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Regulatory Affairs Executive
2 weeks ago
The Offer
- Opportunity to make a positive impact
- A role that offers a breadth of learning opportunities
- Work in a company with a solid track record of performance
The Job
Job Description:
- Dossier preparation as per the ACTD & CTD (Module I, II, III, IV, and V) guidelines.
- Technical documents like Raw Materials and finished products specification, manufacturing process,
- Product development report, stability reports, process validations preparation & review.
- Analytical method validation review as per the ICH guideline.
- Drug Master File review
- Technical query response to the various regulatory authorities.
The Profile
- You have at least 1 year post-qualification experience in a similar role.
The Employer
Our client is a marketing consultant that helps businesses grow their online presence through integrated digital marketing strategies. They combine SEO, PPC, and social media marketing to guide prospects through a unified online journey, enhancing brand impact and boosting leads and conversions.
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