Regulatory Affairs Leader for Medical Device Development

Job Title: Regulatory Affairs Team LeadAbout the Role:We are seeking a highly skilled Regulatory Affairs Team Lead to join our team at Straumann Group. The successful candidate will be responsible for ensuring that all products in scope are designed, manufactured, and distributed in accordance with applicable regulatory requirements.Main Responsibilities:*...

Job Title: Team Leader Regulatory AffairsJob Summary:We are seeking a highly skilled Team Leader Regulatory Affairs to join our team at Straumann Group. As a key member of our regulatory affairs team, you will be responsible for ensuring that our products meet all applicable regulatory requirements and are safe and effective for their intended use.Main...

The RoleWe are seeking a highly skilled Device Engineer to join our team at Roche Technical Development, specifically within the Device Development Department.This department is responsible for the development and support of drug delivery devices for our product portfolio, covering a range of engineering disciplines from requirements definition to...

Job SummaryWe are seeking a highly experienced and skilled Global Regulatory Affairs Leader to join our team at Ironwood Pharmaceuticals. In this role, you will be responsible for developing and implementing regulatory strategies across all phases of product development, ensuring timely development of regulatory strategy and operating plans.

Job Summary:As a Regulatory Affairs Expert at Straumann Group, you will be responsible for ensuring that all products in scope are designed, manufactured, and distributed in compliance with applicable regulatory requirements.Main Responsibilities:Ensure product compliance with regulatory requirementsInteract with authorities and other approving bodiesGuide...

Key Responsibilities:As a crucial member of Ironwood Pharmaceuticals' Regulatory Affairs team, you will develop and implement global regulatory strategies for assigned projects and products, ensuring timely development and submission of regulatory materials. Your expertise will help navigate complex regulatory landscapes, drive strategic planning, and foster...

Stratpharma, a rapidly expanding Dermatology company, is seeking a skilled Global Regulatory Affairs Associate to support their dynamic team. This exciting opportunity allows you to be part of a company experiencing significant growth and expansion globally.This highly successful company boasts an impressive 200% year-on-year growth rate and is undergoing...

Job SummaryWe are seeking a highly experienced and skilled Regulatory Affairs professional to lead our international regulatory strategy and team. The ideal candidate will have a strong background in pharmaceutical regulatory affairs, with a focus on global drug development and EU regulatory compliance.Key ResponsibilitiesDevelop and implement global...

Stratpharma AG, a rapidly growing dermatology company, is seeking an experienced Regulatory Affairs Associate to join their team. With a strong focus on global expansion and product development, this role offers an exciting opportunity for individuals looking to make a meaningful impact.The ideal candidate will have a solid understanding of regulatory...

Stratpharma AG - A Fast-Growing Dermatology CompanyWe are seeking a highly skilled Regulatory Affairs Associate to join our dynamic team in ensuring compliance with regulatory requirements and supporting the global registration and approval process for our products.Key Responsibilities:Manage and maintain product registrations and submissions for global...

Job Description for Regulatory Affairs Director at Ironwood PharmaceuticalsResponsibilities and Expectations Develop and lead global regulatory strategies for assigned projects or products across all phases of product development, ensuring timely development and implementation. Participate in or lead cross-functional task forces and initiatives,...

body {font-family: Arial, sans-serif;}Job SummaryWe are seeking a highly skilled Clinical Trial Regulatory Lead to join our team at Roche. As a key member of our Pharma Development Regulatory organization, you will be responsible for leading the clinical trial regulatory strategy and submissions globally (excluding the US, China, and Japan) for molecules and...

Position Overview:We are seeking a highly skilled Medical Director for Clinical Development to join our team at Ironwood Pharmaceuticals. As a key member of our interdisciplinary development team, you will contribute effectively and independently to the clinical development of our assigned assets.About the Role:This is a high-visibility leadership role that...

Job DescriptionWe are seeking a skilled Device Engineer to join our team at Roche Technical Development in the Device Development Department.About the PositionThe successful candidate will be responsible for the development and support of drug delivery devices, including Prefilled Syringes with Needle Safety Devices, Autoinjectors, and high-volume...

Stratpharma AG, a rapidly expanding dermatology company, is seeking a skilled Global Regulatory Affairs Associate to support their growth.This is an exciting opportunity to join a company that is experiencing significant expansion and has a strong presence in the industry.The successful candidate will play a crucial role in ensuring compliance with...

Stratpharma AG is a fast-growing company in the Dermatology sector seeking a Global Regulatory Affairs Associate to join their dynamic team.This is an exciting opportunity to be part of a company that is expanding globally and is currently looking for a professional to ensure compliance with regulatory requirements and support the global registration and...

Stratpharma AG, a rapidly growing dermatology company, is seeking a Global Regulatory Affairs Associate to join their dynamic team.This is an exciting opportunity to be part of a company that is experiencing rapid growth and expanding globally.The successful candidate will play a crucial role in ensuring compliance with regulatory requirements and supporting...

Aixial Group, a renowned Clinical Research Organization (CRO), is seeking an experienced Lead CMC Dossier Manager to join our team in Basel, Switzerland. Our company specializes in Life Science, providing technical support on clinical projects from phases I to IV and post-market.We are part of the Alten family since 2014 and have been expanding our...

About the RoleWe are seeking a highly skilled Regulatory Strategy and Submissions Lead to join our Pharma Development Regulatory (PDR) organization at Roche. This is an exciting opportunity to develop and maintain licensees that permit us to market and sell life-improving therapies worldwide.As a Clinical Trial Regulatory Lead, you will lead the clinical...

The RoleR oche is recruiting for an experienced Device Engineer to support the development of drug delivery devices, including Prefilled Syringes with Needle Safety Devices, Autoinjectors, and high-volume Patch-injectors.About the TeamThe Device Engineering group is responsible for the design, engineering, testing, and manufacturing of reliable and safe drug...