Medical Device Compliance Manager
1 month ago
We are seeking a highly skilled Regulatory Affairs and Clinical Manager to join our team at Stirling Q&R. As a key member of our regulatory and clinical leadership team, you will be responsible for leading our regulatory and clinical activities to ensure compliance with global regulations and overseeing clinical evaluations for our medical device products.
Main Responsibilities:- Develop and implement regulatory strategies for product approvals in various global markets
- Prepare and submit regulatory documents to health authorities
- Stay up-to-date with changes in regulations, particularly EU MDR, and lead company transition efforts
- Work collaboratively with cross-functional teams to ensure regulatory compliance throughout product lifecycle
- Lead clinical evaluation processes, PMCF, and clinical investigations
- Develop clinical strategies aligned with regulatory requirements and business objectives
- Build and maintain relationships with clinical research organizations and investigators
- Manage and develop a team of regulatory and clinical professionals
- Provide guidance and mentorship to team members
- Collaborate with other departments to ensure alignment of regulatory and clinical activities with overall business goals
- Ensure adherence to quality management systems and SOPs
- Participate in internal and external audits
- Identify and address compliance issues, conducting investigations when necessary
The successful candidate will have a strong background in regulatory affairs and clinical research, with excellent leadership and communication skills. The estimated salary for this position is $140,000 - $200,000 per year, depending on experience and qualifications.
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Product Compliance Engineer
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Mountain Ash, United Kingdom Stirling Q&R Full timeStirling Q&R is a leading company in the medical device industry dedicated to delivering innovative solutions that enhance patient care. We are seeking a highly skilled Product Compliance Engineer to ensure our products meet the highest quality standards and regulatory requirements.The successful candidate will have a strong background in quality engineering...
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Regulatory Affairs and Clinical Strategist
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Mountain Ash, United Kingdom Stirling Q&R Full timeJob OverviewWe are seeking an experienced professional to lead our regulatory and clinical activities at Stirling Q&R. This role is crucial in ensuring compliance with global regulations and overseeing clinical evaluations for our medical device products.Key Responsibilities:Develop and implement regulatory strategies for product approvals in various global...
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Global Regulatory Leader
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Maintenance Technician
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Maintenance Technician
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Maintenance Technician
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Industrial Plant Technician
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Maintenance Operations Coordinator
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Maintenance Technician
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Medical Sales Specialist
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Process Excellence Professional
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Maintenance Professional
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Mountain Ash, United Kingdom Hunter Selection Full timeAt Hunter Selection, we are seeking a talented Maintenance Professional to join our team. This is an exciting opportunity to work with a thriving business that has recently secured major contracts in the medical device sector.The successful candidate will be responsible for ensuring the smooth operation of our equipment and facilities. This includes...
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Quality Assurance Specialist
1 month ago
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Equipment Engineer Position
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Operations Exec
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Senior Health and Safety Advisor
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