:

Main Purpose of the Role

Manages teams within the Regulatory Affairs Sub-Function.

Focus is on policy and strategy implementation and control rather than development.

Typically handles short-term operational/tactical responsibilities.

- Main Responsibilities

As the Manager of the Regulatory Affairs Sub-Function, oversees the strategy implementation and operations for 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.

Qualification

Education

Associates Degree (± 13 years)

Experience / Background

Minimum 7 years The base pay for this position is

N/AIn specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Regulatory Operations

DIVISION:

CRLB Core Lab

LOCATION:

Colombia > Bogota : Building II

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 15 % of the Time

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Not Applicable

📌 Regulatory Affairs Manager - Argentina And Colombia (Bogotá)
🏢 Abbott
📍 Bogotá