Regulatory Affairs

JAMP India Pharmaceuticals Pvt. Ltd. is conducting a Walk-In Interview Drive for experienced and aspiring professionals in Regulatory Affairs. This is an excellent opportunity to join a dynamic pharmaceutical regulatory team working across global markets including **Canada, USA, Australia, New Zealand, UK, and Europe (Preferred Markets).**

*Positions:** 2

* **Role:** Manager / Deputy Manager / Assistant Manager

* **Qualification:** M.Pharm / B.Pharm

* **Experience:** 7–12 years of relevant experience

**Key Responsibilities:**

* Preparation, review, and submission of regulatory dossiers for drug products

* Handling ANDS filings and post-approval changes

* Evaluation and response to regulatory deficiencies

* Coordination with regulatory authorities and internal stakeholders

* Team management and cross-functional collaboration

* Ensuring compliance with global regulatory requirements

### **2. Regulatory Affairs – CMC Canada (Senior Executive Level)**

* **Positions:** 5

* **Qualification:** M.Pharm / B.Pharm

* **Experience:** 4–7 years

**Key Responsibilities:**

* Preparation and submission of ANDS and regulatory documentation

* Compilation and lifecycle management of regulatory submissions

* Handling variations, updates, and deficiency responses

* Supporting GMP-related regulatory activities

* Ensuring compliance with Canadian regulatory guidelines

### **3. Regulatory Affairs – CMC Canada (Trainee Officer Level)**

* **Positions:** 4

* **Qualification:** M.Pharm / B.Pharm

* **Experience:** Freshers or candidates with internship experience preferred

**Key Responsibilities:**

* Assisting in dossier preparation and documentation

* Learning regulatory submission processes

* Supporting team in regulatory compliance activities

* Training in CMC regulatory requirements for Canada and Australia markets

### **4. Regulatory Affairs – eCTD (Publishing & Submissions)**

* **Positions:** 1

* **Role:** Senior Officer / Officer / Trainee Officer

* **Qualification:** M.Pharm / B.Pharm

* **Experience:** 0–3 years

**Key Responsibilities:**

* eCTD compilation, publishing, and submission

* Managing electronic regulatory documents

* Validation and tracking of submissions

* Maintaining regulatory information systems

* Supporting compliance with global submission standards

Date:Sunday, July 5

Time:10:00 AM to 4:00 PM

A-1207, 12th Floor, Navratna Corporate Park,

Ambli–Bopal Road,

Ahmedabad – 380058

## **Important Instructions**

* Candidates must attend the walk-in interview with an updated resume

* Bring passport-size photographs and relevant documents

* Salary slips (last 3 months) and appointment letter (if applicable) required

* Candidates interviewed in the last 30 days are not eligible

* No consultancy or registration fees involved

* Beware of fraudulent job offers or calls

How to Apply

Eligible candidates can directly attend the walk-in interview at the mentioned venue.

Candidates who cannot attend walk-In interview can send their resume to the mail id or via scanning the QR code provided in the below official notification.