Looking for pharma jobs in India? Explore this Regulatory Affairs opportunity at Teva Pharmaceuticals in Navi Mumbai—ideal for professionals in QA jobs, QC jobs, and regulatory careers.
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About the Company
Teva Pharmaceuticals is a globally recognized biopharmaceutical leader with a strong presence in generics and specialty medicines. The company is known for innovation in neuroscience and immunology while maintaining strict regulatory compliance standards.
With operations across multiple countries, Teva offers strong career growth, global exposure, and a collaborative work culture focused on improving patient health worldwide.
Job Details
- Company Name: Teva Pharmaceuticals
- Experience: Varies by role (Regulatory Affairs experience preferred)
- Qualification: Life Sciences / Pharmacy or related field
- Location: Navi Mumbai, India
Job Description
Teva Pharmaceuticals is hiring for a Regulatory Affairs role focused on publishing and managing regulatory submissions. The position involves working with global teams to ensure timely, high-quality submissions aligned with regulatory guidelines.
Regulatory Affairs Specialist II
- Department: Regulatory Affairs
- Market: Global (EU, US, Canada)
- Role: eCTD publishing and regulatory submission management
- Experience: Relevant experience in regulatory affairs preferred
- Education/Qualification: Life Sciences, Pharmacy, or related field
Skills/Qualifications
- Knowledge of ICH guidelines and regulatory submission standards
- Experience with eCTD, NeeS, and paper submissions
- Familiarity with Veeva Vault, Lorenz Validator, and Adobe Acrobat
- Strong document management and quality control skills
- Ability to troubleshoot publishing issues
- Good communication and teamwork skills
- Understanding of global regulatory requirements
Key Responsibilities
- Publish eCTD submissions for EU, US, Canada markets
- Manage lifecycle and post-approval submissions
- Perform quality checks on submission documents
- Troubleshoot document-level publishing issues
- Collaborate with scientific teams for submissions
- Ensure compliance with regulatory timelines
- Maintain publishing standards and documentation accuracy
- Use tools like Veeva Vault and Lorenz Validator
Benefits/Perks
- Competitive salary and benefits package
- Global exposure in regulatory affairs
- Career growth opportunities in pharma industry
- Learning and development programs
- Inclusive and collaborative work environment
- Work on international regulatory submissions
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Teva Pharmaceuticals.
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Interested candidates can apply through the official Teva Pharmaceuticals careers page. You can also explore similar opportunities on Pharma Recruiter: https://pharmarecruiter.in
Apply now to advance your career in regulatory affairs and pharmaceutical careers in India.
Why You Should Join
Teva Pharmaceuticals offers a stable and growth-oriented environment for regulatory professionals. Employees gain exposure to global markets, advanced regulatory systems, and a culture focused on compliance and innovation. This role is ideal for building a long-term career in pharmaceutical regulatory affairs.
FAQs
Who can apply for this role?
Candidates with Life Sciences or Pharmacy backgrounds and regulatory experience can apply.
Is this a remote job?
No, this role is based in Navi Mumbai, India.
How can I apply?
Apply via the official Teva careers portal or visit Pharma Recruiter for updates.
What growth opportunities are available?
Teva offers global exposure, skill development, and career advancement in regulatory affairs.
