They use the latest technologies to improve the manufacturing packaging process every day. Currently this organisation is looking for a Product Specification Manager who will lead the quality-centere...

As Product Specification Manager you will be responsible for the implementation of multiple new customers and products (SKUs) per year. Furthermore you will optimize and automate data & artwork processes and you will contribute to the success of strategic quality projects. You will be working with multiple systems and applications, including BarTender, Docuboxx, and InDesign. Your main working tool will be Veratrak – a blockchain-based tool through which communication with the customers is manag...

• Bachelors degree in a technical or scientific subject. • Demonstrated experience with leading teams and individuals towards growth, professional success and personal improvement. • Experience with analyzing data in optimization projects. • Lean Six Sigma black belt or equivalent experience. • Familiarity and experience with cGMP/cGDP. • Experience with Docuboxx, InDesign and BarTender is an advantage. • Good with planning, scheduling and monitoring work to meet time and quality targets. ...

Temporary senior position for four months at the Global Pharmacovigilance Process Department (Leiden, the Netherlands) ...

The organisation is an international pharmaceutical organisation that has been operating in over 40 countries across Europe, the middle east and Africa. They operate on a global level and most of the teams have a global focus. They do everything in-house: Research, Development, Manufacturing, Warehousing and also Sales and Marketing. It is their hope to change tomorrow’s world and to improve the lives of individuals by providing innovative medicines where there is urgent need for better treatmen...

In the role of Senior Data Assurance Officer you will be responsible for the maintenance of excellency in Regional Process Data Assurance and Medical Consistency. Thereby, you will be responsible for the implementation and execution of various QC measures in ICSR processing, which will contribute to the successful implementation of Regional Pharmacovigilance Process Management goals and objectives. Furthermore, you will ensure that the quality of contracted work is delivered to the Global Pharm...

• Master degree in Life Sciences or equivalent. • Five years of relevant experience. • In-depth knowledge and understanding of PV Process regulatory requirements and ICSR processing procedures both globally and in the assigned region. • Technical expert who has the ability to recommend enhancements to internal policies, processes and procedures based on new requirements and legislation. • Able to maintain case processing and case quality at the highest standards at all times. • Ability to ...

Strategical and high-profile position within an ambitious biopharmaceutical company...

Our client is a research-based biopharmaceutical company with 17 marketed products, a pipeline of late stage drug candidates and patient access programs to ensure medications are available to those who could otherwise not afford them. Their product portfolio consists of products for HIV, Hepatitis, Oncology and Anti-fungal. You will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. By joining this client, you will become part of th...

As Associate Marketing Director HIV you will be responsible for the product marketing of the HIV portfolio. This means that you develop the brand strategy and actions plans for this product. You will partner with Medical Affairs, Government and Public Affairs to ensure effective development and implementation of strategies. Furthermore, you will be leading the promotion review committee process to ensure marketing materials are cleared for promotional use and develop effective working relationsh...

• a Master of Science preferably in Marketing, Health Economics or another relevant field • experience with marketing, product management or brand management in the pharmaceutical industry • demonstrated track record of successful product launches or sustained commercial growth • in-depth ability to work with external agencies including advertising, public relations and medical education vendors to develop programs and materials required • strong analytical skills • driven and proactive • ...

Dé ideale instapfunctie als apotheker in de farmaceutische industrie (Flevoland, Nederland) ...

Onze opdrachtgever levert als onafhankelijke en groeiende onderneming farmaceutisch maatwerk voor specifieke patiëntenbehoeften waardoor er zorg wordt gedragen voor een doelmatige geneesmiddelenvoorziening. Zij zetten zich in om geneesmiddelen met een medische noodzaak beschikbaar te maken en beschikbaar te houden. Dit zijn in bepaalde gevallen geneesmiddelen die voor een specifieke patiëntengroep of indicatie onmisbaar zijn. Op locatie ontwikkelt, produceert en registreert onze opdrachtgever ha...

Als Trainee word je gedurende het eerste jaar van je loopbaan bij allerlei uitdagende en leerzame trajecten betrokken. Je bent verantwoordelijk voor diverse projecten en opdrachten voor verschillende afdelingen. Denk hierbij aan bijvoorbeeld projecten als productie apotheker, RA/QA, beoordelen van bereidingsprotocollen etc.. Verder een unieke kans om alle productieprocessen te leren kennen (vast, vloeibaar, steriel, aseptisch en verpakken). Hierdoor heb je de mogelijkheid om brede kennis en erva...

• afgeronde MSc opleiding farmacie; • maximaal drie jaar werkervaring binnen de farmaceutische sector; • sterke communicatieve vaaridgheden en uistekend kunnen samenwerken; • hebben van een ‘can-do mentaliteit’; • pragmatisch, flexibel, out-of-the-box denken, probleemoplossen, zelfstarter, aanpakker; • ambitieus, leergierig, openstaan voor nieuwe ervaringen. ...

A temporary Quality position as Senior QA Officer at a large pharmaceutical company until September 2021...

Our client is a world leader in the healthcare industry. Through their medicines, vaccines, biological therapies, and support services they offer health solutions for people and animals in over 140 countries. They also demonstrate their commitment to an increasing access to healthcare through far-reaching programs that donate and deliver their products to the people who need them. The organization has three main locations with approximately 4,500 employees. This position is located in Haarlem....

As a Senior Quality Assurance Officer your primary purpose is to ensure cGMP compliance of the manufacturing site and suppliers. You will be part of multidisciplinary projects and will represent the Quality team. Your role is to review, advise and monitor these validation projects. You will ensure validation of cGxP processes, subsystems and suppliers. In addition you will be responsible to take on the Quality role for technical projects, both process-related and IT-related. You will support and...

• B.Sc. or M.Sc. required, with a pharmaceutical or chemical background. • At least three years of relevant experience in a similar QA officer position. • Experience with GMP and/or GDP. • Preferably experience with packaging and/or production. • Attention to details, flexible, result oriented, proactive and able to work independently. • Good communication skills in Dutch and English (verbal, reading and writing)....

Challenging senior position within a new Quality team...

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 s...

As Senior Delegated Qualified Person (QP) you will act as back up of the current manager. In his absence, you will be the first point of contact for the organization and you will coordinate the team activities. The Global External Quality team is responsible for certifying the finished products of the organization within the EU. Also, they ensure that the finished medicinal product batches are manufactured compliant with GMP, the Manufacturing Authorisation (MIA) and the Marketing Authorisations...

• • M.Sc. in (or similar to) Industrial Pharmaceutical Science. • More than 5 years of relevant experience required (in an FDA and EMA approved pharmaceutical environment). • Experience as QP within either biotech or pharmaceutical industry. • Good mathematical and statistical skills, as well as leadership skills. • Able to act decisively, work well under pressure and make confident judgements. • Good communication skills in English and preferably in Dutch (verbal, reading and writing)....

Uitdagende marketingfunctie waarmee je met jouw product de levenskwaliteit van de patiënt kan verbeteren (Amsterdam, Nederland)...

Onze opdrachtgever is één van de 20 grootste farmaceutische bedrijven in de wereld en heeft ongeveer 17.000 medewerkers. In Europa is onze opdrachtgever in twaalf landen actief met ongeveer 2.000 medewerkers. Het Europese hoofdkantoor is gevestigd in München, Duitsland, en niet ver van daar, staat één van de wereldwijde productievestigingen. Deze imposante organisatie verzorgt innovatieve producten en services en heeft jarenlange tradities en een wetenschappelijke achtergrond. Met haar innovatie...

Als Brand Manager Cardiovasculair ben je verantwoordelijk voor de marketing van een oraal antistollingsmiddel en het op effectieve wijze plannen en uitvoeren van de multi-channel middelenmix. Daarnaast ben je verantwoordelijk voor het ontwikkelen van korte- en langetermijnplannen en zorg je voor een goede implementatie, monitoring, follow-up en tijdig aanpassen indien noodzakelijk. Ook neem je deel aan het jaarlijkse budgetproces, houd je je bezig met het nauwkeuring monitoren van de marketingko...

• een afgeronde wo-diploma, bij voorkeur in de richting van marketing; • relevante ervaring in marketing en in de farmaceutische industrie; • ervaring op het gebied van CV en/of trombose is een pre; • ervaring met digitale communicatie en multi/omnichannel klantbenadering; • analytische kijk op data, marktinzichten en in staat om te vertalen naar winnende strategie en tactiek; • goede communicatieve-, sterke sociale- en uitstekende presentatievaardigheden; • analytisch, commercieel, team...

A 2 year temporary Regulatory Affairs assignment at a large pharmaceutical company...

Our client is a world leader in the healthcare industry. Through their medicines, vaccines, biological therapies, and support services they offer health solutions for people and animals in more than 140 countries. They also demonstrate their commitment to an increasing access to healthcare through far-reaching programs that donate and deliver their products to the people who need them. The organisation has three main locations with approximately 4,500 employees. This position is located in Boxme...

As a Senior Regulatory Affairs Specialist your primary purpose is to support the new licensing activities of several major new product ranges, as well as the regulatory maintenance of the existing biological products. You will be part of a subdepartment in the Global Regulatory Affairs team, which is responsible for the biological product portfolio. Your role is to prepare and manage timely submissions of scientific dossiers, variation, and renewal packages for licensing of new biological prod...

• M.Sc. required, preferably followed by Ph.D. in Biomedical Sciences. • Knowledge of the (veterinary) pharmaceutical industry in development and/or maintenance of products. • Knowledge of (or several years experience in) Regulatory Affairs, preferably within the field of biologicals. • Flexible and persistent, ability to work under high pressure and meet deadlines. • Good teamplayer, negotiator and attention to details. • Knowledge of project management. • Good communication skills in E...

A temporary assignment for ten months at a large pharmaceutical company (Haarlem, The Netherlands) ...

Our client is a world leader in the healthcare industry. They aim for a healthy world. Through their medicines, vaccines, biological therapies, and support services they offer health solutions for people and animals in over 140 countries. They also demonstrate their commitment to an increasing access to healthcare through far-reaching programs that donate and deliver their products to the people who need them. The organization has three main locations with approximately 4.500 employees. This p...

As a Supply Chain Fulfilment Coordinator you are responsible for maintaining and building relationships with the assigned customers, the relevant supply sites and other stakeholders (End to End (E2E) Planners, Global Logistics, Finance and Quality). The Supply Chain Fulfilment Coordinator acts as primary contact for the customer; receives, analyses and processes their forecasts and orders; manages their inventory and deliveries and supports new product introductions. This is all done with the o...

• Bachelor or proven equivalent with experience in a related business (Supply Chain, Project Management, Logistics, Planning, Procurement, Business Planning or equivalent). • Two years of experience in a Customer Service environment. • Fluent in English both spoken and written. • Knowledge of and experience in MRP-systems. • Customer-focused, analytical, accurate, able to meet deadlines and a team player. • Basic understanding of working in a GMP and/or GDP environment and basic knowledge ...