Lowongan Kerja sebagai Analytical Dev Supervisor, QC Chemical Analyst, Operator Produksi, QC (Chemical) Supervisor, Operator Warehouse di PT Anvita Pharma Indonesia

Lowongan Pekerjaan Analytical Dev Supervisor, QC Chemical Analyst, Operator Produksi, QC (Chemical) Supervisor, Operator Warehouse

PT. Anvita Pharma Indonesia

Berikut ini adalah Informasi Lowongan Kerja dari PT Anvita Pharma Indonesia untuk posisi:

Job Vacancy!

Analytical Dev. Supervisor
Requirement:

• Bachelor degree 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:

1. Carry out stages of developing API & FDF product analysis methods
2. Supervise the development stages of related product analysis methods in terms of HSE, Quality and Compliance in the QC area
3. Evaluate the need for use of instruments, equipment, change instrument parts, stock materials and other consumables, and also ensure its readiness
4. Coordinate with all departments related to the development stages of analytical methods in the QC area

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:

1. Conducting analysis activities in accordance with scheduling and to be appropriate in terms of HSE, Quality and Compliance in the QC area
2. 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
3. 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)

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:

1. Melakukan kegiatan produksi sesuai dengan penjadwalan
2. Melakukan dokumentasi terhadap semua aktivitas di area Produksi
3. Perawatan fasilitas, mesin, dan peralatan yg mendukung proses produksi di area Produksi

QC (Chemical) Supervisor
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:

1. Supervise related laboratory activities in terms of EHS, Quality and Compliance in the QC area
2. Create SOP documents, protocols, and reports that are relevant to the needs he needs of validation, verification, routine activities, and each project plan
3. Create specification and URS documents, analysis methods as needed
4. Supervise the use of instruments, equipment, stock materials, reagents and other consumables; and also ensure its readiness
5. Make a plan and schedule activities for Analysts and Lab Assistants
6. Coordinate with QA regarding calibration and qualification plans in the QC area

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:

1. Melakukan verifikasi dan evaluasi terhadap data hasil dokumentasi
2. Memberikan laporan mengenai kebutuhan mesin, peralatan, stok bahan dan bahan habis pakai dan jika terdapat ide perbaikan
3. Memberikan laporan jika diketemukan. resiko atau adanya penyimpangan atau pelanggaran dalam hal HSE, Kualitas den Kepatuhan di area Warehouse

If you meet this qualification, please click the link below to apply

https://tinyurl.com/Anvita-Form-Aplikasi-Kandidat

*sumber IG @ loker_kimia.id