Medical Device Validation Specialist

Job OverviewThe Quality Assurance Validation Engineer plays a pivotal role in ensuring the quality and compliance of medical devices at a manufacturing site. If you have experience in Quality / Validation engineering and enjoy working collaboratively with a diverse team, we encourage you to apply.Key Responsibilities:Coordinate and participate in validation...

About This RoleThis position oversees the validation program to guarantee conformity with regulatory requirements, quality standards and industry guidelines.Manage site equipment, utilities, processes and software validation to ensure compliance.Develop and maintain a validation master plan, project plans and schedules.Prepare and submit validation protocols...

Pharmaceutical Engineer Role in West IrelandLocated on the picturesque west coast of Ireland, our pharmaceutical client is seeking a skilled Pharmaceutical Engineer to join their state-of-the-art facility.The successful candidate will be responsible for coordinating and participating in the validation and quality assurance of site equipment, utilities,...

Job Description:We are seeking a highly skilled Validation Specialist to join our team. The successful candidate will be responsible for coordinating and participating in the validation of site equipment, utilities, processes, and software to ensure compliance with regulatory standards. This is an excellent opportunity to work in a dynamic environment and...

Senior Clinical Research Associate Job DescriptionWe are seeking a skilled Senior Clinical Research Associate to manage clinical study activities as part of our clinical team. This is an excellent opportunity to support the development of innovative medical devices in line with ISO standards, FDA regulations, and EU MDR.Key Responsibilities:Coordinate...

Our company is seeking a Senior Clinical Research Associate to manage clinical trials outsourced to CRO's and support the development of innovative medical devices in line with ISO standards, FDA regulations, EU MDR, and other applicable requirements.Key Responsibilities:Coordinate clinical investigation activitiesWork with site staff, consultants, and teams...

Clinical Research Associate OpportunityOur company is seeking a highly skilled Clinical Research Associate to join our team and contribute to the success of our clinical trials. This individual will be responsible for managing clinical study activities as part of the clinical team, supporting the development of innovative medical devices in line with ISO...

Site Validation SpecialistThe ideal candidate for this role will possess a strong understanding of quality assurance and validation principles, as well as experience in implementing and maintaining site validation programs.Key Responsibilities:Coordinate the implementation and active participation in the site Validation Program and general Quality Assurance...

Job Title: QA Validation EngineerWe are seeking a highly skilled professional to coordinate the development and maintenance of our site validation program. As a key member of our team, you will be responsible for ensuring that our processes and systems meet the highest standards of quality and regulatory compliance.Main Responsibilities:Coordinate and...

Product Design SpecialistWe are seeking a seasoned product design specialist to join our team at Collins McNicholas Recruitment, exclusively partnering with Arrotek.The ideal candidate will possess a strong background in medical device design and development, with expertise in product innovation, quality assurance, and regulatory compliance.Key...