Tqm Administrator

5 days ago


Singapore SAMSUNG ELECTRONICS SINGAPORE PTE. LTD. Full time

**OVERVIEW & IMPACT**:
Samsung Electronics Device Solution is a global leader in Memory Semiconductor technology. The TQM Administrator will support the Memory Technical team of our sales office in Singapore office and other ASEAN countries.

The incumbent will be responsible for the daily operations related to the Return Materials Administration.

**JOB RESPONSIBILITIES**:

- Handle the day-to-day RMA Authorization processing as needed
- Respond to customer with RMA request timely.
- Coordinate with tech support to process RMA/Samples cross-ship requests.
- Coordinate with customers/agents/warehouse to request and process RMA shipment.
- Maintain daily RMA records.
- Document and report monthly RMA records to different stakeholders
- Process RMA credits in CRM/ERP system.

**QUALIFICATIONS & REQUIRED SKILLS**:

- Proficient with MS Excel
- Experiences in CRM/ERP software is prefered.
- Detail oriented with good organizational skills
- Ability to multi-task and adapt to changing priorities
- Ability to work independently with minimum supervision
- Applicant is willing to take on 1-year contract role ( extendable)


  • QC Analyst III

    6 days ago


    Singapore NOVARTIS SINGAPORE PHARMACEUTICAL MANUFACTURING PTE. LTD. Full time

    Job Description This role will be responsible for establishing and ensuring testing of drug substance release and stability testing, including testing of intermediates in process control samples. Lab operations must comply with written testing SOPs and local/international regulations. About the Role: Execution of assigned tasks in the quality control...


  • Singapore PSC Biotech Corporation Full time

    Key Responsibilities Manage the storage and inventory of laboratory samples Conduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples Ensure strict compliance with cGxP standards, including data integrity requirements Execute and document stability testing (if not...


  • Singapore beBeeQualityControl Full time

    Job Title: Quality Control Specialist">This is a key role in our organization's quality control laboratory, responsible for ensuring the testing of drug substance release and stability. The successful candidate will be involved in the establishment and execution of assigned tasks in accordance with cGxP regulations.">Key Responsibilities:">">Sample storage...


  • Singapore beBeeLaboratory Full time $80,000 - $120,000

    Key ResponsibilitiesOur team is responsible for managing the storage and inventory of laboratory samples, conducting analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples.We ensure strict compliance with cGxP standards, including data integrity requirements. Our roles also involve...


  • Singapore beBeeAnalytical Full time $60,000 - $80,000

    Job OverviewThis position involves testing drug substance release and stability, including the examination of process control samples.It requires adherence to written testing SOPs and international regulations.Key Responsibilities:Sample storage and management.Analytical testing and documentation of API / drug substance / drug product / finished product /...


  • Singapore beBeeAnalytical Full time

    Job Title: Quality Assurance Specialist About the Role This role involves ensuring the highest standards of quality in laboratory settings within the pharmaceutical industry. As a Quality Assurance Specialist, you will be responsible for managing laboratory samples, conducting analytical testing and documentation, and maintaining compliance with regulatory...

  • QC Analyst III

    24 hours ago


    Singapore Novartis Singapore Full time

    Join to apply for the QC Analyst III (Analytical)role at Novartis Singapore . Summary: Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory-specific activities such as analyses, maintenance, calibration, and qualification of analytical equipment. About The Role: Key Responsibilities:...

  • QC Specialist I

    4 weeks ago


    Singapore Novartis Farmacéutica Full time

    This role will be responsible for establishing and ensuring the testing of drug substance release and stability testing, including testing of intermediates in process control samples. Lab operations must be in accordance with written testing SOPs and local/international regulations. About the Role Key Responsibilities: Sample storage and management....

  • Qc Analyst

    2 weeks ago


    Singapore Novartis Full time

    QC Analyst (QC Biochemist 3) Location - Singapore #LI Hybrid About the Role: Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment. Key Responsibilities: - Analytical testing and...


  • Singapore UMANAH12 TRADING PTE. LTD. Full time

    As a vital team member, you will be responsible for identifying the areas of improvement in our current business processes, developing and implementing new strategies and technologies, and collaborating with stakeholders to ensure alignment and successful adoption of the new procedures. Additionally, you will conduct process audits and performance...