Jobs in Medicine, Dentistry, Pharmacy in Belgium | StepStone

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Sales Representative, Neurovascular - Belgium

Medtronic

Brussels

• Promote Medtronic Neuro Vascular unique value and partnership positioning by proper value propositions, and coordinate the definition and implementation of specific related commercial initiatives - As the key point of contact for a selected group of Key Accounts in Belgium, the Key Account Rep. is responsible for the growth, expansion and protection of Medtronic sales in these accounts through Customer Relationship Management, the promotion and sales of our entire product portfolio and the coordination of all Medtronic functional teams to provide support and valued-added services to our customers, to ensure effective long-term partnership. Responsibility for sales, marketing and service including the design and implementation of marketing and sales strategies, follow-up and evaluation. • Achieve annual sales targets in terms of revenues and margins • Promote Medtronic Neuro Vascular unique value and partnership positioning by proper value propositions, and coordinate the definition and implementation of specific related commercial initiatives - As the key point of contact for a selected group of Key Accounts in Belgium, the Key Account Rep. is responsible for the growth, expansion and protection of Medtronic sales in these accounts through Customer Relationship Management, the promotion and sales of our entire product portfolio and the coordination of all Medtronic functional teams to provide support and valued-added services to our customers, to ensure effective long-term partnership. Responsibility for sales, marketing and service including the design and implementation of marketing and sales strategies, follow-up and evaluation. • Achieve annual sales targets in terms of revenues and margins
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Specialist QA Clinical supply chain/clinical manufacturing

Oxford Global Resources

Breda

As a QA specialist clinical manufacturing/clinical supply chain, you will be mainly responsible for providing QA oversight on the supply chain of clinical trial products, QA guidance and support in the production area and clinical product disposition. In this role, you will be in direct contact with a wide range of stakeholders, and you will be responsible for establishing effective working relationships with Global Clinical Supply Chain (GCSCM), Corporate Quality, Contract Manufacturing Quality and Site Quality, Clinical Research Management, Regulatory Affairs and Clinical Research Associates/Clinical Research Organizations, Clinical Production operators, line leads, warehouse, maintenance and engineering. As a QA specialist clinical manufacturing/clinical supply chain, you will be mainly responsible for providing QA oversight on the supply chain of clinical trial products, QA guidance and support in the production area and clinical product disposition. In this role, you will be in direct contact with a wide range of stakeholders, and you will be responsible for establishing effective working relationships with Global Clinical Supply Chain (GCSCM), Corporate Quality, Contract Manufacturing Quality and Site Quality, Clinical Research Management, Regulatory Affairs and Clinical Research Associates/Clinical Research Organizations, Clinical Production operators, line leads, warehouse, maintenance and engineering.
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PAION Deutschland GmbH: Production Manager API (m/f/d)

Jobs via StepStone.de

Aachen

• Manage production related change controls and deviations internally as well as externally with PAIONs vendors • Provide support to PAION's licensees in production related topics where applicable, including the organisation and support of manufacturing process transfer programs if applicable • Draw up, review and maintain internal and external production-related documents i.e., validation reports, risk assessments, master and executed batch records, as well as SOPs • General management and control of external vendors of PAION and co-ordination of interactions with these vendors in all production related topics - Jobs via StepStone.de * Aachen * Contract duration unspecified * Full Time - PAION is a publicly listed specialty pharmaceutical company focused on developing and commercializing innovative drugs for out-patient and hospital-based sedation, anesthesia and critical care services. • Manage production related change controls and deviations internally as well as externally with PAIONs vendors • Provide support to PAION's licensees in production related topics where applicable, including the organisation and support of manufacturing process transfer programs if applicable • Draw up, review and maintain internal and external production-related documents i.e., validation reports, risk assessments, master and executed batch records, as well as SOPs • General management and control of external vendors of PAION and co-ordination of interactions with these vendors in all production related topics - Jobs via StepStone.de * Aachen * Contract duration unspecified * Full Time - PAION is a publicly listed specialty pharmaceutical company focused on developing and commercializing innovative drugs for out-patient and hospital-based sedation, anesthesia and critical care services.
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Regulatory Affairs Manager

Arsanne Consulting SPRL

Brussel

For one of its client, the affiliate of an entrepreneurial international pharmaceutical group, ARSANNE Consulting is looking for a Regulatory Affairs Manager Benelux (RA, QA and Vigilance Manager). * Ensure regulatory affairs files are maintained to support compliance with regulatory requirements. * Be the local Regulatory Contact Person for Marketing Authorizations. This requires development of regulatory strategies, creating and submitting change notifications to regulatory agencies, updating technical files and design dossiers. * Support internal and external audits by regulatory agencies as required. * Knowledge of BENELUX pharmaceutical regulatory environment is an important asset. * Previous experience in creating and submitting change notifications to regulatory agencies is required. * Previous experience in the development of regulatory strategies is preferred. Arsanne Consulting SPRL * Brussels For one of its client, the affiliate of an entrepreneurial international pharmaceutical group, ARSANNE Consulting is looking for a Regulatory Affairs Manager Benelux (RA, QA and Vigilance Manager). * Ensure regulatory affairs files are maintained to support compliance with regulatory requirements. * Be the local Regulatory Contact Person for Marketing Authorizations. This requires development of regulatory strategies, creating and submitting change notifications to regulatory agencies, updating technical files and design dossiers. * Support internal and external audits by regulatory agencies as required. * Knowledge of BENELUX pharmaceutical regulatory environment is an important asset. * Previous experience in creating and submitting change notifications to regulatory agencies is required. * Previous experience in the development of regulatory strategies is preferred. Arsanne Consulting SPRL * Brussels
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Quality Associate

Oxford Global Resources

Ixelles

We are looking for someone passionate about quality, enjoys working in a fast pace environment and has an eye for detail. Support the Quality departments in Belgium/Luxemburg (SCQ BeLux) & The Netherlands (SCQ NL) with the additional CovVx workload. * product quality incidents; * vendor quality management; * Quality minded, precise, organizational skills, work independently * Previous experience with QMS and pharmaceutical industry quality standards - mainly GDP (Good Distribution Practice) Oxford Global Resources * Ixelles * Contract duration specified * Full Time - Your responsibilities - Do you fit that description? Then this might be the job for you! Job description - Responsibilities * procedure review; * self inspections; * returned goods; * data integrity; * e-repository; * transportation & storage incidents; * etc. Do the above responsibilities fit you like a glove? and motivation letter via the " " button and you can expect feedback from us soon. We are looking for someone passionate about quality, enjoys working in a fast pace environment and has an eye for detail. Support the Quality departments in Belgium/Luxemburg (SCQ BeLux) & The Netherlands (SCQ NL) with the additional CovVx workload. * product quality incidents; * vendor quality management; * Quality minded, precise, organizational skills, work independently * Previous experience with QMS and pharmaceutical industry quality standards - mainly GDP (Good Distribution Practice) Oxford Global Resources * Ixelles * Contract duration specified * Full Time - Your responsibilities - Do you fit that description? Then this might be the job for you! Job description - Responsibilities * procedure review; * self inspections; * returned goods; * data integrity; * e-repository; * transportation & storage incidents; * etc. Do the above responsibilities fit you like a glove? and motivation letter via the " " button and you can expect feedback from us soon.
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Grünenthal GmbH: Pharma Engineer (f/m/d)

Jobs via StepStone.de

Aachen

Pharma Engineer (f/m/d) Jobs via StepStone.de * Aachen * Contract duration unspecified * Full Time - Grünenthal is a global leader in pain management and related diseases. We're driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We're focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. Pharma Engineer (f/m/d) Jobs via StepStone.de * Aachen * Contract duration unspecified * Full Time - Grünenthal is a global leader in pain management and related diseases. We're driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We're focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion.
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Clinical Project Manager (Phase II-III)

SGS Group Belgium

Mechelen

As Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects (late phases). In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Project Manager (Phase II-III). * You have at least 2 years of experience in an International Project Management role, having managed international phase 2 and 3 clinical trials in a pharmaceutical or biotech company or another CRO. SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. As Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects (late phases). In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Project Manager (Phase II-III). * You have at least 2 years of experience in an International Project Management role, having managed international phase 2 and 3 clinical trials in a pharmaceutical or biotech company or another CRO. SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities.
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QA specialist

Brunel Belgium NV

Vlaams-Brabant

At the moment for example, we are looking for a quality assurance specialist to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Vlaams-Brabant * Contract duration unspecified * Full Time - About You - Are you someone who likes trying new things and gaining different experiences? Than life as a consultant might be your thing! As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Advising on the translation of GDP-, GMP- and customer requirements that need to be integrated in the operational processes. Ensure the incorporation of such requirements in the procedures and instructions and provide training when necessary. * Reporting and follow-up of Quality-KPI's. At the moment for example, we are looking for a quality assurance specialist to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Vlaams-Brabant * Contract duration unspecified * Full Time - About You - Are you someone who likes trying new things and gaining different experiences? Than life as a consultant might be your thing! As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Advising on the translation of GDP-, GMP- and customer requirements that need to be integrated in the operational processes. Ensure the incorporation of such requirements in the procedures and instructions and provide training when necessary. * Reporting and follow-up of Quality-KPI's.
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RA Manager

Brunel Belgium NV

Vlaams-Brabant

We are currently looking for a Regulatory Affairs Manager to join the team at our client's. * Ensure that processes, procedures and regulatory files are well documented in up to date and complete applicable archives, databases, repositories and trackers. * Secure timely and adequate information and decision making with regard to regulatory issues that need to be brought to the attention via the RA lead to the Management Team, such as deletions, divestitures and acquisitions. * Take part in affiliate product and launch teams to provide regulatory input and strategy advice. Brunel Belgium NV * Vlaams-Brabant * Contract duration unspecified * Full Time - About You - Your responsibilities * Support implementation locally of new initiatives, management tools or processes in cooperation with EST- RA. * Contribute to the EST-RA and affiliate Quality Management System. We are currently looking for a Regulatory Affairs Manager to join the team at our client's. * Ensure that processes, procedures and regulatory files are well documented in up to date and complete applicable archives, databases, repositories and trackers. * Secure timely and adequate information and decision making with regard to regulatory issues that need to be brought to the attention via the RA lead to the Management Team, such as deletions, divestitures and acquisitions. * Take part in affiliate product and launch teams to provide regulatory input and strategy advice. Brunel Belgium NV * Vlaams-Brabant * Contract duration unspecified * Full Time - About You - Your responsibilities * Support implementation locally of new initiatives, management tools or processes in cooperation with EST- RA. * Contribute to the EST-RA and affiliate Quality Management System.
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Capital Application Specialist - Robotics, Belgium Based

Medtronic

Brussel

Medtronic * Brussels * Contract duration unspecified * Full Time - About Medtronic - At Medtronic, you will find a diverse who bring their unique backgrounds and their individual life experiences to work every day. We work hard to cultivate a workforce that reflects our patients and partners, we believe it's the only way to drive healthcare forward. We want to attract a diverse workforce, regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, veterans, or any other characteristic protected by state or local law. Join us and bring the power of your point of view to our culture of collaboration and innovation. It is through strong diversity, inclusion and engagement that we can remain a leader in medical technology and solutions. Medtronic * Brussels * Contract duration unspecified * Full Time - About Medtronic - At Medtronic, you will find a diverse who bring their unique backgrounds and their individual life experiences to work every day. We work hard to cultivate a workforce that reflects our patients and partners, we believe it's the only way to drive healthcare forward. We want to attract a diverse workforce, regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, veterans, or any other characteristic protected by state or local law. Join us and bring the power of your point of view to our culture of collaboration and innovation. It is through strong diversity, inclusion and engagement that we can remain a leader in medical technology and solutions.
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