Job Title- Regulatory Affairs Associate
Location- Alameda CA 94502
12+ Months of contract role
Shift- 8 am to 5 pm
Job Description
As an individual contributor in the function of a Regulatory Affairs Specialist you will provide support for the Regulatory Affairs department to ensure efficient and compliant business processes and environment. The individual may execute tasks and partner across business functions. The individual will be reviewing Labeling, Advertising and Promotional materials, determining risk, identifying data needed, obtaining data and ensuring that the information is reliable and effectively presented to substantiate claims. You'll also have opportunities to participate in worldwide regulatory submissions. This is a broad scoped position with strong opportunity for growth and career development based on performance.
What You ll Work On CAN ADD/CHANGE
Review and analyze labeling, advertising and promotional materials while working with Marketing teams to provide regulatory strategy and compliance input.
Assist with promotional content development and review for compliance before distribution.
Assist in Regulatory Affairs Ad & Promo SOP development and review.
Assist with activities related to NPI and on market products (510K, PMA, Health Canada submissions and Latin America countries) as needed
Determine and communicate promotional content and approval requirements to cross functional teams.
Assist compliance with product post-marketing approval requirements as needed.
Required Qualifications
Bachelor's degree or an equivalent combination of education and work experience
Minimum of 2 years experience in a regulated industry (e.g., medical products, nutritionals, pharma, food). Regulatory area is preferred but may consider quality assurance,, research and development/support, scientific affairs, operations, or related area.
Communicate effectively verbally and in writing. Communicate with diverse audiences and personnel. Write and edit technical documents.
Work with cross-functional teams. Work with people from various disciplines and cultures.
Write and edit technical documents.
Negotiate internally.
Pay strong attention to detail.
Manage projects. Create project plans and timelines.
Think analytically and critically.
Organize and track complex information.
Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
Apply business and regulatory ethical standards.
Preferred Qualifications
Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), regulatory affairs, engineering, or medical fields.
1+ year of Regulatory Affairs or Quality experience within Medical Devices is preferred. Experience with review of labeling, promotional, and or advertising materials is highly desired.
Prefer some knowledge of Regulatory and/or Quality Systems history, guidelines, policies, standards, practices, requirements and precedents; Regulatory agency structure, processes and key personnel; Principles and requirements of applicable product laws; Principles and requirements of promotion, advertising and labeling; Domestic and international regulatory guidelines, policies and regulations; Ethical guidelines of the regulatory profession, clinical research and regulatory process.
Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.)
Office programs skills to include Word, Excel, PowerPoint, Visio and SharePoint.