37 Job openings found

Roles & Responsibilities:   Identification for Export Exports of Nutraceuticals, veterinary, Products in regulatory countries. Preparation of Dossier as per the legal requirement export   Qualification& Certifications: B.SC or B.sc and MBA (Import & Export) Gender: MALE           Salary: Negotiable   Skills: Must have Experience in Advanced Excel and Power Point Presentation Should have Good command over English (Written and Oral Both)  

works to help a company or organization meet all state, local, federal, international, and industrial regulations that apply to their products. They must have excellent organizational, analytical, project management, and communication skills. They work frequently with other employees and team members to coordinate complex activities, often with competing priorities. Most regulatory affairs positions ...

Job Location : Mahape, Nearest Station Ghansoli (Navi Mumbai)   Look for people from Navi Mumbai or Mumbai Only   Only Female Candidates required   Qualification : B.Pharm / M.pharm   Experience : 1yr – 3yr   Salary : 1.42lpa – 2 .80lpa     Profile : Experience in preparing Dossiers in CTD, ACTD, Country Specific Dossiers.   Countries : ROW and Latum   Job Description: Dossier Preparation along ...

  Identify and develop new business opportunities in international markets (Asia, Africa, LATAM, CIS, Europe, etc.) Manage and grow relationships with existing overseas clients, distributors, and partners Handle export documentation, quotations, and tender submissions Conduct market research and competitor analysis to identify potential customers and product opportunities Coordinate with Regulatory Affairs for dossier submissions, product ...

Quality Inspector - Transmission Tower FabricationJob Summary The Quality Inspector is responsible for ensuring that all steel components andfabricated sections for transmission line towers meet the required specifications, engineeringdrawings, and industry standards (e.g., ASCE, IEC, IS, and customer specifications). This role involvesconducting multi-stage inspections, from raw material receipt through to ...

The following is a general job description for a Documentation Audit Engineer or Quality Control(QC) Documentation Auditor specializing in Transmission Tower Fabrication. Documentation Audit Engineer / QC Documentation Auditor (Transmission Tower Fabrication)Job SummaryThe Documentation Audit Engineer is responsible for independently planning, executing, andreporting on audits of the quality control and project ...

Position:          Regulatory Manager Location:         Mumbai Experience:      5 - 8 Years Industries:       Chemical Responsibilities. Global Product Registration & Dossier Management Lead the full registration lifecycle (pre-market research, submission, renewal) for all target export countries. Compile regulatory dossiers, including 5-batch analysis and efficacy data, ensuring strict adherence to national formats. Serve ...

Position:         RA Trainee(Khopoli) Location:        Khopoli - Raigarh Experience:     0 - 1 Years Industries:      Pharma    Responsibilities: Assist in the preparation and compilation of regulatory dossiers (CTD / ACTD / eCTD) for product registration in various markets. Support the collection and review of technical documents from R&D, QA, QC, and Production ...

Position:          Manager/Sr. Manager - R&D Location:         Vadodara Experience:     10 - 15 Years Industries:       Pharma   Responsibilities: Project & Team Management Lead and manage multiple API development projects across various stages (Route scouting, lab development, scale-up, validation). Plan and allocate resources effectively among chemists and analysts. Mentor and guide junior ...

Position:          Officer/Executive – RA Location:         Paria - Vapi Experience:     2 - 5 Years Industries:       Pharma   Responsibilities: Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions. Handle full lifecycle of product registration including new submissions, renewals. Review technical documentation: ...