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QbD Jobs Overview areas of expertise Medical devices Working at Quality by Design: Medical devices As QbD expert you are our clients' best guarantee of product and process quality You guide your clients in life sciences and healthcare through every life phase of their medical devices: from the initial strategy meeting where you help to map out the concept and feasibility of the Singlehandesly manage all Regulatory Affairs and Quality Compliance activities for the company: 1) Subject Matter Expert for Class A to D Medical Devices regulatory matters 2) Registrant for 60 product owners (still counting) successfully - Registered 5 Class B 2 class C devices -

All regulatory affairs

regulatory affairs - medical device jobs in Canada Sort by Relevance Date Posted Anytime Since yesterday In last two days In last week In last 15 days Employer None Selected Kardium (2) Siemens (2) DSA Consultants (2) Johnson Johnson Family of Companies (2) ORPYX MEDICAL TECHNOLOGIES (1) SBI ALApharma Canada Inc (1) Cardinal Health (1) Artron Bioresearch Inc (1)

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Quality and regulatory affairs manager medical devices bath 40k - 60k benefits flexible working innovative medical device startup Enter your email address to receive alerts when we have new listings available for Part time regulatory affairs jobs You can cancel your email alerts at any time By proceeding you consent to our Legal Notice and acknowledge how we process your personal

Regulatory Affairs In the pharmaceutical biotechnology and medical devices industries quality assurance and regulatory affairs can hardly be dissociated from each other That's why Quality by Design offers you the total package We do not only take care of quality management but also support you throughout the entire drug or medical

Medical devices are products or equipment intended generally for a medical use and are regulated at Member State level The Medical Devices and the In-Vitro Diagnostic Devices Regulations have introduced new responsibilities for the European Medicines Agency (EMA) and national competent authorities in the assessment of certain categories of medical device

Job: Regulatory Affairs Specialist (Medical Devices) at

Communication with company staff the MOH pharmaceutical dept as well as corresponding regulatory affairs responsible in international suppliers in order to get the products that the company needs to be registered and/or imported or cleared as quickly as possible Studying and updating the government regulations and the different export regulations of all our suppliers Keeping and updating

Medical Devices Regulatory jobs Sort by: relevance - date Page 1 of 334 jobs Displayed here are job ads that match your query Indeed may be compensated by these employers helping keep Indeed free for jobseekers Indeed ranks Job Ads based on a combination of employer bids and relevance such as your search terms and other activity on Indeed For more information see the Indeed Terms of

Developed regulatory strategies for new and modified radiological devices Provided guidance and feedback to regulatory affairs management Prepared and submitted internal regulatory file applications and supporting documentation Reviewed medical device labeling and advertising materials for accuracy and completeness

Developed regulatory strategies for new and modified radiological devices Provided guidance and feedback to regulatory affairs management Prepared and submitted internal regulatory file applications and supporting documentation Reviewed medical device labeling and advertising materials for accuracy and completeness

Must have a minimum of 0-3 years of experience in a regulated industry (e g medical devices pharmaceuticals etc ) Regulatory Affairs experience is preferred but may consider quality assurance research and development/support scientific affairs operations or related area Preferred to have knowledge of standards/regulations for MDSAP Countries (US Canada Australia Brazil Japan) and

Regulatory Affairs We work on Regulatory Affairs jobs for global pharmaceutical companies CROs and regulatory consultancies across pharmaceuticals medical devices and cosmetics We place candidates into roles at all levels from Regulatory Affairs Associates through to Senior Regulatory Affairs Managers

TOPRA Jobs - Regulatory affairs vacancies TOPRA Jobs is a specialist job board for regulatory affairs roles in the UK and mainland Europe hosted by our partners at PharmiWeb jobs It is regularly used by a wide variety of global and regional organisations as well as government agencies and consultancies Our jobs cover roles in the human medicines medical devices and veterinary

FDA regulations and policies applying to medical devices and in vitro diagnostic devices including but not limited to requirements for 510(k)s IDEs PMAs labeling and promotional materials and Research Use Only devices Must be able to interpret regulatory requirements determine what is necessary for compliance and effectively communicate this information to stakeholders

Medical Devices Regulatory Affairs Jobs Ireland

Right now we are seeking to hire a Medical Devices Regulatory Affairs Advisor with experience in the medical devices sector We are regarded as one of the most dynamic regulatory consultancy firms in Europe and we work with some of the biggest names in medical devices pharmaceutical and clinical trials on a daily basis Now we are working

MSc Regulatory Affairs (Medical Devices) TOPRA has developed an exciting new MSc in Medical Devices It provides the opportunity for people to combine modules in both pharmaceutical and medical technology regulatory affairs something that might be particularly beneficial for those interested in drug-device combination products as well as consultants and members who are in the early stages of

Must have a minimum of 0-3 years of experience in a regulated industry (e g medical devices pharmaceuticals etc ) Regulatory Affairs experience is preferred but may consider quality assurance research and development/support scientific affairs operations or related area Preferred to have knowledge of standards/regulations for MDSAP Countries (US Canada Australia Brazil Japan) and

Manager Regulatory Affairs Medical Devices Die grte Kategorie in der offen Manager Medical Affairs Jobs erscheinen ist Stellen aus Gesundheitswesen Pflege gefolgt von Stellen aus Wissenschaft Qualittssicherung 75% der aktuellen Stellenangebote sind Vollzeit und 25% davon sind Teilzeitstellen weitere Informationen Neueste Blogeintrge Jobsuche whrend der Corona

Farmapi Bologna divisione specialistica del gruppo Lavoropi Spa cerca un/una regulatory affairs medical devices per azienda di certificazione con sede in provincia sud di Bologna ATTIVITA': - Si occuper del controllo revisione e validazione fascicoli tecnici per conto di clienti del settore medical devices in tutto il mondo - Si interfaccer con il cliente finale e con gli enti

Regulatory Affairs We work on Regulatory Affairs jobs for global pharmaceutical companies CROs and regulatory consultancies across pharmaceuticals medical devices and cosmetics We place candidates into roles at all levels from Regulatory Affairs Associates through to Senior Regulatory Affairs Managers

Medical Devices Regulatory jobs Sort by: relevance - date Page 1 of 334 jobs Displayed here are job ads that match your query Indeed may be compensated by these employers helping keep Indeed free for jobseekers Indeed ranks Job Ads based on a combination of employer bids and relevance such as your search terms and other activity on Indeed For more information see the Indeed Terms of