Senior Regulatory Specialist

Job overview

The Senior Regulatory Specialist role is onsite in Alameda, CA, for a six-month contract, with a 9:00 a.m.–5:00 p.m. schedule. Compensation is not specified. The role supports medical-device regulatory affairs and timely approval of new devices and continued approval of marketed products.

What you'll do

• Assess regulatory changes, apply knowledge of U.S.
• medical-device submissions, and contribute to regulatory strategy, risk management, policy and intelligence, and continuous improvement.
• Represent regulatory affairs on cross-functional teams and advise development and marketing teams on manufacturing changes, line extensions, technical labeling, and applicable regulations.

What we're looking for

Skills & competencies

senior regulatory specialist

regulatory affairs

medical devices

alameda ca

onsite

six-month contract

9:00 a.m.–5:00 p.m.

regulatory change assessments

u.s. submissions

risk management

cross-functional teams

hiretalent

Work arrangement

• Weekend coverage required

Why this role

Requires seven years of medical-device regulatory affairs experience. The contract may be extended.

About the employer

HireTalent is hiring for this role. Industry: Employment Placement Agencies. Sector: 56.