Regulatory Affairs Executive

4 weeks ago


Rajkot Gujarat, India Bombay Ortho Industries Full time

Having Knowledge Regarding ISO 13485, cGMP, GMP and other Regulatory Standard related to Pharma, Medical or Engineering industries.

Handy on Microsoft Office and good Communication Skills and Learning Skills.

Pay: ₹20,000.00 - ₹23,000.00 per month

**Benefits**:

- Provident Fund

Schedule:

- Day shift

Supplemental Pay:

- Overtime pay
- Yearly bonus

**Education**:

- Master's (preferred)

**Experience**:

- total: 3 years (preferred)

Work Location: In person



  • Rajkot, Gujarat, India Lifelancer Full time

    Job Title Regulatory Affairs Executive API PHARMAJob Location Ahmedabad Gujarat IndiaJob Location Type On-siteJob Contract Type Full-timeJob Seniority Level AssociateSkills Regulatory legislation Regulatory Permision Regulatory Guidelines Regulatory Inspection Regulatory Policies Regulatory Practise and SOP Company OverviewSuccess Vibrant Human...


  • Rajkot, Gujarat, India Lifelancer Full time

    Job Title Regulatory Affairs ExecutiveJob Location Ahmedabad Gujarat IndiaJob Location Type On-siteJob Contract Type Full-timeJob Seniority Level Mid-Senior levelSkills ROW Market FDA Guidelines technical documents Review skills Analytic Skills Dossier Preparation Company OverviewBioMatrix Healthcare Private Limited 100 export-oriented company...


  • Ahmedabad, Gujarat, India DF Pharmacy Full time

    **Job Posting: Regulatory Affairs Executive** **Location**: Sola, Ahmedabad **Salary**: ₹10,000 - ₹20,000 per month **Key Responsibilities**: - Prepare, review, and submit regulatory documents (e.g., dossiers, DMFs) to regulatory authorities. - Coordinate with R&D, QA, and production teams to gather necessary documentation for product registration. -...


  • Science City, Ahmedabad, Gujarat, India Vetenza India Pvt Ltd. Full time

    Hiring 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...


  • Bodakdev, Ahmedabad, Gujarat, India Sunchem Industrial Corporation Full time

    Regulatory 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...


  • Rajkot, Gujarat, India Lifelancer Full time

    Job DescriptionWe are seeking a talented Regulatory Affairs Executive to join our team at Lifelancer. This mid-level position requires a candidate with expertise in regulatory standards and processes. The successful candidate will play a crucial role in managing regulatory submissions, ensuring compliance, and facilitating product registrations to support...


  • Vadodara, Gujarat, India Vega Biotec Pvt. Ltd Full time

    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 - 2-4 year's minimum in regulatory affairs Job profile: 1....


  • Vatva Gidc, Ahmedabad, Gujarat, India Samarthhrconsultant Full time

    Regulatory Affairs Executive B.Pharm / M.Pharm 2-4 years vatva Ahrmdabad Pay: From ₹12,000.00 per month **Experience**: - total work: 1 year (preferred) Work Location: In person Application Deadline: 21/01/2025 Expected Start Date: 19/12/2024


  • Gota, Ahmedabad, Gujarat, India Noronic Pharmaceutical Pvt Ltd Full time

    Job Title: Regulatory Affairs Specialist Department: Regulatory Affairs Location: HO Office, Gota Ahmedabad Company name : Noronic pharmaceutical Job Summary: The Regulatory Affairs Specialist is responsible for ensuring compliance with regulatory requirements, overseeing the preparation of technical documents, and supporting product registration and...


  • Ahmedabad, Gujarat, India Fusion Market Research Full time

    _**Regulatory Affairs Manager Responsibilities**_ - Develop and execute regulatory strategies and plans to ensure compliance with applicable laws, regulations, and standards. - Stay updated on changes in regulatory requirements and translate them into actionable steps for the organization. - Collaborate with cross-functional teams including R&D, Quality...


  • Odhav, Ahmedabad, Gujarat, India Nest Healthcare Pvt Ltd Full time

    **Position**: Regulatory Affairs Specialist **Location**: Odhav. Ahmedabad **Department**: Regulatory Affairs **Reports to**: Regulatory Affairs Manager / Director Job Summary: Key Responsibilities: - **Compliance Monitoring**: Monitor changes in regulations and guidelines to ensure ongoing compliance with local and international regulations. -...


  • Ahmedabad, Gujarat, India Contract Pharmacal Corp. Full time

    Responsibilities include, but are not limited to: - Review/approve Master Carton Labels, Pallet Labels, Blister Master Proofs and Printer proofs. - Support and Prepare draft Ingredient Lists. - Support Label Claim Substantiation activities. - Support drug product listing and maintenance, as needed. - Support second sourcing projects, as needed. - Prepare,...


  • Rajkot, Gujarat, India BioMatrix Healthcare Full time

    Company OverviewBBioMatrix Healthcare Private Limited 100 export-oriented company headquartered at Ahmedabad Gujarat India was established in 2007 with a thought of Supporting Life Worldwide The company is engaged in R D and manufacturing of oral solids liquids and dry syrups Our manufacturing facility has been accredited by WHO-GMP successfully...


  • Ahmedabad, Gujarat, India MNR Solutions Private Limited Full time

    **Job Summary**: The primary responsibility for the position is to oversee the daily activities of the Regulatory Affairs. Ensure that deliverables are being met based on planned submission timelines. Directs the development of submission of Product registration Dossiers, amendments, PSUR and Annual reports etc to Regulatory authorities. Queries response...


  • Tandalja, Vadodara, Gujarat, India Sun Pharmaceutical Industries Full time

    **Job Description**At Sun Pharmaceutical Industries, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. The ideal candidate will have 2-10 years of experience in regulatory affairs for the Indian market.Key Responsibilities:Evaluate regulatory strategies for products to be registered in IndiaSubmit applications on online portals...


  • Sola, Ahmedabad, Gujarat, India WEST-COAST PHARMACEUTICAL WORKS LTD Full time

    **We are urgently looking for Regulatory Affairs Executive.** Age criteria: below 30 Qualification - B.pharm/M.pharm Experience: 0 to 2 years only Location: Sola, Ahmedabad Work mode: on site Job role: - ➤ Should have worked in Regulated Market (ROW). ➤ Dossier Submission, Dossier preparation (ACTD & CTD). ➤ Technical Documents review. ➤...


  • Ambli, Ahmedabad, Gujarat, India Rishika Health Full time

    **Job Description**: Prepare, review and submit regulatory dossiers for product registrations. Ensure all necessary documentation is accurate, complete and meets regulatory requirements. Collaborate with cross-functional teams to ensure compliance with global regulatory standards. Conduct regulatory research and stay updated on international regulatory...


  • Bavla, Ahmedabad, Gujarat, India HCP Wellness Full time

    **Job Location**: Bavla Join HCP Wellness Pvt. Ltd., a leading cosmetic, skincare, and oral care manufacturer in India. We have urgent job openings for Quality Assurance (QA) & Regulatory Affairs (RA) at our Bavla manufacturing plant, located near Sanand, Changodar, Moraiya, and Sarkhej industrial zones. **Open Positions**: **Quality Assurance (QA)...


  • Ahmedabad, Gujarat, India Teknow source Full time

    **Designation**: Regulatory affairs -Executive/ Sr. Executive **CTC**: Full time 6-9 lacs/annum **Job Location**:Ahemdabad **Job Type**: Full time **Job Summary**: The primary responsibility for the position is to oversee the daily activities of the Regulatory Affairs. Ensure that deliverables are being met based on planned submission timelines. Directs...


  • Tandalja, Vadodara, Gujarat, India Sun Pharmaceutical Industries Full time

    **Regulatory Affairs Role**Sun Pharmaceutical Industries is looking for an experienced Senior Regulatory Executive to lead our regulatory affairs efforts in India. The successful candidate will have 2-10 years of experience in regulatory affairs for the Indian market.Responsibilities:**Develop and implement regulatory strategies for product registration in...