
Regulatory Affairs Officer/ Executive
5 days ago
**Location : Kandivali WEST**
**Roles and Responsibilities**(API)
- Market : ROW- Education /Qualification : M.Sc. /B. Pharm/M. Pharm
- Experience : 2 to 6 years
- Job Profile:
- DMF filing in regulatory / non regulatory market.
- Co-ordination with site for all the data required for initial filing and queries received.
- To review the documents (Analytical, R&D, PV).
- To check suitability for filing.
- Corrections of gaps found from site
- To plan for analytical validations with QA/ ADL
- Visit the site as and when required.
**Roles and Responsibilities** (Formulation)
- Market : Africa & South Africa, South East Asia, CIS, Brazil and Mexico
- Education /Qualification : M.Sc. /B. Pharm/M. Pharm
- Experience : 1 to 3 years - Job profile:
- Role:
Regulatory Affairs Compliance
- Salary:
Not Disclosed by Recruiter
- Industry:
Pharmaceutical & Life Sciences
- Department:
Legal & Regulatory
- Role Category:
Corporate Affairs
- Employment Type:
Full Time, Permanent
- Key Skills
Regulatory Affairs
dossier
dmf
regulatory guidelines
Skills highlighted with ‘‘ are preferred keyskills
- Education
- UG:
B.Pharma in Any Specialization
- PG:
MS/M.Sc(Science) in Any Specialization,M.Pharma in Any Specialization
Company Profile
- Rusan Pharma
- Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates. The company has its own Research & Development centre at Kandivli (west), Mumbai, state of the art, Bulk Manufacturing Plant at Ankleshwar and Formulation plant at Dehradun and SEZ, Kandla having approval of MHRA (UK), MCC (SA) and other International Health Authorities. March 2008 - 82 Crs., Expected by March 2009 €“ 150 Crs.
Contact Company:
Rusan Pharma
Website:
-
Regulatory Affairs
1 day ago
Mumbai, Maharashtra, India CliniLaunch Research Institute Full timeJob DescriptionPosition: Sr. Executive/Asst. Manager/Deputy Manager-Regulatory Affairs (Domestic).Location: Andheri, Mumbai.Qualification: M. Pharm. (Experienced preferred).JOB DESCRIPTION Regulatory Affairs (Domestic)The role will involve expertise in D & C Act and Rules as well as FSSAI regulations withexperience in FDA related activities. This profile...
-
Executive - Regulatory Affairs - Mumbai
5 days ago
Mumbai, Maharashtra, India Domnic Lewis Pvt. Ltd Full time**Executive - Regulatory Affairs - Mumbai**: **Domnic Lewis has been mandated to hire for Executive - Regulatory Affairs - Mumbai** **Position Title**: Executive - Regulatory Affairs **Grade**: C **Reports to**: Lead/Manager - Regulatory Affairs **Position Purpose**: - Monitor and report the status of all product licenses in a timely and accurate manner -...
-
Regulatory Affairs Officer
5 days ago
Mumbai, India TheTalentforte.com Full time**REGULATORY AFFAIRS EXECUTIVE** Job Location: VIkhroli Mumbai Qualification: B.Pharma / M.Pharma OR MSc + Diploma in Drug Regulatory Affairs Experience: 3 to 4 years in Regulatory Affairs of Pharma Formulations **JOB PROFILE** 1. Preparation and submission of registration dossier in CTD/ACTD /country specific format for countries in CIS, Africa, South...
-
Regulatory Affairs Executive
5 days ago
Mumbai, India Amico Formulations LLP Full time**Post**: RA Executive **Experience**: 5+ Years Experience in Regulatory Affairs in Pharma Industry (Formulation) **Location**: Masjid Bunder, Mumbai - 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...
-
Regulatory Affairs Professional
20 hours ago
Mumbai, Maharashtra, India beBeeRegulatoryAffairs Full time ₹ 90,00,000 - ₹ 1,50,00,000Regulatory Affairs SpecialistMain Purpose of Role:We are seeking a highly experienced and knowledgeable Regulatory Affairs Specialist to join our team. The ideal candidate will have comprehensive knowledge in the area of Regulatory Affairs and be able to execute complex projects.The Regulatory Affairs Specialist will direct the development of product...
-
Regulatory Affairs Executive/pharmaceutical
5 days ago
Mumbai, India Double HR Consultancy Full timeMumbai, Vile Parle, Dombivli East Regulatory Affairs Executive Eligibility: - M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. - Should have good knowledge of preparing registration of Drugs & Feed Supplements in different countries - Minimum 2 years experience in the same industry. **Job Description**: - Managing regulatory...
-
Regulatory Affairs Professional
22 hours ago
Mumbai, Maharashtra, India beBeeRegulatory Full time ₹ 20,00,000 - ₹ 25,00,000Regulatory Affairs Executive RoleJob Summary:We are seeking a highly motivated and experienced Regulatory Affairs professional to join our organization.Main Responsibilities:
-
Regulatory Affairs Specialist
3 days ago
Mumbai, Maharashtra, India beBeeRegulatoryAffairs Full time ₹ 9,00,000 - ₹ 12,00,000Regulatory Affairs Manager Job DescriptionThe role involves developing and executing regulatory strategies, compiling and reviewing regulatory submissions, ensuring product compliance and acting as a key liaison with regulatory agencies.Key Responsibilities:Submission Management: Preparation, review and submission of regulatory documentation (e.g., dossiers,...
-
Regulatory Affairs Executive
4 days ago
Borivali, Mumbai, Maharashtra, India TheTalentforte.com Full timeManufacturer of Pharmaceutical Tablets, Oral Suspension & Pharmaceutical Medicines. A dynamic Pharmaceutical company of approximately turnover of US $ 200 million and operating business in more than 50 countries. **REGULATORY AFFAIRS EXECUTIVE** **Job Location: BORIVILI** **QUALIFICATION** BPharma / MPharma **OR** MSc + Diploma in Drug Regulatory...
-
Regulatory Affairs Executive
5 days ago
Andheri East, Mumbai, Maharashtra, India Career Strategy Solutions Full timeSeeking Drug Regulatory Affairs for a Company into Pharma Industry **Key Responsibilities**: - Research and stay updated on regulatory requirements and guidelines - Coordinate with cross-functional teams to gather necessary documentation and information for regulatory filings - Review and assess product labeling, packaging, and promotional materials to...