Regulatory Affairs Executive

Vega Biotec Pvt Ltd forms part of Vega group companies having state of the art manufacturing company in Vadodara and having presence in over 20 countries. Our export arm has an opening for the following post.1. Senior Regulatory affairs executive-Qualification- Bsc/Msc Chem,B.pharma/M.pharmaExperience- Minimum 4 years in RAJob Profile-1. CTD or ACTD dossier...

**Regulatory Affairs Executive (01 Person)**: **Qualification**: B. Pharm / M. Pharm-RA **Experience**: 2 to 3 Years **Description**: - Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority. - Well versed with the guidelines of ICH and other regulatory. - Preparation of documents for COPP, FSC,...

**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...

“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 /...

1. Preparation, Review and Submission of the Dossiers as per CTD/ACTD guidelines as well a country specific guidelines. 2. Compilation of Dossiers and quality documents as per checklist in the guidelines. 3. Review of artworks as per the Regulatory requirements 4. Inter Department coordination to arrange and review of documents and samples for Regulatory...

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. -...

POSITION :REGULATORY AFFAIRS EXPERIENCE : 0 TO 1 QUALIFICATION : B.PHARM, M.PHARM. JOB LOCATION : AHMEDABAD mo: 7383005000 SHIVANI WINSTON HR SERVICES **Salary**: ₹15,000.00 - ₹20,000.00 per month Schedule: - Day shift **Experience**: - total work: 1 year (preferred) Ability to Commute: - Ahmedabad, Gujarat (required) Ability to...

**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...

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....

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...

Must be required knowledge of GPCB - Must be required knowledge of Methanol (MA - I and MA-II) - Must be required knowledge of GMP and GLP - Must be required knowledge of Regulatory Affair and Country Submission - Must be required knowledge of Dual License - Must be required knowledge of FDA, WHO, Manufacturing License - Must be required knowledge of CDSCO,...

Job Description: Job Description: 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 Administrative & Technical. ? Reviewing the technical documents provided by QA, QC,...

JOB ID: - 240204- Job family- Regulatory- Position Title- Executive - QA and RA (Level I/ II)- Job Type- Full Time- Location- Vadodara, Gujarat- Nature of _Work_ - On-site- Company Name- JC OrthoHeal Private Limited- Updated on- 15.02.2024**Summary**: Executive (QA, RA) (Level I/ II) will _work_ with the regulatory team and formulate or implement regulatory...

JOB ID: 240204 Job family Regulatory Job Type Full Time Location Vadodara, Gujarat Nature of Work On-site Company Name JC OrthoHeal Private Limited **Summary**: Executive (QA, RA) (Level I/ II) will work with the regulatory team and formulate or implement regulatory affairs policies and procedures. **Key Roles and **Responsibility** - Formulate or...

Job Description: Job responsibilities:Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD,ACTD as well as country specific format for countriesPreparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbalproducts for country specific format in countries of African...

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...

Job Description: Job Description: To assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials .  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...

Ø Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD, ACTD as well as country specific format for countries Ø Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal products for country specific format in countries of African Region, Cambodia, Myanmar, CIS Ø To manage...

**Job Types**: Full-time, Regular / Permanent **Salary**: ₹500,000.00 - ₹600,000.00 per year **Benefits**: - Health insurance - Leave encashment - Life insurance - Paid sick time - Paid time off - Provident Fund Schedule: - Day shift - Morning shift Supplemental pay types: - Yearly bonus Ability to commute/relocate: - Vadodara, Gujarat: Reliably...