PT Anvita Pharma Indonesia

PT Anvita Pharma Indonesia adalah perusahaan farmasi yang memiliki visi untuk menjadi pemimpin dalam pengembangan dan produksi bahan baku obat berkualitas tinggi di Indonesia. Didirikan pada tahun 2018, perusahaan ini memiliki peran penting dalam meningkatkan kemandirian Indonesia di sektor farmasi, khususnya dalam hal produksi Bahan Baku Aktif (API).

Sebagai perusahaan farmasi berbasis penelitian, Anvita Pharma terus berinovasi untuk mengembangkan teknologi yang lebih efisien dan efektif dalam proses produksi obat. Fokus utama perusahaan adalah pada molekul kecil, yang merupakan komponen penting dalam banyak jenis obat. Dengan fasilitas produksi yang modern dan bersertifikat GMP, Anvita Pharma berkomitmen untuk menghasilkan produk-produk farmasi yang memenuhi standar kualitas internasional.

Selain berkontribusi pada pengembangan industri farmasi di dalam negeri, Anvita Pharma juga memiliki ambisi untuk memperluas pasarnya ke kawasan Asia Tenggara. Dengan demikian, perusahaan ini tidak hanya berperan dalam memenuhi kebutuhan kesehatan masyarakat Indonesia, tetapi juga berkontribusi pada peningkatan aksesibilitas obat-obatan berkualitas di tingkat regional.

Lowongan Kerja PT Anvita Pharma Indonesia

Validation Staff

Job Description :

• Carrying out activities based on superior assignments, validation, qualification and routine calibration, project-based, or compliance needs, SOP and all GMP documents applicable in the QA area correctly and on time
• Prepare documents [protocols and reports] required for routine, project-based validation, qualification and calibration activities, or compliance needs, SOP and all applicable GMP documents in the QA area correctly and on time
• Conduct observations and sampling of the validation and qualification stages
• Ensuring that all calibration certificate, validation, study and qualification document are available in the form of soft files, ensuring that the original documents are stored in the appropriate place and maintaining document archives
• Conduct verification and evaluation of data resulting from documentation of validation, qualification and calibration activities, work forms and loogbooks, before being given to superiors
• Take corrective action on risks and/or problems iin terms of HSE, quaity and compliance in the QA area
• Prepare the monthly calibration and qualification actualization report based on the current schedule in the VMP

Requirement :

• Min Diploma of Pharmacy / Chemistry / Industry / related fields
• Have Certification related to GMP training or calibration is a plus
• Have knowledge about Validation/Qualification/Calibration in the Pharmaceutical Industry
• min 1 year experience in the field of Quality in the Pharmaceutical Industry
• Have skill in Standard procedures in the GMP/CPOB corridor for the pharmaceutical industry established by the Ministry of Health and BPOM; validation and calibration equipment used in the pharmaceutical industry; Validation, qualification and calibration processes in the pharmaceutical industry; Documentation of validation, qualification and calibration processes in the pharmaceutical industry

Qualification Supervisor

Job Description :

• Verify and evaluate the data of Calibration, Study and Qualification/Validation results (including Installation Qualification, Operational Qualification, and Performance Qualification) in accordance with RIV.
• Verify and evaluate the data from the recapitulation from the QA area; Verify and evaluate the data on relevant work forms from Staff and logbooks.
• Carry out a management system and documentation of Calibration, Studies and Qualifications activities at PT Anvita Pharma Indonesia so that it runs effectively and efficiently
• Prepare the necessary documents for routine, project-based, or compliance activities; such as URS, protocols and reports for Calibration, Studies and Qualifications, SOPs (Standard Operational Procedures), and all applicable GMP documents in the QA area.
• Identify CAPA based on GMP and HSE Audit relevant to the area.
• Involved in internal audits, regular inspections in QA areas and external audits to ensure all aspects comply with HSE and GMP regulations.

Requirement :

• Bachelor Degree of Pharmacy / Chemistry / Industry / Pharmacist/ related fields
• > 2 years experience in the Pharmaceutical Industry
• Have knowledge about Qualification/Calibration in the Pharmaceutical Industry
• Have Certification related to calibration training is a plus
• Have skill in Standard procedures for quality assurance in the GMP/CPOB corridor for the pharmaceutical industry established by the Ministry of Health and BPOM; Quality Management System; GMP [CPOB], GDP [Good Documentation Practice]; Equipment and instruments used in the pharmaceutical industry; Pharmaceutical industry processes and testing procedures

Analyst QC Chemical

Job Description :

• Conduct activities in accordance with analysis methods, SOP and protocols relevant to validation needs, routine activities, and each project plan
• Using instrumentry, equipment, instrument change parts, stock materials and other consumables according to the needs based on scheduling, and also ensure its readiness
• Carry out analysis activities in accordance with scheduling and to be compliant in terms of HSE, Quality and Compliance in the QC area
• Documentation of all activities carried out n the QC area
• Support the audit process of GMP, HSE and other audit carried out at QC area facilities
• Involving participation of Continuous Improvement in QC area
• Fulfilling and improving self competency in QC area
• Complying regulations related to work safety, and maintain work safety supporting equipment to maintain a safe work environment
• Support maintain stability between teams and a conductive work environment in the QC area

Requirement :

• Have skill in Standard procedures for analytical (sampling, instrument types, general analysis and documentation of analysis results) in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM; Chemical analysis process in pharmaceutical industry; documentation
• Bachelor of Vocational School from Pharmacy / Chemistry / Industry / related fields
• Fresh graduate or > 1 years experience in the field of QC in the Pharmaceutical Industry
• Have deep knowledge of QC in the Pharmaceutical Industry
• Have skills in using MS. Office & Basic skill in English

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

Requirement :

• 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

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