Regulatory Affairs Associate
4 days ago
**About Us**:
An established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform **- CLYZO**
**Position
- Regulatory Affairs Associate.**
An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking for Regulatory Affair Executive having experience and knowledge of handling technical queries and regulatory documentation.
**Responsibilities**:
- Handling entire regulatory documents of excipients.
- Resolving technical queries of big pharmaceutical clients
- Handling technical matters & document related work of excipient manufacturer.
- Preparation of in house technical documents, required for promotion of excipient products.
- Should be able to understand & provide specific technical documents, for manufacturer & product qualification.
- Regulatory qualification documents and queries for Excipients / in-actives,
- Co-ordination with Excipients / in-actives manufacturer overseas
- USP/EP/JP Monograph comparison for various excipients / in-actives
- Preparing documents of Pharmaceutical companies, w.r.t Excipients Qualification
- Handling Virtual Audits of Pharma Customers w.r.t Excipients Qualification
- Handling Vendor Qualification Process end to end for Excipients Raw Material Products.
**Skills required**:
- Good Technical Know-how, w.r.t Guidelines / GMP / Testing Methods (for Excipients)
- Vendor management experience
- Minimum 2 years of experience into similar role
- Remuneration and benefits will be best in industry. _
Pay: ₹200,000.00 - ₹400,000.00 per year
**Benefits**:
- Cell phone reimbursement
- Health insurance
- Provident Fund
- Work from home
Application Question(s):
- are you available to join immediate?
**Experience**:
- total work: 2 years (required)
Work Location: In person
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thane, India beBeeRegulatoryAffairs Full timeJob OpportunityWe are seeking a highly skilled Regulatory Affairs Associate to join our team.The ideal candidate will have extensive experience in handling technical queries and regulatory documentation, with a strong understanding of guidelines, GMP, and testing methods for excipients.Key Responsibilities:Handling entire regulatory documents of...
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