Regulatory Affairs Executive

Position: Regulatory Affairs Assistant - Cosmetic Industry Department: Regulatory Affairs Experience Required: 0-2 years Location: Santej, Ahmedabad Salary Range: 2.2 LPA - 3 LPA Roles & Responsibilities: 1. Handling Legal Documents and Regulatory Affairs: - Assist in the preparation, review, and submission of regulatory documents. - Maintain and...

We are Hiring QA/Regulatory Affairs Specialist for Medical Devices (Orthopedic Implants and Instruments) **Role & Responsibilities**: 1. Documents preparation for ISO13485, CE Certificate (As per EU MDR). 2. Work on technical master file. 3. Work on CERs (clinical evaluation report) as per EU MDR. 4. Have knowledge about QMS (quality management systems). 5....

“Job Description” **Position**:Regulatory Affairs - Executive Cum Microbiologist** **Department: Regulatory Affairs / Microbiologist** **Min Qualification: B.Pharm, M.pharm,Bio-Medical Engineer, B.Sc or M.sc with Microbiology** **Min Experience: 3 - 5 Years** **SAARY**: 30,000 To 60,000 **Industries Preferred: Medical Device / Pharma / Bio-Tech /...

Hiring for a **REGULATORY AFFAIRS OFFICER ** for our **Ahmedabad **location. Freshers with good knowledge should apply **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. -...

**Job description** - Good communication skills client handling, Preparing/ checking and submitting technical files and compilation of dossiers in CTD/ACTD format as required for semi regulated countries/markets, - Product life-cycle management in ROW markets, - Handling product registration, - Providing regulatory support for out-licensing projects. -...

Position: Regulatory Affair Executive / Officer Location: Vatva, Ahmedabad Experience: 2- 7 years **Salary**: Hike on current CTC Skills: - Knowledge of Emerging Markets / Regulated Markets Worked on eCTD & CTD dossier OR Share with your friends! **Job Type**: Regular / Permanent **Salary**: ₹240,000.00 - ₹420,000.00 per year Schedule: - Day...

Title/Designation:                   Senior Regulatory ExecutiveBased at:                                 AhmedabadIndustry:                                 Medical Devices manufacturing (Class...

Develops strategies to ensure the company’s production activities comply with government regulations. - Serves as a liaison between regulatory bodies and operating divisions of the company. - Responds to requests for information from regulatory bodies. - Coordinates with operations departments regarding production design and development to ensure...

Title/Designation:                   Senior Regulatory Executive Based at:                                 Ahmedabad Industry:                                 Medical Devices manufacturing (Class III)...

Title/Designation:                   Senior Regulatory ExecutiveBased at:                                 AhmedabadIndustry:                                 Medical Devices manufacturing (Class...

Title/Designation:                   Senior Regulatory ExecutiveBased at:                                 AhmedabadIndustry:                                 Medical Devices manufacturing (Class...

Role Overview: - Responsible to prepare and review the dossier as per country specific guideline or CTD. - Responsible to submit error free dossier within timeline to reporting Manager - Responsible to prepare regulatory submission for international projects. - To resolve queries within timeline received from regulatory authorities. - To ensure company’s...

Experince: 2 Yrs to 3 yrs Qualification: Bpharm **Salary**: Depend on Interview. Designation: Regulatory Officer & Regulatory Excutive. **Salary**: ₹18,000.00 - ₹25,000.00 per year Schedule: - Day shift Ability to commute/relocate: - Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required) **Experience**: -...

Title/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,...

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The 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,...

AG 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...

The 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...

1. Preparation of dossiers, compilation of data 2. Aware of ACTD, CTD and coutry wise guidelines 3. Filing dossier to different countries for product registration 4. Query and responses

Experience of 1 to 3 years for ROW Market