ตำแหน่ง Admin RA

บริษัท Ortho Clinical Thailand Ltd.

ที่อยู่บริษัท Interrink Tower

เงินเดือน สำหรับสมาชิกเท่านั้น

ลักษณะงานที่ทำ
- Managed Regulatory documentation such as Licenses,
Certification of ISO FDA registration
- Writing clear arguments and explanations for new product licenses and licenses renewals
- Keeping up-to-date with changes in regulatory legislation and guidelines
- Studying scientific and legal documents
- Liaising and negotiating with regulatory authorities
- Ensuring that quality standards are met and submissions meet strict deadlines
- Prepared and submitted Report Import and Sale in System
FDA Thai
- Provide general administration support to RA Manager

ตำแหน่ง Administration Executive

บริษัท ZUELLIG PHARMA (HOE Pharmaceutical)

ที่อยู่บริษัท BB Building

เงินเดือน สำหรับสมาชิกเท่านั้น

ลักษณะงานที่ทำ
- Prepare document use Cash Voucher by adding vat and withholding and checking the invoices and receipts received from the staff and supplliers reimbursement by forwarding to the accounting officer to continue paying the staff and suppliers.
- Report update for employment to office HR at Hoe Pharmaceutical at Malaysia
- Prepare document Free Sale for Medical device contact Food and Drug Administration for approval Free Sale
- Report Assets in office every quarter by send email to accounting officer at Malaysia and make petty cash messenger fee and Postage (Project team Marketing)
- Composes and prepares written documentation and Correspondence for the FDA Thai
- Negotiating with regulatory authorities for marketing authorization
- Specifying storage, labeling and packaging requirements
- Assist in organizing and updating department files and database for General Manager and Sale Manager and Support team Sale and team Marketing in Payment Allowance and other
- Reply to email Product Complaints to Manufacture in Malaysia
Reasons of leaving: They want out of business and get laid off.

ตำแหน่ง Regulatory Affairs

บริษัท Smith and Nephew Co.,Ltd

ที่อยู่บริษัท The nine พระราม เก้า

เงินเดือน สำหรับสมาชิกเท่านั้น

ลักษณะงานที่ทำ
 Managed Regulatory documentation such as License,
Certification of ISO and Fee sale, to proceed FDA registration
 Writing clear arguments and explanations for new product licences and licence renewals
 Keeping up-to-date with changes in regulatory legislation and guidelines
 Studying scientific and legal documents
 Liaising and negotiating with regulatory authorities
 Ensuring that quality standards are met and submissions meet strict deadlines
 Prepared Monthly Summary Report to RA Global
 Provide administration general support to RA Manager
 Prepared catalog for submission medical such as Orthopedic,surgery,Wound & Care etc