Post by tarek on Sept 14, 2015 14:23:09 GMT
HUMAN RESSOURCES DEPARTMENT
JOHNSON AND JOHNSON HEALTHCARE
September 14,2015
Job opportunity
Are you ready for that next step in your career and want to take the opportunity to become part of the success story behind one of the world’s most comprehensive and broadly based manufacturer of health care products and related services?
Responsibilities
:
-prepares regulatory submissions for different medical devices "MRI, Scanner"
- Develops and executes regulatory strategy for assigned projects and interacts with regulatory authorities.
- Ensures compliance to ANSM Quality System Regulations and internal Quality System.
- Reviews and approves product labeling and advertising/promotional material.
- Maintains awareness of global regulatory legislation and assesses impact of changes to the business.
- Consults and provides training related to regulations and regulatory requirements.
- Participates in audits and inspections by regulatory authorities and certification/accreditation bodies.
Required Knowledge/Skills, Education, and Experience:
- Knowledge and experience with global registrations and development of medical devices
- Strong leadership, interpersonal, communication and organizational skills required.
- Must possess a high level of critical and strategic thinking skills and be a detail oriented team player with ability to influence multi-discipline teams and successfully negotiate with regulatory authorities.
- a minimum of 1 year of relevant experience is preferable
The ideal candidat for this position will have Master’s degree in Regulatory affairs of Medical Devices
Valued but not required competencies:
.Experience working in an ISO 13485/ ISO 9001 and ANSM regulated environment.
.Fluent in additional languages
To apply
Please send via email only a letter explaining why you are applying for this post and an up-to-date copy of your CV/resume to tareksalouane@jnj.com
For the full position description and additional information about us please visit our website at www.jnj.com
JOHNSON AND JOHNSON HEALTHCARE
September 14,2015
Job opportunity
Position | .Regulatory affairs specialist in the field of medical devices |
Compagny | .Johnson & Johnson |
Job Location | .Paris, France |
Employement type | .Fulltime |
Related Categories | .Regulation /Quality |
Start date | ASAP |
Are you ready for that next step in your career and want to take the opportunity to become part of the success story behind one of the world’s most comprehensive and broadly based manufacturer of health care products and related services?
Responsibilities
:
-prepares regulatory submissions for different medical devices "MRI, Scanner"
- Develops and executes regulatory strategy for assigned projects and interacts with regulatory authorities.
- Ensures compliance to ANSM Quality System Regulations and internal Quality System.
- Reviews and approves product labeling and advertising/promotional material.
- Maintains awareness of global regulatory legislation and assesses impact of changes to the business.
- Consults and provides training related to regulations and regulatory requirements.
- Participates in audits and inspections by regulatory authorities and certification/accreditation bodies.
Required Knowledge/Skills, Education, and Experience:
- Knowledge and experience with global registrations and development of medical devices
- Strong leadership, interpersonal, communication and organizational skills required.
- Must possess a high level of critical and strategic thinking skills and be a detail oriented team player with ability to influence multi-discipline teams and successfully negotiate with regulatory authorities.
- a minimum of 1 year of relevant experience is preferable
The ideal candidat for this position will have Master’s degree in Regulatory affairs of Medical Devices
Valued but not required competencies:
.Experience working in an ISO 13485/ ISO 9001 and ANSM regulated environment.
.Fluent in additional languages
To apply
Please send via email only a letter explaining why you are applying for this post and an up-to-date copy of your CV/resume to tareksalouane@jnj.com
For the full position description and additional information about us please visit our website at www.jnj.com