Profil Perusahaan
Medifarma Laboratories adalah perusahaan farmasi manufaktur tol yang berbasis di Indonesia yang didirikan pada tahun 1975, dengan fasilitas produksi seluas 36.595 meter persegi.
Fasilitas produksi dan operasi kami telah disertifikasi oleh Badan Pengawas Obat dan Makanan Indonesia (Badan Pengawasan Obat dan Makanan), dengan standar praktik manufaktur yang ditemukan sesuai dengan standar Cara Pembuatan yang Baik serta memenuhi standar yang disyaratkan oleh Inspeksi Farmasi. Skema Kerjasama (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.
Alamat
Jl. Raya Jakarta-Bogor KM. 33,
Kelurahan Curug, Kecamatan Cimanggis
Kota Depok, Jawa Barat 16453
Phone: +6221 874-0659
Email: info.mli@medifarma.biz
Social Media
PT Medifarma Laboratories saat ini sedang membuka kesempatan untuk posisi:
1. PPIC Supervisor
Responsibilities
- Responsible for MPS and MRP running at MLI Plant
- Responsible to the availability of materials for production planning
- Responsible for monitoring finished products supply (PO fulfillment)
- Responsible for supporting in launching new products
- Review PPIC reports
Qualifications
- Apothecary with minimum 2-3 years working experiences in PPIC or Production
- Strong in data analysis
- Have received training and understand the Good Manufacturing Practices (CPOB)
- Have leadership skills
- Able to work individually and with team as well
- Fluent in English both speaking and writing
2. Production Supervisor
Responsibilities
- Create a weekly schedule based on requests from PPIC/ Marketing approved by the Production Manager
- To control/supervise implementation of GMP, SOP, Halal guarantee system
- To organize and supervise the work of subordinates and additional job in particular time
- Responsible for monitoring the processing and packaging process
- Overcaming problems that arise during the all process (trouble shooting)
Qualifications
- Apothecary with minimum 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
3. QC Supervisor
Responsibilities
- Handling related to protocol validation of analytical methods and verification of analytical methods
- Handling related to microbiological testing samples, raw material, finished goods, and stability
- Review related to worksheet for stability and finished goods
- Review regarding analytical procedures
Qualifications
- Apothecary/Chemistry with minimum 3 years experience
- Strong experience in analytical development
- 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
4. QC Starting Material Supervisor
Responsibilities
- Monitoring and control of sampling and inspection implementation of starting material (RM & PM)
- Review and give the recommendation disposition to starting material
- Release and reject starting material on exact system
- Monitoring internal & external CAPA
- GMP observation and monitoring of deviation
- Review technical documents related to starting material
Qualifications
- Apothecary with minimum 3 years experience
- High motivated to work in starting material
- 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
5. QA Validation Calibration Supervisor
Responsibilities
- 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.
Qualifications
- 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
6. QA Validation Staff
Responsibilities
- Create protocol document and monitoring of process validation, packaging validation, cleaning validation, performance qualification or computerized 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
Qualifications
- 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
7. Packaging Development
Responsibilities
- 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
Qualifications
- 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
8. Engineering Supervisor
Responsibilities
- Coordinating the task of Maintenance team every day so that the maintenance and repair work of production machines can run effectively and efficiently
- Coordinating the Head Utility Unit, Utility Technicians and Utility Operators so that utility support to the production room and others can run properly
- Evaluating the implementation of maintenance programs and trying to make improvements with the approval of the Engineering Manager
- Evaluate its implementation and make changes if necessary, with the Engineering
- Manager's approval
- Arrange a work shift schedule for all technicians
- Provide support for company programs
Qualifications
- Bachelor’s degree from Mechanical/Electrical
- Preferably with 2-3 years experience
- Responsible, hard worker, fast learner, and strong leadership
- Able to work individually and with team as well
- Fluent in English both speaking and writing
9. Operational Excellence Specialist
Responsibilities
- 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
Qualifications
- 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
Submit your latest CV to
Only suitable applicants will be contacted.
Sumber: Nada Fitria Siregar
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