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| Job Location | Manchester |
| Education | Not Mentioned |
| Salary | 50,000 - 70,000 per annum, negotiable, inc benefit |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
If you are looking for a permanent job within Reg affairs and if you have experience covering different markets including any of EU, APAC, North America or South America, this job could be ideal for you!If you are interested, please read on for more info. You can apply by responding with your up to date CV (in word format) to me on Day to day responsibilities:- Managing a RA team- Manage and lead IVD planning and transition for the business- Support regulatory approval for worldwide support to FDA, TGA, HC, ANVISA or other regulatory bodies- Lead and create regulatory documentation for product licence- Conduct all work in compliance with GMP, ISO9001, 13485 and other regulatory standards.Are you right for the role- You will have experience in IVD fields- You will have experience within Reg affairs management positions- You will have experience covering different markets including APAC, North/South America and Europe- You will have experience in working on ISO13485For more information regarding the role or an informal discussion, please do not hesitate in contacting me and arranging a further discussion over phone, email or video call.Alternatively, if this is not right for you, but you know someone who would be interested, please make the most out of ourrefer a friend bonus by referring suitable individuals.