EU MDR Compliance Specialist

Job Title: EU MDR Regulatory Content SpecialistAbout DEV-X Consulting LLCDEV-X Consulting LLC is a leading provider of medical device regulatory consulting services. Our team of experts helps clients navigate the complex EU MDR landscape and ensure compliance with all relevant regulations.Job SummaryWe are seeking a highly skilled EU MDR Regulatory Content...

Job Title: EU MDR Project Manager SpecialistWe are seeking an experienced project manager to oversee the planning, coordination, and implementation of projects within a highly regulated industry. The ideal candidate will have a strong understanding of CERs within EU MDD MDR compliance and excellent communication skills to effectively monitor and present...

Job OverviewWe are seeking a highly organized and skilled project manager to oversee EU MDR projects from planning to implementation. This is an excellent opportunity for individuals with experience in the medical device or pharmaceutical industry.The successful candidate will have strong business acumen, excellent communication skills, and a solid...

Job SummaryThe EU MDR Marketing Claims Specialist will play a critical role in ensuring the success of our EU MDR program. The successful candidate will have excellent project management skills and be able to work effectively in a fast-paced environment.Key Responsibilities:Coordinate the defined cadence of the EU MDR program work for claims with other copy...

Project Manager - EU MDRWe are seeking a seasoned project manager to lead our EU MDR projects from concept to completion. This is a unique opportunity to work in a highly regulated industry and contribute to the development of innovative medical devices.The successful candidate will have a strong background in project management, excellent communication...

Project Manager Role at DEV-X Consulting LLCWe are searching for a highly motivated and experienced project manager to join our team at DEV-X Consulting LLC. As a key member of our team, you will play a critical role in driving project success.The salary for this role is estimated to be around $90,000 - $120,000 per year, depending on experience and...

About the RoleThis is a high-visibility project that requires exceptional time management and coordination skills. The ideal candidate will have experience working in a regulated industry and possess a solid understanding of EU MDR compliance.As a project manager, you will be responsible for setting project timelines, monitoring deliverables, and providing...

Job DescriptionIn this role, you will lead the execution of projects related to EU MDR compliance and medical devices.As a seasoned project manager, you will be responsible for ensuring that all aspects of the project are completed on time, within budget, and to the required quality standards.You will work closely with clients, stakeholders, and project team...

About the RoleWe are looking for a highly organized and detail-oriented Marketing Claims Coordinator to coordinate the defined cadence of the EU MDR program work with other copy review workstreams such as active CAPAs. The ideal candidate will have experience in medical devices within the EU MDD and/or EU MDR regulations.

Company Overview: DEV-X Consulting LLC is a leading consulting firm that specializes in providing expert services to companies operating in highly regulated industries. Our team has extensive experience in managing complex projects and ensuring compliance with regulatory requirements.Job Description: As a Regulatory Affairs Project Coordinator, you will play...

Job Title: Medical Device Marketing Communications CoordinatorAbout DEV-X Consulting LLCAt DEV-X Consulting LLC, we are passionate about helping medical device companies succeed in the EU MDR landscape. Our team of experts provides customized regulatory consulting services to meet the unique needs of each client.Job SummaryWe are seeking a highly skilled...

Computer Systems Compliance Specialist Job DescriptionWe are seeking a skilled Computer Systems Compliance Specialist to join our team in Exton, PA. As a Software Validation Engineer at Pharmaron, you will play a critical role in ensuring the compliance of our computer systems with regulatory requirements. With a strong background in software validation and...

Quality Assurance Director Job DescriptionThis key leadership position oversees the quality assurance function, ensuring compliance with regulatory requirements and industry standards. The ideal candidate will have a strong background in pharmaceutical quality assurance and leadership.Key Responsibilities:Develop and implement quality management systems to...

Overview:West Pharmaceutical Services is a leading global company dedicated to developing innovative pharmaceutical solutions. As a Senior Quality Engineer, Integrated Systems, you'll play a critical role in ensuring the quality of our products and processes.Key Responsibilities:Develop and implement quality systems and procedures to ensure compliance with...

About Zenith LifeScience:Zenith LifeScience is a leading provider of life sciences solutions, dedicated to delivering high-quality products and services to our customers. We are committed to excellence in all aspects of our business, including quality assurance, regulatory compliance, and customer satisfaction.We are seeking a highly experienced Quality...

RequirementsTo succeed in this role, you will need:Minimum 7 years direct construction safety experience requiredDegree in a safety-related field preferredOSHA 511 and or 501 a plusCSP certification preferredExcellent written and verbal communication skills requiredProficient Microsoft Office skillsAbility to embody HazTek's Core Values of Integrity,...

About the RoleAs an Occupational Health Specialist at HazTek Inc., you will play a vital part in ensuring best practices are implemented and safety compliance requirements are met across various projects. This role requires someone with a strong background in construction safety, preferably with 7 years of direct experience.We offer a competitive...

Job DescriptionWe are seeking a highly skilled Clinical Data Management Specialist to join our team at Frontage Laboratories, Inc. in Exton, PA.About the Job:Manage data transfers between Frontage and clients, adhering to company SOPs and relevant regulations.Develop and maintain data management templates for internal reporting and external transfer.Work...

Job Title: Patient Registration SpecialistRole Overview:We are seeking an experienced Patient Registration Specialist to join our team at The Center for Orthopedic and Research Excellence. In this role, you will be responsible for registering patients, managing patient data, and ensuring a seamless patient experience.Responsibilities:Greet patients, verify...

Job Title: Senior Computer Systems Validation SpecialistAbout Us:Frontage Laboratories is a leading contract research organization offering a range of services in drug development, including bioanalytical, pharmacokinetics/pharmacodynamics, safety and toxicology, chemistry and manufacturing controls, and core laboratory services for clinical trials.Job...