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Open nowPosted yesterday

Associate Manager - CMC Regulatory

Elanco389 open roles

Where
IN - Bangalore
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Your applicationOpen nowAssociate Manager - CMC RegulatoryElanco · IN - Bangalore

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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. Elanco postings stay open a median of 48 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted yesterday

Elanco median: 48 days open

The posting

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Job Description

Your Role: Associate Manager - CMC Regulatory

The purpose of Associate Manager, CMC Regulatory, is to work cross functionally with Elanco manufacturing and quality to develop regulatory strategy, oversee submission preparation and meet the reporting requirements for the maintenance of registrations/approvals of new animal drug with global regulatory agencies. These roles also execute CM&C regulatory functions necessary to provide supplements/variations, renewals, and annual reporting requirements for approved products. The person must have a strong knowledge of FDA/CVM and EMA guidelines with the understanding of developing regulatory strategy in the other major geographical regions.

Your Responsibilities:

  • Proven track record of overseeing end to end Life cycle management (LCM) of Small and/or Large Molecules/Complex dosage forms/Sterile preparations/Products derived from Biotechnology/Fermentation and Specialized dosage forms etc.,
  • Design/develop CMC regulatory strategy for marketed products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance
  • Maintain a positive collaboration and partnership with internal groups in R&D, Quality, Manufacturing and with global regulatory business partners of Elanco
  • Lead CMC submission preparation to provide high quality submissions to multiple geographies
  • Proactively communicate CMC regulatory strategy, key issues and any other critical topics throughout the life cycle in an adequate and timely manner to interdisciplinary project teams, while applying the global strategy into submissions.
  • Ensure the required documentation and any content, quality and/or timelines for global submissions are communicated to the appropriate teams and tracked according to the functional procedures
  • Author high-quality CMC documentation for submission, applying CMC global regulatory strategies, assuring regulatory compliance.
  • Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends
  • Provide trainings and mentorship to CMC team members, as necessary

What You Need to Succeed (minimum qualifications):

  • Degree in Science (MSc, B. Pharm/M.Pharm, Postgraduate in Vet Sciences etc.,)
  • 3 to 5 years in Global Regulatory Affairs, direct hands-on experience in post-approval CMC Life Cycle Management is preferred.

What will give you a competitive edge (preferred qualifications):

  • Strong knowledge of FDA/CVM, EMA and VICH guidelines
  • Experience with CMC registrations in the US and/or Europe and/or Rest of the World
  • Experience in managing multiple pharmaceutical dosage forms
  • Strong communication skills, both written and oral
  • Ability to make decisions when there is no clear right or wrong answer
  • Self-starter, takes initiative
  • Timeline driven
  • Attention to detail
  • Quality and customer focused mindset
  • Strong organizational skills and an ability to handle multiple projects at different phases of development at the same time
  • Understanding of the cGMP requirements
  • Experience working with Regulatory Information Management Tools and Systems

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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