Beranda LOKER SMA/SMK PT Medifarma Laboratories

PT Medifarma Laboratories

- 2024-09-25, 21:40

PT Medifarma Laboratories adalah perusahaan farmasi yang berkantor pusat di Indonesia. Kantor pusatnya berada di Depok, di pinggiran selatan Jakarta, ibu kota Indonesia. Didirikan pada tahun 1975, fasilitas produksi kami saat ini seluas 36.595 m2. Berikut ini adalah Lowongan Kerja PT Medifarma Laboratories.

Fasilitas produksi dan operasi kami telah disertifikasi oleh Badan Pengawas Obat dan Makanan Indonesia, dengan standar praktik manufaktur yang ditetapkan sesuai dengan standar Praktik Manufaktur yang Baik saat ini serta memenuhi standar yang dipersyaratkan oleh Skema Kerjasama Inspeksi Farmasi (PIC/s) dan Organisasi Kesehatan Dunia (WHO).

Medifarma mengekspor produknya ke Filipina, Singapura, Malaysia, Hong Kong, Myanmar, Kamboja, dan Vietnam. Kami berkomitmen untuk mempertahankan standar kualitas tertinggi untuk semua yang kami produksi.

Lowongan Kerja PT Medifarma Laboratories

Saat ini PT Medifarma Laboratories memberikan kesempatan untuk dapat bergabung bersama dengan posisi sebagai berikut:

1. Operational Excellence Specialist

Requirement :

Bachelor’s degree from Industrial/Management Engineering
Minimum 2-3 years of working experience in a related field in Manufacturing Company, preferably Pharmaceutical/Food Industry
Experience with training/background in operational excellence & LEAN; SQC Tools, Six Sigma & Lean Sigma Belt holder
Individual Contributor
Fluent in English both speaking and writing

Job Description :

Leads Operational Excellence Boot Camps, Assessment and initiatives for the plants
Leads/Supports Budget planning, direction setting and KRA setting exercises for the division
Handles capacity management and volume analysis requirements for plants
Ensures that reports for key performance indicators are generated monthly
Ensure that all requests for master recipe and production versions are generated and updated
Leads project requirements initiated by Plant Head

2. MTU Supervisor

Requirement :

Apothecary with minimum 2 – 3 years working experiences
Has received training and understands Good Manufacturing Practices (CPOB) and the Halal Assurance System (SJH)
Have leadership skills
Have active command of the English language

Job Description :

Reviewing formulas and supporting documents to be worked on by the subordinate can be applied in laboratory scale and pilot scale experiments
Carry out subordinate supervision in conducting formula experiments on both a laboratory scale and a pilot scale
Prepare Bill of Material and Bill of Operation (BOMBOO) for the calculation of COGS calculations and inform Finance
Participates in reviewing and providing recommendations for changes in specifications for finished drugs, specifications for raw materials and specifications for packaging materials used.
Perform status updates related to the NPD, ASD, Improvement and Reformulation and Technology Transfer projects
Reviewing the Proof Print from MTU Packaging Development
Review the Standard Operating Procedure of the MTU department and ensure that it is carried out correctly

3. QA Supervisor

Requirement :

Apothecary with minimum 2-3 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 :

Providing input to the QA Manager in making the Validation Program and matters related to Validation for the preparation of Budget Quality Assurance
Prepare process validation protocols and reports for the production scale and pilot scale for existing products, validate procedures for cleaning equipment and machines
Coordinate with related Supervisors in carrying out Process Validation, Validation of equipment and machine cleaning procedures and Validation of Supporting Facilities
Coordinate with the IT Department in preparing and implementing computerized system validation
Monitor the implementation of sampling, testing and inspection during the validation process in accordance with SOP

4. QC Pharmacist Staff

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

5. QA Validation Staff

Requirement :

Apothecary with experience in the same role
High motivated, responsible, hard worker, and fast learner
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 :

Create protocol document and monitoring of process validation, packaging validation,cleaning validation, performance qualification or computerised system validation
Recording validation data in accordance with the validation protocol
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

6. Business Development Senior Staff

Requirement :

Apothecary with experience in the same role
High motivated, responsible, hard worker, and fast learner
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 :

Helping Buss.Dev Supervisor communicate with customers regarding New Product Development
Responsible with Medifarma’s internal team regarding New Product Development
Helping Buss.Dev Supervisor in monitoring the progress of New Product Development and ensuring all stages have been carried out according to the time line agreed upon with the customer
Hold monthly meetings with all internal teams to discuss the progress of New Product Development
Carry out other duties assigned from time to time by BD Supervisor

7. QC IPC Inspector

Requirement :

Minimal Sekolah Menengah Farmasi atau Sekolah Menengah Analis Kimia
Memiliki pengetahuan dan pengalaman mengenai pekerjaan yang sama lebih disukai
Telah mendapatkan pelatihan Cara Pembuatan Obat yang Baik
Dapat bekerja secara tim ataupun individu

Job Description :

Melakukan sampling dan inspeksi pada awal, pertengahan, dan akhir proses produksi atau selama proses produksi pada produk antara, ruahan, dan jadi sesuai dengan prosedur yang berlaku
Membuat laporan hasil inspeksi pada awal, pertengahan, dan akhir proses produksi atau selama proses produksi pada produk antara, ruahan dan jadi
Mencatat temuan dan penyimpangan yang ditemukan selama melakukan sampling & inspeksi dalam form yang telah ditentukan, dan melaporkannya kepada QC In-Process Control Coordinator atau QC Supervisor

8. QC Analyst RM

Requirement :

Minimal Sekolah Menengah Atas dan yang sederajat atau Sekolah Menengah Analis Kimia atau Sekolah Menengah Analis Kesehatan
Dapat bekerja secara tim ataupun individu
Telah mendapatkan pelatihan dan memahami Cara Pembuatan Obat yang Baik

Job Description :

Melakukan pengujian fisika, kimia, dan mikrobiologi terhadap sample bahan baku, produk jadi dan pembuatan laporannya
Melakukan pengembangan metode analisa baru, validasi metode analisa dan pembuatan laporannya
Melakukan pencatatan pada logbook/ logsheet terhadap semua aktivitas
Melakukan verifikasi terhadap alat ukur (neraca analistis, ph meter, konduktiviti meter, dll)
Melakukan pembuatan pereaksi sekunder termasuk indikator kimia dalam pengujian

9. QC Analyst Stability

Requirement :

Minimal Sekolah Menengah Atas dan sederajat atau Sekolah Menengah Analis Kimia atau Sekolah Menengah Analis Kesehatan
Dapat bekerja secara tim ataupun individu
Telah mendapatkan pelatihan dan memahami Cara Pembuatan Obat yang Baik

Job Description :

Melakukan pengujian fisika-kimia terhadap sample produk jadi dan pembuatan laporannya
Melakukan pencatatan pada logbook/ logsheet terhadap semua aktivitas
Melakukan verifikasi terhadap alat ukur (neraca analistis, ph meter, konduktiviti meter, dll)
Melakukan pembuatan perekasi sekunder termasuk indikator kimia dalam pengujian

10. Warehouse RM Staff

Requirement :

Minimal SMU atau sederajat
Pengalaman kerja minimal 1 (satu) tahun sebagai Warehouse Staff
Telah mendapatkan pelatihan Cara Pembuatan Obat yang Baik (CPOB)
Terbiasa dalam bekerja secara tim atau individu

Job Description :

Menerima, menyimpan dan mengirimkan produk dengan baik dan benar sesuai SOP
Memisahkan material antara status Quarantine dengan status Released dan menempatkannya sesuai dengan area masing-masing
Memastikan kesesuaian data antara sistem, lembar kerja dan fisik barang saat serah terima barang
Inventory Record Accuracy (IRA) 100% pada area tangggung jawabnya
Membantu petugas QC, untuk mengembalikan hasil sampling pada wadahnya
Mengirim permintaan material yang “siap kirim” ke produksi
Membantu Warehouse Supervisor untuk pemenuhan target CAPA sehingga dapat terpenuhi sebelum due date

Tata Cara Melamar:

Bagi peserta yang ingin melamar dan memenuhi kriteria, segera melakukan registrasi melalui link di bawah :

1. Operational Excellence Specialist	DAFTAR
2. MTU Supervisor	DAFTAR
3. QA Supervisor	DAFTAR
4. QC Pharmacist Staff	DAFTAR
5. QA Validation Staff	DAFTAR
6. Business Development Senior Staff	DAFTAR
7. QC IPC Inspector	DAFTAR
8. QC Analyst RM	DAFTAR
9. QC Analyst Stability	DAFTAR
10. Warehouse RM Staff	DAFTAR