Regulatory Affairs
1 week ago
**Qualification**: B.Pharma - Pharmacy or M.Pharma - Pharmacy
**Experience**: 2.0 Year **To** 4.0 Year **( Must have experience in Pharma Formulations)**
1. Preparing dossiers as per country specific guidelines
2. Countries knowledge
- Africa, South East Asia
They must have excellent organizational, analytical, project management, and communication skills.
They work frequently with other employees and team members to coordinate complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory Responsibility means a duty or responsibility, assigned to an individual by management.
Regulatory compliance is when a business follows state, federal, and international laws and regulations relevant to its operations, Regulatory compliance involves following external legal mandates set forth by state, federal, or international government.
ensure that a company's products comply with the regulations of the regions where they want to distribute them.
keep up to date with national and international legislation, guidelines and customer practices.
collect, collate and evaluate scientific data from a range of sources.
develop and write clear arguments and explanations for new product licences and licence renewals.
prepare submissions of licence variations and renewals to strict deadlines.
monitor and set timelines for licence variations and renewal approvals.
work with specialist computer software and resources.
write clear, accessible product labels and patient information leaflets.
liaise with, and make presentations to, regulatory authorities.
negotiate with regulatory authorities for marketing authorization.
**Requirements**:
Minimum 2 years in regulatory affairs and should be well versed with Dossier making process as per individual country requirement (ROW market )
**Job Types**: Full-time, Permanent
**Salary**: ₹150,000.00 - ₹300,000.00 per year
**Benefits**:
- Health insurance
- Provident Fund
Supplemental pay types:
- Yearly bonus
**Experience**:
- total work: 2 years (preferred)
Work Location: In person
**Speak with the employer**
+91 9328903541
-
Regulatory Affairs
2 days ago
Vadodara, Gujarat, India Sai Placement Full time ₹ 6,00,000 - ₹ 12,00,000 per yearURGENT OPENING FOR REGULATORY AFFAIRS OFFICER/ SR OFFICER LOCATION VADODARA Position:-Regulatory Affairs Officer/ Sr OfficerLocation:-VadodaraExperience:-1 to 3 Yrs (Formulation)Qualification :- B.Pharm/ M.Pharm Required Candidate profilePreparing dossiers as per country-specific guidelines.Compiling and reviewing documents.Coordinating with QA for...
-
Regulatory Affairs Executive
9 hours ago
Vadodara, Gujarat, India Ami Lifesciences Full time**Role & responsibilities** - EU Dossier preparation and submission to Europe market. - EU ASMF and CEP preparation and submission to Europe with post-approval activities - Handling of EDQM Agency Queries. - Brazilian DMF Preparation and Deficiency response. - China DMF Preparation and Deficiency response. - eCTD publishing in EDUCE software with PDF...
-
Regulatory Affairs Executive
6 days ago
Vadodara, India Amico Formulations LLP Full time**Post**: RA Executive **Experience**: 5+ Years Experience in Regulatory Affairs in Pharma Industry (Formulation) **Location**: Vadodara - Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. - Preparation, Compilation & Review of Registration documents that include...
-
Regulatory Affairs Officer
1 week ago
Alkapuri, Vadodara, Gujarat, India Novopharm Formulation Full timeGood communication and teamwork abilities. - Basic understanding of **regulatory affairs** in the pharmaceutical industry. - Strong **documentation and organizational skills**. - Knowledge of **CTD/eCTD submissions** is a plus. - Assist in the **preparation and submission of regulatory documents**, including dossiers for product registrations, variations,...
-
Executive - Regulatory Affairs
4 days ago
Tandalja, Vadodara, Gujarat, India Sun Pharmaceutical Industries Ltd Full time**Title**:Executive - Regulatory Affairs**: - Date: Sep 26, 2025 - Location: Tandalja - R&D - Company: Sun Pharmaceutical Industries Ltd **Job Title**: Executive - Regulatory Affairs **Business Unit**: R&D1 Regulatory Affairs **Job Grade** G12A **Location** Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering...
-
Executive - Regulatory Affairs
4 days ago
Tandalja, Vadodara, Gujarat, India Sun Pharmaceutical Industries Ltd Full time**Title**:Executive - Regulatory Affairs**: - Date: Jul 4, 2025 - Location: Tandalja - R&D - Company: Sun Pharmaceutical Industries Ltd - Preparation, reviewing, timely submission and coordination of implementation of labeling based on FDA notifications and/or RLD labeling updates. - Coordination of labeling related activities with cross functional teams...
-
Regulatory Affairs Executive
2 weeks ago
Vasna Road, Vadodara, Gujarat, India Vega Biotec Pvt. Ltd Full time**Vega Biotec Pvt Ltd** a part of Vega group of companies having global presence and state of the art manufacturing pharmaceutical factory is having an opening for the following post. Qualification - B.Pharm/ M. Pharm Experience - 3+ years of experience in regulatory affairs for ROW market (Rest of the world) **Job Summary**: The Regulatory Affairs...
-
Regulatory Affairs Officer
6 days ago
Odhav, Ahmedabad, Gujarat, India Nest Healthcare Pvt Ltd Full time**Position**: Regulatory Affairs Specialist **Location**: Odhav. Ahmedabad **Department**: Regulatory Affairs **Reports to**: Regulatory Affairs Manager / Director Job Summary: Key Responsibilities: - **Compliance Monitoring**: Monitor changes in regulations and guidelines to ensure ongoing compliance with local and international regulations. -...
-
Regulatory Affairs Officer
2 weeks ago
Ahmedabad, Gujarat, India Swastik Placement Agency Full time**Position : Regulatory Affairs Officer/Executive (Female)** **Education : B Pharm (Preferably)** **Experience : 1-2 Years** **Work Profile**: 1. Preparation & Checking of Dossiers of formulation products for product registration in other countries. 2. Co-ordination with Manufacturer & our partner in country (With their regulatory person) 3. Travel may...
-
Regulatory Affairs Executive
6 days ago
Vadodara, India RG HR Solutions Full timeStudying scientific and legal documents - Gathering, evaluating, organising, managing and collating information in a variety of formats - Ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA) - Maintaining familiarity with company product ranges - Planning, undertaking and overseeing product trials and...