A temporary position for the period of four months at a global pharmaceutical company (Haarlem, The Netherlands)...

Our client is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Their employees are at the core of their success, with colleagues in over 80 countries, delivering the world’s largest medicine cabinet to 200 million people every day. They offer a uniquely diverse portfolio of products and solutions for patients and they have built a promising pipeline centered around their c...

As Qualified Person you will handle compliance activities in Quality Center NL in alignment with the business unit, in order to ensure that commercial products are handled compliant and distributed to the Netherlands and other European countries by meeting GMP & GDP, regional, local standards and customer needs. This means that you have to ensure QP batch certification according to GMP Annex 16 for products for the Dutch market as well as European countries. Furthermore, you will have to adminis...

• Master´s Degree in Pharmacy, Medicines, Biology is required or an equivalent combination of education and experience to the functional role to register as a QP • minimum of 5 year experience as a QP in a pharmaceutical company or importer/distributor • knowledge of pharmaceutical industry as it relates to QP regulations and Quality Compliance • in-depth understanding of cGMP & GxP's regulations • experience with development and implementation of Quality Systems and application of risk asse...

A challenging position at a biopharmaceutical company...

The organisation is a (bio)pharmaceutical company based in Noord-Brabant. They are currently facing the next stage of the clinical phase because of which they need to expand their team with another expert. Therefore the organisation is looking forward to get in touch with a flexible and collaborative QC Technician....

In the position of QC Technician you will be responsible for a broad range of duties. You will be responsible to ensure that all relevant samples are tested in a timely manner to support batch release, stability studies and clinical studies. You will perform qualification and validation of analytical methods and equipment. You work in close collaboration with QA-, Production-, RA- department and Qualified Person to perform tests on QC-samples. It is also your responsibility to ensure qualificati...

• at least a Bachelor’s degree • a minimum of two years of experience within GMP environment • at least two years of experience in flow cytometry analytical testing • independent and able to work in small teams • good writing skills in English ...

Veelzijdige kwaliteitsrol bij een ondernemende, creatieve, ambachtelijke en toegewijde organisatie (Flevoland) ...

Onze relatie ontwikkelt en produceert een breed assortiment aan voedingssupplementen, cosmetica en farmaceutische producten. De producten zijn te koop bij drogisterij- en supermarktketens binnen en buiten Europa. Het assortiment omvat meer dan duizend producten, varierend van A-merken tot private label producten. ...

Als QA Manager ben je verantwoordelijk voor de kwaliteit van de producten die onze opdrachtgever produceert. Samen met je team van 4 fte draag je zorg dat de producten voldoen aan wettelijke richtlijnen, wensen en eisen van de klant en de kwaliteitseisen van de organisatie. Om dit te kunnen garanderen, houd je de ontwikkeling betreffende wetgeving en internationale richtlijnen over de productcategorieën nauwlettend in de gaten en ben je verantwoordelijk voor de incorporatie van deze ontwikkeling...

Onze relatie ontwikkelt en produceert een breed assortiment aan voedingssupplementen, cosmetica en farmaceutische producten. De producten zijn te koop bij drogisterij- en supermarktketens binnen en buiten Europa. Het assortiment omvat meer dan duizend producten, varierend van A-merken tot private label producten. ...

Fulltime dynamic opportunity at a world’s leading medical technology company (Amsterdam, the Netherlands)...

Our client is one of the world’s leading medical technology company and is driven to make healthcare better. They offer innovative products and services in a wide field in the healthcare industry that helps improve patient and hospital outcomes. As Tender and Contract Specialist you will join a multi-disciplinary team that enjoys collaborating to bring the Commercial Department of the Netherlands to the next level....

As Tender and Contract Specialist you will be responsible for managing all tender submissions of our client’s location in the Netherlands. You will also be responsible for the contract set-up and overall contract management. In collaboration with the Commercial Services Manager, you will manage the entire tender process (identification, response and evaluation). You will lead the tender process, in collaboration with Legal, Sales, Finance and Product Management. For customer contracts you will b...

• bachelor’s degree level of working and thinking (preferably Business Administration/Economics/Law) • at least five years of relevant work experience in Tenders & Contracts • good knowledge of MS Office (Word, PowerPoint & Excel) • the ability to multi-task and juggle multiple projects simultaneously • a high level of discipline and being able to meet strict deadlines, structured and organizational planner • good with numbers and process-oriented • team-player focusing on making deadlines...

(geen informatie)

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 Data Analyst you are responsible for implementing the StS Supplier Enablement efforts and you have to ensure the organisation reaches supplier enablement targets. In this position you will coordinate closely with all regions to ensure that the Supplier Enablement approach is consistent. This means that you have to define a plan to onboard suppliers to Ariba, and that you have to act as an ambassador for the Streamline project and the system Ariba. Besides that, you have to cleanse the data an...

• bachelor degree is preferred • high proficiency in Microsoft Office products • knowledge about SAP at a beginners level • experience with working in a team setting • ability to work under pressure to meet deadlines • ability to make decisions • strong analytical, verbal and written communications and organization skills • excellent skills in English, both oral and written...

(geen informatie)

The organisation is an international pharmaceutical company that is operating in more than 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 research, development, manufacturing, warehousing but also sales and marketing. They hope to change ‘tomorrow’ and improve the lives of individuals by providing innovative medicines in areas of health where there is an urgent need for better treatments. The organisation ...

As Project Coordinator you will deliver support to global pharmacovigilance departments across the organisation. You will therefore be responsible for schedule meetings and circulate agendas for safety-related meetings. You will document these meeting minutes and circulate them for review. Thereby, you will assist in drafting reports and presentations in support of safety deliverables and assist with requesting case reports from the safety database. Next to this you manage SharePoint Sites, for ...

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A temporary position for two years 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 Associate Specialist you will participate in a multidisciplinary project team. The goal of the project is to ensure that all regulatory submissions within the EU are following the upcoming New Veterinary Regulations (NVR) and systems are in line with the new EU Telematics landscape. You will support the implementation of a new business processes to adhere to the NVR and update/create relevant SOPs. Besides that, you will support the Global Regulatory Affairs teams in collecting and analyzing ...

• bachelor degree or proven related working experience of minimum 2,5 years in the pharmaceutical industry • experience in participating in multi-disciplinary project teams • (preferred) knowledge on EU Telematics landscape (IDMP, UPD, SPOR, CESSP) • preferred experience with regulatory information systems and platforms (i.e.: CESSP, Veeva) • experience with registration processes (e.g. document management lifecycle and regulatory procedures; knowledge on dossier content to be able to compar...

Temporary position for 12 months in pharmacovigilance at a pharmaceutical company...

The organisation is an international pharmaceutical organisation that is operational in at least 40 countries across Europe, the Middle East and Africa. The operate on a global level and most of the teams have a global focus. They have everything in house like research, development, manufacturing, warehousing, but also sales and marketing. It is their hope to change tomorrow and to improve the lives of individuals like men, women and children, by providing innovative medicines in areas of health...

As a PV Process Configuration Manager you will be responsible for aspects of excellence in Regional PV Process Distribution & Submissions. You will work together with a small team in the Netherlands and report to the Lead Regional. It is an international role where you work extensively with PV Information Management within the region to ensure the quality of outputs as well as system configuration to strengthen the correct functioning of PV Systems, supporting the ongoing assurance of the safety...

• minimum BA/BS, preferably with an advanced professional degree • minimum of 5 years relevant experience in the pharmacovigilance or combined PV/RA/QA, and/or clinical development • in-depth knowledge and understanding of PV Process regulatory reporting requirements and guidelines in assigned region • in-depth understanding of PV, data management and adverse event reporting • experience in managing multiple projects in a heavily matrixed and/or cross-functional environment • a quality mi...

Temporary position for 12 months in pharmacovigilance at a pharmaceutical company...

The organisation is an international pharmaceutical organisation that is operational in at least 40 countries across Europe, the Middle East and Africa. The operate on a global level and most of the teams have a global focus. They have everything in house like research, development, manufacturing, warehousing, but also sales and marketing. It is their hope to change tomorrow and to improve the lives of individuals like men, women and children, by providing innovative medicines in areas of health...

As a ICSR Management Liaison Manager you will be responsible to ensure PV requirements are incorporated in protocol design for interventional as well as non-interventional studies and Market Research Programs and/or Safety Management Plans for clinical studies or organized data collection programs conducted in (assigned) region. You will build and maintain close relationships with DSOs, Regulatory Affairs, Clinical and Medical Affairs functions in the assigned region. Also you will be responsibl...

• minimum BA/BS in Life Sciences • minimum of 5 years relevant experience in the pharmacovigilance or combined PV/RA/QA, and/or clinical development • in-depth understanding of safety regulations for both marketed and investigational products, and excellent knowledge of global health authority requirements including ICH, CFR 21, FDAAA, EU GVP module, JP regulations • in-depth knowledge and understanding of PV Process regulatory requirements and guidelines in the assigned region • proven ex...

Responsible and high-profile position within ambitious biopharmaceutical...

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 Director Market Access & Reimbursement you will be responsible for the development and implementation of the Market Access Strategy including pricing and reimbursement for the entire product portfolio in The Netherlands. You will ensure that access strategy across the portfolio supports product pricing and reimbursement objectives and will work in close collaboration with the cross-functional teams to ensure alignment on strategy and implementation. Furthermore, as an individual you will have...

• a Master of Science or PhD degree preferably in Economics, Health Economics, Business studies, Medicine, Pharmacy, or another relevant field • experience with market access and/ or health economics work (in the industry or elsewhere) • extensive understanding of Market Access processes and the goals and strategies of payers and other stakeholders in The Netherlands • strong analytical skills, driven and proactive • demonstrates the ability to prioritize and persist, despite obstacles and o...