Quality Control Manager

17141 Bekasi, West Java IDR8 Annually WhatJobs

Posted 8 days ago

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Job Description

full-time
Our client, a rapidly growing manufacturing firm specializing in consumer goods, is seeking an experienced and meticulous Quality Control Manager to join their team in **Bekasi, West Java, ID**. This role is critical in ensuring that all products manufactured meet the highest standards of quality, safety, and customer satisfaction. You will be responsible for developing, implementing, and overseeing the company's quality control systems and procedures, leading a dedicated team of quality inspectors.

Key responsibilities include:
  • Developing and implementing comprehensive quality control plans and protocols for all stages of the manufacturing process.
  • Establishing quality standards and specifications in line with industry best practices and customer requirements.
  • Supervising and training a team of quality inspectors, assigning tasks, and monitoring performance.
  • Conducting regular inspections of raw materials, in-process products, and finished goods.
  • Analyzing quality data, identifying trends, and implementing root cause analysis for non-conformities.
  • Developing and implementing corrective and preventive actions (CAPA) to address quality issues.
  • Ensuring compliance with relevant quality certifications and regulatory standards (e.g., ISO 9001).
  • Collaborating with production, R&D, and engineering departments to resolve quality-related problems.
  • Managing the calibration and maintenance of quality control equipment.
  • Preparing detailed quality reports for senior management, highlighting key findings and areas for improvement.
  • Fostering a quality-focused culture throughout the manufacturing facility.
  • Driving continuous improvement initiatives to enhance product quality and reduce defects.

The ideal candidate will possess a Bachelor's degree in Engineering, Science, or a related technical field, with a strong understanding of quality management systems. Proven experience in a Quality Control or Quality Assurance role within a manufacturing environment is essential. Experience with quality tools such as Six Sigma or Lean Manufacturing principles is highly desirable. Excellent analytical, problem-solving, and leadership skills are required. Strong communication and interpersonal skills are necessary to effectively liaunt with various departments and manage a team. You must have a keen eye for detail and a commitment to upholding rigorous quality standards. This is a significant opportunity to impact product excellence at a leading manufacturing site in **Bekasi, West Java, ID**.
This advertiser has chosen not to accept applicants from your region.

operator quality control

Bekasi, West Java Mayora group

Posted 10 days ago

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Job Description

Lowongan Kerja Terbaru PT MAYORA INAH TBK

PT Mayora Indah Tbk adalah perusahaan swasta nasional yang bergerak dalam bidang produksi makanan dan minuman. Dengan fokus produksinya berupa biskuit atau roti, permen, wafer, cokelat, makanan kesehatan serta kopi.

Produk dan kualitas dari Mayora sudah tidak diragukan lagi, berbagai penghargaan dan sertifikat halal sudah diperoleh perusahaan.

Hal ini tentunya menjadi kepuasan tersendiri pada konsumen yang biasa mengkonsumsi produk perusahaan. Tidak hanya itu, perusahaan juga sangat memperhatikan keselamatan dan kesehatan lingkungan kerja.

Saat ini PT Mayora Indah Tbk (Mayora Group) sedang membuka lowongan kerja untuk mengisi beberapa posisi yang akan ditempatkan di pabriknya, berikut ini kualifikasi dan tatacara melamarnya.

Lowongan Kerja SMA/SMK PT Mayora Indah Tbk (Mayora Group)

1. Posisi : Oреrаtоr Prоdukѕі
Kuаlіfіkаѕі :

  • Pеndіdіkаn Mіnіmаl SMK atau SMA Semua Juruѕаn.
  • Memiliki Pengalaman di Arеа Operator Prоdukѕі minimal 1 tahun jadi nilai tambah
  • Mеmіlіkі Ketelitian, Disiplin dan Tanggung Jawab.
  • Tеrbіаѕа Bеkеrjа dengan Sіѕtеm Monoton (Tidak Mudаh Bosan).
  • Dараt Bеkеrjа Sесаrа Indіvіdu аtаuрun Berkelompok.
  • Bersedia Bеkеrjа dеngаn Sistem Shіft.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

2. Jabatan: Staf Administrasi
Kualifikasi:

  • Pendidikan Mіnіmаl SMA/SMK/D3/S1
  • Menguasai Mісrоѕоft Offісе, Menguasai Kеаrѕіраn, Mеnguаѕаі Alur dan Proses Surаt Mеnуurаt
  • Mengerti Sistem SAP
  • Tеlіtі, Cеkаtаn dаn bіѕа bеkеrjа ѕаmа ѕесаrа іndіvіdu maupun kelompok
  • Bersedia bekerja dengan sistem Shift
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

3. Posisi : Operator Packing
Kualifikasi :

  • Luluѕаn SMA/SMK Sederajat
  • Mеmіlіkі kеtеlіtіаn уаng baik, dіѕірlіn dаn bеrtаnggung jawab.
  • Dapat kerja dі bаwаh tekanan
  • Bersedia bekеrja sіѕtеm shift
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

4. Posisi : Operator QC (Quality Control)
Kualifikasi :

  • Pendidikan Minimal SMA/SMK/D3
  • Mеmіlіkі Pеngаlаmаn dі bіdаng уаng ѕаmа mіnіmаl 1 tahun.
  • Jujur, Fоkuѕ dаn bisa mеlаkukаn kеrjа sama dеngаn kеlоmроk.
  • Bersedia bekerja dengan sistem kerja Shift.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

5. Posisi : Staff Gudang (Warehouse)
Kuаlіfіkаѕі :

  • Lulusan SMA/SMK/D3/S1
  • Memiliki реngаlаmаn kеrjа mіnіmаl 1 tahun.
  • Mеngеrtі Inventory sederhana.
  • Lebih dіѕukаі apabila dараt mеnguаѕаі fоrklіft dаn memiliki SIO (аktіf)
  • Jujur, Rajin, Teliti, Bеrtаnggung jаwаb, dіѕірlіn, multіtаѕkіng, сераt bеlаjаr, mudаh dіаrаhkаn dаn memiliki іnіѕіаtіf.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

Informasi Pendaftaran :
Apabila kamu memenuhi kualifikasi diatas dan berminat bekerja di PT Mayora Indah Tbk, Silahkan kirim surat lamaran beserta CV dan foto terbaru kamu via web berikut :

Website Rekrutmen PT Mayora Indah Tbk  LAMAR DI SINI 


Jika kamu memenuhi kualifikasi, kamu akan dipanggil untuk mengikuti test seleksi.
Lowongan kerja terbuka untuk umum

Lowongan kerja ini tidak dipungut biaya. Lamaran yang tidak memenuhi kualifikasi diatas tidak akan diproses. Hanya kandidat terbaik yang akan dipanggil untuk mengikuti seleksi tahap selanjutnya.

Alamat PT Mayora Indah (Mayora Group)

Head Office Gedung Mayora Group Headquarter
Jl. Daan Mogot KM 18, Cengkareng, Jakarta

Tangerang Factory Jl. Daan Mogot Km 19,
Batuceper, Tangerang

Jl. Raya serang Km. 12,5 Desa Bitung Jaya,
Kecamatan Cikupa, Tangerang

Cibitung Factory Kawasan Industri MM2100
Jl. Jawa Blok H No. 10, Cibitung, Bekasi

Jl. Raya Tajur No.89, RT.01/RW.07, Kecamatan Pakuan. Bogor Sel., Kota Bogor

This advertiser has chosen not to accept applicants from your region.

Pharmaceutical Quality Control Analyst

17111 Bekasi, West Java IDR7 Monthly WhatJobs

Posted 2 days ago

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Job Description

full-time
Our client , a leading pharmaceutical company dedicated to producing high-quality medicines, is seeking a meticulous and driven Pharmaceutical Quality Control Analyst to join their fully remote team. This role is essential in ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements before they reach the market. The ideal candidate possesses a strong background in pharmaceutical sciences, analytical chemistry, and quality control methodologies, coupled with a keen eye for detail and a commitment to accuracy. This position is conceptually tied to operations in Bekasi, West Java, ID , but offers a fully remote work arrangement, providing excellent flexibility and the opportunity to contribute to critical quality assurance processes from anywhere.

As a remote Pharmaceutical Quality Control Analyst, your responsibilities will include performing laboratory tests on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy). You will be responsible for accurately documenting test results, preparing reports, and investigating any deviations or out-of-specification results. This role requires strict adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will collaborate with the quality assurance team to ensure compliance with all regulatory guidelines, including those set forth by national and international health authorities. We are looking for a highly organized, self-motivated individual with strong analytical and problem-solving skills. The ability to work independently and manage multiple tasks effectively in a remote setting is crucial. This is an exciting opportunity to contribute to the development and production of life-saving medications and uphold the highest standards of pharmaceutical quality. Your dedication to precision and quality will be vital to our company's mission.

Key Responsibilities:
  • Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
  • Utilize analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, and others.
  • Document all laboratory test results accurately and maintain detailed records.
  • Prepare Certificates of Analysis (CoA) for approved materials and products.
  • Investigate out-of-specification (OOS) results and deviations, identifying root causes.
  • Ensure all laboratory activities comply with GLP and GMP regulations.
  • Participate in the validation and calibration of analytical equipment.
  • Collaborate with Quality Assurance personnel to ensure product quality and regulatory compliance.
  • Stay updated on pharmacopeial standards (e.g., USP, EP) and regulatory guidelines.
  • Contribute to process improvements within the Quality Control laboratory.
  • Maintain a safe and organized laboratory environment, even in a remote setup.
  • Review and approve batch records from a quality control perspective.
Qualifications:
  • Bachelor's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related science field.
  • Minimum of 3 years of experience in pharmaceutical Quality Control (QC) or Quality Assurance (QA).
  • Hands-on experience with common analytical laboratory techniques and instrumentation (HPLC, GC, etc.).
  • Strong understanding of pharmaceutical manufacturing processes and regulatory requirements (GMP, GLP).
  • Excellent analytical, problem-solving, and documentation skills.
  • Proficiency in data analysis and interpretation.
  • Detail-oriented with strong organizational and time management abilities.
  • Ability to work independently and manage workload effectively in a remote environment.
  • Good communication skills in Bahasa Indonesia and English.
  • Familiarity with pharmacopeial standards and regulatory submissions.
This advertiser has chosen not to accept applicants from your region.

Automotive Quality Control Inspector

16525 Bekasi, West Java IDR7500000 Annually WhatJobs

Posted 8 days ago

Job Viewed

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Job Description

full-time
Our client, a prominent automotive manufacturing facility located in Bekasi, West Java, ID , is seeking a detail-oriented Automotive Quality Control Inspector. This role is crucial in ensuring that all manufactured vehicles and components meet the highest quality standards before they reach our customers. You will perform rigorous inspections, identify defects, and work closely with production teams to implement corrective actions. The ideal candidate possesses a strong understanding of automotive manufacturing processes and quality control methodologies. A keen eye for detail and a commitment to excellence are paramount for success in this position.

Key Responsibilities:
  • Conduct visual and instrumental inspections of finished vehicles and their components during various stages of production.
  • Identify and document any defects, deviations from specifications, or non-conformities.
  • Utilize various testing equipment and gauges to verify product quality and performance.
  • Compare finished products against quality standards, blueprints, and technical drawings.
  • Collaborate with production supervisors and line workers to address identified quality issues promptly.
  • Implement and monitor corrective action plans to prevent recurrence of defects.
  • Maintain accurate and organized records of inspection results and quality reports.
  • Participate in root cause analysis investigations for quality failures.
  • Ensure compliance with internal quality procedures and relevant industry standards.
  • Contribute to continuous improvement initiatives aimed at enhancing product quality and production efficiency.
  • Perform final inspection of vehicles prior to shipment.

This position requires a high school diploma or equivalent, preferably with a technical background in automotive technology or manufacturing. Previous experience in a quality control or inspection role within the automotive industry is highly preferred. Strong understanding of automotive systems and assembly processes is essential. The ability to interpret technical documents and use measurement tools effectively is required. Excellent observational skills and a methodical approach to problem-solving are key attributes for this role. Our client is committed to producing high-quality vehicles and offers a stable working environment with opportunities for advancement within the quality assurance department.
This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst (Pharmaceutical)

16111 Bekasi, West Java IDR8 Monthly WhatJobs

Posted 8 days ago

Job Viewed

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Job Description

full-time
Our client, a reputable pharmaceutical manufacturer, is seeking a meticulous Quality Control Analyst to join their dedicated team. This role is essential for ensuring the quality, safety, and efficacy of pharmaceutical products manufactured at their facility in **Bekasi, West Java, ID**. You will be responsible for performing a range of analytical tests on raw materials, in-process samples, and finished products according to established specifications and standard operating procedures (SOPs). Key responsibilities include operating and maintaining laboratory equipment, documenting test results accurately, and identifying any deviations from quality standards. The ideal candidate will have a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. Previous experience in pharmaceutical quality control or a GMP (Good Manufacturing Practice) environment is highly desirable. Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and wet chemistry methods is required. Excellent attention to detail, accuracy, and organizational skills are crucial for this position. You must be proficient in data recording and analysis, and able to work effectively both independently and as part of a team. Compliance with regulatory requirements and company policies is paramount. This is a vital role in safeguarding public health by ensuring that all products meet the highest quality standards.
This advertiser has chosen not to accept applicants from your region.

loker quality control makanan

Bekasi, West Java Mayora group

Posted 10 days ago

Job Viewed

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Job Description

Lowongan Kerja Terbaru PT MAYORA INAH TBK

PT Mayora Indah Tbk adalah perusahaan swasta nasional yang bergerak dalam bidang produksi makanan dan minuman. Dengan fokus produksinya berupa biskuit atau roti, permen, wafer, cokelat, makanan kesehatan serta kopi.

Produk dan kualitas dari Mayora sudah tidak diragukan lagi, berbagai penghargaan dan sertifikat halal sudah diperoleh perusahaan.

Hal ini tentunya menjadi kepuasan tersendiri pada konsumen yang biasa mengkonsumsi produk perusahaan. Tidak hanya itu, perusahaan juga sangat memperhatikan keselamatan dan kesehatan lingkungan kerja.

Saat ini PT Mayora Indah Tbk (Mayora Group) sedang membuka lowongan kerja untuk mengisi beberapa posisi yang akan ditempatkan di pabriknya, berikut ini kualifikasi dan tatacara melamarnya.

Lowongan Kerja SMA/SMK PT Mayora Indah Tbk (Mayora Group)

1. Posisi : Oреrаtоr Prоdukѕі
Kuаlіfіkаѕі :

  • Pеndіdіkаn Mіnіmаl SMK atau SMA Semua Juruѕаn.
  • Memiliki Pengalaman di Arеа Operator Prоdukѕі minimal 1 tahun jadi nilai tambah
  • Mеmіlіkі Ketelitian, Disiplin dan Tanggung Jawab.
  • Tеrbіаѕа Bеkеrjа dengan Sіѕtеm Monoton (Tidak Mudаh Bosan).
  • Dараt Bеkеrjа Sесаrа Indіvіdu аtаuрun Berkelompok.
  • Bersedia Bеkеrjа dеngаn Sistem Shіft.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

2. Jabatan: Staf Administrasi
Kualifikasi:

  • Pendidikan Mіnіmаl SMA/SMK/D3/S1
  • Menguasai Mісrоѕоft Offісе, Menguasai Kеаrѕіраn, Mеnguаѕаі Alur dan Proses Surаt Mеnуurаt
  • Mengerti Sistem SAP
  • Tеlіtі, Cеkаtаn dаn bіѕа bеkеrjа ѕаmа ѕесаrа іndіvіdu maupun kelompok
  • Bersedia bekerja dengan sistem Shift
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

3. Posisi : Operator Packing
Kualifikasi :

  • Luluѕаn SMA/SMK Sederajat
  • Mеmіlіkі kеtеlіtіаn уаng baik, dіѕірlіn dаn bеrtаnggung jawab.
  • Dapat kerja dі bаwаh tekanan
  • Bersedia bekеrja sіѕtеm shift
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

4. Posisi : Operator QC (Quality Control)
Kualifikasi :

  • Pendidikan Minimal SMA/SMK/D3
  • Mеmіlіkі Pеngаlаmаn dі bіdаng уаng ѕаmа mіnіmаl 1 tahun.
  • Jujur, Fоkuѕ dаn bisa mеlаkukаn kеrjа sama dеngаn kеlоmроk.
  • Bersedia bekerja dengan sistem kerja Shift.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

5. Posisi : Staff Gudang (Warehouse)
Kuаlіfіkаѕі :

  • Lulusan SMA/SMK/D3/S1
  • Memiliki реngаlаmаn kеrjа mіnіmаl 1 tahun.
  • Mеngеrtі Inventory sederhana.
  • Lebih dіѕukаі apabila dараt mеnguаѕаі fоrklіft dаn memiliki SIO (аktіf)
  • Jujur, Rajin, Teliti, Bеrtаnggung jаwаb, dіѕірlіn, multіtаѕkіng, сераt bеlаjаr, mudаh dіаrаhkаn dаn memiliki іnіѕіаtіf.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

Informasi Pendaftaran :
Apabila kamu memenuhi kualifikasi diatas dan berminat bekerja di PT Mayora Indah Tbk, Silahkan kirim surat lamaran beserta CV dan foto terbaru kamu via web berikut :

Website Rekrutmen PT Mayora Indah Tbk  LAMAR DI SINI 


Jika kamu memenuhi kualifikasi, kamu akan dipanggil untuk mengikuti test seleksi.
Lowongan kerja terbuka untuk umum

Lowongan kerja ini tidak dipungut biaya. Lamaran yang tidak memenuhi kualifikasi diatas tidak akan diproses. Hanya kandidat terbaik yang akan dipanggil untuk mengikuti seleksi tahap selanjutnya.

Alamat PT Mayora Indah (Mayora Group)

Head Office Gedung Mayora Group Headquarter
Jl. Daan Mogot KM 18, Cengkareng, Jakarta

Tangerang Factory Jl. Daan Mogot Km 19,
Batuceper, Tangerang

Jl. Raya serang Km. 12,5 Desa Bitung Jaya,
Kecamatan Cikupa, Tangerang

Cibitung Factory Kawasan Industri MM2100
Jl. Jawa Blok H No. 10, Cibitung, Bekasi

Jl. Raya Tajur No.89, RT.01/RW.07, Kecamatan Pakuan. Bogor Sel., Kota Bogor

This advertiser has chosen not to accept applicants from your region.

kerja staff quality control

Bekasi, West Java Mayora group

Posted 12 days ago

Job Viewed

Tap Again To Close

Job Description

Lowongan Kerja Terbaru PT MAYORA INAH TBK

PT Mayora Indah Tbk adalah perusahaan swasta nasional yang bergerak dalam bidang produksi makanan dan minuman. Dengan fokus produksinya berupa biskuit atau roti, permen, wafer, cokelat, makanan kesehatan serta kopi.

Produk dan kualitas dari Mayora sudah tidak diragukan lagi, berbagai penghargaan dan sertifikat halal sudah diperoleh perusahaan.

Hal ini tentunya menjadi kepuasan tersendiri pada konsumen yang biasa mengkonsumsi produk perusahaan. Tidak hanya itu, perusahaan juga sangat memperhatikan keselamatan dan kesehatan lingkungan kerja.

Saat ini PT Mayora Indah Tbk (Mayora Group) sedang membuka lowongan kerja untuk mengisi beberapa posisi yang akan ditempatkan di pabriknya, berikut ini kualifikasi dan tatacara melamarnya.

Lowongan Kerja SMA/SMK PT Mayora Indah Tbk (Mayora Group)

1. Posisi : Oреrаtоr Prоdukѕі
Kuаlіfіkаѕі :

  • Pеndіdіkаn Mіnіmаl SMK atau SMA Semua Juruѕаn.
  • Memiliki Pengalaman di Arеа Operator Prоdukѕі minimal 1 tahun jadi nilai tambah
  • Mеmіlіkі Ketelitian, Disiplin dan Tanggung Jawab.
  • Tеrbіаѕа Bеkеrjа dengan Sіѕtеm Monoton (Tidak Mudаh Bosan).
  • Dараt Bеkеrjа Sесаrа Indіvіdu аtаuрun Berkelompok.
  • Bersedia Bеkеrjа dеngаn Sistem Shіft.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

2. Jabatan: Staf Administrasi
Kualifikasi:

  • Pendidikan Mіnіmаl SMA/SMK/D3/S1
  • Menguasai Mісrоѕоft Offісе, Menguasai Kеаrѕіраn, Mеnguаѕаі Alur dan Proses Surаt Mеnуurаt
  • Mengerti Sistem SAP
  • Tеlіtі, Cеkаtаn dаn bіѕа bеkеrjа ѕаmа ѕесаrа іndіvіdu maupun kelompok
  • Bersedia bekerja dengan sistem Shift
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

3. Posisi : Operator Packing
Kualifikasi :

  • Luluѕаn SMA/SMK Sederajat
  • Mеmіlіkі kеtеlіtіаn уаng baik, dіѕірlіn dаn bеrtаnggung jawab.
  • Dapat kerja dі bаwаh tekanan
  • Bersedia bekеrja sіѕtеm shift
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

4. Posisi : Operator QC (Quality Control)
Kualifikasi :

  • Pendidikan Minimal SMA/SMK/D3
  • Mеmіlіkі Pеngаlаmаn dі bіdаng уаng ѕаmа mіnіmаl 1 tahun.
  • Jujur, Fоkuѕ dаn bisa mеlаkukаn kеrjа sama dеngаn kеlоmроk.
  • Bersedia bekerja dengan sistem kerja Shift.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

5. Posisi : Staff Gudang (Warehouse)
Kuаlіfіkаѕі :

  • Lulusan SMA/SMK/D3/S1
  • Memiliki реngаlаmаn kеrjа mіnіmаl 1 tahun.
  • Mеngеrtі Inventory sederhana.
  • Lebih dіѕukаі apabila dараt mеnguаѕаі fоrklіft dаn memiliki SIO (аktіf)
  • Jujur, Rajin, Teliti, Bеrtаnggung jаwаb, dіѕірlіn, multіtаѕkіng, сераt bеlаjаr, mudаh dіаrаhkаn dаn memiliki іnіѕіаtіf.
  • Bеrѕеdіа di tempatkan dі Plant Mayora Group Jakarta, Tangerang, Bekasi dan BogorLAMAR DI SINI

Informasi Pendaftaran :
Apabila kamu memenuhi kualifikasi diatas dan berminat bekerja di PT Mayora Indah Tbk, Silahkan kirim surat lamaran beserta CV dan foto terbaru kamu via web berikut :

Website Rekrutmen PT Mayora Indah Tbk  LAMAR DI SINI 


Jika kamu memenuhi kualifikasi, kamu akan dipanggil untuk mengikuti test seleksi.
Lowongan kerja terbuka untuk umum

Lowongan kerja ini tidak dipungut biaya. Lamaran yang tidak memenuhi kualifikasi diatas tidak akan diproses. Hanya kandidat terbaik yang akan dipanggil untuk mengikuti seleksi tahap selanjutnya.

Alamat PT Mayora Indah (Mayora Group)

Head Office Gedung Mayora Group Headquarter
Jl. Daan Mogot KM 18, Cengkareng, Jakarta

Tangerang Factory Jl. Daan Mogot Km 19,
Batuceper, Tangerang

Jl. Raya serang Km. 12,5 Desa Bitung Jaya,
Kecamatan Cikupa, Tangerang

Cibitung Factory Kawasan Industri MM2100
Jl. Jawa Blok H No. 10, Cibitung, Bekasi

Jl. Raya Tajur No.89, RT.01/RW.07, Kecamatan Pakuan. Bogor Sel., Kota Bogor

This advertiser has chosen not to accept applicants from your region.
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Senior Quality Control Engineer - Manufacturing

40542 Bekasi, West Java IDR18000000 Monthly WhatJobs

Posted 6 days ago

Job Viewed

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Job Description

full-time
Our client, a prominent player in the manufacturing sector, is seeking a highly skilled Senior Quality Control Engineer to join their production facility in Bekasi, West Java, ID . This role is critical in upholding the company's commitment to producing high-quality products that meet stringent industry standards and customer expectations. You will be responsible for developing, implementing, and managing comprehensive quality control systems and procedures throughout the manufacturing process. This includes raw material inspection, in-process quality checks, and final product verification. The ideal candidate will possess a strong analytical mindset, meticulous attention to detail, and extensive experience in quality assurance methodologies within a manufacturing environment. You will lead a team of quality technicians, providing guidance, training, and performance management to ensure adherence to quality protocols. Your responsibilities will involve analyzing production data to identify trends, root causes of defects, and areas for improvement. You will collaborate closely with production, engineering, and R&D teams to implement corrective and preventive actions (CAPA) and drive continuous improvement initiatives. This position requires a deep understanding of statistical process control (SPC), Six Sigma principles, and relevant quality management systems (e.g., ISO 9001). The successful candidate will be adept at conducting internal audits, managing customer quality concerns, and ensuring compliance with all relevant regulations. This is an excellent opportunity for a seasoned quality professional to make a significant impact on product excellence and operational efficiency.

Responsibilities:
  • Develop and implement robust quality control plans and procedures for manufacturing operations.
  • Oversee the inspection and testing of raw materials, in-process materials, and finished products.
  • Lead and mentor the quality control team, ensuring effective execution of quality checks.
  • Utilize statistical process control (SPC) techniques to monitor and improve production processes.
  • Conduct root cause analysis for product defects and implement effective corrective and preventive actions (CAPA).
  • Collaborate with production and engineering teams to resolve quality issues and enhance product quality.
  • Perform internal audits to ensure compliance with quality standards and regulatory requirements.
  • Manage customer complaints and quality-related inquiries, ensuring timely resolution.
  • Contribute to the continuous improvement of quality management systems (QMS).
  • Prepare detailed quality reports and present findings to management.
  • Ensure all quality control activities comply with industry standards (e.g., ISO 9001).
Qualifications:
  • Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or a closely related discipline.
  • Minimum of 6 years of experience in quality control and assurance within a manufacturing setting.
  • Proven experience with Six Sigma methodologies (Green Belt or Black Belt certification preferred).
  • Strong knowledge of statistical analysis tools and software.
  • Experience with various inspection and testing equipment.
  • Familiarity with ISO 9001 or other relevant quality management systems.
  • Excellent problem-solving, analytical, and decision-making skills.
  • Strong leadership and team management capabilities.
  • Effective communication and interpersonal skills for cross-functional collaboration.
  • Proficiency in technical documentation and reporting.
This advertiser has chosen not to accept applicants from your region.

Senior Pharmaceutical Quality Control Analyst

17111 Bekasi, West Java IDR12000000 Annually WhatJobs

Posted 8 days ago

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Job Description

full-time
Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their team in **Bekasi, West Java, ID**. This role is critical in ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong background in analytical chemistry, pharmaceutical regulations, and laboratory operations. You will be responsible for conducting various tests, interpreting results, and maintaining accurate records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). This hybrid role offers a blend of on-site laboratory work and flexibility for remote data analysis and reporting.

Key Responsibilities:
  • Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, spectroscopy, titration).
  • Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH).
  • Prepare reagents, solutions, and standards required for testing.
  • Analyze and interpret test results, documenting all findings accurately and thoroughly in laboratory notebooks and electronic systems.
  • Identify and investigate Out-of-Specification (OOS) results, determining root causes and recommending corrective and preventive actions (CAPAs).
  • Maintain laboratory equipment, ensuring proper calibration, qualification, and routine maintenance.
  • Ensure all laboratory activities comply with GMP, GLP, and other relevant regulatory requirements.
  • Write and review Standard Operating Procedures (SOPs), test methods, validation protocols, and reports.
  • Participate in internal and external audits, providing necessary documentation and explanations.
  • Collaborate with R&D, manufacturing, and regulatory affairs departments to resolve quality issues.
  • Train and mentor junior QC analysts, providing technical guidance and support.
  • Contribute to continuous improvement initiatives within the QC department.

Qualifications:
  • Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific discipline.
  • Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
  • Extensive hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer titrators.
  • Thorough understanding of pharmaceutical quality systems, GMP, and GLP guidelines.
  • Proficiency in method validation and transfer.
  • Strong data analysis and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Detail-oriented with a commitment to accuracy and quality.
  • Familiarity with electronic laboratory notebooks (ELNs) and LIMS is a plus.
This advertiser has chosen not to accept applicants from your region.

Senior Pharmaceutical Quality Control Analyst

40512 Bekasi, West Java IDR15000000 Annually WhatJobs

Posted 8 days ago

Job Viewed

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Job Description

full-time
Our client, a leading innovator in the pharmaceutical sector, is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their dynamic team in **Bekasi, West Java, ID**. This is a critical role responsible for ensuring the consistent quality and safety of our pharmaceutical products through rigorous testing and analysis. The successful candidate will play a pivotal role in maintaining compliance with stringent regulatory standards and contributing to the development of life-changing medicines.

Responsibilities:
  • Conduct comprehensive analytical testing of raw materials, in-process samples, and finished products using advanced laboratory techniques and instrumentation (e.g., HPLC, GC, UV-Vis spectroscopy, dissolution testing).
  • Develop, validate, and transfer analytical methods according to pharmacopeial standards and internal protocols.
  • Analyze and interpret test data, generate detailed reports, and identify any deviations from specifications.
  • Troubleshoot analytical equipment and resolve technical issues to ensure accurate and reliable results.
  • Maintain meticulous laboratory records and documentation in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Participate in internal and external audits, and support regulatory submissions.
  • Collaborate with R&D, Production, and Regulatory Affairs departments to address quality concerns and implement corrective actions.
  • Stay abreast of current industry trends, regulatory changes, and advancements in analytical technologies.
  • Mentor and train junior QC analysts, fostering a culture of continuous improvement and scientific excellence.
  • Ensure a safe and organized laboratory environment, adhering to all safety protocols.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific field.
  • Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
  • In-depth knowledge of analytical techniques, instrumentation, and pharmaceutical regulatory guidelines (e.g., BPOM, FDA, EMA).
  • Proficiency in data analysis software and laboratory information management systems (LIMS).
  • Strong problem-solving skills, attention to detail, and the ability to work independently and as part of a team.
  • Excellent written and verbal communication skills.
  • Experience with method validation and stability studies is highly desirable.
  • Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
This hybrid role offers a unique opportunity to contribute to a vital industry and grow your career within a supportive and forward-thinking organization located in **Bekasi, West Java, ID**. If you are a passionate scientist dedicated to quality and driven by innovation, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
 

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