Total 6,171 quality control manager job vacancies in Quality Assurance / Control category in The United States of America

The incumbent must ensure the quality, safety, and compliance of products throughout the processing and production stages. Besides, the incumbent needs to pay attention to detail when inspecting products, conducting tests, and recording data accurately.

Job Responsibilities:

·         To inspect bird condition before and after process (ante mortem & postmortem)

·         Check and record stunner, bleeding time, scalder temperature for every process.

·         To ensure all processes follow the standard operation procedure.

·         Check, record and maintain spinechiller and chicken temperature during process.

·         Check and record the lorry’s temperature and condition before the loading process.

·         To ensure all product in good quality before delivering to customers.

·         Receive and check any incoming material.

·         To participate and assist during audit from authorities or customer.

·         To report any finding of non-compliance to management team.

·         Perform any other duties assigned by superior/management from time to time.

Job Requirements:

·         A Bachelor's Degree in a relevant field such as Food Science, or a related discipline is preferred.

·         Familiarity with ISO standards, GMP, HACCP and HALAL are added advantages.

·         Effective communication skills are essential to collaborate with other departments, report findings, and explain quality issues and solutions.

Perks & Benefits

• Medical insurance
• Open culture

Responsibilities:

• Determine quality improvement parameters.
• Identify statistical methods relevant to manufacturing processes.
• Identify sample size and acceptable error.
• Establish statistical reliability and perform reliability demonstration tests.
• Analyze data by completing hypothesis, normal distribution, and process capability analysis tests.
• Prepare reports by collecting, analyzing, and make recommendations.

Requirements:

• Excellent numerical skills and understanding of data analysis/statistical methods.
• Good knowledge of MS Office and databases.
• Exceptional communication skills.
• Good attention to detail and a results driven approach.
• Reliable and Trustworthy.
• Possess at least a Bachelor's Degree in Business Administration or relevant field.
• Certification of quality control is a strong advantage (ISO 9000 etc.).

Perks & Benefits

• Commission and bonus
• Allowance (travel stipends, transportation, etc.)
• Work visa sponsorship
• Personal development opportunities
• Annual Leave up to 21 day per year

Responsibility:

1)      Project Development

• Development of equipment, jig and tool drawings.
• Testing to check the suitability of the products together with Production Engineer.
• Preparation of customer’s documentation.
• Etc.

2)      Production Process

• Setup new production method and process.
• Monitor and improve the current production method and process.
• Monitor in-process product in production area to ensure quality products are delivered to the customers.
• Record and analyze the production rejection rate on all items.
• Etc.

3)      Quality Issue and Improvement

• To investigate customer complaints and non-conformance issues arise (internal
• To develop, recommend and monitor corrective and preventive actions
• Preparation of document which is required by customer.
• Preparation of quality control plan, PFMEA and etc.
• Keep records of quality reports, statistical reviews and relevant documentation.
• Promote quality awareness and commitment to quality across the company and ensure all employees follow the quality requirements.
• Etc.

4)      Incoming & Outgoing Quality Documents

• Managing the incoming quality documents, ie COA, COC, Incoming Raw Material & Goods Check Sheet, etc.
• Preparation of Outgoing Quality Check Sheet.
• Etc.

5)      Calibration of Equipment, Jigs & Tools

• Monitor the schedule of calibration.
• Ensure the relevant parties are using the calibrated equipment, jig & tool and keep it properly.
• Etc.

6)      ISO Documentation and Audit Process

• Review and update relevant quality system procedures and work instructions.
• To coordinate and support on-site internal and external audits.
• To evaluate audit findings and implement appropriate corrective actions.

7)      Chemical Substances Management

• Consolidate the relevant information and documents, ie. ROHS report, ICP report, SOC report of the materials.
• Submission of relevant report to the customer.
• In charge of chemical handling & abnormalities.
• Ensure chemical management awareness on the shop floor.

8)      Any other tasks assigned by the Management from time to time.

Authority:

1. Release of new inspection jig.
2. Release of the calibrated measuring equipment.
3. Release of finished goods.
4. Suspend and stop the production process due to nonconformity and abnormality found.
5. Decide the action on the rejected parts that have a rejection rate is less than 3%.
6. Acknowledgement of Incoming Raw Material & Goods Check Sheet.

Perks & Benefits

• Commission and bonus
• Allowance (travel stipends, transportation, etc.)
• Casual dress code
• Medical insurance
• Personal leave

Responsibilities:

• Plan procedures to inspect and report quality issues.
• Oversee all operations that affect quality.
• Monitor and guide inspectors, technicians and other staff.
• Reaffirm the reliability and consistency of production by checking processes and final output.
• Appraise customers' requirements and make sure they are satisfied.
• Report all malfunctions to production executives to ensure immediate action.
• Facilitate proactive solutions by collecting and analyzing quality data.
• Review current standards and policies.
• Document records of quality reports, statistical reviews and relevant documentation.
• Ensure all legal standards are met.
• Interact with external quality assurance officers during on-site inspections.

Requirements:

• Proven experience as a quality assurance manager or relevant role.
• Exceptional knowledge of methodologies of quality assurance and standards.
• Outstanding numerical skills and understanding of data analysis/statistical methods.
• Good knowledge of MS Office and databases.
• Excellent communication skills.
• Good attention to detail and a results driven approach.
• Exemplary organizational and leadership abilities.
• Reliable and Trustworthy.
• Possess at least Bachelor's Degree in Business Administration or relevant field.
• Certification of quality control is a strong advantage (ISO 9000 etc.).

Perks & Benefits

• Allowance (travel stipends, transportation, etc.)
• Flexible working hours
• Casual dress code
• Medical insurance
• Personal leave

JOB SCOPE :

-        Monitoring operations to ensure that they meet production standards.

-        Recommending adjustments to the assembly or production process. Inspecting, testing, or measuring materials or products being produced. 

-        Responsible for QC department document filling system.

-        To compile of daily QC record and compute into QC daily report.

-        To undertake any other related job such as typing, report, Preparation, etc

REQUIREMENT :

-        Must possess minimum Secondary School / SPM / “O” level / Diploma or equivalent.

-        At least 1 year experience required.

-        PC literate and proficient in Microsoft Office with good typing skills.

-        Knowledge of the requirement of ISO 9001:2015 is essential. 

-        Responsible for completing finished product quality checks for assembly lines, tracking of non-conforming materials and products and documentation of daily paperwork

-        Responsible for reviewing products and materials during Operation to make sure they meet client requirements.

-        Perform sampling quality inspection on the prepared stock based on the client specification / requirement before release for storage / delivery.

-        Reject all products and materials that fail to meet quality expectations.

-        Read Work Instruction and product specifications to understand the requirements of the products and services.

-        Recommend improvements to the production process to ensure quality control.

-        Document inspection outcomes by completing detailed reports and performance records.

-        Teach or guide the production team about quality control concerns to improve product excellence.

-        Resolve quality-related issues in a timely manner.

-        Assist in internal audits and external audits (SGS audit, client / customer audit, regulatory audit)

-        Other tasks as and when required by the HOD

-        Perform regular quality assessments on all incoming materials from vendors

5 working days (Regular Hour)

Dental Subsidy

The incumbent must ensure the quality, safety, and compliance of products throughout the processing and production stages. Besides, the incumbent needs to pay attention to detail when inspecting products, conducting tests, and recording data accurately.

Job Responsibilities:

·         To inspect bird condition before and after process (ante mortem & postmortem)

·         Check and record stunner, bleeding time, scalder temperature for every process.

·         To ensure all processes follow the standard operation procedure.

·         Check, record and maintain spinechiller and chicken temperature during process.

·         Check and record the lorry’s temperature and condition before the loading process.

·         To ensure all product in good quality before delivering to customers.

·         Receive and check any incoming material.

·         To participate and assist during audit from authorities or customer.

·         To report any finding of non-compliance to management team.

·         Perform any other duties assigned by superior/management from time to time.

Job Requirements:

·         A Bachelor's Degree in a relevant field such as Food Science, or a related discipline is preferred.

·         Familiarity with ISO standards, GMP, HACCP and HALAL are added advantages.

·         Effective communication skills are essential to collaborate with other departments, report findings, and explain quality issues and solutions.

Perks & Benefits

• Medical insurance
• Open culture

職責：

• 規劃檢查和報告品質問題的程序。
• 監督所有影響品質的操作。
• 監督和指導檢查員、技術人員和其他工作人員。
• 透過檢查流程和最終輸出來重申生產的可靠性和一致性。
• 評估客戶的要求並確保他們滿意。
• 向生產主管報告所有故障，以確保立即採取行動。
• 透過收集和分析品質數據來促進主動解決方案。
• 審查現行標準和政策。
• 品質報告、統計審查和相關文件的記錄記錄。
• 確保符合所有法律標準。
• 在現場檢查期間與外部品質保證官員互動。

要求：

• 具備擔任品質保證經理或相關角色的豐富經驗。
• 對品質保證和標準的方法有豐富的了解。
• 出色的數字技能和對數據分析/統計方法的理解。
• 熟悉 MS Office 和資料庫。
• 高超的溝通技巧。
• 注重細節和以結果為導向的方法。
• 模範的組織和領導能力。
• 可靠且值得信賴。
• 至少擁有工商管理或相關領域的學士學位。
• 品質控制認證是一個強大的優勢（ISO 9000 等）。

津貼和福利

• 津貼（旅費、交通費等）
• 彈性的工作時間
• 休閒著裝要求
• 醫療保險
• 事假

Job Responsibilities:

1. New product registration:

• Prepare and compile registration dossiers in accordance with relevant regulatory requirements including: 
  

  • Constructing/ editing letters of response/ justification/ declaration and clinical documentation for submission packages in accordance with guidelines checklists.

  • Compile/ review/check material for dossier prior to submission, incorporate feedback from relevant stakeholders.

  • Conduct checks on artworks to ensure in compliance with local regulation.

• Submit product registration applications to local health authorities  according to target submission timelines.
• Liase with and respond to additional requests or queries from health authorities and follow up (when necessary) until approval per target timelines.
• Liase with enternal and external stakeholders/ departments to build rapport and to achieve target outcomes.

2. Comply with regulatory requirements: to maintain validity of existing licenses/ certification/ authorization (e.g, product licenses, manufacturing licenses, establishment license, GDPMD licenses, import/ export license) through timely variations and/ or renewals to ensure supply continuity.

3. Keep abreast of regulatory updates from health authorities in the drugs, cosmetics, and medical device space.

• Assess regulatory updates on impact to business and communicate insights on approach to handle affairs.
• Propose solutions to arising issues.

4. Update and maintain database of regulatory and product registration information.

5. Good maintenance of final submitted documentation and local repository.

6. Ensure compliance with quality procedures stipulated for regulatory affairs, its administartive maintenance, and plan/ suggest improvements to operations.

7. Support any audits or inspections.

8. Guide/ oversee work performance and development of direct report.

9. Provide input for periodic operation metrics/ budget initiatives by managing  operating expenses within approved budget for the year.

10. Handle any other assingment as advised by supervisor.

Requirements: 

• Possess a Bachelor Science
• Work experience in regulatory affairs.
• Familiar with drugs/ cosmetics/ medical device regulatory landscape and GxP related matters.
• Proficiency in Microsoft Office Applications and relevant regulatory system software.
• Adopt good practices in documentation and communication.

Perks & Benefits

• Allowance ( mileage,transportation)
• Medical insurance

工作範圍 ：

- 監控操作以確保其符合生產標準。

- 建議調整組裝或生產流程。檢查、測試或測量正在生產的材料或產品。

- 負責QC部門文件填寫系統。

- 編制每日QC記錄並計算成QC日報。

- 承擔任何其他相關工作，如打字、報告、準備等

要求 ：

- 必須至少擁有中學/SPM/“O”水準/文憑或同等學歷。

- 需至少 1 年經驗。

- 懂電腦，精通 Microsoft Office，並具備良好的打字能力。

- 了解 ISO 9001:2015 的要求至關重要。

- 負責完成裝配線的成品品質檢查、不合格材料和產品的追蹤以及日常文書工作的記錄

- 負責在營運期間審查產品和材料，以確保其滿足客戶要求。

- 在放行儲存/交貨之前，根據客戶的規格/要求對準備好的庫存進行抽樣品質檢驗。

- 拒絕所有不符合品質期望的產品和材料。

- 閱讀工作指導和產品規格，以了解產品和服務的要求。

- 建議改善生產流程以確保品質控制。

- 透過完成詳細的報告和績效記錄來記錄檢查結果。

- 教導或指導生產團隊有關品質控制問題，以提高產品卓越性。

- 及時解決品質相關問題。

- 協助內部審核和外部審核（SGS審核、客戶/客戶審核、監管審核）

- HOD要求時的其他任務

- 對供應商的所有進料進行定期品質評估

5個工作天（正常時間）

牙科補貼

職責：

• 確定品質改進參數。
• 確定與製造過程相關的統計方法。
• 確定樣本大小和可接受的誤差。
• 建立統計可靠性並進行可靠性論證測試。
• 透過完成假設、常態分佈和製程能力分析檢定來分析資料。
• 透過收集、分析和提出建議來準備報告。

要求：

• 出色的數字技能和對數據分析/統計方法的理解。
• 熟悉 MS Office 和資料庫。
• 優秀的溝通技巧。
• 注重細節和以結果為導向的方法。
• 可靠且值得信賴。
• 至少擁有工商管理或相關領域的學士學位。
• 品質控制認證是一個強大的優勢（ISO 9000 等）。

津貼和福利

• 佣金和獎金
• 津貼（旅費、交通費等）
• 工作簽證贊助
• 個人發展機會
• 年假最多 21 天

工作職責：

1、新產品註冊：

• 根據相關監管要求準備和編制註冊檔案，包括：
  

  • 根據指南清單建立/編輯提交包的回應/理由/聲明和臨床文件。

  • 在提交之前編譯/審查/檢查檔案資料，納入相關利害關係人的回饋。

  • 對藝術品進行檢查，以確保符合當地法規。

• 根據目標提交時間表向當地衛生部門提交產品註冊申請。
• 與衛生當局聯絡並回應其他請求或詢問，並跟進（必要時）直至按照目標時間表獲得批准。
• 與內部和外部利害關係人/部門聯絡，建立融洽關係並實現目標成果。

2. 遵守監管要求：透過及時變更和/或更新來維持現有許可證/認證/授權（例如產品許可證、製造許可證、企業許可證、GDPMD許可證、進出口許可證）的有效性，以確保供應連續性。

3. 隨時了解衛生當局在藥品、化妝品和醫療器材領域的最新監管動態。

• 評估監管更新對業務的影響，並就處理事務的方法傳達見解。
• 針對出現的問題提出解決方案。

4.更新和維護監管和產品註冊資訊資料庫。

5. 妥善維護最終提交的文件和本機儲存庫。

6. 確保遵守監管事務、行政維護規定的品質程序，並規劃/建議營運改善。

7. 支持任何審計或檢查。

8. 指導/監督工作績效和直接報告的發展。

9. 透過在年度核准的預算內管理營運費用，為定期營運指標/預算計畫提供輸入。

10. 處理主管建議的任何其他分配。

要求：

• 擁有科學學士學位
• 監管事務方面的工作經驗。
• 熟悉藥品/化妝品/醫療器材監管環境和 GxP 相關事宜。
• 熟練Microsoft Office應用程式和相關監管系統軟體。
• 在文件和溝通方面採用良好的做法。

津貼和福利

• 津貼（里程、交通）
• 醫療保險

Unique Fire Holdings Berhad focuses on the assembly, manufacture and distribution of active fire protection systems, equipment, and accessories. Our comprehensive range of products continue to reliably serve customers in Malaysia and abroad. Our export markets include ASEAN countries and the Middle East.

After our public-listing exercise, we are currently undergoing major expansion and we invite all enthusiasts and energetic individuals to join our growing team.

Job Description:

• Oversee the quality control activities including inspection/testing records on incoming goods (IQC), process inspection (PQC), final inspection (FQC), and product performance test.
• Raise defective product complaint reports to suppliers, especially on receiving product defects, in- process inspection, and product improvement.
• Conduct inspection on nonconformance products “Discrepant Material Report” (DMR) and register into the Epicor system on manufacturing products.
• Investigate defective products in production and customer complaints (RMA) and follow up with corrective actions taken to ensure effectiveness.
• Identify the cause of product failure and recommend a “Corrective Action Request” (CAR).
• Monitor and verify data collection on the “Overall Equipment Effectiveness” system (OEE) in Manufacturing/Production.
• Monitoring validation/calibration equipment (internal and external calibration provider).
• Assist internal and external audits such as SIRIM, ISO Management System, etc.
• Ensure all controlled documents and quality records are maintained according to procedures.
• Perform report, product inspection/testing samples from the vendor/research & development purpose
   

Job Requirements:

• At least 2 years of working experience in safety preferably from the manufacturing industry
• Sound knowledge of Occupational Safety and Health Regulations (OSH)
• Proactive and resourceful
• Able to communicate effectively in English and Bahasa Malaysia

The perks:

• Career & development opportunities - networking events, conferences, training, and certification sponsored by the company.
• Overtime and travel allowance.
• Company engagement activities (annual dinner, team building, festive celebration etc)
• Medical, optical and dental benefits (in-panel clinic)
• Rewards and recognitions

Benefit:

• 5 Working Days
• Birthday Leave
• OT & Attendance Allowance 

企業必須確保產品在整個加工和生產階段的品質、安全和合規性。此外，任職者在檢查產品、進行測試、準確記錄數據時需要注意細節。

工作職責：

· 檢查加工前後的家禽狀況（宰前和宰後）

· 檢查並記錄每道工序的致暈劑、泌水時間、燙燙溫度。

· 確保所有流程均遵循標準作業程序。

· 加工過程中檢查、記錄並保持脊椎冷卻器和雞的溫度。

· 裝貨前檢查並記錄卡車的溫度和狀況。

· 確保所有產品在交付給客戶之前保持良好的品質。

· 接收並檢查任何傳入的材料。

· 參與並協助當局或客戶的審核。

· 向管理團隊報告任何不合規情況。

· 履行上級/管理階層不時指派的任何其他職責。

工作要求：

· 擁有食品科學等相關領域或相關學科的學士學位者優先。

· 熟悉 ISO 標準、GMP、HACCP 和 HALAL 是額外優勢。

· 有效的溝通技巧對於與其他部門合作、報告調查結果以及解釋品質問題和解決方案至關重要。

津貼和福利

• 醫療保險
• 開放文化

✔ Quality Engineer (Assembly Test)

✔ Gelang Patah, Johor Bahru

✔ Optical product manufacturer

✔ Monday - Friday

✔ 8.00am - 5.30pm

✔ Min Degree in Optics, Materials Science, Mechanical Engineering or any related field

✔ Min 5 years of working experience in manufacturing environment and handling QA systems, processes and audit

✔ Basic salary can be up to RM7000

Job Responsibilities :

• Conduct thorough inspections of optical components, lenses, metal barrels, and related materials
• Utilize specialized testing equipment to verify optical characteristics
• Monitor the assembly process to identify any deviations from established procedures or specifications, ensuring correct alignment and mounting
• Conduct interferometric tests to assess the surface quality and shape of optical components
• Perform final inspections on completed optical systems with metal barrels to ensure they meet all specified quality requirements

Requirements :

• Min Degree in Optics, Materials Science, Mechanical Engineering or any related field
• Min 5 years of working experience in manufacturing environment and handling QA systems, processes and audit
• Have experience in QA within optical lens assembly with metal components
• Knowledgeable in optics principles, lens manufacturing processes, and optical testing techniques
• Proficient in handling precision measurement tools, and metal testing equipment
• Proficient in using quality management software and tools
• Willing to travel for the audit suppliers
• Relevant certifications in optics, metallurgy, or quality assurance (ASQ Certified Quality Engineer, Optical Society of America certifications) is an added advantage

Benefits :

• Quarterly bonus
• Flexi bonus
• AWS
• Salary increment

✔ 品質工程師（組裝測試）

✔ 振林山, 新山

✔ 光學產品製造商

✔ 週一至週五

✔ 上午 8.00 至下午 5.30

✔ 光學、材料科學、機械工程或任何相關領域的最低學位

✔ 至少 5 年製造環境和處理 QA 系統、流程和審核的工作經驗

✔ 底薪可達 RM7000

工作職責 ：

• 對光學元件、鏡頭、金屬鏡筒和相關材料進行徹底檢查
• 利用專業測試設備驗證光學特性
• 監控組裝過程，識別與既定程序或規範的任何偏差，確保正確對齊和安裝
• 進行干涉測試以評估光學元件的表面品質和形狀
• 對帶有金屬鏡筒的完整光學系統進行最終檢查，以確保它們符合所有指定的品質要求

要求 ：

• 光學、材料科學、機械工程或任何相關領域的最低學位
• 至少5 年製造環境以及處理 QA 系統、流程和審核方面的工作經驗
• 具備金屬零件光學鏡片組裝品質保證經驗
• 熟悉光學原理、鏡頭製造流程和光學測試技術
• 熟練操作精密測量工具、金屬檢測設備
• 熟練使用品質管理軟體和工具
• 願意為審核供應商出差
• 光學、冶金或品質保證的相關認證（ASQ 認證品質工程師、美國光學協會認證）是額外優勢

好處 ：

• 季度獎金
• 靈活獎金
• AWS
• 加薪