Talent.com
Graviti Pharmaceuticals - Regulatory Affairs Professional
Graviti Pharmaceuticals - Regulatory Affairs ProfessionalGraviti Pharmaceuticals • Hyderabad, India
Graviti Pharmaceuticals - Regulatory Affairs Professional

Graviti Pharmaceuticals - Regulatory Affairs Professional

Graviti Pharmaceuticals • Hyderabad, India
2 days ago
Job description

Title : Regulatory Affairs Professional

Location : Hyderabad, Telangana

Experience : 5-8 years

Employment Type : Full-time, On-site

About Graviti Pharmaceuticals :

Graviti Pharmaceuticals, headquartered in Hyderabad, India, is a research-driven pharmaceutical organization specializing in the development and manufacturing of high-quality, complex generic formulations. With expertise in modified-release formulations, bio and stability-sensitive molecules, and innovative drug delivery systems, the company is committed to providing affordable and superior healthcare solutions.

Graviti Pharmaceuticals consistently adheres to stringent international regulatory standards, ensuring excellence, reliability, and transparency across all operations. These core values drive the organizations long-standing partnerships and its reputation for quality within global markets.

Role Overview :

The Regulatory Affairs Professional will play a critical role in managing regulatory submissions, ensuring compliance with regional and international guidelines, and supporting product development for key global markets, specifically Europe and the United States.

This is an on-site position requiring close collaboration with cross-functional teams, including R&D, QA, QC, Formulation Development, and Manufacturing. The ideal candidate will be skilled in dossier preparation, lifecycle management, regulatory strategy, and communication with regulatory authorities.

Key Strategy & Compliance :

  • Develop, implement, and maintain regulatory strategies for assigned products targeting EU and US markets.
  • Ensure adherence to regional regulatory requirements (EMA, MHRA, FDA) for complex generic formulations.
  • Monitor, interpret, and communicate regulatory changes, guidelines, and updates to internal stakeholders.

Dossier Preparation & Submissions :

  • Prepare, review, and compile high-quality regulatory submissions, including : ANDAs, MAAs, Variations
  • Renewals, Amendments and responses to queries

  • Manage the lifecycle of regulatory dossiers to ensure their timely submission and approval.
  • Document Management & Coordination :

  • Coordinate with Formulation, Analytical, QA, and Manufacturing teams to gather accurate and complete documentation.
  • Maintain regulatory documentation, submission records, and regulatory databases.
  • Support product development teams by providing regulatory insights throughout the project lifecycle.
  • Authority Interactions :

  • Liaise with global regulatory authorities (FDA, EMA, MHRA, and other EU agencies) to ensure efficient communication and timely resolution of regulatory queries.
  • Prepare and support teams during regulatory inspections or audits pertaining to Collaboration :
  • Provide regulatory guidance to R&D teams during product development to ensure alignment with EU / US regulatory requirements.
  • Support quality and compliance activities related to regulatory submissions, product launches, and post-approval changes.
  • Qualifications & Skills :

    Educational Background :

  • Bachelors or Masters degree in Pharmacy, Life Sciences, or a related discipline (preferred).
  • Technical Expertise :

  • Strong understanding of regulatory guidelines and frameworks applicable to US FDA and EU regulatory submissions.
  • Hands-on experience in dossier preparation (Modules 15), including CTD format.
  • Familiarity with regulatory submission portals such as ESG (FDA), eCTD, and EU Submission Gateway.
  • Professional Experience :

  • 5-8 years of experience in Regulatory Affairs within the pharmaceutical industry.
  • Proven experience with regulatory submissions for Europe and US markets is essential.
  • Exposure to complex generics, modified-release formulations, or innovative drug delivery systems is highly desirable.
  • Core Skills :

  • Excellent organizational and analytical skills with the ability to manage multiple projects simultaneously.
  • Strong problem-solving ability and attention to detail.
  • Effective written and verbal communication skills for cross-functional collaboration and regulatory correspondence.
  • Ability to adapt to evolving regulatory landscapes and anticipate potential challenges.
  • Why Join Graviti Pharmaceuticals :

  • Opportunity to work with a rapidly growing, innovation-driven pharmaceutical company.
  • Exposure to global regulatory frameworks and complex formulation strategies.
  • Collaborative and transparent work culture rooted in scientific excellence.
  • Career growth in one of the most critical and respected functions within the pharmaceutical industry.
  • (ref : iimjobs.com)

    Create a job alert for this search

    Pharmaceutical • Hyderabad, India

    Related jobs
    Regulatory Affairs Representative I (Plastics)

    Regulatory Affairs Representative I (Plastics)

    Eastman • Hyderabad, Republic Of India, IN
    The Product Steward is the key link between Eastman’s Advanced Materials segments (Specialty Plastics, Advanced Interlayers, and Performance Films) and the larger Global Product Stewardship & Regul...Show more
    Last updated: 13 days ago • Promoted
    Senior Analyst - Regulatory Compliance

    Senior Analyst - Regulatory Compliance

    ValueLabs • Hyderabad, Republic Of India, IN
    Immediate opening for Senior Business Analyst and Product owner.As a Senior Business Analyst, you will be the critical strategic link between our business stakeholders (spanning Compliance, Treasur...Show more
    Last updated: 24 days ago • Promoted
    Regulatory Compliance Analyst

    Regulatory Compliance Analyst

    People Prime Worldwide • Hyderabad, Republic Of India, IN
    Greetings from #People Prime worldwide.Job Title : Statutory Compliance Specialist.People Prime is a 13-year’s recruiting company providing innovative IT solutions to Fortune 500 clients.We speciali...Show more
    Last updated: 7 hours ago • Promoted • New!
    Pharmacologist

    Pharmacologist

    PI Health Sciences Ltd • Hyderabad, Telangana, India
    Role - Research Scientist - In Vitro ADME.Master’s degree in pharmacology, Biochemistry, Pharmaceutical Sciences, or related discipline. ADME laboratory (pharma / biotech / CRO).To generate high-quality...Show more
    Last updated: 4 days ago • Promoted
    Tax and Regulatory Support Specialist

    Tax and Regulatory Support Specialist

    V Nagarajan & Co. • Hyderabad, Republic Of India, IN
    Chartered Accountant firm based in Hyderabad, offering over 40 years of expertise in financial clarity, compliance, and strategic growth. We cater to individuals, startups, NGOs, corporates, and int...Show more
    Last updated: 23 days ago • Promoted
    Regulatory Manager

    Regulatory Manager

    Confidential • Hyderabad / Secunderabad, Telangana, India
    Job Title : Regulatory Manager – Europe Market.Yashoda Group of Hospitals, Hyderabad.Graviti channels a significant share of its revenue into. As part of our global expansion, we are now entering the...Show more
    Last updated: 12 days ago • Promoted
    Clinical Research Regulatory Coordinator

    Clinical Research Regulatory Coordinator

    Stryde Research • Hyderabad, IN
    We're a Site Management Organization operating 20+ clinical research sites across Dallas-Fort Worth, Houston, Louisiana, New York, and New Jersey. M+ patients through 100+ specialized clinics with d...Show more
    Last updated: 1 day ago • Promoted
    Pharmaceutical Compliance Program Lead

    Pharmaceutical Compliance Program Lead

    GBIT (Global Bridge InfoTech Inc) • Hyderabad, Republic Of India, IN
    The Manager of Pharma Mystery / Secret Shopping is responsible for leading compliance testing programs across online pharmaceutical and healthcare platforms. This role ensures compliance with prescr...Show more
    Last updated: 30+ days ago • Promoted
    Regulatory Affairs Professional

    Regulatory Affairs Professional

    Confidential • Hyderabad / Secunderabad, Telangana, India
    Graviti Pharmaceuticals, established in Hyderabad, India, is a research-driven company specializing in the production of high-quality and complex generic formulations. The organization focuses on de...Show more
    Last updated: 1 day ago • Promoted
    Manager, Regulatory

    Manager, Regulatory

    Confidential • Hyderabad / Secunderabad, Telangana, India
    Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.At Velocity, we align o...Show more
    Last updated: 28 days ago • Promoted
    Regulatory Affairs Specialist – (APAC & RoW)

    Regulatory Affairs Specialist – (APAC & RoW)

    vueverse. • Hyderabad, IN
    Regulatory Submissions & Compliance.Author, compile, and submit regulatory dossiers to global health authorities, including USFDA, EMA, MHRA, TGA, HSA, NPRA, Thai FDA, Taiwan FDA, CDE, NMPA, PMDA, ...Show more
    Last updated: 23 days ago • Promoted
    MSN Laboratories - Regulatory Project Manager

    MSN Laboratories - Regulatory Project Manager

    MSN Laboratories Pvt Ltd • Hyderabad, India
    We are seeking a highly organized and detail-oriented Regulatory Project Manager to be the central point of contact between our Head Office (HO) and our Emerging Market country teams.This critical ...Show more
    Last updated: 18 days ago • Promoted
    Bristol Myers Squibb - Senior Manager - Established Brands Regulatory Lead

    Bristol Myers Squibb - Senior Manager - Established Brands Regulatory Lead

    Bristol Myers Squibb • Hyderabad, India
    The Senior Manager, Established Brands Regulatory Lead takes ownership of one or more Established Brands and oversees the lifecycle of marketed products, ensuring compliance with global / regional re...Show more
    Last updated: 11 days ago • Promoted
    Graviti Pharmaceuticals - Regulatory Manager

    Graviti Pharmaceuticals - Regulatory Manager

    Graviti Pharmaceuticals Pvt Ltd • Hyderabad, India
    Title : Regulatory Manager - Europe Market.Industry : Pharmaceuticals / Healthcare.About the Pharmaceuticals is a sister concern of the prestigious Yashoda Group of Hospitals, Hyderabad.Focused on i...Show more
    Last updated: 11 days ago • Promoted
    Manager, Regulatory Affairs

    Manager, Regulatory Affairs

    Confidential • Hyderabad / Secunderabad, Telangana, India
    Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing uniq...Show more
    Last updated: 26 days ago • Promoted
    Shri Kartikeya Pharma - Manager / Senior Manager - Global Regulatory Affairs

    Shri Kartikeya Pharma - Manager / Senior Manager - Global Regulatory Affairs

    SHRI KARTIKEYA PHARMA • Hyderabad, India
    Company : Shri Kartikeya Pharma is one of Indias leading nutraceutical companies, specializing in the manufacture of high-quality dietary supplement...Show more
    Last updated: 8 days ago • Promoted
    Regulatory reporting - Senior Manager

    Regulatory reporting - Senior Manager

    State Street Corporation • Hyderabad, India
    We are looking for a result driven individual to manage the Regulatory Reporting team responsible for assessing regulatory reporting requirements, identifying SSGM change as a result of those requi...Show more
    Last updated: 30+ days ago • Promoted
    Bristol Myers Squibb - Associate Director - Regulatory Affairs

    Bristol Myers Squibb - Associate Director - Regulatory Affairs

    Bristol Myers Squibb • Hyderabad, India
    Us : - Challenging.Those aren't words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happe...Show more
    Last updated: 8 days ago • Promoted