Specialist Regulatory Affairs
Abbott · Delhi
- Experience1–2 yrs
- SalaryNot disclosed
- Work modeonsite
- Leveljunior
- Posted9 Sept 2026
About Abbott
Abbott is hiring in Delhi in healthcare. This role looks for around 1+ years of experience.
Skills
- Regulatory Affairs
- Product Registration
- Regulatory Strategy
- Regulatory Compliance
- Medical Devices
- Pharmaceuticals
- Biologics
- Chemistry Manufacturing Controls
- Technical Labeling
The role
A regulatory affairs specialist at a healthcare products company develops regulatory submissions and strategies, manages product registration and regulatory liaison, and advises on medical device and pharmaceutical compliance.
Full job description
MAIN PURPOSE OF ROLE
Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Regulatory Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
Main Responsibilities
As the Experienced professional in the Regulatory Affairs Sub-Function, possesses well developed skills 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
Associates Degree (± 13 years)
Experience/Background
Minimum 1 year