SHARE YOUR UPDATED RESUME AT *varun.j...@diverselynx.com*
<varun.j...@diverselynx.com>

 Dear Recruiter,

Hope you are doing fine. We have an urgent requirement for  *Regulatory
Affairs Specialist at **Irvine*, *CA* for a *6- 12 months Contract* role.
Please go through the same and let us know if you have anyone matching the
below role. Please send your responses to *varun.j...@diverselynx.com*
<varun.j...@diverselynx.com> with your candidate resume and contact details.

 SHARE YOUR UPDATED RESUME AT *varun.j...@diverselynx.com*
<varun.j...@diverselynx.com>

 *Title* – Regulatory Affairs Specialist

*Location* – Irvine, CA

*Duration* – 6+ Months Contract
 SHARE YOUR UPDATED RESUME AT *varun.j...@diverselynx.com*
<varun.j...@diverselynx.com>



*Technical/Functional Skills*



The Regulatory Affairs Specialist should provide direct World Wide
Regulatory support to various projects and products. Candidate should
support for strategic planning and product development efforts, provide
Regulatory support for existing products with respect to product
changes/modifications, labeling and promotional material review and
approval.



·         Knowledge of FDA regulations and CE

·         Excellent communication skills, both verbal and written.

·         Good organizational skills.

·         Good analytical thinking, problem solving and investigative skills



Additionally, experience supporting Japan, Russia, China, Brazil,
Australia/New Zealand, and Canada are highly desirable.



*Roles & Responsibilities*



·         Writes, coordinates and completes the submission of Regulatory
documents to FDA and other Regulatory agencies (e.g. EPA). Includes
international documents (e.g. tech files, etc.)

·         Prepares responses to FDA questions and other Regulatory
correspondence

·         Provides direct Regulatory support to project teams including the
creation of detailed Regulatory Plans

·         Includes in-depth team involvement including Core Team membership

·         Conducts product labeling and advertising review and approvals

·         Evaluates proposed product modifications for Regulatory impact.
Completes Regulatory Assessments as needed

·         Other activities as assigned by supervisor including special
projects, as needed

·         Perform other work-related duties as assigned by the manager of
the role

·         510(k)s and determinations as to whether a device modification
may trigger the need for a new 510(k)

·         European Technical Files, including maintenance and change
assessments.









Thanks and Regards,

Varun Jain

Diverse Lynx LLC



Email is the best way to reach me…

Phone: 732-452-1006  ext 288

Fax: 732-452-0684

Email – *varun.j...@diverselynx.com* <varun.j...@diverselynx.com>

*Linkedin -  *https://www.linkedin.com/in/varun-jain-928487b9/



Diverse Lynx LLC |300 Alexander Park|Suite #200|Princeton , NJ 08540



“For our open jobs please visit Diverselynx Jobs
<http://jobs.diverselynx.com/candidates/myjobs/searchjobsdone.jsp?a=9xjdnw687b7a7nvvdyut936kpjlgy0023blrozaecads0pdnwppcswnaaku8ji2g>
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“Note: Diverse Lynx LLC is an Equal Employment Opportunity employer. All
qualified applicants will receive consideration for employment without
regard to race, religion, color, sex, age, national origin or disability.
All applicants will be evaluated solely on the basis of their ability,
competence, and performance of the essential functions of their positions.
We promote and support a diverse workforce at all levels in the company.
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