SR. REGULATORY AFFAIRS SPECIALIST

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About this role

Company Description

Pharmaceutical / Biotech

Job Description

SR. REGULATORY AFFAIRS SPECIALISTΒ 

California Santa Clara



EXP 7-10 yrs

DEG Bach

RELO

BONUS


Job Description.

We are searching for an experienced regulatory professional to work within the Companion Diagnostics (CDx) team. Reporting to the Sr. Director, Regulatory Affairs (CDx), the successful candidate must have global regulatory experience working in IVD, Medical Devices or Pharmaceutical, with a history of successful regulatory submissions, registrations, 510(k)’s and PMA approvals in US and Asia. The preferred candidate has experience in Companion Diagnostics, and has lead company-sponsored interactions with regulatory bodies, especially FDA. The candidate must have excellent oral and written communication skills. The candidate will represent Regulatory Affairs on project teams and in close collaboration with pharmaceutical partners.


Responsibilities


1) Provide expertise in regulatory affairs leading to the successful regulatory registrations and approvals of Companion Diagnostic products in global markets.

2) With Regulatory Sr. Management, develops regulatory strategies related to CDx product development.

3) Provides regulatory assessments and plans for international product registrations and approvals.

4)Interacts and collaborates with pharmaceutical partners in joint meetings.

5)Ensures the accurate and timely preparation of regulatory submissions and reporting in accordance with Company goals, regulatory requirements and partnership contracts.

6)Works across the organization to ensure alignment of regulatory processes, standards and compliance. Provide expertise and advice in obtaining CDx product registrations and approvals in the Pacific Asian market.

7) Represents the Company in 3rd party meetings, especially the FDA, and regulatory associations.

8) Stays abreast of global IVD regulations and guidances, especially those relevant to Companion Diagnostics.


Bachelors or Masters Degree or University Degree or equivalent.

Typically 8+ years relevant experience for entry to this level. Post-graduate and/or certification/ license may be required.

Requires specialized depth and/or breadth of expertise in job. Not a natural progression from Advanced level.


Qualifications

Additional Information

All your information will be kept confidential according to EEO guidelines.

Direct Staffing Inc


Frequently Asked Questions

Is the salary disclosed for the SR. REGULATORY AFFAIRS SPECIALIST position at dstaff?
The salary for this SR. REGULATORY AFFAIRS SPECIALIST role at dstaff is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the SR. REGULATORY AFFAIRS SPECIALIST position at dstaff located?
This SR. REGULATORY AFFAIRS SPECIALIST role at dstaff is based in CA, Santa Clara, Santa Clara, CA, United States, us. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the SR. REGULATORY AFFAIRS SPECIALIST role at dstaff full-time or part-time?
This is listed as a Full time position. It is posted as a SR. REGULATORY AFFAIRS SPECIALIST role at dstaff.
How do I apply for the SR. REGULATORY AFFAIRS SPECIALIST position at dstaff?
Click the "Apply Now" button on this page. You will be redirected to dstaff's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the SR. REGULATORY AFFAIRS SPECIALIST job at dstaff posted?
This SR. REGULATORY AFFAIRS SPECIALIST position at dstaff was posted on Mar 26, 2015. Apply as soon as possible β€” early applications are often reviewed first.
SR. REGULATORY AFFAIRS SPECIALIST
dstaff
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