Regulatory Affairs Trainee

Flamingo Pharmaceuticals is inviting applications from M.Pharm Freshers for the position of Regulatory Affairs Trainee. This is an excellent opportunity for fresh M.Pharm graduates who wish to build a successful career in pharmaceutical regulatory affairs and product registrations.

Candidates with a basic understanding of regulatory documentation, CTD/eCTD submissions, and international regulatory guidelines are encouraged to apply.

Company: Flamingo Pharmaceuticals

Position:Regulatory Affairs Trainee (Fresher)

Job Location: Mumbai (All Areas)

Experience: 0–1 Year (Freshers Eligible)

Qualification: M.Pharm (Any specialization)

Selected candidates will be responsible for:

* Assisting in the preparation of CTD/eCTD dossiers.

* Supporting regulatory documentation for pharmaceutical product registrations.

* Working on registration activities for Oral Solid Dosage (OSD) products such as tablets and capsules.

* Coordinating documentation as per regulatory requirements.

* Learning and implementing global regulatory submission practices.

* Supporting the Regulatory Affairs team in day-to-day activities.

Candidates should possess:

* Basic knowledge of CTD/eCTD documentation.

* Familiarity with ICH, CDSCO, USFDA, and MHRAregulatory guidelines.

* Knowledge of pharmaceutical regulatory affairs and product registration processes.

* Good communication and interpersonal skills.

* Proficiency in Microsoft Office applications.

* Strong willingness to learn and build a career in Regulatory Affairs.

* Regulatory Compliance

* Product Registration

* Artwork Review

* Documentation Management

* M.Pharm in M.Pharm (Any specialization)

* Freshers are welcome to apply.

* Candidates should have good communication skills and a positive learning attitude.

Why Join Flamingo Pharmaceuticals?

* Excellent opportunity to begin a career in Regulatory Affairs.

* Hands-on experience in global regulatory documentation and submissions.

* Exposure to international regulatory standards including USFDA, MHRA, ICH, and CDSCO.

* Learn from experienced regulatory professionals in a reputed pharmaceutical organization.