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)....

Vind jij het als Senior Buyer een uitdaging om je nieuwe werkgever te helpen bij de transitie naar een Lead Buyership-organisatie? Heb jij werkervaring als inkoper in de farmaceutische of biotechnologische industrie? Voor onze klant in Nijmegen zijn wij op zoek naar een Senior Buyer. Deze geneesmiddelenproducent staat na jaren van onderzoek op het punt om volgend jaar nieuwe medicatie op de markt te brengen....

Vind jij het als Senior Buyer een uitdaging om je nieuwe werkgever te helpen bij de transitie naar een Lead Buyership-organisatie? Heb jij werkervaring als inkoper in de farmaceutische of biotechnologische industrie? Voor onze klant in Nijmegen zijn wij op zoek naar een Senior Buyer. Deze geneesmiddelenproducent staat na jaren van onderzoek op het punt om volgend jaar nieuwe medicatie op de markt te brengen. ...

De afdeling Procurement & Supply Chain is verantwoordelijk om de organisatie te voorzien van de juiste middelen om alle (kern) processen te ondersteunen. Kortom; De R&D-organisatie en de teams ondersteunen met alle benodigde materialen, tools & services op het juiste moment op de juiste plek. Je participeert en adviseert in grote Capital Expenditures (CAPEX) projecten op de locatie in Nijmegen. Ze zijn geïnteresseerd in resultaatgerichte mensen met een scherpe ondernemersgeest, die kunnen bijdra...

We zijn op zoek naar een ambitieuze kandidaat, een teamspeler met sterke onderhandelingsvaardigheden en diepgaande kennis van inkoopprocessen. Je focust op het opbouwen van relaties met leveranciers, bezit een pragmatische aanpak en met je diepgaande SAP-kennis, GMP-bewustzijn en analytische mindset help je mee de inkoopbehoeften van onze R&D-organisatie te bepalen. Contractmanagement (MSA / LSA) is je tweede natuur. •HBO of WO-opleiding bedrijfskunde, bedrijfseconomie of vergelijkbaar; • Mi...

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 ...

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)....

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...

Handling CMC dossiers for gene and cell therapy...

Our client is a multinational pharmaceutical company with EMEA headquarters based in London and affiliates throughout Europe. The client is engaged in Research and Development (R&D), Manufacturing and Sales and Marketing. The EMEA region is important and growing because they have key strengths in the various therapy areas. In the organisation they believe that nurturing a good relationship with employees delivers good business results. They are aiming to become recognized as an Employer of Choic...

A suitable candidate will be responsible for developing submission plans for assigned projects and provides input for RA strategy. You identify and collect data required for registration packages, often including initial IND submissions for later stage development products. You will take responsibility for the development and implementation of Regulatory processes within the department. As a Regulatory Manager you are responsible for independently managing complex technical documents. You prepar...

• At least a Bachelor’s degree in a scientific or related discipline. • At least 7 years of industry experience combined with 4 years in RA. • Expert level of scientific knowledge in chemistry, general biological/physical science, and ability to apply that knowledge to Regulatory issues and product development. • Recognized as skilled in an aspect of pharmaceutical drug development, with RA skills. • Full knowledge of FDA and ICH regulations and guidelines, and the ability to provide inte...

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...

Ben jij een gediplomeerd recovery verpleegkundige en wil jij werken in een omgeving die het beste bij jou past? Bij HMC kan dat! Of je nu een belangrijke bijdrage wil leveren bij acute en grote trauma’s of juist bij oncologische of topklinische ingrepen. Wij gaan graag het gesprek met jou aan en kijken samen hoe wij jouw ambities waar kunnen maken! Lees snel verder en solliciteer direct. Hebben we een klik? Dan ligt er voor jou een contract voor onbepaalde tijd klaar! ...

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Als Recovery Verpleegkundige heb je een zeer belangrijke rol tijdens het opvangen, begeleiden, observeren, bewaken, verplegen en verzorgen van de operatiepatiënt in de pré- en postoperatieve fase. Binnen onze operatiekamers leveren wij traumazorg op het hoogste niveau volgens de landelijke criteria. Gezien het grote aantal polytrauma-patiënten, onze expertise in de traumazorg en onze infrastructuur, zijn wij hét traumacentrum van Haaglanden en omgeving. HMC staat bekend om haar acute, onc...

Wat vragen wij van jou? Je bent een gediplomeerd recovery verpleegkundige Je hebt patiëntgerichtheid hoog in het vaandel staan Je toont initiatief, bent enthousiast, communicatief vaardig, gemotiveerd en iemand die uitstekend kan samenwerken Kom je bij ons werken? Dan vragen wij om een VOG (verklaring omtrent gedrag). ...

Within FrieslandCampina, LQS serves as independent central laboratory for QC-analyses in raw materials, intermediate and finished products, packaging material, process water and waste water for the FrieslandCampina Opco’s. ...

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As a PAT Specialist, you will be part of the PAT team in the department of business support. Business Supports operates in an international environment and supports more than 50 production locations worldwide with QC related expertise in microbiology, sensory, chemical and process analytic technology. The PAT cluster within Business Support is a growing team that plays an essential role in developing the FrieslandCampina strategy of moving towards product qualification/fingerprinting techniques...

What we ask Msc or PhD degree in chemical engineering or physical chemistry or food technology Strong expertise in spectroscopy (NIR, Raman) and other analytical techniques for inline process measurements Experience with inline or atline measurement of physical properties like viscosity and particle size distribution Experience with processing spectroscopic data processing techniques (PLS, PCA) and the required software tools for this ( for example matlab or Simca) ...