Post by claire on Sept 14, 2015 15:30:08 GMT
Regulatory Affairs Assistant - San Diego - competitive
• Job type: Permanent
• Salary: competitive
• Location: San Diego
• Reference: M2ARDM15163
The Regulatory Affairs Assistant will assist the manager in doing plan, coordinate, conduct, and report on company Regulatory Affairs Programs. This includes activities such as preparation of clearance/approval/registration/licensure documentation for regulatory submissions to government agencies (U.S. and worldwide), performing tasks associated with obtaining and maintaining product clearances licenses and registrations, and leading pre-market activities associated with product import/export.
The Regulatory Affairs Assistant works on problems of high complexity and diverse scope, in which data analysis requires evaluation of identifiable factors.
* Creates and executes regulatory strategies for US and global registrations and compliance activities of high complexity.
* Participates in business interactions and negotiations with regulatory agencies on premarket submission requirements, formats, labeling claims, etc. Participate to the meetings with regulators, including development of agendas and training/preparation of company personnel attending the meetings.
* Monitors FDA and other government agency laws and regulations through websites and publications, and identifies and communicates items needed for interpretation for impact to company regulated products.
Qualifications:
* A minimum of a Bachelor's of Science degree
* 1 years' experience working in a medical device environment will be considered relevant
* An experience working on product regulatory submissions
would be an advantage.
About 3M:
Do you see the world differently? Are you inspired by how a simple shift can result in big change? Do you share your ideas in the hopes of coming up with something even better by working together? Then join 3M! With 88,000 people around the world in more than 70 countries and $30 billion in sales, 3M is committed to building on our rich heritage by bringing our best to the innovations we create. Be part of improving how people live and work every day. Be part of what’s next at 3M!
3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Contact us:
If you are interested in this role please email your CV to M2ipil.english@gmail.com
For further details about this role or other opportunities within Regulatory Affairs please contact Nath P or Claire C on 001 212 440 96 87 or send a copy of your CV to M2ipil.english@gmail.com
• Job type: Permanent
• Salary: competitive
• Location: San Diego
• Reference: M2ARDM15163
The Regulatory Affairs Assistant will assist the manager in doing plan, coordinate, conduct, and report on company Regulatory Affairs Programs. This includes activities such as preparation of clearance/approval/registration/licensure documentation for regulatory submissions to government agencies (U.S. and worldwide), performing tasks associated with obtaining and maintaining product clearances licenses and registrations, and leading pre-market activities associated with product import/export.
The Regulatory Affairs Assistant works on problems of high complexity and diverse scope, in which data analysis requires evaluation of identifiable factors.
* Creates and executes regulatory strategies for US and global registrations and compliance activities of high complexity.
* Participates in business interactions and negotiations with regulatory agencies on premarket submission requirements, formats, labeling claims, etc. Participate to the meetings with regulators, including development of agendas and training/preparation of company personnel attending the meetings.
* Monitors FDA and other government agency laws and regulations through websites and publications, and identifies and communicates items needed for interpretation for impact to company regulated products.
Qualifications:
* A minimum of a Bachelor's of Science degree
* 1 years' experience working in a medical device environment will be considered relevant
* An experience working on product regulatory submissions
would be an advantage.
About 3M:
Do you see the world differently? Are you inspired by how a simple shift can result in big change? Do you share your ideas in the hopes of coming up with something even better by working together? Then join 3M! With 88,000 people around the world in more than 70 countries and $30 billion in sales, 3M is committed to building on our rich heritage by bringing our best to the innovations we create. Be part of improving how people live and work every day. Be part of what’s next at 3M!
3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Contact us:
If you are interested in this role please email your CV to M2ipil.english@gmail.com
For further details about this role or other opportunities within Regulatory Affairs please contact Nath P or Claire C on 001 212 440 96 87 or send a copy of your CV to M2ipil.english@gmail.com