Regulatory Affairs Specialist II

Job OverviewThis role is an exciting opportunity to join our team as a Regulatory Affairs Specialist II.As a key member of our Infectious Disease business unit, you will be responsible for preparing documentation for EU Technical Files and international product registrations.

We are seeking a Regulatory Affairs Specialist to join our team in the Infectious Disease business unit.The successful candidate will be responsible for preparing documentation for EU Technical Files and international product registrations.This is an excellent opportunity for a skilled Regulatory Affairs professional to take their career to the next level...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Collabera. As a key member of our Infectious Disease business unit, you will be responsible for preparing documentation for EU Technical Files and international product registrations.

We are seeking a highly skilled Regulatory Affairs Expert to join our team at Collabera, a Global Digital Solutions Company.Job OverviewCollabera is a leading provider of Software Engineering Solutions for the world's most tech-forward organizations in areas such as Engineering, Cloud, and Data/AI. With operations across 60 locations in 11 countries, we...

About the RoleThis Regulatory Affairs Specialist position involves technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR). You will provide regulatory support for diagnostic product development and commercial diagnostic products, developing regulatory strategies for products in development and for modified products...

We are seeking a highly motivated Compliance Officer II to join our team in the Infectious Disease business unit.The successful candidate will be responsible for ensuring compliance with regulatory requirements and developing regulatory strategies for products.Key Responsibilities:Analysis of regulatory requirements and development of compliance...

About the RoleThe estimated salary for this position is $120,000 - $180,000 per annum.We are seeking a highly skilled Medical Affairs Manager to join our team at Collabera. The successful candidate will be responsible for defining medical affairs strategy and conducting medical activities related to the IVDR process.Key responsibilities include:Supporting...

We are seeking a highly skilled EU Regulatory Compliance Manager to join our team at Collabera. As a key member of our Regulatory Affairs department, you will be responsible for ensuring compliance with EU regulatory requirements for our Infectious Disease business unit.This is an exciting opportunity for a talented professional to develop their skills in...

About PSG Global Solutions CareersWe are a leading clinical development company with 20+ years of experience in clinical research and strategic resourcing.

About Abbott LaboratoriesAs a global healthcare leader, Abbott Laboratories helps people live more fully at all stages of life. Our diverse portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.We have 114,000 colleagues...

About Our CompanyKyyba is a leading provider of high-quality resources and top-notch recruiting services. With a global presence and headquarters in Farmington Hills, MI, we enable businesses to effectively respond to organizational changes and technological advances. Our core values of value, passion, excellence, empowerment, and happiness create a vibrant...

About the JobThis is an exciting opportunity for a skilled professional to join our team as a Regulatory Compliance Officer II. In this role, you will work closely with our manufacturing team to ensure that all products meet regulatory requirements.Key ResponsibilitiesDevelop and implement quality control processesConduct regular audits to ensure compliance...

Job OverviewWe are seeking an experienced Regulatory Compliance Specialist to ensure the quality and compliance of GxP-regulated software solutions. This role involves oversight of the Software Lifecycle deliverables, collaboration with cross-functional teams to build compliance capabilities, and supporting audits.Key Responsibilities:SOC and SLC Deliverable...

About UsAbbott Laboratories is a global healthcare leader dedicated to helping people live more fully at all stages of life. Our diverse portfolio spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.We empower smarter medical and economic decision-making to help...

Collabera is seeking a highly motivated and experienced Technical Writing Expert to join our team. As a key member of our Regulatory Affairs department, you will be responsible for developing regulatory documents, including EU Technical Files and international product registrations.This is an excellent opportunity for a talented writer to leverage their...

About the RoleWe are looking for a skilled Clinical Research Associate to join our team in Lake Forest, IL.The successful candidate will be responsible for managing sites through the life of trial and close-out, ensuring compliance with applicable Corporate and Divisional Policies and Procedures.Key Responsibilities:Conduct site qualification and initiation...

Key ResponsibilitiesThe successful candidate will be responsible for:Preparing documentation for EU Technical Files and international product registrationsProviding regulatory support for diagnostic product development and commercial diagnostic productsDeveloping regulatory strategies for products in development and for modified productsResearching and...

About the Role:Aunt Martha's Health and Wellness Inc. is seeking a dedicated Community Support Specialist II to join our team. This exciting opportunity will allow you to make a positive impact on the lives of at-risk youth in our community.Job Summary:The Community Support Specialist II will be responsible for providing assessment, counseling, and service...

OverviewAbbott Laboratories is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.We have an opportunity for a Global Product Lead for...

About the RoleWe are seeking a skilled Quality Assurance Specialist to join our team at Kyyba. As a Quality Assurance Specialist, you will play a critical role in ensuring the quality of our medical devices and maintaining compliance with regulatory requirements.Key ResponsibilitiesEnter records in eQMS systems such as Isotrain, Trackwise, Veeva, Agile,...