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...

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)....

Als Laborant Biochemie ga je verschillende biochemische assays uitvoeren waaronder ELISA, SDS-PAGE en sequencing ter karakterisering van nieuwe vaccins...

Dit bedrijf is gespecialiseerd in translationeel vaccin onderzoek en ontwikkeling en hier werken 150 medewerkers.

...

Als Laborant Biochemie ga je verschillende biochemische assays uitvoeren waaronder ELISA, SDS-PAGE en sequencing ter karakterisering van nieuwe vaccins

Als Laborant Biochemie ga je verschillende biochemische assays uitvoeren waaronder ELISA, SDS-PAGE en sequencing ter karakterisering van nieuwe vaccins

• Je draagt bij aan de ontwikkeling van analysemethoden om de kwaliteit van een vaccin te kunnen vaststellen (volgens ICH-richtlijnen).
• Je voert de werkzaamheden...

Voor de functie van Laborant Biochemie zoeken wij een enthousiaste HBO kandidaat met minimaal 2 jaar relevante ervaring met biochemische, immunochemische en moleculaire assays

• Relevante technieken zijn ELISA, Western Blot, SDS PAGE, DNA sequencing, qPCR
• Ervaring met het werken in een BSL-II laboratorium is een absolute pré
• Ervaring met GraphPad Prism is gewenst, evenals GMP

...

Als HBO Chemisch Analist ga je verschillende analytisch chemische en biofysische methoden opzetten voor de karakterisatie van nieuwe vaccins ...

Dit bedrijf is gespecialiseerd in translationeel vaccin onderzoek en ontwikkeling en hier werken 150 medewerkers.

...

Als HBO Chemisch Analist ga je verschillende analytisch chemische en biofysische methoden opzetten voor de karakterisatie van nieuwe vaccins

Als HBO Chemisch Analist ga je verschillende analytisch chemische en biofysische methoden opzetten voor de karakterisatie van nieuwe vaccins

• Toegepaste chemische analyses zijn zijn HPLC, GC, NMR, SEC en biofysische technieken (circulair dichroïsme, fluorescentie spectrometrie, DLS, DSC, FFF- MALS)
• Je gaat methoden o...

Voor de functie van HBO Chemisch Analist zoeken wij een enthousiaste HBO kandidaat met minimaal 1-3 jaar ervaring met relevante technieken

• Relevante technieken zijn NMR, Chromatografie (HPLC, SEC), circulair dichroïsme en fluorescentie spectrometrie
• Ervaring in methode ontwikkeling en validatie is een absolute pré
  
• Als persoon ben je flexibel ingesteld
  
• Je spreekt zowel Nederlands als Engels
  

...

This is your opportunity for a change in scenery to the best of what Australia has to offer!...

Our client is a specialized Bioanalytical laboratory which offers services for a range of clients across the pharmaceutical and biotechnology industry. They have an ever-expanding range of services within their specialized laboratories, including Immunoassays, Biomarkers and LC-MS Bioanalysis. Continued year on year growth underpinned by a government R&D Tax initiative. Their facilities operate to FDA and GLP standards, as well being NATA and ISO accredited. Their facilities are based in Adelai...

As a Study Director you ensure timelines are firstly set appropriately considering, company and external stakeholder requirements and once set, ensure timelines are achieved. You are the communication line between internal and external stakeholders. Also, you ensure the scientific, integrity and regulatory compliance of study date by the review of all runs. Troubleshoot scientific issues by liaising with appropriate groups including Research & Development (R&D), Operations and Management. Furthe...

• Bachelor’s degree in life sciences • Minimum 5 years of experience in a regulated Bioanalytical position, ideally in a pharmaceutical or CRO environment. • Preferably at least 2 years work experience as a Study Director. • Proven ability to review SOPs and ALMs. • Experience with immunoassay development or Immunobiology. • Ambitious, entrepreneurial and communicative....

Are you a motivated candidate with strong experience in Sample management within the pharmaceutical industry? In this role as a Sample Managment Specialist (COVID-19) you will use your expertise to support the manufacturing of biopharmaceutical products including the COVID-19 vaccine. Apply now!...

An international pharmaceuticial company involved in the manufacturing of biopharmaceutical products. The team you will work in is responsible for Sample Management and execution of all analytical test methods using various techniques. Sample Management will support in process control and both product release and stability.

...

Are you a motivated candidate with strong experience in Sample management within the pharmaceutical industry? In this role as a Sample Managment Specialist (COVID-19) you will use your expertise to support the manufacturing of biopharmaceutical products including the COVID-19 vaccine. Apply now!

As a Sample Management Specialist you will support the required Sample Management activities. Additionally, you will handle quality and compliance related topics and you will contribute t...

For the position as a Sample Management Specialist we are looking for a motivated candidate with expertise on sample management.

• HBO or MSc degree in a relevent discipline such as biosciences, pharmacy, biotechnology or equivalent
  
• Multiple years of experience in a cGMP environment (QC/QA/manufacturing).
• Strong experience with sample management and appropriate software
• Experience with (c)GMP compliance
  
• Deviation management experienc...

We’re looking for a professional working in auditing, consultancy or internal control, who is ready for a career change to our Danone CBS Finance Benelux team! This Internal Controller role is the perfect switch for you to grow your Danone career. Why? Because we want to offer you the possibility to learn the fundamentals of our Internal Control practices and join us in the ambitions for further increasing the maturity level of our risk & control practices in Danone Benelux. This is a hi...

Danone’s mission is bringing health through food to as many people as possible and we want to invite people to join the movement for a healthier world. We recognize the power people have to impact the world through their daily choices. Healthy food needs a healthy planet, and this is what our new signature One Planet One Health embodies....

Your mission is to support the Danone Benelux business units and services with process & control evaluations and to drive improvements as a member of the CBS Internal Control team. The CBS Internal Control team consists of the Head of Internal Control and 10 people in the team (Internal Controller Managers, Internal Controllers and Interns). In this role, your assignment will focus on multiple business units and business services within our Benelux organisation where you will bring their inte...

To be successful in this role, you have a relevant Academic background in Finance, IT (Business Information Technology, Operational Auditing) or Accountancy or ACCA/CPA equivalent); you will bring 3-5 years working experience in an Auditing, Internal Control role or Process Improvements and knowledge and experience with processes and controls in the area of Intercompany, Financial Control (FP&A), Human Resources, General Services (including Compliance/GDPR) will be considered as a plus. We wi...

Are you a Packaging Innovator with deep expertise in metal/tin packaging development? Do you want to be part of how we lead the packaging transformation into the next frontier of technologies and experiences that will be critical to engaging our vulnerable consumers – infants, toddlers, expecting mothers, the elderly and patients? As a Senior Packaging Technologist you will be part of establishing a leading innovation practice, and, fostering collaborative internal and external partnersh...

Danone’s mission is bringing health through food to as many people as possible and we want to invite people to join the movement for a healthier world. We recognize the power people have to impact the world through their daily choices. Healthy food needs a healthy planet, and this is what our new signature One Planet One Health embodies. Nutricia Research is part of Danone. R&D is an important basis of the work we do in nutrition and health. We collaborate with partners, for example in a...

Build packaging center of excellence for tin knowledge and expertise on material science, processes and manufacturing skills. Create/maintain overview of internal and external technologies for defined packaging area (material / design / process); Translate business strategy to needed technology development by delivering approved briefing and business cases; Influence the development programs of our strategic suppliers towards the needed technology developments; Have a global network of suppl...

You are an experienced Packaging Engineer and have rich experience in metal / tin packaging development and innovation. Next to that, you bring: At least 7 years of experience in packaging development and medium- long term innovation Bachelor's or Master's Degree in packaging engineering, mechanical engineering, material engineering or similar discipline. A high degree of technical knowledge balanced with creative ability Experience in working with early stage product development, and i...

Pragmatische leider op de vloer. Efficiency en productiviteit op alle fronten....

Dynamische familiale KMO specialist in zijn vak. Enkele jaren geleden werd de nieuwe site in gebruik genomen met de recentste technologieën en duurzame ontwikkelingen doorheen het volledige verwerkingsproces. Om de onderneming in zijn sterke groei verder te ondersteunen is er de vacature Productieleider.

Deze familiale onderneming heeft de Werving en Selectie voor de vacature Productieleider exclusief uitbesteed aan CeresRecruitment. Voor meer informatie kun je terecht bij...

Ben je graag op de werkvloer en stuur je graag je team? Vertoef je graag in een productieomgeving en ben je gepassioneerd door de voedingsindustrie? Ben je hands-on en trek je graag optimalisatieprojecten? Dan is deze vacature voor jou!

Functie

Efficiency en productiviteit op alle fronten  

• Je bent verantwoordelijk voor de dagdagelijkse leiding en planning van de productie en stuurt hierbij de operatoren aan.
• Je bewaakt en optim...

Pragmatische leider op de vloer

 

Functie-eisen

 

• Bachelor of Masterdiploma of gelijkwaardig door ervaring.
• Minimaal 5 jaar ervaring in een leidinggevende functie in een productieomgeving, in de FMCG of voedingsindustrie is een plus.
• Goede kennis van Nederlands, Frans en Engels.

 

Competenties

 

• Analytisch en proactief.
• Leidinggevende en organisatorische vaardigheden.
• Geen 9-to-5 m...

Ben jij een enthousiaste laborant en heb jij ervaring met celkweek? In deze functie als Laborant celkweek ga je nieuwe cellijnen ontwikkelen en verschillende cellijnen onderhouden. Lijkt dit jou wat? Solliciteer dan direct!...

Farmaceutisch bedrijf gespecialiseerd in de ontwikkeling van vaccins. De groep waarin je gaat werken is verantwoordelijk voor het kweken en onderhouden van cellen die worden gebruikt voor testen van assays en testen voor de vrijgiften van producten.

...

Ben jij een enthousiaste laborant en heb jij ervaring met celkweek? In deze functie als Laborant celkweek ga je nieuwe cellijnen ontwikkelen en verschillende cellijnen onderhouden. Lijkt dit jou wat? Solliciteer dan direct!

Als Laborant Celkweek ga je nieuwe cellijnen ontwikkelen, optimaliseren en onderhouden (zoals A549 en HEK293). Daarnaast word je verantwoordelijk voor:

• Het uitvoeren van assays zoals GPT en Control Cell
  
• Het onderhouden van een ho...

Voor de functie van Laborant Celkweek zoeken wij een enthousiaste mbo kandidaat met werkervaring in celkweek.

• Je hebt affiniteit met medicinale producten
  
• Je hebt ervaring met kwaliteitsrichtlijnen, met name cGMP
  
• Je bent accuraat, pro-actief en een teamspeler
  
• Je bent sterk in verbale en schriftelijke communicatie in zowel Engels als Nederlands
  

Bij voorkeur heb je:

• Ervaring in een omgeving gedreven doo...