Teva Pharmaceuticals Hiring Regulatory Affairs Specialist II – Apply Now

Teva Pharmaceuticals is hiring for the role of Regulatory Affairs Specialist II at its Navi Mumbai location. This opportunity is ideal for regulatory professionals with hands‑on experience in eCTD publishing, lifecycle management submissions, and post‑approval regulatory activities for global markets such as EU, US, and Canada. The role offers exposure to complex regulatory publishing projects and collaboration with cross‑functional scientific teams in a global regulatory environment.

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🏢 About the Firm

Teva Pharmaceuticals is one of the world’s leading pharmaceutical companies, committed to improving access to high‑quality medicines globally. Operating across multiple regions, Teva combines scientific innovation with strong regulatory and quality frameworks. Working at Teva means being part of a diverse, global organization that supports continuous learning, career flexibility, and employee well‑being.

📊 Job Description

• Company Name: Teva Pharmaceuticals
• Job Role: Regulatory Affairs Specialist II
• Employment Type: Full‑Time
• Experience Required: B.pharm(2 years), M.pharm(0 to 1 year)
• Functional Area: Regulatory Affairs / Regulatory Publishing
• Job Location: Navi Mumbai

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📋 Primary Responsibilities

As a Regulatory Affairs Specialist II, your responsibilities may include:

• Publishing and dispatching major and complex lifecycle management eCTD submission projects for EU, US, and Canada
• Handling post‑approval regulatory submissions, including publishing and transmitting high‑quality submissions to health authorities
• Performing document‑level publishing activities and troubleshooting technical or document‑related issues
• Conducting quality control (QC) checks on submission‑ready documents in line with agency requirements
• Collaborating closely with scientific, regulatory, and technical teams for submission planning and execution
• Maintaining up‑to‑date knowledge of internal and external regulatory publishing standards
• Applying basic knowledge of ICH guidelines and submission formats such as eCTD, NeeS, and paper submissions
• Working with regulatory IT systems and publishing tools to support compliant submissions

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🎓 Who is Eligible

Candidates applying for this role should meet the following criteria:

• B.Pharm:
  • Minimum 2 years of experience in Regulatory Affairs
• M.Pharm / Master’s in Life Sciences:
  • 0 to 1 year of experience in Regulatory Affairs

🧠 Skills Required

The following skills are essential for success in this role:

• Strong understanding of regulatory publishing processes
• Good knowledge of eCTD and related regulatory specifications
• Awareness of regulatory guidelines governing submissions (ICH, eCTD, NeeS)
• Hands‑on experience or familiarity with regulatory systems such as:
  • Global Insight
  • Veeva Vault
  • ISI Toolbox
  • Adobe Acrobat
  • Lorenz Validator
• Good understanding of regulatory IT systems
• Command over spoken and written English
• Ability to work effectively in a culturally diverse, global organization

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⭐ Work Summary

The Regulatory Affairs Specialist II role at Teva provides exposure to global regulatory submissions and advanced publishing systems. Professionals in this role contribute directly to the lifecycle management of medicines marketed worldwide. This position is particularly valuable for candidates seeking growth in regulatory publishing, technical regulatory operations, and global regulatory strategy.

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🎯 Ideal Applicants

This opportunity is suitable for:

• Regulatory Affairs professionals with experience in eCTD publishing
• Pharmacy or life sciences graduates seeking growth in global regulatory roles
• Candidates interested in post‑approval submission and lifecycle management activities
• Professionals comfortable working with regulatory IT systems and tools

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🎁 What TEVA offers

At Teva, employee well‑being and career development are key priorities. From the first day, employees are supported through benefits and development opportunities designed to help them thrive both professionally and personally.

Key highlights include:

• Generous annual leave entitlements
• Competitive reward and benefits plans
• Flexible working arrangements (role dependent)
• Access to tailored health and well‑being support
• Opportunities to give back to the community
• Twist, Teva’s career development platform, offering:
  • Learning programs
  • Short‑term projects
  • Internal career growth opportunities
• A culture that encourages continuous learning, flexibility, and personal growth

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📈 Growth Path

With experience and performance, professionals can prWith experience and performance, professionals in this role can progress into positions such as:

• Senior Regulatory Affairs Specialist
• Regulatory Publishing Lead
• Global Regulatory Operations Roles
• Regulatory Strategy or Compliance positions

Teva supports internal mobility and long‑term career development.

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💰 Expected Salary

• Expected salary for Regulatory Affairs Specialist II Teva jobs:
  ₹6 – ₹12 LPA (Approx.) depending on experience and skills

Actual compensation depends on experience, skill set, and internal policies.

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🔗 Application Link

Interested candidates should apply only through the official company career website using the link provided below.

Important Disclaimer:This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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