marketing, communications, events, PR, marketing manager jobs in the Biotechnology & Pharmaceuticals industry

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Page Personnel Belgium - Zaventem(2 days ago)
For their Headquarters in Zaventem, they are currently looking for a Public Relations Specialist. Client Details My client is a growing US based company, quoted on the New York Stock Exchange. Active in the cosmetic, pharmaceutic sector. Based in Zaventem. Description Be the spokesman product specialist for the company in the assigned region (West Europe) Develop media relations strategy, seeking ...
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Profile Group - 4800, Verviers(5 hours ago)
Vous êtes titulaire d"un bachelier ou d"une expérience professionnelle équivalente en gestion d"équipes de venteVous avez d"excellentes connaissances en néerlandais et en anglaisVous êtes orienté ....
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Arcq - 1000, Brussel(7 days ago)
Job content As a Marketing Associate, you take on the marketing of a mix of established and new products for the management of Diabetes/Immunology on the BeLux market. You are responsible for executing customer/brand plans by delivering unparalleled customer experience in order to prepare together with the Brand Manager an excellent launch of products in the future. The role combines a clear focus...
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Arcq - 3020, Herent(1 day ago)
Job content Your role will be to maximize sales performance by creating superior brand equity in a digital environment. To develop and implement adequate digital strategy in the Immunology therapeutic area. You will drive execution of strategies through implementation of new or existing tactics and solutions through the use of multiple e-channels (mail, virtual P2P, webcasts, social media, ….). Ha...
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Arcq - Herent(1 day ago)
Job content The Quality Analyst will be responsible for facilitating management of Quality Events and Quality Risks through application of the company's Quality Event Management program, and the analysis of quality data including but not limited to internal/external audit, regulatory inspections, and QEM program. Translating data into knowledge and making best use of knowledge are essential to ach...
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VALESTA - Multiple locations(1 day ago)
Since we are frequently looking for experienced Medical science liaisons (MSL) to reinforce our team, don't hesitate to apply if you recognize yourself in following criteria: Do you have previous experience as MSL, or another experience within the pharmaceutical industry, f.e. as a medical writer, within medical information, as CRA, as medical representative.? Do you have a strong scientific backg...
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Pauwels Consulting NV - 2830, Willebroek(5 days ago)
Job description Our client is a global market leader in the field of kidney failure with a fully integrated range of products and services within dialysis care and direct care for dialysis patients. In addition, innovative solutions are offered within therapeutic apheresis and in the field of liver problems. In the times of digitalization and integration of equipment and software in hospitals, wor...
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Arcq - Herent(7 days ago)
Job content The Quality Analyst will be responsible for facilitating management of Quality Events and Quality Risks through application of the company's Quality Event Management program, and the analysis of quality data including but not limited to internal/external audit, regulatory inspections, and QEM program. Translating data into knowledge and making best use of knowledge are essential to ach...
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Progressive Recruitment - Antwerp(2 days ago)
Ben jij een QA ingenieur en werk je graag in de farmaceutische sector? Een van onze toonaangevende eindklanten zoekt een QA ingenieur. Als jij een eerste ervaring hebt binnen kwaliteit en / of validatie en het leuk vindt aan kwaliteitsprojecten te werken bij een farmaceutische speler waar jij binnen een multidisciplinair team de QA ingenieur rol vervult dan past deze vacature bij jou. Wij zoeken e...
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Pauwels Consulting NV - 2870, Puurs(13 days ago)
Functieomschrijving We zijn op zoek naar een QE (Quality Engineer) Process Automation om aan de slag te gaan in Puurs. Als QE Process Automation heb je volgende verantwoordelijkheden: Verantwoordelijk voor het onderhouden van bestaande en uitwerken van nieuwe procedures onder het systeem Computer Systems Opstellen van validatie documenten GMP trends volgen op het vlak van automatisatie en software...
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Pauwels Consulting NV - Job location not provided(2 days ago)
Functieomschrijving The Process Efficiency Improvement Engineer – On-Market Product Support works under guidance and supervision of the Business Excellence Lead and will intensively work with stakeholders. Management of events in the context of On-Market Product support (linked to – be it not exclusively - the Quality Event Management process), i.e.: Customer Inquiries Complaints Discordance repor...
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Pauwels Consulting NV - 6281AB, MECHELEN(10 days ago)
Company description Pauwels Consulting is a Belgian consulting firm with more than 520 experts in engineering, life sciences and IT. We offer consulting, project management and recruitment services to leading companies in Belgium and beyond. We have offices in Belgium, France, Germany and Switzerland (https://www.pauwelsconsulting.com/about/contact/) . Job description Provide input from a quality ...
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The European Society of Anaesthesiology (ESA) - 1000, Brussel(5 hours ago)
The European Society of Anaesthesiology (ESA) is the leading European association for Anaesthesia, Critical Care, Pain and Perioperative Medicine. It is a not-for-profit company which promotes the exchange of qualitative information between European anaesthesiologists, in order to improve safety and quality of patient care. The complexity of the business and the number of stakeholders makes this o...
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Arcq - Herent(1 day ago)
You manage clinical trials from start to finish: you carry out pre-study visits, you initiate the trial, you are responsible for routine monitoring and closing visits about the quality standards and timelines You obtain and update essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations both in a Trial Master File (eTMF) and Investigator Study File (ISF) You a...
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Hays Wavre - Flemish Brabant(1 day ago)
* Quality Event and Risk Management * GCP/GLP/GMP * Belgium, Flemish Brabant area Hays Life Sciences is looking for a Clinical Quality Systems Analyst - GCP (Good Clinical Practice) & GLP (Good Laboratory Practice) to join the Quality Assurance team in a global clinical contract research organization. As a Quality Systems Analyst, you will be responsible for facilitating management of Quality Even...
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GlaxoSmithKline - 1330, Rixensart(1 day ago)
GSK is looking for a Scientist (M/F) Requisition ID: WD201814 Your Responsibilities: The incumbent will be responsible of the design of filling and devices process evaluation/ experimental protocols in collaboration with Drug Product (DP) Belgium (BE) project referent, for the experimental realizations and the redaction of the related reports. The person will collaborate with Early & Late projects...
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Pauwels Consulting NV - Mont-St-Guibert(2 days ago)
Job description The Clinical Study Manager is responsible for coordinating all operational aspects of a clinical trial. The main responsibilities are the following: Collaborate with Medical and Clinical Affairs department and with all other departments in the overall study management of a clinical trial Write or contribute to preparation of clinical protocols, amendments, informed consent forms, s...
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Pauwels Consulting NV - 1435, Mont-St-Guibert(2 days ago)
Job description The Clinical Study Manager is responsible for the oversight of multiple clinical trials from the protocol concept to the clinical study report, ensuring the quality of the trial and the completion of study deliverables. The main responsibilities include: Collaborate with Medical and Clinical Affairs department and with all other departments in the overall study management of a clin...
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Pauwels Consulting NV - Job location not provided(2 days ago)
Job description Follow up of the day to day operational activities that are executed by the 3PL service provider. This includes the physical activities as well as the documentation/admin/shipping activities. Identify operational performance issues and manage the swift resolution in close collaboration with the 3PL and the Site Operation Manager Act as coordinator and facilitator with EDN CS & RIT ...
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Pauwels Consulting NV - Job location not provided(2 days ago)
Bedrijfsomschrijving Pauwels Consulting is a Belgian consulting firm with more than 520 experts in engineering, life sciences and IT. We offer consulting, project management and recruitment services to leading companies in Belgium and beyond. We have offices in Belgium, France, Germany and Switzerland (https://www.pauwelsconsulting.com/about/contact/) . Functieomschrijving For one of our high-tech...
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Michael Page Belgium - 1000, Brussels(2 days ago)
Regulatory Affairs Specialist - OTC Products Global FMCG & OTC company Client Details Our client is one of the main actor within the FMCG & OTC world. In order to sustain their growth, they are today looking for a new regulatory affairs specialist in order to take care of the Regulatory Authorities on the Belgian Markets for their range of products. Description The successful candidate will have t...
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Arcq - 2627, Schelle(6 days ago)
Job content The QA/QC Officer is responsible for all quality related matters in our BENE affiliate. Your main tasks and responsabilities: Prepare and coordinate the administrative releases of the pharma products for distribution. QC of locally outsourced activities (e.g. re-labeling) and internal GDP/ISO 9001 related activities. Supplier qualification/maintenance. Participate in the maintenance of...
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Pauwels Consulting NV - Job location not provided(6 days ago)
Company description Pauwels Consulting is a Belgian consulting firm with more than 520 experts in engineering, life sciences and IT. We offer consulting, project management and recruitment services to leading companies in Belgium and beyond. We have offices in Belgium, France, Germany and Switzerland (https://www.pauwelsconsulting.com/about/contact/) . Job description Develop and maintain maintena...
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Hays Wavre - Bruxelles(6 days ago)
Hays Life Sciences is recruiting a Real World Evidence (RWE) Data Scientist to join a Global Biopharmaceutical Company. The position is based preferably in Belgium, in the Brussels area, but other locations may be considered. * Epidemiology * Pharmacovigilance * Outcome research * Skilled in written and oral scientific presentations The RWE Data Scientist is a Lead Scientist position that will sup...
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Hays Wavre - Brabant Flamand(6 days ago)
* Quality Event and Risk Management * GCP/GLP/GMP * Belgium, Flemish Brabant area Hays Life Sciences is looking for a Clinical Quality Systems Analyst - GCP (Good Clinical Practice) & GLP (Good Laboratory Practice) to join the Quality Assurance team in a global clinical contract research organization. As a Quality Systems Analyst, you will be responsible for facilitating management of Quality Even...
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