Regulatory Compliance Labeling Specialist for Medical Devices

Overview:RQM+ provides comprehensive regulatory and quality services to the MedTech industry. Our expertise spans 40 years, and we have worked with numerous top medical device manufacturers and IVD companies. As a Regulatory Labeling Project Manager, you will play a critical role in ensuring compliance and quality in our clients' labeling processes.Key...

We are seeking a highly skilled Senior Labeling Project Specialist to join our team at Pharmavise Corporation. As a key member of our organization, you will play a critical role in planning, managing, training, and directing the creation and revision of product literature and labeling.The ideal candidate will have excellent communication skills and be able...

About RQM+RQM+ is a leading MedTech service provider with the world's largest global team of regulatory and quality experts.With 40 years of regulatory expertise, we provide comprehensive clinical trial, lab and reimbursement services - reducing risk and supporting market access throughout the entire product lifecycle for medical devices, digital...

OverviewBoston Scientific is seeking an experienced professional to lead its IT SOX program, ensuring compliance with regulatory standards and best practices in the medical device industry.Salary Range: $100,700 - $191,300 per yearAbout the Role: As an IT SOX Program Lead, you will be responsible for overseeing the company's IT SOX, internal controls, and...

Job OverviewThe Regulatory and Quality Assurance Specialist II plays a vital role in ensuring the company's compliance with regulatory agencies, including FDA, state, local, and AABB. This position requires a high level of expertise in quality systems and regulatory aspects.Key Responsibilities:Implement, monitor, and maintain the company's Quality System to...

Lead Design Assurance and Quality Engineering ExpertWe are seeking an experienced Senior Quality Assurance Specialist to join our medical device development team at Michael Page. As a key member of our cross-functional team, you will play a critical role in ensuring the quality and safety of our innovative electrophysiology products.About the Role:Provide...

Job Summary:The Senior Sterilization Specialist will play a critical role in ensuring the quality and safety of our medical devices. This position requires a strong understanding of sterilization processes, quality systems, and regulatory requirements.Responsibilities:Validate sterilization processes to ensure compliance with industry standards.Manage clean...

At Sartorius AG, we seek a dedicated Quality Control Lead to drive the success of our initiative in creating innovative solutions.Job OverviewThe successful candidate will oversee quality control activities ensuring the quality and compliance of our emerging therapy services.This includes management of QC microbology testing, environmental monitoring,...

Role OverviewBioTalent is seeking a highly skilled Product Safety and Compliance Specialist to join our team. This role plays a critical part in ensuring the quality and safety of our medical devices.Key ResponsibilitiesQuality Assurance: Oversee the product development lifecycle, including risk management, design verification, and validation, to guarantee...

About the RoleWe are looking for a seasoned Medical Devices Development Specialist to join our team at IPG Photonics. In this role, you will be responsible for developing and integrating software / hardware solutions and products related to an Endoscope system with image processing, laser, and fluid management in surgical endoscopy.The ideal candidate will...

Compunnel Inc. is seeking a talented Validation Expert - Medical Devices to join our team.The estimated salary for this position is $110,000-$170,000 per year, depending on experience and qualifications.About the Position:This role involves performing Test Method Validation and Equipment Qualification, leading root cause analysis, and investigations on test...

We are looking for a talented Design Assurance Specialist to provide design assurance support for new product development and on-market medical devices at Mastech Digital.Responsibilities Include:Facilitating design validation, risk management, and regulatory compliance.Leveraging cross-functional teams to drive manufacturability...

Job DescriptionThe Regulatory and Quality Assurance Specialist II is responsible for implementing and maintaining quality systems, document control, and compliance with federal and state regulations.This includes:Implementing, monitoring, and improving the company's Quality SystemEnsuring appropriate licensure is held and maintained by the...

Role SummaryThis is a key role within US Fertility, LLC, responsible for overseeing the implementation and maintenance of the company's Quality System, ensuring compliance with regulatory agencies.Key Accountabilities:Implement, monitor, and maintain the Quality System to ensure compliance with regulations.Develop and implement a document control system to...

Job SummaryWe are seeking an experienced Program Management Expert to lead the development of our medical devices. This role requires strong project management skills, expertise in design control and risk management, and a proven track record of delivering complex projects on time and within budget.About IPG Photonics CorporationIPG Photonics Corporation is...

Company Overview: At Mastech Digital, we are dedicated to delivering exceptional results and value to our clients. As a leading provider of IT staffing services, we understand the importance of quality and compliance in the medical device industry.Job Description: We are seeking a highly skilled Design Assurance Engineer to support new product development,...

Cynet Systems is looking for a motivated and detail-oriented Laboratory Technician to support our biomedical research efforts. In this role, you will be responsible for conducting in vitro hemocompatibility testing of medical devices, as well as assisting senior team members with data analysis and record-keeping.Key Qualifications:Bachelor's degree in...

Company OverviewIPG Photonics is a leading developer of next-generation medical products based on cutting-edge technology. Our mission is to create innovative medical device laser solutions that improve lives and drive a sustainable future for our company and society.

Company Overview">A leading medical device manufacturer in the US, with a strong presence in the national market. They have expanded their operations through strategic acquisitions, focusing on specific product categories.">Job Summary">We are seeking an experienced Manufacturing/ NPI Engineer to join our team in Marlborough, MA. The successful candidate...

Job OverviewThe Medical Device Development Engineer will play a pivotal role in the development of essential medical device products through design, development, and manufacturing. Our client is a nationally recognized medical device design and manufacturing organization with a proven track record in great customer service and new innovation.