Regulatory Affairs Associate

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...

Company OverviewRenown Pharmaceuticals Pvt. Ltd. is a reputable soft gelatin contract manufacturer with a state-of-the-art facility in Vadodara, India. The company upholds the highest quality standards and aims to be a top producer of soft gelatin capsules in India. Renown Pharma is known for its adherence to regulatory standards like MHRA, TGA, and WHO-GMP,...

Company OverviewRenown Pharmaceuticals Pvt. Ltd. is a reputable soft gelatin contract manufacturer with a state-of-the-art facility in Vadodara, India. The company upholds the highest quality standards and aims to be a top producer of soft gelatin capsules in India. Renown Pharma is known for its adherence to regulatory standards like MHRA, TGA, and WHO-GMP,...

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,...

Vega Biotec Pvt Ltd forms part of Vega group companies involved in manufacturing and exporting of finished pharmaceutical products and having global presence in 20+ countries. We have an opening for the following post. 1. Regulatory Affairs Executive - Qualification - B.pharma/M.pharm Experience - 0 to 1 year Job profile: 1. To assist manager in dossier...

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...

**Job Description Description**: **Qualification: B.Pharma - Pharmacy; M.Pharma - Pharmacy** **Tablet and capsule** - Hand on experience in preparation of CTD section as per regulatory requirements of different region - Having experience in preparation of query response and PAS, CBE and annual report. - Have ability to co-ordinate with cross functional...

Duties and Responsibilities: - Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy - Timely compile materials for license renewals, updates and registrations - Maintain regulatory files/database and chronologies in good order. Establish and...

Position : Exe / Sr. Exe (Regulatory Affairs, Baroda) Grade – G12A/G11B Education – B.Pharm / M. Pharm Experience – 4 to 6 years Location – R&D - Baroda Job Description: Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for...

Position : Exe / Sr. Exe (Regulatory Affairs, Baroda) Grade – G12A/G11B Education – B.Pharm / M. Pharm Experience – 4 to 6 years Location – R&D - Baroda Job Description: Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various...

Vega Biotec Pvt.Ltd part of Vega group of companies having state of the art manufacturing pharmaceutical formulation factories and having global presence in 25+ countries. We have an opening in the export division. 1. QA/RA executive - Experience - Fresher or 6 months experience Qualification - Msc. chem/ B. Pharma/ M. Pharma Job Profile: 2. Artwork proof...

Job D Job Description A Position Overview Position Title Business Associate Manager Department Business Associate Model – Agency Sales Level/ Band Assistant Manager / Manager Role Summary: Identify, recruit and build a team of business associates and advisors to drive business objectives on a month on month...

PR FLEXMAKE PRIVATE LIMITED (P+caRe) is hiring for Quality Control & Regulatory Affairs JOB DESCRIPTIONMaintenance of QM, SOP, Device and Plant Master Files, Quality certification audits, documentation, Manufacturing license for medical devices (Class A&B), Inspecting the final output, model, specifications and design and approving the final productsREQUIRED...

Job Title: Lead - CAPA Effectiveness Department: Corporate Quality Job Description: • Responsible to plan, co-ordinate and schedule the site visits for CAPA effectiveness review activities based on review plan.  • Responsible for CAPA effectiveness review associated with commitments provided to regulatory authorities across Sun manufacturing sites...

Alembic Pharmaceuticals Limited is looking for professionals in senior business development roles for expanding our presence in European markets based at Corporate Office Vadodara.Responsibilities:Conduct comprehensive market research to discern trends, competitors, and growth opportunities within the European pharmaceutical sector.Execute strategic business...

Alembic Pharmaceuticals Limited is looking for professionals in senior business development roles for expanding our presence in European markets based at Corporate Office Vadodara. Responsibilities: Conduct comprehensive market research to discern trends, competitors, and growth opportunities within the European pharmaceutical sector. Execute strategic...

Alembic Pharmaceuticals Limited is looking for professionals in senior business development roles for expanding our presence in European markets based at Corporate Office Vadodara.Responsibilities:Conduct comprehensive market research to discern trends, competitors, and growth opportunities within the European pharmaceutical sector.Execute strategic business...

Alembic Pharmaceuticals Limited is looking for professionals in senior business development roles for expanding our presence in European markets based at Corporate Office Vadodara.Responsibilities:Conduct comprehensive market research to discern trends, competitors, and growth opportunities within the European pharmaceutical sector.Execute strategic business...

**Roles and Responsibilities** **Maintenance Services**: - Ensure instrument maintenance of the equipments as per checklist and instruction / Feedback from Eng. service Head/Executive. - Prepare instrument maintenance schedule for all the plant as per direction of engineering head/2nd line. - Check the I.M.T.E. (Instruments Measuring Testing Equipments) as...

Position Title: Associate Professor, or Professor (Department of Quality Assurance )Job Summary:We are seeking dynamic and experienced individuals to join our esteemed faculty in the Department of Quality Assurance. The successful candidates will be responsible for delivering high-quality education, conducting research, and contributing to the academic and...