Medical Device Regulatory Compliance Specialist

Job DescriptionThis role is designed to support the regulatory department in ensuring efficient and compliant business processes and environment. As a Regulatory Affairs Specialist, you will execute tasks to evaluate product and software changes in consideration of regulatory guidance documents and regulations.Your responsibilities will include providing...

Job DescriptionWe are seeking a Senior Quality Professional to join our team at Kyyba. As a Senior Quality Professional, you will be responsible for ensuring the quality of our medical devices and maintaining compliance with regulatory requirements.ResponsibilitiesManage supplier quality metrics and performance monitoring.Investigate and resolve...

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 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...

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...

Key ResponsibilitiesThe Trade Compliance Special Projects TCRS4206 will be responsible for overseeing special projects for the Trade Compliance Department, ensuring seamless execution of tasks and meeting established deadlines.Key responsibilities include:Supporting the import export compliance program by handling special projects

About the RoleWe are looking for a skilled Assembling Medical Devices Specialist to join our 2nd shift team in Lake Zurich, IL.The ideal candidate will have a strong background in medical device assembly and be comfortable working in a fast-paced environment.Key Responsibilities:Assemble medical devices with attention to detail and precision.Conduct quality...

Job OverviewWe are seeking a Regulatory Compliance Expert in Software Development to join our team at Collabera.This is an exciting opportunity to work with a leading provider of IT consulting and staffing services, delivering high-quality solutions to clients across various industries.ResponsibilitiesEnsure the quality and compliance of regulated...

Job OverviewExperis IT ManpowerGroup is seeking a highly skilled Quality Engineer to join our team. This is a unique opportunity to work with a leading Medical device organization.We offer a competitive pay rate and a 12-month contract with the possibility of extension or hiring.This role involves collaborating with cross-functional teams to build compliance...

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,...

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.

About the Job Are you passionate about ensuring quality and safety in medical devices? Do you have experience with design verification, risk management, and quality control? Look no further! Experis has partnered with a leading medical device organization in Lake County, IL to fill a Quality Assurance Specialist role. As a member of our team, you will play a...

We are seeking a highly skilled Regulatory Affairs Specialist II to join our team at Collabera. As a key member of our Infectious Disease business unit, you will play a crucial role in preparing documentation for EU Technical Files and international product registrations.This is an exciting opportunity for a talented professional to develop their skills in...

Job OverviewWe are seeking a Clinical Contract Assistant to join our team at The Fountain Group. As a key member of our team, you will be responsible for reviewing and editing clinical research contracts to ensure compliance with company policies and regulations.Responsibilities:Review and edit contracts for complianceAnalyze and resolve technical contract...

Job Summary: As a Medical Device Industry Liaison, you will play a critical role in building strong relationships with healthcare customers and providing them with exceptional support. Your expertise in customer service, combined with your knowledge of medical devices, will enable you to deliver tailored solutions that meet their unique...

What You'll DoYou will be responsible for managing investigations and CAPAs for the Quality department, providing oversight and approvals for compliance across all plant operations. Additionally, you will own and approve change controls within the Quality department, ensuring alignment with existing compliance requirements.In this role, you will also provide...

Regulatory Support Professional:Collabera is seeking a highly motivated and detail-oriented Regulatory Support Professional to join our team. The successful candidate will be responsible for providing regulatory support to ensure efficient and compliant business processes and environment. This includes evaluating proposed software, hardware and manufacturing...

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...

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...

Regulatory Compliance Role:Synectics Inc seeks a talented and detail-oriented individual to fill the position of Commercial Compliance Analyst in our US Commercial Compliance department. This role offers a unique opportunity to make a significant impact on our company's regulatory compliance efforts and contribute to the growth and success of our...