Pam Segale

Principal

Since 2010, Pam Segale has been working in Simpirica Spine. Pam is an experienced Vice President RA, CA and QA with over six years of work experience. According to Pam's CV and work profile, this expert has worked at more than three companies with diverse backgrounds and gained various skills. Pam attended school at the Santa Clara University from 1998 to 2001. Pam can be found in San Francisco, California – where this expert is currently located. You can search for this person's phone number and email. We can also provide you with additional contact information upon request.
Name variants:
Pamela Segale
Last updated Jun 11, 2024

Contact Information

Last Update
Jul 8, 2022
Location
San Francisco, CA

Workplace

Vice President RA, CA and QA

Industry

Medical Devices

Work History

Vice President RA, CA and QA

from Feb 2010

Sr. Director RA and QA

Feb 2008 — Feb 2010

Director, Regulatory Affairs

Jul 2004 — Feb 2008

Occupations

Professor
School Principal
Executive
Vice President
Director
School Administrator
Educational Manager
Chief Executive
Operations Manager

Skills

Clinical Research
Medical Devices
510 K
Fda
Iso 13485
Ce Marking
Capa
Regulatory Affairs
Quality Systems
Regulatory Submissions
Clinical Trials
Design Control
Pma
Spine
Regulatory Strategy

FAQs about Pam Segale

What's the main profession of Pam Segale?

Pam is a Principal.

What are the profession of This professional?

These person's professions are Professor and School Principal

Where is Pam Segale located?

Pam is currently located in San Francisco, California.

Where did Pam Segale work?

Pam Segale worked at Simpirica Spine, Medtronic.

What education does Pam Segale have?

Pam studied at the Santa Clara University from 1998 to 2001.

What is professional industry that Pam Segale is connected to?

Pam works in Medical Devices industry.

Are there any skills, that Pam Segale has?

Pam has the following skills: Clinical Research, Medical Devices, 510 K, Fda, Iso 13485, Ce Marking, Capa, Regulatory Affairs, Quality Systems, Regulatory Submissions, and Clinical Trials.
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