13/05/2026
๐ฒ๐ ๐ถ๐๐ ๐ป๐พ๐๐พ๐๐!!
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QA & RA Executive
Responsibilities
โข Conduct thorough checks and evaluations of dossiers, documents, and samples as part of the registration process for Pharmaceuticals, food supplements, cosmetics, and medical devices.
โข Responsible for the submission of dossiers, samples, queries, letters, and other related forms to the MFDA and monitoring the process to maintain the timelines.
โข Ensure to stay updated with changes in FDA guidelines and announcements in order to provide regulatory support and advice to management teams and partner companies.
โข Maintain records of mandatory documents and data required in the registration process.
โข Handle all kinds of regulatory activities including NDA application, Renewal registration, one-time recommendations and DIAC attachments application to the MFDA.
โข Must possess excellent communication skills in both spoken and written English and Act as a liaison with different companies abroad to fulfill registration process requirements.
โข Conducting quality assessment measures of all the imported products to ensure that all products meet the companyโs quality standards and comply with all relevant regulations and keeping records.
โข Build good cooperation and collaboration with all stakeholders including but not limited to regulatory, QA and supply chain functions,
Qualifiations:
- Have proficient computer skills, and be able to work well within a team environment.
- Ability to travel to Nay Pyi Taw as and when required.
- Graduated ( B. Pharm )
- Must have 2 years experience in related field
Interested candidates can send their resumes to
[email protected], [email protected]
09 796895718 (Viber)
We shall be pleased to connect with all the Short-listed candidates!
