Regulatory Affairs Specialist

About the RoleAs a highly skilled Regulatory Affairs Specialist, you will be responsible for ensuring the successful start-up and regulatory compliance of clinical trials. With your expertise in the pharmaceutical industry, you will play a key role in managing study start-up and regulatory deliverables.

Regulatory Affairs SpecialistJohnson and Johnson is seeking a skilled Regulatory Affairs Specialist to join our team in Madrid. This role offers a hybrid working model and is an exciting opportunity to contribute to our company's mission to build a world where complex diseases are prevented, treated, and cured.Key ResponsibilitiesSupport the growth of our...

Job OverviewVision Achievement is seeking an experienced Life Sciences Regulatory Affairs Specialist to join our team. As a key member of our consulting group, you will be responsible for planning and delivering life science consulting engagements related to quality and regulatory affairs infrastructure.

Job Title: Regulatory Affairs Specialist at EricssonAbout the Role:We are seeking a highly skilled Compliance Manager to join our team in Sao Paulo, Brazil. As a key member of our organization, you will play a crucial role in ensuring that we maintain the highest standards of compliance and regulatory adherence.About You:To be successful in this position,...

**Company Overview:** Vision Achievement is a leading provider of regulatory and quality consulting services to the life sciences industry. Our team is dedicated to helping clients navigate complex regulatory landscapes and achieve compliance with industry standards.**Compensation:** $85,000 - $110,000 per year, depending on experience and qualifications....

Job Description: Ferring Pharmaceuticals seeks a Quality Assurance & Regulatory Affairs Specialist to support and contribute to the Quality and Regulatory Affairs team. Key responsibilities include managing the company's system of procedures, preparing and reviewing SOPs, and monitoring submitted variations to obtain approvals. Requirements:- Health Sciences...

About KenvueKenvue is a global leader in the development of innovative consumer goods. Our team of experts is passionate about delivering high-quality products that meet the needs of our customers.Job SummaryWe are seeking a highly motivated Regulatory Affairs Specialist to join our team in Spain. As a key member of our regulatory affairs department, you...

Job DescriptionWe are seeking a skilled Regulatory Affairs Specialist to join our team at Zentiva Group, a.s. as part of our regulatory affairs department.About the RoleThis is a challenging and rewarding opportunity for an experienced professional to contribute to the company's success by ensuring compliance with regulatory requirements and guidelines. The...

Regulatory Affairs InternWe are currently recruiting for a Regulatory Affairs intern at Kenvue. As a member of our global team, you will contribute to the development and implementation of regulatory strategies for our products. Your responsibilities will include coordinating and compiling new drug applications, cosmetics, and medical devices for submission...

Galderma is a pioneering dermatology company with a rich legacy and commitment to innovation. With operations in approximately 90 countries, we deliver a diverse portfolio of premium brands and services that cater to the evolving needs of the dermatology market.We are seeking an expert Regulatory Affairs CMC Specialist to join our team in Barcelona. As a key...

At Ferring Pharmaceuticals, we are seeking a motivated and detail-oriented Regulatory Affairs & Quality Assurance Specialist to join our team. This temporary position will support the Quality and Regulatory Affairs team in Madrid, covering maternity leave.About UsWe are a global pharmaceutical company dedicated to helping people build families and live...

Company Overview: Vision Achievement, a leading provider of life sciences consulting services, is seeking an experienced Regulatory Affairs Specialist to join our team. This exciting opportunity allows you to leverage your expertise in RA/QA matters related to medical devices, in vitro diagnostics, pharmaceuticals, and cosmetics.Job Description: As a...

About the CompanyErgomed Group is a rapidly expanding full-service CRO specializing in Oncology and Rare Disease, with operations in Europe, North America, and Asia.We value employee experience, well-being, and mental health, acknowledging that a healthy work-life balance is crucial for employee satisfaction and high-quality client service.Job DescriptionThe...

Oatly, the original oatmilk company, is expanding its presence in North America and seeks a highly skilled Regulatory Affairs Manager to join our team. As the leader of our US-based regulatory affairs function, you will provide expert guidance on food law and compliance matters.About the Role:This role involves leading the Oatly North America Regulatory...

About the RoleErgomed is a rapidly expanding full-service CRO specializing in Oncology and Rare Disease. As a Senior Specialist, Study Start Up and Regulatory, you will be responsible for completing study start-up and regulatory deliverables based on an established SSU RA management plan.The ideal candidate will serve as a liaison between SSU/regulatory...

OverviewKenvue is a leading company in the healthcare industry, dedicated to delivering innovative products and services that improve people's lives. Our team is passionate about science and care, and we're committed to making a positive impact on the world.Job DescriptionWe're seeking a highly motivated and detail-oriented Regulatory Affairs intern to join...

About the RoleBitfinex is a leading digital asset trading platform seeking an experienced Senior Regulatory Affairs Specialist to join its regulatory licensing team.Job DescriptionThis role will be responsible for managing regulatory licensing engagements from planning to completion, engaging with regulatory consultation processes in different countries, and...

Kenvue, a leading company in the pharmaceutical industry, is seeking a highly skilled Regulatory Affairs Professional to join its team in Madrid, Spain. As a key member of our regulatory department, you will be responsible for ensuring compliance with regulatory requirements and guidelines for new drug applications, cosmetics, medical devices, food...

Parexel, a leading Clinical Research Organization (CRO), is seeking an experienced Regulatory Affairs Consultant to drive success in post-approval Chemistry, Manufacturing, and Controls (CMC) activities.This exciting opportunity is based in various European locations, offering the chance to work remotely or from our office. As a Principal Regulatory Affairs...

Job Description:    At Vision Achievement, we are seeking an experienced Regulatory Compliance Specialist to join our team. This exciting role offers a unique opportunity to work with clients in the life sciences industry, providing expert guidance on quality and regulatory affairs.About the Role:    As a Regulatory Compliance Specialist, you will be...