Agent
Jobs
Applied
Tracker
Profile
    1. Jobs for you
    2. Job

    Job · 12746145

    Lonza logo

    Regulatory Affairs Specialist

    Lonza · Hyderabad · onsite · Posted 63d ago

    Not disclosed6–8 yrsfulltimeSourced fromFoundit

    About a minute. You'll make an account on the way through.

    About this role

    India, Hyderabad

    Job Title: Regulatory Affairs Specialist

    Location: Hyderabad, India (Hybrid)

    • Relocation assistance is available for eligible candidates and their families, if needed.

    Summary

    Join Lonza's Global Capability Center (GCC) in Hyderabad and play a key role in global regulatory submissions. As a Specialist in Regulatory Affairs (CMC), you will be responsible for site and customer CMC writing actvities for clinical trial application and product lifecycle support.

    What You Will Get

    • An agile career and dynamic working culture.
    • An inclusive and ethical workplace.
    • Compensation programs that recognize high performance.
    • Opportunities to collaborate with global cross-functional teams.
    • Ongoing learning and professional development opportunities.
    • Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits .

    What You Will Do

    • Support the site and customer related regulatory dossier activities for clinical trial applications.
    • Write CMC regulatory dossiers for Bioconjugates, Microbial, Cell Gene Therapy , Vaccine or Biologicals using source documents, ensuring accuracy, completeness, and compliance.
    • Support product lifecycle management activities
    • Collaborate with Lonza network Regulatory teams to co-ordinate the regulatory submissions to achieve successful submission outcomes.

    What We Are Looking For

    • Degree in Chemistry, Biology, or related Life Sciences discipline with 6+ years of experience in a regulatory industry.
    • Strong knowledge of global regulatory requirements and CMC documentation (clinical and commercial submissions).
    • Experience with Veeva Vault, eCTD publishing, and document management systems.
    • Strong project management skills with the ability to manage multiple priorities and timelines.
    • Excellent communication skills with business fluency in English and ability to influence stakeholders.
    • Collaborative, proactive, and solution-oriented mindset with strong accountability and ownership.

    About Lonza

    At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

    Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers breakthrough ideas into viable therapies, we look forward to welcoming you on board.

    Ready to shape the future of life sciences Apply now.

    Reference: R78620

    Apply

    Similar Jobs

    R78616

    R78617

    R78618

    Sourced from foundit

    Skills

    CMC regulatory dossiersBioconjugatesMicrobial Cell Gene TherapyVeeva vaultDocument management systemseCTD Publishingglobal regulatory requirementsProject ManagementBiologicalsvaccine

    About Lonza

    Lonza logo

    Lonza

    Pharma

    174

    employees

    1897

    129 years old

    Basel

    Switzerland

    About

    A prominent provider of healthcare solutions, focusing on innovative therapies for disease prevention and specialized ingredients for various industries.

    Industries

    PharmaChemicals / Agri InputsManufacturing

    Employee ratings

    36 reviews

    3.5/ 5

    Culture

    3.4

    Career growth

    2.5

    Work-life

    4.1

    Employees rate it well for

    Senior Management4Career Growth4Work Life Balance4

    Find them on

    WebsiteLinkedInAmbitionBox reviews

    Regulatory Affairs Specialist · waiting for your command