MAIN PURPOSE OF THE ROLEExperienced qualified 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 skilled 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 recent 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.QUALIFICATIONSEducationEducation Level Major/Field of Study or EquivalentAssociates Degree (± 13 years)Experience/BackgroundExperience Experience DetailsMinimum 1 year

📌 Assistant Manager – Submission Publishing Maharashtra
🏢 Abbott Laboratories
📍 Maharashtra