Senior Regulatory Affairs Manager

MAIN PURPOSE OF ROLE

Summarize the main purpose of the role.

Specialist professional individual contributor with comprehensive knowledge in the area of Regulatory Affairs.

Ability to execute highly complex or specialized projects.

Adapts precedent and may make significant departures from traditional approaches to develop solutions.

MAIN RESPONSIBILITIES

As the Specialist in the Regulatory Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization in directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports.

Interacts with regulatory agency to expedite approval of pending registration.

Serves as regulatory liaison throughout product lifecycle.

Participates in some of the following: product plan development and implementation, regulatory strategy, risk management, chemistry manufacturing control (CMC).

Ensures timely approval of new drugs, biologics or medical devices and continued approval of marketed products.

Serves as regulatory representative to marketing, research teams and regulatory agencies.

Advises development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations.

QUALIFICATIONS

Education

Education Level Major/Field of Study Or Education Level

Associates Degree ( 13 years)

Experience/Background

Experience Experience Details

Minimum 7 years

Role: Head - Regulatory Affairs

Industry Type: Medical Devices & Equipment

Department: Legal & Regulatory

Employment Type: Full Time, Permanent

Role Category: Corporate Affairs

Education

UG: Any Graduate

PG: Any Postgraduate