Titan Pharma Hiring Regulatory Affairs Manager
- Regulatory Affairs Manager Vacancies – Titan Pharma
- Company Overview
- Job Role & Responsibilities
- Deputy Manager – Regulatory Affairs (Regulated Markets)
- Manager / Senior Manager – Regulatory Affairs (Regulated Markets)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
Regulatory Affairs Manager Vacancies – Titan Pharma
Titan Pharma hiring Deputy Manager to Sr. Manager in Regulatory Affairs for regulated markets. Apply today.
Titan Pharma is expanding its Regulatory Affairs division and is hiring experienced professionals to support global regulatory submissions for regulated markets. If you have strong dossier preparation skills, hands-on experience with CTD/eCTD formats, lifecycle management expertise and the ability to lead regulatory strategy for global filings, these openings offer a solid career path in an established pharmaceutical organisation.
Company Overview
Titan Pharma is an integrated pharmaceutical group known for its high-quality formulations, strong regulatory presence and a disciplined approach to compliance. The company works across global regulated markets and maintains a robust portfolio supported by data-driven development, reliable manufacturing practices and a focus on patient-centric product safety.
The Regulatory Affairs division drives global submissions, manages product lifecycle activities and works closely with R&D, QA and manufacturing to ensure alignment with stringent regulatory requirements.
Job Role & Responsibilities
Deputy Manager – Regulatory Affairs (Regulated Markets)
Key responsibilities:
- Prepare, review and submit dossiers for regulated markets.
- Manage CTD/eCTD submissions, variation filings and renewals.
- Coordinate with R&D, QA and manufacturing for documentation readiness.
- Track regulatory guidelines, assess impact of updates and ensure compliance.
- Support responses to regulatory queries within defined timelines.
Skills required:
- Strong understanding of global regulatory frameworks.
- Experience in RA for regulated markets.
- Ability to interpret and apply guidelines to real-time projects.
Manager / Senior Manager – Regulatory Affairs (Regulated Markets)
Key responsibilities:
- Lead regulatory strategy for new submissions and lifecycle management.
- Oversee dossier compilation, data evaluation and cross-functional coordination.
- Guide teams on regulatory expectations and documentation standards.
- Manage regulatory timelines, deficiency responses and agency communication.
- Ensure compliance with global guidelines across product portfolios.
Skills required:
- Advanced expertise in CTD/eCTD submissions.
- Proven leadership in regulatory planning and execution.
- Ability to identify regulatory risks and propose mitigation strategies.
Eligibility / Qualifications
Required education:
- B.Pharm / M.Pharm or equivalent pharmaceutical science qualifications.
Preferred background:
- Experience exclusively in Regulatory Affairs for regulated markets.
- Strong understanding of international guidelines (ICH, EU, USFDA).
Experience:
- Deputy Manager: Mid-level RA experience
- Manager / Sr. Manager: Senior-level RA leadership experience
Location & Salary
Salary is competitive and based on experience. Candidates with substantial exposure to regulated markets, dossier management and lifecycle activities may receive higher compensation.
Application Process
Interested candidates may apply by sending their CV to:
Application tips:
- Mention the position you are applying for in the subject line.
- Attach your updated resume and any certifications related to Regulatory Affairs.
- Ensure your experience in regulated markets is clearly highlighted.
FAQs
Q: Are these roles for regulated markets only?
Yes. Experience in regulated market submissions is mandatory.
Q: What type of dossiers should candidates be familiar with?
CTD/eCTD formats, variations, renewals and responses to agency queries.
Q: Is remote work available?
Roles generally require office-based collaboration.
Q: Is prior team leadership required for the Manager roles?
Yes, especially for the Senior Manager position.
Q: What documents should be included in the application?
Updated CV, experience summary and any regulatory certifications.
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| Company | Titan Pharma |
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| Vacancies | Deputy Manager, Manager, Sr. Manager – Regulatory Affairs |
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| Required Education | B.Pharm, M.Pharm, PG Diploma in Regulatory Affairs |
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| Experience | Mid to senior level RA experience in regulated markets |
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To apply for this job email your details to vaibhavi.b@titanpharma.com