Regulatory Submissions Director with Expertise in Life Sciences

**Vision Achievement**: A Top-Rated Team for Life Sciences Consulting ExpertsWe are seeking highly organized and self-starting individuals with significant experience in RA/QA aspects of life sciences industry sub-sectors such as medical devices, in vitro diagnostics, lab developed tests, pharmaceuticals, and cosmetics.The role involves designing,...

Company Overview: At Vision Achievement, we pride ourselves on delivering top-notch consulting services to the life sciences industry. With a strong focus on quality and regulatory affairs, we help our clients navigate complex regulations and ensure compliance with industry standards.Salary: $120,000 - $150,000 per year, depending on experience.Job...

Job Title:Regulatory Assurance Specialist - Life SciencesAbout Us:Vision Achievement is a leading provider of regulatory and quality assurance services to the life sciences industry.Compensation:The estimated annual salary for this position is $120,000 - $180,000, depending on experience.Job Description:We are seeking an experienced Regulatory Assurance...

Job Summary: We are seeking a highly experienced Regulatory Affairs expert to join our team at United Staff Source. This role is ideal for individuals with significant experience in RA/QA aspects of life sciences industry sub-sectors such as medical devices, in vitro diagnostics, lab-developed tests, pharmaceuticals, clinical manufacturing, and...

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...

Job Summary: We are seeking a highly experienced Regulatory Submissions Project Manager Lead to join our team at IQVIA. This role will lead a worldwide delivery team responsible for the development and harmonization of the Regulatory Submissions Process.About the Role: The Associate Director – Regulatory Submissions has experience working with QRDs, CTDs,...

Job DescriptionWe are seeking an experienced independent contractor with a strong background in Regulatory Affairs (RA) and Quality Assurance (QA) within the life sciences industry. This role involves providing expert consulting services in the RA/QA domains, specifically focusing on medical devices, in vitro diagnostics, lab-developed tests,...

Company OverviewVision Achievement is a leading provider of regulatory and quality assurance services to the life sciences industry. Our team of experts works closely with clients to ensure compliance with relevant regulations and standards.">About the RoleThis exciting opportunity is for an independent contractor or contract-for-hire with significant...

Company Overview: At Vision Achievement, we are committed to delivering exceptional consulting services that drive patient safety and population health improvement. Our team of experts works closely with clients to provide tailored solutions that meet their unique needs.Salary: We offer competitive compensation packages for our consultants, with an estimated...

Job DescriptionVision Achievement is seeking a highly experienced Clinical Auditor to join our team as an independent contractor. This exciting role offers the opportunity to work on various life sciences consulting engagements related to quality and regulatory affairs infrastructure, with a focus on patient safety and population health improvement.Key...

We are seeking experienced independent contractors with a robust background in Regulatory Affairs (RA) and Quality Assurance (QA) within the life sciences industry. This role involves providing expert consulting services in the RA/QA domains, specifically focusing on medical devices, in vitro diagnostics, lab-developed tests, pharmaceuticals, and...

Deliver high-quality regulatory submissions translation and localization projects to completion while ensuring our standards are met. As a Regulatory Submissions Project Manager, you will work closely with the wider project management team to coordinate and manage multiple projects simultaneously from receipt to completion.About UsIQVIA is a leading global...

**Company Overview:**   Vision Achievement is a leading life sciences consulting firm dedicated to helping clients navigate complex regulatory landscapes and improve patient safety. Our team of experts provides tailored solutions for companies operating in the medical device, in vitro diagnostics, pharmaceuticals, and cosmetics industries.**Salary:**...

About Vision AchievementWe are a top-rated team of independent contractors who specialize in providing high-quality consulting services to the life sciences industry. Our mission is to help our clients achieve their goals by providing expert advice and support in areas such as quality assurance, regulatory affairs, and compliance.Compensation PackageWe offer...

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 Overview**Vision Achievement is seeking a highly experienced Quality Assurance Specialist to join our team as an independent contractor. This exciting role offers the opportunity to work on various projects related to quality and regulatory affairs in the life sciences industry.**Estimated Salary:** $120,000 - $180,000 per year, depending on experience...

About Our CompanyBAS Life Science is a global consulting enterprise working exclusively in the life sciences industry. We are a company that values diversity, collaboration, and innovation, and we are seeking a talented Life Sciences Data Leader to join our team.As a Life Sciences Data Leader, you will lead our data architecture and analytics efforts,...

Lead Regulatory Affairs for a Leading Pharmaceutical CompanyWe are seeking an experienced Regulatory Affairs Associate Director to join our team at Mcr International. This strategic role is based in Madrid, Spain and offers the opportunity to shape and implement groundbreaking regulatory strategies on a global scale.Key Responsibilities:Spearhead the...

Company OverviewSalve Consulting is a leading consulting firm specializing in life sciences transactions. Our team of experts provides exceptional service and solutions to clients across the industry.Salary RangeWe offer a competitive salary range of $120,000 - $180,000 per year, commensurate with experience.Job DescriptionWe are seeking a Senior Life...

About the Role: As a Salesforce Architect at Base Life Science A/S, you will be responsible for leading the design and development of Salesforce solutions tailored to the unique needs of our pharmaceutical and healthcare clients. This role requires a deep understanding of Salesforce capabilities, healthcare industry practices, and strong consulting...