PT Anvita Pharma Indonesia

Lowongan Kerja – PT Anvita Pharma Indonesia adalah perusahaan farmasi swasta yang didirikan pada tahun 2018 dan berlokasi di Kawasan Industri Karawang New Industry City, Kabupaten Karawang, Jawa Barat. Perusahaan ini berfokus pada pengembangan dan produksi Bahan Farmasi Aktif (API) berbasis molekul kecil untuk memenuhi kebutuhan industri farmasi di Indonesia serta pasar regional ASEAN.

Dengan fasilitas produksi bersertifikasi GMP di area seluas sekitar 25.000 m², PT Anvita Pharma Indonesia menyediakan layanan menyeluruh sebagai Contract Development & Manufacturing Organization (CDMO), mencakup pengembangan hingga manufaktur API dan formulasi obat jadi. Perusahaan mengedepankan nilai kolaborasi, integritas, inovasi, dan akuntabilitas dalam menjalankan seluruh kegiatan operasionalnya.

Baca: Info Lowongan Kerja untuk Lulusan Baru

Sumber Daya Manusia (SDM) merupakan asset yang sangat berharga atau sebuah investasi besar yang akan menjadi faktor utama yang menentukan suatu keberhasilan sebuah perusahaan/instansi. Pengelolaan Manajemen Sumber Daya Manusia (MSDM) yang tepat bagi sebuah perusahaan/instansi akan menjadi faktor utama dan membawa kesuksesan yang maksimal. Kreatifitas dan dedikasi para ahli dibidangnya adalah kunci keberhasilan sebuah perusahaan/instansi. Apresiasi yang tinggi atas kontribusi para karyawan menumbuhkan lingkungan kerja yang produktif, inovatif, kreatif dan dinamis.

Maka dari itu PT Anvita Pharma Indonesia kembali membuka rekrutmen lowongan kerja terbaru untuk sejumlah posisi yang dibutuhkan. Calon kandidat yang memenuhi kualifikasi, memiliki semangat dan dedikasi yang tinggi serta keinginan untuk berkembang meningkatkan keterampilan dan pengalamannya. Berikut adalah posisi dan kualifikasi lowongan yang tersedia pada saat ini.

Lowongan Kerja PT Anvita Pharma Indonesia

1. Warehouse Admin

Requirement :

• Min Diploma from Pharmacy/ Chemistry/ Industry/ related fields
• ≥ 1 years experience in the Pharmaceutical Industry
• Have deep knowledge of warehouse and supply chain pharmaceutical industry
• Have skill in material handling procedures [receiving, storing, weighing and shipping] in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM; Equipment used in  the pharmaceutical industry; Pharmaceutical industry processes; Documentation
• Have skills in using MS Office & excellent skill in English
• Placement : Karawang

Job Description :

• Ensure compliance with HSE, quality, and warehouse compliance procedures
• Input and update incoming and outgoing stock data
• Prepare and manage warehouse reports and documentation
• Monitor stock availability and conduct stock opname/cycle count
• Coordinate operational activities with related departments
• Operate warehouse/ERP systems such as SAP and Microsoft Dynamics
• Ensure data accuracy and completeness of shipping and warehouse documents

2. Quality Assurance

Requirement :

• Have skill in standard procedures in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM
• = 1 year of experience in the field of QC in the pharmaceutical industry
• Have deep knowledge of document management systems in the pharmaceutical industry
• Bachelor’s Degree in Pharmacy / Chemistry / Industry / related fields
• Have skills in using MS Office & excellent skill in English
• Have knowledge and skill in statistical analysis is an advantage, but not mandatory
• Placement : Karawang

Job Description :

• Carrying out activities based on superior assignments, project-based, or compliance needs, SOP [Standard Operational Procedure] and all GMP documents applicable in the QA area correctly and on time.
• Ensure the completeness and content of product release documents from the production and QC departments before submitting them to TT & EBR Supervisor.
• Ensuring that all document are available in the form of soft files [scanned], ensuring that the original documents are stored in the appropriate place and maintaining document archives.
• Collect documentation error data in product release document and updating data in the batch release logbook & Storing batch record archives [hard copy and soft copy] until a predetermined deadline.
• Report to supervisor if there is a risk or deviation or violation in terms of HSE, Quality and Compliance in the QA area, as soon as possible.
• Conduct verification and evaluation of data resulting from documentation, before being given to superiors.
• Involved in internal audits [if required] and regular inspections in QA Area, to ensure all aspects comply with HSE and GMP regulations.
• Conduct inspection and evaluation on imported product
• Assist QA Supervisor in collecting and analyzing data for Product Quality Review and any other report that needed statistical analysis

3. Production Operator

Requirement :

• SMK Farmasi, Kimia, Industri, atau terkait
• Dapat bekerja dalam sistem kerja shift
• Mampu mengoperasikan Ms. kemampuan dasar dalam B. Inggris Office,
• Memiliki pengalaman min. 1 tahun di bidang produksi di Industri Farmasi
• Placement : Karawang

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

4. QC Chemical Supervisor

Job Description :

• Supervise and evaluate the stages of analysis terms of HSE, Quality and Compliance in the QC Chemical area
• Plan and ensure the use of machines/instruments, equipment, stock materials and consumables required to carry out activities and compliance in the QC Chemical area
• Creates SOPs, protocols, and working instruction that are relevant to validation needs, routine activities, and each project plan
• Create specifications and analysis methods as needed
• Create URS documents as needed
• Supervising the use of machines/instruments, equipment, machines/instruments change parts, stock of materials and other consumables; and also ensure its readiness
• Planning and scheduling the activities of the Analyst and Inspectors
• Create, review, assess and determine the impact of proposed changes relating to and relating to products, facilities and machines/instruments in QC Chemical area
• Coordinate cross-functionally with QA, Production, Engineering, and Supply Chain to ensure effective planning and execution of sampling activities, calibration, qualification, environmental monitoring, as well as maintenance, repair, and spare part management for machines and instruments in the QC Chemical area

Requirements :

• Bachelor Degree of Pharmacy / Chemistry / Industry / related fields (Aphothechary Competency Certificate is a plus)
• Have deep knowledge of QC in the Pharmaceutical Industry
• = 2 years experience in the field of QC in the Pharmaceutical Industry
• Have skills in using MS. Office & Excellent skill in English
• Have skill in Standard procedures for quality control in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM; Quality Management System; GMP [CPOB], GDP [Good Documentation Practice] and GLP [Good Laboratory Practice]; Laboratory equipment/instrument used in the pharmaceutical industry; pharmaceutical chemical analysis; Root cause analysis
• Placement : Karawang

Bagi yang berminat dan memenuhi kualifikasi, Silahkan melakukan pendaftaran secara online.

NOTE :

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• Proses rekrutmen dilakukan tanpa biaya (GRATIS!!!).
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