PT Medifarma Laboratories: Komitmen terhadap Standar Farmasi Global

PT Medifarma Laboratories merupakan perusahaan farmasi terkemuka di Indonesia yang berafiliasi dengan United Laboratories, Inc., produsen farmasi terbesar di Filipina. Selain itu, perusahaan ini juga berhubungan erat dengan Darya-Varia Laboratoria sebagai sister company di Indonesia. Dengan jaringan yang kuat ini, Medifarma mampu memanfaatkan sumber daya dan keahlian internasional sambil tetap fokus pada pasar domestik.

Selanjutnya, Medifarma Laboratories menjalankan fasilitas produksi yang telah memperoleh sertifikasi dari Badan POM (Badan Pengawas Obat dan Makanan) Indonesia. Proses manufakturnya tidak hanya memenuhi standar CPOB (Cara Pembuatan Obat yang Baik) secara ketat, tetapi juga sesuai dengan persyaratan Pharmaceutical Inspection Co-operation Scheme (PIC/s) dan Organisasi Kesehatan Dunia (WHO). Dengan demikian, setiap produk yang dihasilkan menjamin keamanan, kualitas, dan efektivitas bagi konsumen.

Selain itu, Medifarma tidak hanya berfokus pada pasar domestik, tetapi juga memperluas ekspornya ke berbagai negara, termasuk Filipina, Singapura, Malaysia, Hong Kong, Myanmar, dan Kamboja. Ekspansi ini menunjukkan kepercayaan pasar global terhadap kualitas produk Medifarma. Perusahaan ini secara konsisten menerapkan pengawasan mutu yang ketat pada setiap tahap produksi, mulai dari pemilihan bahan baku hingga proses distribusi.

Lebih lanjut, Medifarma Laboratories terus berinovasi dalam pengembangan produk untuk memenuhi kebutuhan kesehatan yang terus berkembang. Perusahaan ini memproduksi berbagai jenis obat, mulai dari generik, branded generic, hingga produk khusus yang ditujukan untuk terapi tertentu. Dengan dukungan penelitian dan pengembangan yang kuat, Medifarma mampu menghadirkan solusi farmasi yang efektif dan terjangkau.

Di samping itu, komitmen Medifarma terhadap tanggung jawab sosial juga tercermin dalam berbagai program kesehatan masyarakat. Perusahaan ini aktif berpartisipasi dalam kampanye edukasi kesehatan dan menyediakan akses obat-obatan penting bagi masyarakat yang membutuhkan. Dengan demikian, Medifarma tidak hanya berorientasi pada bisnis, tetapi juga berkontribusi terhadap peningkatan kualitas hidup masyarakat.

Ke depan, PT Medifarma Laboratories berencana untuk terus memperluas kapasitas produksi dan jaringan distribusinya. Perusahaan ini bertekad untuk mempertahankan posisinya sebagai salah satu pemain utama di industri farmasi Indonesia sekaligus meningkatkan daya saing di pasar global. Dengan integritas, inovasi, dan standar kualitas yang tinggi, Medifarma siap menghadapi tantangan industri kesehatan yang dinamis.

Requirement:

• Minimum bachelor’s degree in biology, preferably with minimum 2 years working experiences
• Has obtained training and understanding Good Manufacturing Practices (GMP)
• Fluent in English
• Have good leadership and Communication

Job Description:

• Review disposition of microbiology analysis results
• Review disposition of water monitoring result physically, chemically, and microbiologically
• Prepare monthly trend analysis report of microbiology and chemical regarding environmental monitoring of production, water, and supporting departments
• Prepare plan to propose media and bacterial purchase, and reagent
• Conduct verification regarding analyst/logbook/logsheet in microbiology testing area
• Receive sample from sample delivery officer and distributing sample to analyst of checking microbiology
• Prepare PJE (Engineering Service Request) if any damage occurred or modification which could be repaired by internal technician
• Call external technician in regards of any damage happened or modification which could be repaired by external technician

Requirement:

• Apothecary with minimum 1-2 years working experiences
• Have received training and understand the Good Manufacturing Practices (CPOB)
• Have graphic design application / software skills
• Responsible, hard worker and fast learner
• Proficiency with English both passive and active
• Able to work individually and with team as well

Job Description:

• Prepare documents on artwork for both local and export registration purposes
• Make a packaging trial report, packaging specification, packaging standard and ensure its correctness
• Prepare a packaging design for export (if the country concerned asks for the same packaging design as the existing product)
• Collaborating with purchasing, sourcing and suppliers to accelerate the development process of packaging material
• Cooperate with production for the trial process of new packaging materials and alternate suppliers of packaging material
• Looking for and requesting packaging material from suppliers for new products

Requirement:

• Apothecary with minimum 1-2 years working experiences
• Have received training and understand the Good Manufacturing Practices (GMP) 
• Responsible, hard worker and fast learner
• Proficiency with English both passive and active
• Able to work individually and with team as well

Job Description:

• Create protocol document of process validation, packaging validation, cleaning validation, performance qualification or computerised system validation
• Monitoring the implementation of process validation
• Recording validation data in accordance with the validation protocol
• Create report document of process validation
• Perform physical testing checks during process validation, packaging validation or cleaning validation according to the validation protocol
• Assist the QA Validation and Calibration Supervisor in providing training to other inspectors

Requirement:

• Apothecary with minimum 1-2 years experience
• Responsible, hard worker, fast learner, and strong leadership
• Able to work individually and with team as well
• Have received training and understand the Good Manufacturing Practices (CPOB)
• Fluent in English both speaking and writing

Job Description:

• Responsible for conducting all testing to sample P&G according to procedures / SOP that has been approved along with using specification-met tools and materials
• Assist QC Manager in managing all activites and human resources available in order to optimize output of QC Department
• Review disposition of Stability and Managing storage and scheduling stability sampling
• Prepare protocol and P&G stability testing report
• Monitor the temperature and temperature of the chamber and reviewing data from thermohygro, as well as evaluating if there is a deviation
• Actively participate in supporting “best practice” execution available in PT. Medifarma Laboratories

Requirement:

• Apothecary with 1 year experience
• Responsible, hard worker, fast learner, and strong leadership
• Able to work individually and with team as well
• Have received training and understand the Good Manufacturing Practices (CPOB)
• Fluent in English both speaking and writing

Job Description:

• To control/ monitoring implementation of GMP, SOP, Halal guarantee system
• Responsible for monitoring the processing and packaging process (solid product)
• Overcaming problems that arise during the all process (trouble shooting)

Jika Anda memenuhi kualifikasi di atas dan berminat menjadi bagian dari perusahaan, ikuti langkah berikut:

1. Klik tombol “Lamar Sekarang” menuju portal recruitment perusahaan.
2. Isi formulir pendaftaran dengan lengkap dan unggah CV terbaik Anda.
3. Pastikan seluruh informasi yang Anda berikan akurat dan sesuai dengan kualifikasi yang diminta.

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