null In this role, you have the opportunity to Lead one of the Regulatory Affairs groups within the Device group of the Image Guided Therapy Business Unit within Philips. You will be leading individual contributors, generally operating at a more senior level, establishing team development plans and clear communication processes are key, formulating the medium term regulatory policy for his/ her sub discipline and processes results into a regulatory strategic plan, while also being involved in de...

Job Title: Regulatory Affairs Manager Location: Vantaa, Finland Requisition ID: 115828BR   When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $24 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make signi...

Job Title: Regulatory Affairs Specialist Requisition ID: 110780BR   Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of more than $20 billion and approximately 75,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory...

The Regulatory Affairs Coordinator is a 100% office based professional with Scientific and Clinical expertise, who is responsible for the regulatory activities associated with AZ-Divestment projects and license maintenance through-out product’s life-cycle. The Regulatory Affairs Coordinator is responsible for ensuring the registration files are prepared according to the local registration guidelines, communication with both global teams and local agents, follow up through-out submission and appr...

Regulatory Affairs Specialist- 12 month Fixed Term Contract   When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of $20 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world. &nbs...

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do.  A dynamic, global company founded in 1995, we bring together more than 2,000 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description Join our international team and support regulatory aspects of clinical research projects, streamlining communic...

En todo el mundo, nuestros empleados están unidos por nuestra misión de salvar y mantener vidas. Juntos creamos una cultura que incentiva a los colegas a ir en pos de carreras gratificantes, una cultura en la que todos tienen la oportunidad de hacer un trabajo significativo como parte de un equipo que respetan, en un entorno que valora las contribuciones de cada persona. Estamos felices de que a usted le interese continuar su viaje profesional con Baxter. Objetivo: Apoyará el desarrollo de nuevo...

The Mission Within Patheon, part of Thermo Fisher Scientific in Tilburg, we are responsible for the development and production of commercial medicines in dosed forms (soft gel capsules). You can think of products such as paracetamol, ibuprofen, but also various supplements. The soft gel capsules are available at pharmacies and drug stores but also on a doctor's prescription. Because everyone contributes to the development and production of our soft gel capsules, we are all responsible to make th...

Around the world, our employees are united by our mission to save and sustain lives. Together, we create a culture that encourages colleagues to pursue rewarding careers -- where everyone has the opportunity to do meaningful work as a part of a team they respect, in an environment that values each person’s contributions. We’re happy you’re interested in continuing your career journey with Baxter. Summary Responsible for the implementation of complex regulatory strategies, obtain and maintain mar...

Around the world, our employees are united by our mission to save and sustain lives. Together, we create a culture that encourages colleagues to pursue rewarding careers -- where everyone has the opportunity to do meaningful work as a part of a team they respect, in an environment that values each person’s contributions. We’re happy you’re interested in continuing your career journey with Baxter. Essential Duties and Responsibilities.  This section contains a list of five to eight primary respon...

Career Category Regulatory Job Description Regulatory Affairs Manager Regulatory Manager Affiliate--China Reporting to: Senior, Regulatory Affairs Manager Based in: Beijing Job Description: Purpose: -- Ensure that Amgen acquires and maintains all the required licenses in order to trial investigational medicinal products as well as market commercially approved medicinal products. --Ensure that only high quality products and their supporting information are presented to patients and healthcare pro...

T-BOMA Trenton-BOMA Limited Pharmaceutical Distribution   Regulatory Affairs Executive   The Company: A pharmaceutical distributor established in Year 2000in HKfor the marketing of top generic pharmaceuticals & biopharmaceuticals imported from Europe, Canada and Asia. Our product range includes over 200 products and our distribution coverage spreads across private doctors, private hospitals, the Hospital Authority, pharmacies and chain drugstores.   The Job: Opportunity for a career in regul...

Job Description Summary The Regulatory Affairs Specialist (RAS) demonstrates ability to create and communicate global regulatory requirements throughout the product lifecycle working closely with a cross functional team. The RAS is able to interpret and communicate regulatory changes to ensure the business is aware of opportunities, risks and issues. The RAS is responsible for ensuring compliance with the regulations and Bard Peripheral Vascular processes and procedures. The RAS utilizes project...

Position Purpose Regulatory Affairs Manager is responsible for the plan and implementation of product registration, maintaining the approved product licenses and coordinating regulatory Affairs activities in compliance with Health Authority’s regulations and Company’s Standard Operating Procedures (SOPs). She (he) needs to liaise with Pfizer colleagues for supports and guidance. She (he) should keep good relationship with the regulatory authority, provide knowledge and experience to junior colle...

Category: Regulatory Location: Tianjin, Tianjin, CN Education Background: 1.Bachelor or above degree of pharmaceutical, medical, chemistry, or related life-science discipline 2.Fluent in written and spoken English Professional Experience: 1.More than 10 years of proven track record of regulatory experience in the pharmaceutical company 2.Well understand China registration policies and procedure, strong expertise in Drug Technology Transfer (DTT) Key areas of responsibility: The senior specialist...

Position Summary: As an internal reviewer, check the submission documents according to regulation and best practice, give reasonable comments. Focus on regulation environment changes, improve review standard and transfer to stakeholders accordingly. Create and update related SOP/WI and share best practice among BUs. Mange product change notification process and organize discussion with stakeholders accordingly. Principal Accountabilities: Develop the submission check plan according to priority a...

深圳市 Job Title Regulatory Affairs Manager Job Description In this role, you have the opportunity to Lead regulatory team/resource to ensure timely product registration, regulatory planning for new product introductions and product changes, and assist in maintaining regulatory compliance. Plan, generate and coordinate product submission for global licensing; You are responsible for Leads regulatory team/ resource to ensure timely product registration, regulatory planning for new product introducti...

北京市 Role Summary: This position provides subject matter guidance. He/she works within a team of Regulatory Affairs professionals to ensure GEHC establishes best practices in compliance with regulatory requirements. The Regulatory Affairs Leader will be involved with regulatory activities in the areas such as premarket submissions, post-market reporting, regulatory intelligence, regulatory requirements flow-down advertising and promotion review, product labeling compliance, etc., Essential Respon...

Regulatory Affairs Specialist (Hong Kong)  Our client is a Global Pharmaceuticals and Medical Devices group with offices all over the world. They are seeking a Regulatory Affairs Specialist for their Hong Kong Offices. The RAS will specialize in drug & medical device registrations and variations in accordance with relevant regulations and develop the strategy to obtain the product approval within the target timeframe.   Role Purpose: The main duty of the Regulatory Affairs Specialist will be...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use. Job Description Responsibilities: In accordance with the company’s product launch strategy and department’s work plan, take full responsibility of the product registration and application for approval and develop the plan by stage. Contribute to decision making on drug registration leading to minimal registra...