Senior Life Sciences Regulatory Affairs Consultant

At Vision Achievement, we're seeking a seasoned Senior Life Sciences Consultant to join our team. With a strong background in regulatory affairs and quality assurance, you'll play a crucial role in delivering high-quality consulting engagements related to quality/regulatory affairs infrastructure.This exciting opportunity comes with an estimated salary of...

Vision Achievement is seeking an experienced Senior Life Sciences Consultant to lead regulatory affairs and quality assurance initiatives in the medical devices, pharmaceuticals, and cosmetics industry. About the Role:As a Senior Life Sciences Consultant with Vision Achievement, you will provide expert guidance on regulatory and quality assurance...

Job DescriptionIn this exciting role with Vision Achievement, you will work as an independent contractor, leveraging your expertise in RA/QA to deliver high-quality consulting services. As a Regulatory Affairs Consultant - Quality Assurance Expert, you will plan and execute life science consulting engagements related to quality/regulatory affairs...

Consulting Opportunities with Vision AchievementWe are seeking experienced consultants to join our team at Vision Achievement, where you will have the opportunity to leverage your expertise in RA/QA matters related to life sciences industry sub-sectors. This exciting role is ideal for independent contractors with significant experience in designing,...

We are seeking a highly skilled Senior Quality Assurance Consultant to join our team at Vision Achievement. This exciting role is for independent contractors with significant experience in the RA/QA aspects of life sciences industry sub-sectors such as medical devices, in vitro diagnostics, lab developed tests, pharmaceuticals, and cosmetics.You will likely...

Company Overview">Vision Achievement is a top-rated consulting firm dedicated to providing exceptional services to the life sciences industry. Our team of experts is passionate about patient safety and population health improvement.SalaryWe offer competitive compensation, defined by project, with an estimated annual salary range of $85,000-$110,000,...

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...

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 OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Spain. This role will be responsible for delivering site activation readiness within assigned countries/sites and ensuring compliance with international and local regulations.The ideal candidate will have a strong understanding of clinical trial regulations,...

About the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our teams in Spain and contribute to the development of our local regulatory presence.Key ResponsibilitiesProvide guidance and support for managing submissions and requests from clients regarding Spain.Contribute to regulatory activities, including pre-licensing, new registration,...

About the RoleWe are seeking a highly experienced Senior Regulatory Affairs Officer to join our team at QbD Group in Spain. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with pharmaceutical legislation and regulations.With a strong background in regulatory affairs, you will have expertise in ICH...

Job Summary:We are seeking a skilled Regulatory Compliance Specialist to join our team at Vision Achievement. As a key member of our life sciences team, you will be responsible for providing expert guidance on regulatory and quality assurance infrastructure, ensuring compliance with relevant regulations and standards.In this role, you will conduct thorough...

STRAGO Healthcare is a leading global consultancy that provides top-tier talent services to major Healthcare and Life Sciences organizations worldwide.We are seeking an experienced Clinical Strategy Director - Regulatory Affairs to provide expert strategic advice on clinical and regulatory matters for global drug development projects. In this role, you will...

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...

Regulatory Affairs Role OverviewAs a Regulatory Affairs Specialist at IQVIA, you will play a critical role in supporting clinical trial and marketing authorization activities for both internal and external clients. Your expertise will be instrumental in preparing and reviewing regulatory submissions to ensure compliance with regulatory requirements.Key...

Location: 100% Remote, in the USA. Residency: US Citizen/permanent resident required for US status. Independent Contractor Role with Vision Achievement. This exciting opportunity is for independent contractor quality assurance experts with significant experience in RA/QA aspects of life sciences industry sub-sectors such as medical devices, in vitro...

Job DescriptionThis is a highly specialized role for an experienced Regulatory Affairs professional, with expertise in biopharmaceuticals and biosimilars. You will be responsible for ensuring the adequacy of CMC documentation for global regulatory submissions, including regional registration processes.The ideal candidate will have broad knowledge of global...

**Company Overview**ICON Plc is a world-leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.We are currently seeking a Clinical Research Associate Director -...

Company OverviewQbD Group is a knowledge-based company specializing in development, clinical, regulatory, and compliance services for the life sciences industry. Our team is dedicated to providing tailored solutions that meet the unique needs of our clients.Salary and BenefitsWe offer an attractive and competitive salary package tailored to individual needs,...

Role Overview: As a Senior Manager of Government Affairs and Policy at Bristol Myers Squibb, you will be responsible for developing and executing strategies to shape healthcare policies and regulations in favor of the company's interests. This involves building relationships with government officials, policymakers, and stakeholders, and aligning strategies...