we are recruiting for the role of Regulatory Affairs Manager. *
Fantastic opportunity for someone to bring their skills to this
company. In return you get autonomy, flexibility and the option to
work remotely.
As a Regulatory Affairs Manager, you will be responsible for all
Quality and Regulatory issues within the company. You will oversee the
ongoing management of an ISO **Apply on the website** quality
management system, as well as preparing and co-ordinating regulatory
submissions for products outside the EU.
We are looking for a qualified candidate that has worked in Regulatory
Affairs with significant working knowledge of ISO **Apply on the
website** and project management or product development experience.
Reporting to the CEO, you will manage the representative for external
audit whilst performing internal and external audits. Great
opportunity to join a successful and established company offering a
stimulating work environment and training.
To be considered for this superb position, you must have:
? A third level qualification in a science or engineering discipline
(minimum NFQ level 8)
? At least five years&#**Apply on the website**; experience in a
similar role with a working knowledge of ISO **Apply on the website**
? Project management or product development experience
? Knowledge of FDA regulations and/or submissions and familiarity
with electronic submissions
? Proficiency in MS Office and document management systems
Additionally, as a Regulatory Affairs Manager, you must possess first
class communication and interpersonal skills, both verbal and written,
coupled with a strong multi-tasking ability. You also must have an
analytical nature and plenty of business acumen.
For full details contact Tina or call 1 or
Thornshaw Scientific is a division of the CPL Group. *On behalf of my client, a medical devices company based in Dublin,
we are recruiting for the role of Regulatory Affairs Manager. *
Fantastic opportunity for someone to bring their skills to this
company. In return you get autonomy, flexibility and the option to
work remotely.
As a Regulatory Affairs Manager, you will be responsible for all
Quality and Regulatory issues within the company. You will oversee the
ongoing management of an ISO **Apply on the website** quality
management system, as well as preparing and co-ordinating regulatory
submissions for products outside the EU.
We are looking for a qualified candidate that has worked in Regulatory
Affairs with significant working knowledge of ISO **Apply on the
website** and project management or product development experience.
Reporting to the CEO, you will manage the representative for external
audit whilst performing internal and external audits. Great
opportunity to join a successful and established company offering a
stimulating work environment and training.
To be considered for this superb position, you must have:
? A third level qualification in a science or engineering discipline
(minimum NFQ level 8)
? At least five years&#**Apply on the website**; experience in a
similar role with a working knowledge of ISO **Apply on the website**
? Project management or product development experience
? Knowledge of FDA regulations and/or submissions and familiarity
with electronic submissions
? Proficiency in MS Office and document management systems
Additionally, as a Regulatory Affairs Manager, you must possess first
class communication and interpersonal skills, both verbal and written,
coupled with a strong multi-tasking ability. You also must have an
analytical nature and plenty of business acumen.
For full details contact Tina or call 1 or
Thornshaw Scientific is a division of the CPL Group.
We need : English (Good)
Type: Permanent
Payment:
Category: Others
