Profil Perusahaan
PT Anvita Pharma Indonesia adalah perusahaan farmasi berbasis penelitian yang bertujuan untuk menjadi yang terdepan sebagai pengembang dan produsen bahan baku obat berkualitas tinggi untuk kebutuhan industri farmasi Indonesia dan untuk ekspor ke pasar ASEAN.
Anvita Pharma telah berhasil mengembangkan teknologi yang mengurangi risiko, waktu, dan biaya dalam pengembangan obat untuk obat-obatan penyelamat jiwa. Teknologi-teknologi ini diintegrasikan ke dalam pabrik manufaktur API kami yang canggih, dibangun di atas lahan seluas 25.000 meter persegi di dalam KNIC, kawasan industri terintegrasi kelas dunia dekat Jakarta di Indonesia.
Alamat
Karawang New Industry City
Blok B No. 8
Karawang, Indonesia
Social Media
PT Anvita Pharma Indonesia is hiring:
1. OPERATOR WAREHOUSE
REQUIREMENT:
- SMK Farmasi, Kimia, Industri, atau bidang terkait
- Dapat bekerja dalam sistem kerja shift
- Mampu mengoperasikan Ms. Office, kemampuan dasar dalam B. Inggris
- Memiliki pengalaman min. 1 tahun di area gudang atau distribusi di Industri Farmasi
JOB DESCRIPTION:
- Melakukan verifikasi dan evaluasi terhadap data hasil dokumentasi
- Memberikan laporan mengenai kebutuhan meşin, peralatan, stok bahan dan bahan habis pakai dan jika terdapat ide perbaikan
- Memberikan laporan jika diketemukan resiko atau adanya penyimpangan atau pelanggaran dalam hal HSE, Kualitas dan Kepatuhan di area Warehouse
2. OPERATOR PRODUKSI
REQUIREMENT:
- SMK Farmasi, Kimia, Industri, atau terkait
- Dapat bekerja dalam sistem kerja shift
- Mampu mengoperasikan Ms. Office, kemampuan dasar dalam B. Inggris
- Memiliki pengalaman min. 1 tahun di bidang produksi di Industri Farmasi
JOB DESCRIPTION:
- Melakukan kegiatan produksi sesuai dengan penjadwalan
- Melakukan dokumentasi terhadap semua aktivitas di area Produksi
- Perawatan fasilitas, mesin, dan peralatan yg mendukung proses produksi di area Produksi
3. QC (CHEMICAL) SPV.
REQUIREMENT:
- Pharmacist with min. 2 years experiences in QC Chemical in the Pharmaceutical Industry
- Have in-depth knowledge of standard QC procedures in the corridors of GMP/ CPOB for the pharmaceutical industry stipulated by the Kemenkes and BPOM
- Have a strong understanding of analytical method validation & verification concepts
- English proficiency
JOB DESCRIPTION:
- Supervise related laboratory activities in terms of EHS, Quality and Compliance in the QC area
- Create SOP documents, protocols, and reports that are relevant to the needs of validation, verification, routine activities, and each project plan
- Create specification and URS documents, analysis methods as needed
- Supervise the use of instruments, equipment, stock materials, reagents and other consumables; and also ensure its readiness
- Make a plan and schedule activities for Analysts and Lab Assistants
- Coordinate with QA regarding calibration and qualification plans in the QC area.
4. QC CHEMICAL ANALYST
REQUIREMENT:
- Vocational School in Pharmacy, Chemistry, Microbiology, Industry, or related fields
- Fresh graduate or experience in laboratory
- Good in handling laboratory techniques, research skill, and critical thinking
JOB DESCRIPTION:
- Conducting analysis activities in accordance with scheduling and to be appropriate in terms of HSE, Quality and Compliance in the QC area
- Conduct activities in accordance with analysis methods, SOPS and protocols that are relevant to the needs of validation, verification, routine activities, and each project plan
- Carry out work activities based on routine analysis schedules, project-based, or compliance needs and all applicable GMP documents in the QC area correctly (Right First Time)
5. SALES MARKETING SUPERVISOR
REQUIREMENT:
- Pharmacist or Medicine with min. 2 years experiences in sales/marketing of API, imported/ locally manufacture in the Pharmaceutical Industry
- Have in-depth knowledge of pharma market, product knowledge, and market territory
- English proficiency
JOB DESCRIPTION:
- Manage and coordinate sales of Active Pharmaceutical Ingredients (APIs/ BBO) for the local Indonesian market and export.
- Drive sales growth through direct customer engagement, marketing events, and efficient operations
- The role includes active engagement and coordination with internal teams to ensure alignment and prompt processing of customer needs
- Succeeding Government's program (API Change Source) promoting API to prospectus local/ MNC Pharma companies
6. ANALYTICAL DEV. SUPERVISOR
REQUIREMENT:
- S1 of Pharmacy, Chemis, Microbiology, or a related field with 2 years experience in QC/ RnD in Pharmaceutical company.
- Have in-depth knowledge of standard quality control procedures in the GMP/ CPOB corridor for the pharmaceutical industry established by the Ministry of Health and BPOM
- English proficiency (written and oral)
- Have a good understanding of the Quality Management System
JOB DESCRIPTION:
- Carry out stages of developing API & FDF product analysis methods
- Supervise the development stages of related product analysis methods in terms of HSE, Quality and Compliance in the QC area
- Evaluate the need for use of instruments, equipment, change instrument parts, stock materials and other consumables; and also ensure its readiness
- Coordinate with all departments related to the development stages of analytical methods in the QC area
7. ENGINEERING TECHNICIAN
REQUIREMENT:
- SMK Mekatronika/ Elektro/ Mesin
- Dapat bekerja dalam sistem kerja shift
- Mampu mengoperasikan Ms. Office, kemampuan dasar dalam B. Inggris
- Memiliki pengalaman dalam perawatan mesin, instalasi listrik di Industri Farmasi
- Memiliki kemampuan menganalisa, merubah, dan membuat back up program PLC
- Memiliki kemampuan menggambar teknik, manual dan AutoCAD
JOB DESCRIPTION:
- Melaksanakan semua kegiatan maintenance sesuai dengan SOP yg berlaku
- Bertanggung jawab terhadap pemeliharaan mesin/ alat di Produksi, Warehouse, dan QC
- Bertanggung jawab terhadap dokumentasi kegiatan Engineering baik GMP dan Non GMP
8. HSE MANAGER
REQUIREMENT:
- Min. S1 in K3/ Public Health/ Industry/ other relevant field
- >5 years of experience as SPV/ Ass. Mgr. in the pharmaceutical/ chemical/ relevant industry
- Handling ISO 140001, SMK3 and ISO 45001
- English proficiency
- Have knowledge and experience in planning, compiling, assessing, making decisions, and monitoring all activities related to the implementation of HSE policies at the site; evaluate performance security and pest control systems.
- Strong leadership skill and analytical thinking
JOB DESCRIPTION:
- Assess and make decisions related to HSE policies, security system and pest control.
- Plan, assess, make decisions and monitor all matters related to budget, documentation and activities related to HSE policies, security system and pest control.
- Assess and make decisions relating to members of the HSE department.
- Evaluate HSE departement in terms of facilities, equipment and 'human resources then provide recommendations to the Plant Manager.
- Responsible for the implementation of HSE policies in accordance with strict compliance with GMP and HSE regulations with the required time and costs.
- Manage and control the implementation of the ISO 45001 (Occupational Health and Safety Management System) and ISO 14001 (Environmental Management System) in all areas and take necessary actions to improve processes.
9. HSE SUPERVISOR
REQUIREMENT:
- S1 in K3/ Public Health/ Industry/ other relevant field with 2 years experience HSE Supervisor in Pharmaceutical company.
- Have knowledge and experience in planning, compiling, assessing, and monitoring all activities related to the implementation of HSE policies at the site; evaluate performance security and pest control systems
- English proficiency (written and oral)
- Handling ISO 140001, SMK3, and ISO 45001
JOB DESCRIPTION:
- Carry out HSE activity plans, supervise of security systems, pest control, and related documents in the site area.
- Use and cleaning machinery, equipment, stock of materials and consumables necessary to carry out activities and compliance in the site area.
- Documentation required for the routine, project based, or compliances activities that apply in the site area.
Lamar melalui link berikut:
https://tinyurl.com/Anvita-Form-Aplikasi-KandidatSumber: Ririn Marthianingsih
