Lonza

Regulatory Affairs Specialist

Lonza  •  Hyderabad, IN (Onsite)  •  2 months ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

Location: Hyderabad, India

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 using source documents, ensuring accuracy, completeness, and compliance.
  • Support product lifecycle management activities
  • Manage regulatory workflows, trackers, and document systems (e.g., Veeva) to ensure timely and controlled submissions.
  • 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
  • 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.

Lonza

About Lonza

Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.

Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.

For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Basel, CH
Year Founded
1897
Website
lonza.com
Social Media