Primary Responsibility
- Manage the final product submissions, negotiate and communicate effectively with regulatory authorities to obtain timely product approvals
- Ensure the availability to the affiliate of all relevant registration dossier on new and existing products (filing and archiving) in a secure place within company premise
- Advise on promotional materials and campaigns to ensure adherence to BPOM regulations
- Provide project teams with regulatory input in order to obtain timely regulatory approvals for the products as part of the product development planning
- Develop & maintain regulatory knowledge of relevant international regulations
Qualification
Qualification
- Age 25 - 35 Year
- Bachelor’s degree in Pharmacy
- Minimum one year of experience in pharmacy company would be preferred
- Having STRTTK (letter mark registration Pharmaceutical Technical Staff) is still valid
- Excellent in written and verbal english communication skills and computer literacy
- A thorough understanding of the drug registration processing at BPOM and have extensive experience in the regulatory field
- Show excellent communication, inter-personal skills, and personal influence
- Has effective time management skill and able to set priority in task planning
- Be able to resist any influence which would hamper decision making
- Willing to be placed in TANGERANG
Benefit :
- Fixed salary
- Allowance
- Meal Allowance
- Transport Allowance
- BPJS Kesehatan & Ketenagakerjaan
Informasi lebih lanjut
Bidang Pekerjaan |
Status Kepegawaian |
Farmasi/Makanan Olahan, Farmasi/Makanan Olahan
|
Full-Time
|
Pendidikan Terakhir |
Gaji |
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Sesuai Peraturan Perusahaan
|
Tingkat Jabatan |
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