2,573 Quality Control Analyst jobs in Indonesia

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

About the role:

In your daily routine, you'll conduct physical and chemical analysis of pharmaceutical products and samples, ensuring data integrity and quality documentation.

• Analyze in-process, bulk, finished products, and trial/stability samples in accordance with GMP, GLP, and internal procedures.
• Record and validate data in LIMS; ensure accurate logbook entries, calculations, and documentation.
• Prepare reagents/media/mobile phases and maintain documentation according to SOPs.
• Operate analytical equipment such as HPLC, UV-Vis, IR, AAS, GC-MS, KF, and Dissolution Tester.
• Promptly report any discrepancies or non-conformities and fill out OOS forms.
• Maintain lab order, cleanliness, and equipment verification (balances, pH meters, etc.).

Who you are

• A candidate with prior lab/QC experience in a pharmaceutical or related industry.
• Proficient in GMP/GLP practices and capable of operating analytical instruments.
• Detail-oriented, disciplined, and proactive in reporting and documentation.
• Able to work independently and on shifts.
• Can join immediately, and a 6-month contract may be extended based on performance.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

Job Description:

• Melakukan inspeksi kualitas produk (bulk & finished goods) sesuai standar.
• Monitoring sampel retain, suhu & kelembapan area penyimpanan.
• Menangani non-conformity (sampling AQL & panel test).
• Membuat laporan hasil inspeksi secara akurat & tepat waktu.
• Menginput material usage di sistem WMS.
• Memberikan keputusan release/reject produk.

Qualifications:

• Minimal pendidikan SMA/SMK jurusan IPA/Farmasi/Kimia.
• Pengalaman QC di kosmetik/farmasi menjadi nilai tambah.
• Teliti, detail-oriented, tidak buta warna.
• Mampu mengoperasikan Microsoft Office (Excel).
• Komunikatif, tegas, dan mampu bekerja dalam tim.

"As part of the Quality Control team, you will perform analysis for samples in QC Laboratory, manage standard using the Sample Management system, also support instruments calibration and performance check regularly, perform Good Laboratory Practice and part of continuous improvement"

Qualification :

• Minimum Diploma in Food Technologies/Chemistry/Chemical Engineering.
• Minimum 1 year experience as Quality Control Analyst .
• Experience in Food, Dairy, and Pharmacy Industry would be an advantage.
• Good knowledge in ISO 17025, ISO 17025 training certificate is preferable.
• Experience handling Laboratory.
• Good competence in English written and speaking.
• Good Analytical and problem solving skills, communication and teamwork
• Has good personality, high curiousity and initiative

Responsibilities

• Provide coaching and monitor departments such as Collection, Customer Service (CS), Telemarketing, and Credit Assessment (CA).
• Conduct training sessions and act as a trainer.
• Prepare training materials based on departmental needs.
• Develop agents by observing and analyzing training outcomes.
• Ensure a positive impact and morale after coaching and training sessions.
• Perform other tasks as assigned.
• Monitor and ensure all operational department activities align with company rules.
• Author and manage documentation related to quality control processes.
• Investigate complaints and ensure timely resolution.
• Generate routine quality control reports and handle administrative tasks.
• Inspect products or systems to ensure they meet set specifications and Standard Operating Procedures (SOPs).
• Collaborate cross-functionally with teams including Operations, Marketing, and Finance to accomplish goals.

Qualifications

• Minimum Diploma degree in any field.
• Conversational English proficiency is required.
• At least 1 year of experience as a QC & Trainer in Collection, CS, or Telemarketing.
• Independent, proactive, and positive attitude.
• Strong communication and negotiation skills.
• Ability to work individually and as part of a team.
• Strong attention to detail with the ability to quickly adapt to new changes.
• Ability to handle confidential information with discretion.
• Proficient time management skills and ability to multi-task.

Quality Control Analyst - Bali based

About us

With over 200 brands sold in nearly 180 countries, we're the world's leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you'll test new ideas, learn and grow, and unlock a brighter, more exciting future.

Join us to create a career worth celebrating.

Key Tasks / Accountabilities:

• As part of leadership team in LKJ plant organization to carry out strategic objectives in governance, Aware for environment-health-safety (EHS), quality, cost, responsiveness and people development to achieve plant vision and support DIAGEO business in market
• Control and validate the quality of product specific in raw material, blending of bulk liquid, until validate the liquid in finished product during bottling process
• Control and validate sanitation process
• Control and maintain the lab equipment for physio-chemical and microbiology analysis
• Prepare analysis form, standard operating procedure (SOP), and work instruction (WIT) related to validation of quality process
• Conduct stabilization tests and analysis based on microbiological parameters for raw materials, sample / product produced, RO water, and rinse the results of CIP process (Mo)
• Ensuring products are produced according to the standards
• Ensuring the cleanliness of the work area
• Familiar with process production, 5S standard, Food Safety Standard Requirement, Personal Hygiene and GMP (ISO TS and HACCP, VACCP, TACCP (ISO
• Support raw data for Key Performance Indicator (KPI) Quality Department
• Active on tier 1 meeting and coordinate with production team for issue during process
• Record the data analysis in form and documented/input data in the SAP system
• Conduct maintenance and calibration of laboratory instrument
• Responsible to new instrument installation and documented all the information related the instrument (manual book, SOP, WIT)
• Inventory stocks of chemical, spare part, and microbiology equipment
• Prepared and standardize the chemical solution to support the process of analysis
• Refreshment sensory performed within a period of periodically of the panellist
• Monitoring wastewater treatment plant performance by conduct wastewater analysis and report the result to related team member
• Support for qualification process raw and packaging material

What will you bring to the table?

ESSENTIAL:

• Strong leadership capabilities as per DIAGEO Leadership standard
• Minimal D3 Chemical Analyst/ Bachelor of Food Technology, Biology, Microbiology, or Chemistry

PREFERABLE:

• Minimum 1 year in the food & beverages industry or a recent bachelor's degree graduate
• Understanding of alcoholic beverage production processes
• Familiarity with chemical handling and laboratory analysis procedures
• Knowledge of production processes, 5S standards, GMP/PRP, and HACCP
• Ability to operate laboratory instruments
• Understanding of sampling plans (AQL)
• Computer literacy
• Experience operating SAP
• Capability to lead or work effectively in cross-functional teams
• Ability to work within diverse cultures, religions, and languages

Working with us

Flexibility is key to success. From part-time and compressed hours to different locations our people work flexibly in ways to suit them. Talk to us about what flexibility means to you, and

we'll work together so that you're supported from day one.

We recognise and value performance, offering our people a highly competitive Rewards and Benefits package.

Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.

We embrace diversity in the broadest possible sense. This means that you'll be welcomed and celebrated for who you are just by being you. You'll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.

Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.

Feel inspired? Then this may be the opportunity for you.

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

About The Role
In your daily routine, you'll conduct physical and chemical analysis of pharmaceutical products and samples, ensuring data integrity and quality documentation.

• Analyze in-process, bulk, finished products, and trial/stability samples in accordance with GMP, GLP, and internal procedures.
• Record and validate data in LIMS; ensure accurate logbook entries, calculations, and documentation.
• Prepare reagents/media/mobile phases and maintain documentation according to SOPs.
• Operate analytical equipment such as HPLC, UV-Vis, IR, AAS, GC-MS, KF, and Dissolution Tester.
• Promptly report any discrepancies or non-conformities and fill out OOS forms.
• Maintain lab order, cleanliness, and equipment verification (balances, pH meters, etc.).

Who You Are

• A candidate with prior lab/QC experience in a pharmaceutical or related industry.
• Proficient in GMP/GLP practices and capable of operating analytical instruments.
• Detail-oriented, disciplined, and proactive in reporting and documentation.
• Able to work independently and on shifts.
• Can join immediately, and a 6-month contract may be extended based on performance.

What we offer:
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

Tanggung jawab utama:

Melakukan pemeriksaan semua produk jadi seperti filling kemas primer (sediaan semi solid, liquid), siap kemas primer (sediaan solid) (obat, suplemen, kosmetik, pangan, obat tradisional) dengan tepat, teliti, akurat, sesuai dengan prosedur yang berlaku dan batas waktu yang telah ditetapkan.

Kualifikasi:

1. SMK Analis Kimia/ D3 Analis Kimia/ S1 Farmasi atau Kimia
2. Lebih diutamakan mempunyai pengalaman minimal 1 tahun sebagai Analis di Industri Farmasi, Obat Tradisional, Bahan Kimia atau sejenisnya
3. Terbiasa menggunakan Instrumen seperti HPLC dll
4. Mempunyai pengetahuan terkait GLP, CPOB, CPOTB, CPKB, CPPOB, SJH.
5. Dapat mengoperasikan komputer

Lokasi kerja: Kawasan Pulogadung, Jakarta Timur

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products using methods such as HPLC, GC, UV-Vis, IR, and titration.
• Analyze test results, interpret data, and prepare detailed analytical reports.
• Calibrate and maintain laboratory equipment to ensure accuracy and reliability.
• Ensure all laboratory activities comply with GMP, GLP, and other relevant regulatory standards.
• Document all testing procedures, results, and deviations meticulously in compliance with SOPs.
• Investigate out-of-specification (OOS) results and participate in deviation investigations.
• Assist in the validation of analytical methods and equipment.
• Maintain a clean and organized laboratory environment.
• Contribute to the continuous improvement of quality control processes.
• Participate in internal and external audits as required.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related science field.
• Minimum of 3 years of experience in pharmaceutical quality control or analytical laboratory testing.
• Proficiency with analytical instrumentation commonly used in the pharmaceutical industry (HPLC, GC, etc.).
• Strong understanding of GMP, pharmaceutical regulations, and quality control principles.
• Excellent attention to detail, accuracy, and documentation skills.
• Ability to work independently and as part of a collaborative team.
• Strong problem-solving and analytical thinking abilities.
• Proficiency in Bahasa Indonesia and English is required.