838 Qc Analyst jobs in Indonesia

Job Requirement :

1. Min. D3/S1 Teknologi Pangan/ Kimia Analis
2. Berpengalaman sebagai QC min. 2 tahun (lebih diutamakan dari perusahaan makanan & minuman)
3. Memiliki kemampuan koordinasi, analisa dan perencanaan yang baik
4. Menguasai metode analisa bahan baku, kemasan dan produk
5. Memahami teknik sampling bahan baku, kemasan dan produk
6. Diutamakan berdomisili di Ciawi, Bogor, Jawa Barat

Job Description :

1. MONITORING QUALITY CONTROL

a.    Melakukan pemeriksaan kesesuaian jumlah, kelengkapan dokumen dan kondisi kendaraan saat penerimaan atau pengiriman bahan baku/bahan kemas/produk jadi

b.    Melakukan pengambilan sampel bahan baku/bahan kemas/produk jadi untuk kebutuhan analisa

c Melakukan pelaporan identitas prasampling bahan baku/bahan kemas/produk jadi di Satelite QC

d.    Melakukan analisa bahan baku/bahan kemas/produk jadi sesuai dengan spesifikasi yang ada pada ClickData

e Melakukan pelaporan hasil analisa bahan baku/bahan kemas/produk jadi di Satelite QC

f Melakukan analisa (PPQ (Pemerksaan Pemeriksaan QC)) ketidaksesuaian terhadap bahan baku/bahan kemas/produk jadi

g.    Melakukan analisa sampel retent dan reference sesuai periode Analisa

h.    Melakukan kalibrasi alat yang dilakukan internal

i Melakukan monitoring terhadap kebersihan area Gudang bahan baku/bahan kemas/produk jadi dan ruang repack

j Melakukan monitoring dan evaluasi rekapitulasi suhu dan RH Gudang bahan baku/bahan kemas/produk jadi dan ruang repack

k. Verifikasi sanitasi dan hygiene sebelum dan sesudah proses

1. MENDORONG PROSES IMPROVEMENT

a Memantau dan mengukur tingkat kepuasan pelanggan internal sehubungan dengan layanan QC

b.    Melakukan tindakan perbaikan yang diperlukan untuk meningkatkan layanan QC

Kualifikasi :

• D3/S1 Kimia
• Berpengalaman di industri Petrokimia selama 3 tahun
• Mampu mengoperasikan dan mengkalibrasi peralatan laboratorium (GC, AAS, IC, dll)
• Memiliki pengetahuan dalam hal kimia dasar dan instrumentasi
• Memahami dan memiliki pengalaman dalam hal pengelolaan sample dan pengawasan sample
• Mampu melakukan maintenance dasar pada alat-alat laboratorium, termasuk pemeriksaan kalibrasi dan pembersihan
• Bersedia untuk bekerja secara shift apabila dibutuhkan
• Bersedia untuk melakukan setiap tahapan seleksi secara offline di PT PON
• Mampu berbahasa Inggris dengan baik

Tugas dan Tanggung Jawab :

• Melakukan analisa sample dari raw material, intermediate proses sampai final produk
• Melakukan pengambilan dan/atau analisa sample incoming material sesuai dengan spesifikasi
• Melakukan perawatan rutin terhadap peralatan laboratorium serta menjaga kebersihannya
• Secara rutin cek dan mencatat status stok gas dan checmical

SK Plasma has grown steadily on the foundation of PDMP (plasma-derived medicinal products) business starting from 1970. In 2015, SK Plasma resolved to build a state-of-the-art plasma fractionation plant and has spun off from SK Chemicals Life Science biz., aiming to improve competitiveness in the global PDMP market. SK Plasma is planning to build a plasma fractionation plant in order to improve the self-sufficiency of PDMP in Indonesia through a joint venture with capable business partners under the support of the Indonesian government.

Role Description :

• Physicochemical, biochemical, microbiological, and utility testing

• Quality testing of raw materials, and intermediate/final drug products, IPC test

• HPLC, GC, AAS, FT/IR, UV Spectrophotometer, Kjeldahl, Titrator, Electrophoresis, Endotoxin, TOC, Densitometer, Microplate Reader, Raman, ELISA, etc.

• Sterility Tests, Microbial Limit Tests, etc.

• EM(HVAC, PW/WFI, compressed air, nitrogen, ethanol, etc.) sampling and testing

• Method Validation

• Laboratory management

• Qualification and maintenance of analytical equipment

• Management of test requests, reagents, reference standards, and test samples

• Preparation of SOPs and specification

Required :

• Higschool Graduate or Diploma Degree in Biology, Microbiology, Chemistry, Biotechnology / Life Sciences Engineering, Chemical Engineering and other related fields
• Experienced in Quality Control(QC) within the Pharmaceutical Industry
• Proficiency in English

Preferably :

• Experience in Quality Control(QC) within the biopharmaceutical industry
• Experience in the initial setup and operation of QC in a newly constructed biopharmaceutical facility
• Experience in performing method validation
• Experience in technology transfer processes
• Proficiency in Korean

Key Responsibility :

• Product Specification - Monitoring and controlling raw materials / semi finished / finished goods / water treatment according to Product Specification FFI, responsible for all analyzes done in micro laboratories.
• Shift Report - Makes a shifty report about the results of the analysis and deviation occurring in the micro laboratory and gives it to his superiors.
• Analyze - Analyze and control the result against raw material / semi finished / finished goods and able to perform quick method analysis using instrument.
• Documentation - Ensuring that all analysis results are written in the analysis book, all deviations are well communicated and ensuring all analysis results are inputted in the ORS on time.
• Communications - Communicate to relevant departments regarding problematic analysis results as soon as possible so that corrective action can be done and inform the boss if there is a problematic production analysis result on the spot.
• Hygiene / Safety - Maintain worker hygiene and safety in the work area, understand personnel hygiene & safety in the work area (use PPE when to factory, change clothes when entering high care area.), and keep the work area clean.
• Quality Management - Implementing the system has been established by companies such as GMP, ISO 17025, ISO 9001 (quality management), FOQUS FSQ, and FSSC food safety) relevant to their work.
• Teamwork- Able to work with the team work so that all analysis should be done on his shift able to be resolved properly.
• Safety Health Management (OHSAS 18001, ISO 14001 & FOQUS SHE), Grow awareness of aspects of occupational safety such as LSR, use of PPE, hazard factors present in the workplace, correct and safe ways and attitudes, Implement the system of LSR, SHRA, ERA applicable in work area, and others referring to SHE training matrix, Reporting the incident "Near Miss" to the related party (superiors)

Job Requirements :

• Candidate must possess at least a Diploma, Bachelor's Degree in Biology, Food Science, Agriculture or equivalent.
• Min. 1 year of experience in quality control role of manufacturing business.
• Required language(s): English, Bahasa Indonesia.
• Willing to be based in Pasar Rebo, East Jakarta.
• Willing to undergo 12-months contract of employment.

URGENTLY NEEDED

Company Benefit:-

• BPJS Ketenagakerjaan  (Work Accident Insurance, Death Insurance, Old Age insurance, Pension Insurance)
• BPJS Kesehatan (Full cover health insurance for 1 family (Husband / Wife, 3 Children)
• Lunch Provided
• Medical Benefit

Working Location : Indonesia - Jawa Barat – Kabupaten Bekasi - Delta Silicon 3, Lippo Cikarang.

Job Description

·    Conduct routine and non-routine analysis of raw materials, packaging materials, intermediate product, bulk products, finished products, water monitoring, environment monitoring and stability studies samples. (Melakukan analisis rutin dan non-rutin bahan baku, bahan kemas, produk setengah jadi, produk curah, produk jadi, pemantauan air, pemantauan lingkungan dan sampel stabilitas)

·    Conduct testing on process validation sample according to test method. (Melakukan pengujian terhadap sampel validasi proses sesuai dengan prosedur analitik).

·    Maintain and use laboratory equipment and instrument according to the determined procedure, including identifies and troubleshoots equipment problems. (Memelihara dan menggunakan peralatan dan instrumen laboratorium sesuai dengan prosedur yang ditentukan, termasuk mengidentifikasi dan memecahkan masalah mengenai peralatan/instrumen)

·    Able to do mobile phase preparation and sample preparation, able to calculate the results of analysis in the HPLC system. (Mampu melakukan preparasi fase gerak dan preparasi sampel, mampu melakukan perhitungan hasil di sistem KCKT)

·    Able to read chromatogram data, understand the suitability of the HPLC system, troubleshooting when there are analysis problem and able to handling columns (Mampu membaca data kromatogram, memahami kesesuaian sistem pada KCKT, mampu memecahkan masalah ketika terdapat permasalahan analisa, dan mampu menangani kolom)

Requirements : (Persyaratan) :

· Candidate must possess at least Diploma in Chemical Analysis or other relevant certificate (Calon harus memiliki setidaknya pendidikan Diploma Analisis Kimia atau sertifikat dari jurusan yang berkaitan)

· At least have 1 Year (s) of working experience in the related fieldis required for this position (Preferably in the Pharmaceutical Industry) (Setidaknya mempunyai 1 Tahun pengalaman kerja di bidang terkait yang diperlukan untuk posisi ini (Lebih disukai dari Industri Farmasi))

· Has thinking logic & the ability to test in instrumental analytical chemical (Mempunyai logika berpikir dan kemampuan pengujian secara kimia analisis instrumental)

· Proactive, full of initiatives, high integrity, creative and attention to detail. (Proaktif, penuh inisiatif, integritas tinggi, kreatif, dan perhatian terhadap detail)

· Familiar, Able to operate and prepare sample by using analysis instruments especially HPLC (Terbiasa, Mampu mengoperasikan dan preparasi sampel menggunakan instrument analisa khususnya KCKT)

· Willing place in Cikarang, West Java (Bersedia ditempatkan di Cikarang, Jawa Barat)

Key Responsibility :

• Product Specification - Monitoring and controlling raw materials / semi finished / finished goods / water treatment according to Product Specification FFI, responsible for all analyzes done in micro laboratories.
• Shift Report - Makes a shifty report about the results of the analysis and deviation occurring in the micro laboratory and gives it to his superiors.
• Analyze - Analyze and control the result against raw material / semi finished / finished goods and able to perform quick method analysis using instrument.
• Documentation - Ensuring that all analysis results are written in the analysis book, all deviations are well communicated and ensuring all analysis results are inputted in the ORS on time.
• Communications - Communicate to relevant departments regarding problematic analysis results as soon as possible so that corrective action can be done and inform the boss if there is a problematic production analysis result on the spot.
• Hygiene / Safety - Maintain worker hygiene and safety in the work area, understand personnel hygiene & safety in the work area (use PPE when to factory, change clothes when entering high care area.), and keep the work area clean.
• Quality Management - Implementing the system has been established by companies such as GMP, ISO 17025, ISO 9001 (quality management), FOQUS FSQ, and FSSC food safety) relevant to their work.
• Teamwork- Able to work with the team work so that all analysis should be done on his shift able to be resolved properly.
• Safety Health Management (OHSAS 18001, ISO 14001 & FOQUS SHE), Grow awareness of aspects of occupational safety such as LSR, use of PPE, hazard factors present in the workplace, correct and safe ways and attitudes, Implement the system of LSR, SHRA, ERA applicable in work area, and others referring to SHE training matrix, Reporting the incident "Near Miss" to the related party (superiors)

Job Requirements :

• Candidate must possess at least a Diploma, Bachelor's Degree in Biology or equivalent.
• Required skill(s): Microbiology, Bio Chemistry, Biology.
• Required language(s): English, Bahasa Indonesia

Job Description:

• Conduct Sampling & Routine Testing: Perform sampling of materials (incoming, in-process & finished products); conduct various analytical tests and assays using established methods and instrumentation.
• Quality Inspection: Inspect and evaluate the physical and chemical attributes of quality control samples to determine compliance with established quality standards and specifications.
• Instrumentation and Equipment: Operate and maintain laboratory equipment, including HPLC and other analytical instruments, ensuring their calibration and optimal working conditions.
• Troubleshooting: Identify and resolve technical issues that may arise during testing, working collaboratively with the team to ensure accurate results.
• Data Analysis: Accurately record, analyze, and interpret test results, ensuring data integrity and consistency throughout the testing process.
• Method Validation: Participate in the validation of analytical methods to ensure the accuracy, precision, and reliability of testing procedures.
• Documentation: Maintain comprehensive and organized records of test methods, procedures, results, and any deviations observed during testing, in accordance with applicable procedures and guidelines. Endure timely testing and integrity of data and documentation for product release
• Compliance: Adhere to cGMP (current Good Manufacturing Practices) and applicable regulatory guidelines while conducting testing and maintaining laboratory practices, including maintaining inventory of QC retention & stability samples.
• Safety: Adhere to all safety protocols and guidelines while working with hazardous chemicals, reagents, and equipment.
• Continuous Improvement: Contribute to the enhancement of good laboratory processes, procedures, and practices to optimize efficiency and effectiveness.

Requirements & Qualifications:

• Degree / Diploma in Chemistry/Chemical Sciences, Food Technologies/ Food Science or related field.
• Minimum 3 years of working in a Food Quality Control Laboratory.
• Proficiency in analytical techniques such as physical and/or chemical techniques.
• Familiarity with food industry standards (e.g., CPOB, FSSC 22000, ISO 9001, Halal, Kosher, Physical & Chemical Inspection) and cGMP requirements.
• Strong attention to detail and accuracy in recording and interpreting data.
• Good communication skills and ability to collaborate with cross-functional teams.
• Problem-solving skills to troubleshoot issues during testing and analysis.
• Knowledge or experience in QC laboratory software and data analysis tools.
• Bilingual in Bahasa Indonesia and English.
• Computer literate.
• Willing to work in shifts.
• Willing to be placed in Romokalisari, Surabaya.

• Melakukan pengujian fisika-kimia terhadap sample bahan baku serta produk jadi dan pembuatan laporan produk
• Melakukan pengembangan metode analisa baru, validasi metode analisa dan pembuatan laporan
• 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

Qualifications:

1. Willing to be placed in Mojoagung, Jombang
2. Educated at least D3/S1 Chemical Analyst/Chemical Engineering.
3. Experienced in the chemical industry for at least 3 years
4. Understand ISO 9001, 45001, 14001, 5R
5. Fluent in English
6. Have good communication skills
7. Mastering chemical analysis techniques and instruments
8. Understanding the formulation and basic characteristics of agrochemical products
9. Have MS Office skills

Objective:

1. Ensuring that all products manufactured meet quality standards, from raw materials and production processes to finished goods, as well as conducting tests, analyzing and reporting test results to prevent defective products from reaching consumers

Job Description:

1. Conduct testing and analysis of raw material samples, semi-finished products, and finished products in accordance with Standard Operating Procedures
2. Conducting periodic inspections on the production line to ensure that processes are running according to quality standards
3. create and report all laboratory test results in logbook or information system
4. Managing equipment and performing laboratory equipment calibration
5. Comply with all K3 regulations and policies
6. Make improvement proposals