APCER Life Sciences is hiring for the position of Senior Associate – Regulatory Affairs in Noida. Candidates with an M.Pharm qualification, at least 3 years of experience, and knowledge of US/EU regulatory affairs, including pre-approval and post-approval activities, can apply.
Job Details
| Particulars | Details |
|---|---|
| Company | APCER Life Sciences |
| Job Title | Senior Associate – Regulatory Affairs |
| Industry | CRO / Pharmaceutical |
| Job Location | Noida |
| Experience | 3+ years |
| Qualification | M.Pharm (mandatory) |
| Regulatory Market | US/EU |
| Application Email | deepa.kharel@apcerls.com |
Position
Senior Associate – Regulatory Affairs
The role focuses on regulatory affairs activities for the US and EU markets, with experience in both pre-approval and post-approval activities required.
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Eligibility and Qualifications
Candidates must meet the following criteria:
- M.Pharm qualification is mandatory.
- Minimum 3 years of professional experience.
- Experience in US/EU regulatory affairs.
- Experience in pre-approval and post-approval activities.
Regulatory Affairs Experience Required
Applicants should have relevant experience in:
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- US and EU regulatory affairs.
- Pre-approval regulatory activities.
- Post-approval regulatory activities.
How to Apply
Interested and eligible candidates can share their updated CV via email.
Email: deepa.kharel@apcerls.com