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Location: Head Office (Wokingham UK)
Contract Type: Permanent
Job Type: Full time
Salary: £25,000 - £30,000 per annum
Benefits: Family feel company • Flexible working hours • Training and progression opportunities • Annual performance and salary review • Competitive annual leave entitlement • Generous Company contribution toward gym membership • Matched pension contributions with length of service • Cycle to Work Scheme
Closing date: 13-06-2024
An exciting opportunity has arisen for a Standards Compliance Coordinator to join our thriving UK medical manufacturing company.
The important role, reporting to the Standards Compliance Manager, involves providing standards support, and coordinating actions to help ensure precision and adherence to all applicable global standards and processes. The role includes championing a culture of compliance and contributing to the continued success and growth of the company.
The successful candidate will work as part of a team developing new respiratory care products and maintaining standards conformity for existing product technical files. Working in a busy and evolving environment, you will have interactions throughout the business.
The role involves proactively suggesting improvements to the standards process, and attending webinars to ensure the process is effective and up to date with applicable state-of-the-art.
Experience/Qualifications:
• Experience within the medical device industry, with knowledge of MDD 93/42/EEC, EU MDR (2017/745) and ISO 13485 is desirable
• Experience working with technical documentation and data management
• Experience working on multiple projects simultaneously
Key Skills:
• Excellent technical reading comprehension
• High levels of attention to detail
• Able to function in a highly regulated environment with a focus on compliance
• Organised, efficient and strong administration skills
• Have a can-do attitude with an enthusiastic approach
• Good people skills and excellent communication
Hours of Work:
• 40 hours per week
• Monday to Friday (flexibility to start and finish times)
**No Agencies please**
You will be joining a company where our people work together to meet our company goals. We have a strong family feel, a friendly working environment and extend a warm welcome to all new employees. We are looking for commitment, a strong work ethic and flexibility in all our people and reward those that demonstrate these qualities. Intersurgical is only as good as the people who work for us, and we value all of our employees.
You may also have experience in the following: Compliance Officer, Legislation, Regulation, Policy Officer, Compliance, etc. Compliance Coordinator, Compliance Advisor, Compliance Officer, Quality Advisor, Quality Assurance, Quality Assurance Coordinator, QA Coordinator, Health and Safety Officer, Audit, Medical Compliance, MDD 93/42/EEC, EU MDR (2017/745) ISO 13485 etc
REF-214 133
Contract Type: Permanent
Job Type: Full time
Salary: £25,000 - £30,000 per annum
Benefits: Family feel company • Flexible working hours • Training and progression opportunities • Annual performance and salary review • Competitive annual leave entitlement • Generous Company contribution toward gym membership • Matched pension contributions with length of service • Cycle to Work Scheme
Closing date: 13-06-2024
An exciting opportunity has arisen for a Standards Compliance Coordinator to join our thriving UK medical manufacturing company.
The important role, reporting to the Standards Compliance Manager, involves providing standards support, and coordinating actions to help ensure precision and adherence to all applicable global standards and processes. The role includes championing a culture of compliance and contributing to the continued success and growth of the company.
The successful candidate will work as part of a team developing new respiratory care products and maintaining standards conformity for existing product technical files. Working in a busy and evolving environment, you will have interactions throughout the business.
The role involves proactively suggesting improvements to the standards process, and attending webinars to ensure the process is effective and up to date with applicable state-of-the-art.
Experience/Qualifications:
• Experience within the medical device industry, with knowledge of MDD 93/42/EEC, EU MDR (2017/745) and ISO 13485 is desirable
• Experience working with technical documentation and data management
• Experience working on multiple projects simultaneously
Key Skills:
• Excellent technical reading comprehension
• High levels of attention to detail
• Able to function in a highly regulated environment with a focus on compliance
• Organised, efficient and strong administration skills
• Have a can-do attitude with an enthusiastic approach
• Good people skills and excellent communication
Hours of Work:
• 40 hours per week
• Monday to Friday (flexibility to start and finish times)
**No Agencies please**
You will be joining a company where our people work together to meet our company goals. We have a strong family feel, a friendly working environment and extend a warm welcome to all new employees. We are looking for commitment, a strong work ethic and flexibility in all our people and reward those that demonstrate these qualities. Intersurgical is only as good as the people who work for us, and we value all of our employees.
You may also have experience in the following: Compliance Officer, Legislation, Regulation, Policy Officer, Compliance, etc. Compliance Coordinator, Compliance Advisor, Compliance Officer, Quality Advisor, Quality Assurance, Quality Assurance Coordinator, QA Coordinator, Health and Safety Officer, Audit, Medical Compliance, MDD 93/42/EEC, EU MDR (2017/745) ISO 13485 etc
REF-214 133
