Sun Pharma is hiring experienced pharmaceutical professionals for its Regulatory Affairs – US Group function in Vadodara, Gujarat. The opening is suitable for candidates with an M.Pharm qualification and 2 to 7 years of relevant regulatory affairs experience.
Candidates with experience in new submissions for oral and non-oral dosage forms and new ANDA submissions for regulated markets including the US, Europe, Canada and Australia are encouraged to apply.
This is a strong opportunity for professionals looking for Regulatory Affairs jobs in Vadodara, particularly those with expertise in US regulatory submissions and ANDA filing activities.
Job Details
| Particular | Details |
|---|---|
| Company | Sun Pharma |
| Function | Regulatory Affairs – US Group |
| Position | Regulatory Affairs Professional |
| Qualification | M.Pharm |
| Experience | 2–7 years |
| Job Location | Vadodara, Gujarat |
| Industry | Pharmaceutical |
| Employment Type | Full-time |
| Relevant Areas | New Submissions, ANDA, US Regulatory Affairs |
| Application Email | Rosemary.varghese@sunpharma.com |
Key Responsibilities
The selected candidate is expected to contribute to regulatory submission activities, including:
- Preparing and supporting new regulatory submissions for oral and non-oral dosage forms.
- Working on new ANDA submissions for the US market.
- Supporting regulatory submissions for US, European, Canadian and Australian markets.
- Reviewing regulatory documentation for completeness and submission readiness.
- Coordinating with cross-functional teams involved in regulatory submissions.
- Ensuring submission documents are prepared according to applicable regulatory requirements.
- Supporting responses and follow-up activities related to regulatory submissions.
- Maintaining appropriate regulatory documentation and submission records.
Eligibility Criteria
Candidates applying for this Sun Pharma Regulatory Affairs vacancy should meet the following requirements:
- Qualification: M.Pharm.
- Experience: 2–7 years of relevant experience.
- Experience in new submissions for oral and non-oral dosage forms.
- Hands-on exposure to new ANDA submissions.
- Experience working with regulatory submissions for the US, Europe, Canada and/or Australia will be relevant.
- Strong understanding of regulatory documentation and submission processes is preferred.
Why Apply for This Regulatory Affairs Job?
This opportunity can be particularly relevant for professionals seeking to build or advance their careers in US Regulatory Affairs, ANDA submissions and global regulatory submissions. The role offers exposure to multiple regulated markets and dosage-form submission activities.
Professionals with 2–7 years of experience can use this opportunity to strengthen their expertise in pharmaceutical regulatory affairs and international drug registration.
How to Apply
Eligible candidates should prepare an updated resume highlighting their experience in Regulatory Affairs, ANDA submissions, new drug submissions and international regulatory markets.
Send your updated CV to:
Email: Rosemary.varghese@sunpharma.com