regulatory affairs
4 weeks ago
We are hiring for Regulatory Affairs Executive.
Qualification: B.pharm/M.pharm
Age criteria: below 30
Experience - 0 to 2 years only
Location - Sola, Ahmedabad
Work mode - on site
:
Should have worked in Regulated Market (ROW).
Dossier Submission, Dossier preparation (ACTD & CTD).
Technical Documents review.
Preparation and Checking of Artwork as per guidelines.
FDA work e.g. PP, COPP etc.
Local candidates are 1st preferred.
-
Regulatory Affairs Officer
4 weeks ago
Ahmedabad, 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
4 weeks ago
Science City, Ahmedabad, Gujarat, India Vetenza India Pvt Ltd. Full timeHiring for a **REGULATORY AFFAIRS EXECUTIVE** for our **Ahmedabad **location. **Key Responsibilities**: - Assist in the preparation, compilation, and submission of regulatory documents, such as drug master files (DMFs), technical dossiers, and regulatory filings, to health authorities and regulatory agencies. - Maintain and update regulatory documentation...
-
Officer - Regulatory Affairs
4 weeks ago
Bodakdev, Ahmedabad, Gujarat, India Sunchem Industrial Corporation Full timeRegulatory affairs executive - B Pharm or M Pharm with 2 years plus experience. **Job description**: - Preparing Dossiers for registration of products in various ROW markets and query response submission - Legalization of FDCA documents for respective country registration - Arrangement of Sample for registration submission from respective team - Prior...
-
Regulatory Affairs Executive
6 days ago
Bodakdev, Ahmedabad, Gujarat, India Sunchem Industrial Corporation Full timeRegulatory affairs executive - B Pharm or M Pharm with 2 years plus experience in similar profile or work area. **Job description**: - Preparing Dossiers for registration of products in various ROW markets and query response submission - Legalization of FDCA documents for respective country registration - Arrangement of Sample for registration submission...
-
Regulatory Affairs Executive
4 weeks ago
Ahmedabad, Gujarat, India Winston HR Services,Ahmedabad Full timePOSITION : REGULATORY AFFAIRS QUALIFICATION : B. PHARM, M. PHARM, (B.S.C, M.S.C) EXPERIENCE : 0.6 TO 3 JOB LOCATION : AHMEDABAD MO. 7383005000 SHIVANI WINSTON HR SERVICES **Salary**: ₹20,000.00 - ₹30,000.00 per month Schedule: - Day shift **Experience**: - total work: 1 year (preferred) Work Location: In person **Speak with the...
-
Regulatory Affairs Executive
3 days ago
Ahmedabad, Gujarat, India Sunrise Remedies Full timeSunrise Remedies Job Opening for Regulatory Affairs Executive (RA). **Experience**: 0 To 1 Year **(Fresher and Experience Can Also Apply)** **Industries**: Pharmaceutical Company **Education**: B.Sc. / M.Sc / B.Pharm / M.Pharm **Job Location**: Santej Ahmedabad **Key Responsibilities**: - Regulatory Affairs Specialists assist in obtaining and maintaining...
-
Regulatory Affairs Executive
4 weeks ago
Ahmedabad, India Advanov Pharma Pvt. Ltd. Full time**Job description** Key Responsibilities: - **1. Dossier Preparation**_ a) Review documents received from the manufacturing facilities b) Compilation of documents as per guidelines of the respective country c) Compilation of dossier as per country guideline d) Follow up with the sites for documents, samples, and artwork e) Resolving query raised by...
-
Senior Regulatory Affairs Officer
1 week ago
ahmedabad, India Aegis Lifesciences Pvt Ltd Full timeTitle/Designation: Senior Regulatory ExecutiveBased at: AhmedabadIndustry: Medical Devices manufacturing (Class...
-
Senior Regulatory Affairs Officer
1 week ago
ahmedabad, India Aegis Lifesciences Pvt Ltd Full timeTitle/Designation: Senior Regulatory Executive Based at: Ahmedabad Industry: Medical Devices manufacturing (Class III)...
-
Senior Regulatory Affairs Officer
1 week ago
Ahmedabad, India Aegis Lifesciences Pvt Ltd Full timeTitle/Designation: Senior Regulatory ExecutiveBased at: AhmedabadIndustry: Medical Devices manufacturing (Class...
-
Senior Regulatory Affairs Officer
1 week ago
Ahmedabad, India Aegis Lifesciences Pvt Ltd Full timeTitle/Designation: Senior Regulatory ExecutiveBased at: AhmedabadIndustry: Medical Devices manufacturing (Class...
-
Regulatory Affairs
7 days ago
Ahmedabad, India Pharmazone Full time**Designation**: - Senior Manager- Having a total of 10 to 15 years of RA experience. Out of which at least 6 years of the regulated market such as USA/EU/UK or CA market dossier submission experience, multiple market experience is an advantage.- Having good written and verbal English communication skills- Having team handling experience- Should be aware of...
-
Ahmedabad, India Aegis Lifesciences Pvt Ltd Full timeTitle/Designation:Senior Regulatory Executive Based at:Ahmedabad Industry:Medical Devices manufacturing (Class III) Qualification:Postgraduate or equivalent in Pharma/Medical Devices domainExperience:5-6 years min. Reports to:Head of QA/RA About us: Aegis Lifesciences, established in 2008, is a distinguished manufacturer and exporter of medical devices,...
-
Regulatory Affairs Executive
4 weeks ago
Ahmedabad, India Snaphunt Full timeThe OfferOpportunity to make a positive impactA role that offers a breadth of learning opportunitiesWork in a company with a solid track record of performanceThe JobJob Description:Dossier preparation as per the ACTD & CTD (Module I, II, III, IV, and V) guidelines.Technical documents like Raw Materials and finished products specification, manufacturing...
-
Regulatory Affairs Executive
3 weeks ago
ahmedabad, India Snaphunt Full timeThe Offer Opportunity to make a positive impact A role that offers a breadth of learning opportunities Work in a company with a solid track record of performance The Job Job Description: Dossier preparation as per the ACTD & CTD (Module I, II, III, IV, and V) guidelines. Technical documents like Raw Materials and finished products specification,...
-
Regulatory Affairs Executive
3 weeks ago
ahmedabad, India AG Digital Marketing Full timeAG Digital Marketing is a marketing consultant that helps businesses grow their online presence through integrated digital marketing strategies. We combine SEO, PPC, and social media marketing to guide prospects through a unified online journey, enhancing brand impact and boosting leads and conversions. #agdigitalmarketing #agdigitalmarketinglife...
-
Regulatory Affairs Executive
4 weeks ago
Ahmedabad, India AG Digital Marketing Full timeAG Digital Marketing is a marketing consultant that helps businesses grow their online presence through integrated digital marketing strategies. We combine SEO, PPC, and social media marketing to guide prospects through a unified online journey, enhancing brand impact and boosting leads and conversions. #agdigitalmarketing #agdigitalmarketinglife...
-
Regulatory Affairs Executive
4 weeks ago
Ahmedabad, India Saga Lifesciences Limited Full timeExperience of CTD, ACTD dossiers for ROW, Latin America, South America, Asia, Africa market. Experience in preparing documents for FDCA work. **Salary**: ₹12,426.17 - ₹39,556.43 per month **Benefits**: - Provident Fund Schedule: - Day shift Supplemental pay types: - Overtime pay Ability to commute/relocate: - Ahmedabad, Gujarat: Reliably commute...
-
Regulatory Affairs Executive
4 weeks ago
Ahmedabad, Gujarat, India Saga Lifesciences Limited Full timeExperience of CTD, ACTD dossiers for ROW, Latin America, South America, Asia, Africa market. Experience in preparing documents for FDCA work. Pay: ₹25,426.17 - ₹39,556.43 per month **Benefits**: - Provident Fund Schedule: - Day shift Supplemental pay types: - Overtime pay Ability to commute/relocate: - Ahmedabad, Gujarat: Reliably commute or...
-
Regulatory Affairs Executive
7 days ago
Sola, Ahmedabad, Gujarat, India WEST-COAST PHARMACEUTICAL WORKS LTD Full time➤ Should have worked in Regulated Market (ROW). ➤ Dossier Submission, Dossier preparation (ACTD & CTD). ➤ Technical Documents review. ➤ Preparation and Checking of Artwork as per guidelines. ➤ FDA work e.g. PP, COPP etc. **Salary**: ₹10,000.00 - ₹25,000.00 per month Schedule: - Day shift Supplemental pay types: - Yearly...