Regulatory Affairs Vacancy At GYPTO PHARMA

☑ 𝐆𝐘𝐏𝐓𝐎 𝐏𝐇𝐀𝐑𝐌𝐀… 𝐭𝐡𝐞 𝐞𝐱𝐩𝐞𝐫𝐭 𝐡𝐮𝐛 𝐟𝐨𝐫 𝐩𝐡𝐚𝐫𝐦𝐚𝐜𝐞𝐮𝐭𝐢𝐜𝐚𝐥𝐬 𝐢𝐧 𝐭𝐡𝐞 𝐫𝐞𝐠𝐢𝐨𝐧 𝐬𝐞𝐜𝐮𝐫𝐢𝐧𝐠 𝐭𝐡𝐞 𝐜𝐮𝐫𝐫𝐞𝐧𝐭 𝐚𝐧𝐝 𝐞𝐯𝐨𝐥𝐯𝐢𝐧𝐠 𝐡𝐞𝐚𝐥𝐭𝐡𝐜𝐚𝐫𝐞 𝐧𝐞𝐞𝐝𝐬,
𝐝𝐮𝐞 𝐭𝐨 𝐨𝐮𝐫 𝐞𝐱𝐩𝐚𝐧𝐬𝐢𝐨𝐧 𝐢𝐧 𝐭𝐡𝐞 𝐄𝐠𝐲𝐩𝐭𝐢𝐚𝐧 𝐦𝐚𝐫𝐤𝐞𝐭 ; 𝐰𝐞 𝐢𝐧𝐯𝐢𝐭𝐞 𝐪𝐮𝐚𝐥𝐢𝐟𝐢𝐞𝐝 𝐚𝐧𝐝 𝐡𝐢𝐠𝐡𝐥𝐲 𝐭𝐚𝐥𝐞𝐧𝐭𝐞𝐝 𝐚𝐩𝐩𝐥𝐢𝐜𝐚𝐧𝐭𝐬 𝐭𝐨 𝐣𝐨𝐢𝐧 𝐨𝐮𝐫 𝐭𝐞𝐚𝐦

𝐓𝐢𝐭𝐥𝐞 : Regulatory Affairs Specialist

𝐉𝐨𝐛 𝐃𝐞𝐬𝐜𝐫𝐢𝐩𝐭𝐢𝐨𝐧

•Collect and coordinate information and prepare regulatory CTD documentation for submission to regulatory agencies, authorities or to commercial partners.
•Expertise proficiency with software tools and matrices for CTD submission.
•Select and prepare CTD for products according to management instructions.
•Coordinate with the R&D, Q.C, Q.A, Production, Supply chain and Marketing team members regarding the different registration issues and documents required for CTD preparation.
•Ensure confidentiality in respect of CTD registration files contents.
•Review carefully compiled CTD files to ensure that content, quality; accuracy and format of submission comply with applicable regulations of different markets.
•Perform other related duties as assigned.

𝘛𝘩𝘦 𝘤𝘳𝘪𝘵𝘦𝘳𝘪𝘢 𝘢𝘴 𝘧𝘰𝘭𝘭𝘰𝘸𝘪𝘯𝘨:

1) Bachelor’s degree in pharmacy
2) From 2 – 3 years of experience
3) CTD Experience is a must
4) Good user of MS office
5) Excellent of English language

📎 𝘏𝘰𝘸 𝘵𝘰 𝘢𝘱𝘱𝘭𝘺: 𝘐𝘧 𝘺𝘰𝘶 𝘧𝘶𝘭𝘧𝘪𝘭𝘭 𝘵𝘩𝘦 𝘢𝘣𝘰𝘷𝘦 𝘤𝘳𝘪𝘵𝘦𝘳𝘪𝘢, 𝘱𝘭𝘦𝘢𝘴𝘦 𝘴𝘦𝘯𝘥 𝘺𝘰𝘶𝘳 𝘤𝘷: 𝘩𝘳@𝘨𝘺𝘱𝘵𝘰𝘱𝘩𝘢𝘳𝘮𝘢.𝘤𝘰𝘮
𝘮𝘦𝘯𝘵𝘪𝘰𝘯 𝘵𝘩𝘦 𝘫𝘰𝘣 𝘵𝘪𝘵𝘭𝘦 𝘪𝘯 𝘵𝘩𝘦 𝘦𝘮𝘢𝘪𝘭 𝘴𝘶𝘣𝘫𝘦𝘤𝘵.