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Regulatory and Compliance Executive - Medical Devices - Scotland
Salary: 25,000 -£28,000 plus benefits
A great career opportunity has arisen for Regulatory and Compliance Executive to come and join a global Medical Devices organisation. This growing organisation embraces excellent quality and regulatory standards and has substantial amount growth and development within the company maximising their compliance within the industry and governmental standards.
The Regulatory Affairs team require an enthusiastic and motivated professional to be apart of the coordinating and directing compliance issues within the Regulatory Affairs department to ensure a consistent approach is taken to resolving quality issues including regulatory gap analysis, CAPAs, and audits, compliance of product packaging, labelling and IFU's when nessarsary . You will also be apart of reviewing regulatory and clinical studies and submission of compliance.
They are looking for a talent that is technically qualified at a higher education level, or experience of working within a high volume highly regulated manufacturing environment with full membership of a recognised professional Engineering. Experience within a regulated industry, preferably medical devices. Proven knowledge of engineering and audting. Analytical and problem solving skills, in order to quickly and effectively respond to engineering related quality issues. Ability to take prompt action to accomplish objectives and to work under own initiative. Ability to adhere to codes of conduct and ethical principles and to use, generate and communicate data with integrity. Proven ability to work effectively and cooperatively with others and to communicate well at all levels of the business. Proven track record of technical report auditing. Show the ability to demonstrate initiative and attention to detail, good organisational skills and the ability to work to deadlines across multiple simultaneous projects.
If successful, you will be rewarded with a completive salary, company pension scheme. If you want to be a part of this exciting opportunity, Please contact Ekta Multani, Medical Devices Recruitment consultant at Paramount Recruitment on 0121 616 3474.
Keywords: Regulatory Affairs, Regulatory Compliance, Medical Devices, ISO 13485 jobs, FDA, 21 CDR Part 820 jobs, Scotland, research, 510k, Auditing, SOPs, QMS, Quality Management Systems, Clinical Studies,
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