regultory affairs officer medical device cv

Regulatory Affairs Specialist Resume Example | LiveCareer Strongly reliable and focused Regulatory Affairs Specialist with great depth and breadth of experience in medical device review and evaluation. Superb multitasker able to handle multiple projects efficiently and accurately. Effective independent worker as well as excellent coordinator with other members of a regulatory affairs team. Regulatory Affairs Officer Resume Samples | Velvet Jobs 3 to 5 years of relevant experience in the field of medical device regulatory affairs Ability to work in various projects in parallel and know basic project management skills (cross several time zones) munication in a multi cultural environment Microsoft Outlook & Office skills mandatory Systematic and good in time management Regulatory Affairs Associate Resume Example Rapid Medical ... Regulatory Affairs Associate 02 2001 to 07 2016 Rapid Medical – Atlanta, GA. Rapid Medical Research, Pfizer, Ultragenyx, GSK, Genentech, J & J Contracts ; Wrote, reviewed, and edited scientific manuscripts, clinical study reports, plan outlines, protocols, and documents for regulatory submissions (e.g.meeting packages, investigational new drug [INDs] applications, and sections of marketing ... DOWNLOAD: Regulatory Affairs Resume Example for 2020 ... This FREE Regulatory Affairs resume example combines job responsibilities, experience, achievements, summary of qualifications, technical skills and soft skills generated from a database of successful resume models. Use the Regulatory Affairs resume sample below, replace the information with relevant data about you and match your skill set ... Regulatory Affairs Resume Samples | Velvet Jobs Must have requisite training or certification in medical device regulatory affairs through on the job training, seminars, training. RAC certification preferred Must have experience managing medical device quality systems in compliance with US FDA regulations (21 CFR) and ISO 13485. Quality system or auditing certifications highly desirable Chief Medical Officer Resume Sample Medical Affairs Managed 50 multidisciplinary scientists within the global Regulatory Affairs Department as part of a worldwide expansion to grow the regulatory business. Achieved targeted growth domestically and internationally Delivered successful outcomes for numerous clients and reported these achievements into the Chief Medical Officer Regulatory Affairs Specialist CV Template | CV Samples ... Provided guidance and feedback to regulatory affairs management. Prepared and submitted internal regulatory file applications and supporting documentation. Reviewed medical device labelling and advertising materials for accuracy and completeness. Created and submitted state and federal licensing applications. June 2006 to May 2010 Baines ... Manager Regulatory Affairs Resume Sample | MintResume Ideally 3 years of Medical Device Regulatory Affairs experience in a similar or more junior role Experience in Regulatory Affairs Five (5) or more years of effective, decision making, results delivery, team building, and the ability to stay current with relevant technology and innovation Regulatory Affairs Manager Resume Sample | MintResume Work related experience in quality management system regulatory affairs experience in the medical or consumer device industry Analytical skills: accuracy, reliability, attention to detail List of Typical Responsibilities For a Regulatory Affairs Manager Resume The Role of Regulatory Affairs in the Medical Device Industry Medical device companies also rely on their regulatory affairs team after a device is cleared or approved. In the postmarket setting, the regulatory function is involved in device surveillance, ensuring that any adverse events or malfunctions are appropriately reported to FDA. Regulatory Affairs Specialist Resume Examples | JobHero Regulatory Affairs Specialist Resume Examples. Regulatory Affairs Specialists work in regulated industries, such as energy, telecom, banking, or health care industries. These professionals need to ensure that their companies follow all regulations in the field and advise executives on the regulatory climate they need to consider when making ... Regulatory Specialist Resume Examples | JobHero Regulatory Specialists are in charge for licensing and marketing pharmaceutical and medical products to ensure their safety and efficacy. Specific responsibilities of a Regulatory Specialist are complying with legislation in the field, assessing scientific data, handling license renewals, assessing scientific data, coordinating teams of colleagues, and making presentations to regulatory ... 10 tips to improve your CV for a regulatory affairs ... If you are lucky enough to have regulatory affairs experience in multiple industries, such as pharmaceuticals and medical devices, be sure to focus more on the industry for which you are applying. If possible, try to include the job title for the position you are applying to somewhere in your CV. Medical Device Regulatory Jobs in Dublin January 2021 ... Use for to create your resume on Indeed and apply to jobs quicker. Save your resume. ... Medical Device Regulatory jobs in Dublin. Sort by: relevance date. Page 1 of 113 jobs. ... Regulatory Affairs Officer. Talent Source. South Dublin, County Dublin. €55,000 a year. Medical Device Regulatory Affair Manager Jobs, Employment ... 1,059 Medical Device Regulatory Affair Manager jobs available on Indeed . Apply to Regulatory Affairs Manager, Liaison, Medical Writing Manager and more! Regulatory Affairs Diagnostic and Medical Device CV Regulatory Affairs Diagnostic and Medical Device CV 1. CURRICULUM VITAE JASPREET SINGH VIRDI E Mail : virdisinghjaspreet@gmail Contact No. : 9868764273 PRESENT ADDRESS House Number : 4 Road number : 18 East Punjabi Bagh 110026 Career Interest : It is my heartfelt desire to join the industry and prove my credentials to the hilt Can work effectively in team as well as individually Have good ... Medical Device Regulatory Affairs Consultant | CECON LLC Medical Device Regulatory Affairs Consultant Technical Consultant #1656 Expertise. Summary. Twenty plus years working in the medical industry in the areas of regulatory affairs, quality assurance, clinical studies, research and development, test, manufacturing and technical service. Regulatory Affairs officer for medical devices 848 ... Regulatory Affairs officer for medical devices 848. Description. To develop a new project we are looking for a Regulatory Affairs officer for medical devices. Responsibilities. Writing Technical files for CE marking, regulation 2017 745, Class IIa medical devices, ... C.V Resume Upload * Download Free CV Templates Regulatory Affairs CV Templates. Download as ... Life Science Microbiology Regulatory Affairs Clinical Research Cork Engineering Medical Device Clinical Research Galway Quality Assurance Life Science Scientific Nurse Associate Connected Health Biopharmaceutical Dublin Contract EHS Engineer Medical Affairs ... Regulatory Affairs | Tel: 353 1 685 4848 | Fax: 353 ... CURRICULUM VITAE PROFILE Professional Experience Senior ... CURRICULUM VITAE (name, contact info) PROFILE A global regulatory professional with twenty two years clinical drug development experience, seventeen of which within global regulatory affairs. Broad experience across various therapeutic areas including CNS, anti infective, ophthalmology, GUGI, respiratory and oncology. Regulatory Affairs Jobs | Regulatory Affairs Careers April ... work closely with the Quality & Regulatory Affairs Manager to develop and deliver a range of proactive and responsive QMS initiatives. Job Title: Regulatory Affairs Officer. Job Type: Permanent. Location: Buckinghamshire. Salary: Up To £35,000. Job Summary. To support the medical devices, supply chain … more Job Offer: Regulatory Affairs Officer Medical Devices The Regulatory Affairs Officer – Medical devices will be in charge of the timely and correct execution of projects according to defined timelines: Work with direct reports to develop successful global regulatory strategies to ensure timely device approvals: roadmaps, viability analysis, clinical evaluation, risk management A career in regulatory affairs | New Scientist Jobs A graduate in science with a desire to make a difference will find the world of Regulatory Affairs (RA) very rewarding. Regulatory Affairs was introduced by government authorities to monitor and regulate the development, manufacture, testing and marketing of drugs, medical devices, food products, cosmetics and veterinary products. Regulatory specialist medical devices Jobs | Glassdoor The Senior Specialist, Regulatory Affairs for TMTT will complete and maintain clinical and commercial regulatory approvals of Class III implantable products in the US, Canada and EU, focused…Coursework, seminars, and or other formal government and or trade association training is required Experience preparing domestic and international product submissions for medical device products is ... Regulatory Affairs Officer Jobs on Irishjobs Reporting to the Director of Quality and Regulatory Affairs the Senior Regulatory Affairs will take an active role in developing the Regulatory strategy in Europe and the US and interacting with the relevant Regulatory and Notified Bodies. * Proven track record in a similar role with a minimum of 5 years in medical device Regulatory Affairs Regulatory Affairs Medical Device Jobs, Employment ... 2,235 Regulatory Affairs Medical Device jobs available on Indeed . Apply to Regulatory Specialist, Medical Consultant, Regulatory Affairs Talent munity Remote and more! Regulatory affairs officer Sample Resume With Objective Preparation and review of the dossiers as per the current prescribed guidelines of the respective regulatory authorities. Collection of various pharmacological, pre clinical & toxicological data. Review of the quality and analytical data as per the pharmacopoeia, specification, MOA, STP, batch records, Stability, Finished product Packaging material data for the purpose of compilation of the ... Regulatory affairs officer: job description | TARGETjobs A list of courses and MScs are also available on The Organisation for Professionals in Regulatory Affairs (TOPRA) website. Postdoctoral research, practical research or laboratory work experience is also beneficial. Regulatory affairs experience is particularly sought after. Key skills for regulatory affairs officers. IT skills; Negotiation skills How to get a job in regulatory affairs | Proclinical blogs Regulatory affairs is a vital function in safeguarding the health and wellbeing of millions of people worldwide but regulatory affairs jobs can be a difficult to attain for graduates and even those looking to move from other specialities with relatable skills. Regulatory affairs manager medical devices Jobs | Glassdoor The Regulatory Affairs Specialist will assist and coordinate the compilation, preparation and assembly of regulatory submission and support files for medical devices and in vitro diagnostics… promotional material Product IFUs FUJIFILM Irvine Scientific Website Primary back up to the Senior Regulatory Affairs Manager Experience Education: Bachelor’s… Senior Regulatory Affairs Officer Jobs in January 2021 ... A Regulatory Affairs Officer is required to work for a world class medical device … £30M turnover, this is a great opportunity for a Regulatory Affairs professional to add a … Reporting to the Regulatory Affairs Director, you will provide a service to ensure … Sr Regulatory Affairs Specialist Medtronic Careers Must Have: Minimum Requirements . To be considered for this role, please ensure the minimum requirements are evident on your resume. Bachelor’s degree with 4 years of experience in regulatory affairs and or regulated industry (medical device, pharma, biotech) OR Advanced degree with 2 years of experience in regulatory affairs and or regulated industry (medical device, pharma, biotech).

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