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7 jobs found for quality control

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    • permanent
    • S$4,500 - S$6,000, per month, + VB + transport allowance
    • full-time
    about the companyOur client is a global leading supplier of semi-finished copper and copper alloy products, serving the semiconductor, automotive, datacom, consumer and industrial/factory automation industries. They’re on a look out for a reliable Senior QA/Customer Quality Engineer to join the team during an exciting time in their development.about the jobReporting into the QA Manager, this person will be responsible for:Resolve customer complaints (onsite & off site) for existing and new customer accountsCustomer Field Application Failure Claim resolutionFacilitate Non-conforming Product disposal (EW, EAF, RMA)Liaise with inter-department on Customer Claim issues, i.e. RTV, payment, retain sample.Plans and coordinates with Production on non-conformance product screening.Conduct containment measures and MRB controls.Conduct Specification Review (Product and Corporate)Lead Customer Audit / Visits Review and oversee Improvement Plans, Projects and Technology Roadmaps update.Establish visit programs to customersProvide engineering support to Internal Departments on quality and technical issues.Participate in Internal Quality Audit programDevelop Systems, optimize Work processes for Operational excellenceProcess Change Management (ECN, PCN, PPAP)Training of junior staffjob requirementDegree/Diploma in Material Science/Mechanical/Precision Engineering/Chemical Processing/Quality ManagementMinimum 3 years of relevant experience Experience in metal fabrication, precision engineering, etching or tool & die industry will be an added advantageProficient with MS OfficeGood knowledge or hands on with SAP is an advantageExpert on ISO Standards and ISO Internal AuditingWilling to work in the West (Pioneer/Jurong/Joo Koon)If you are interested in exploring this position, kindly send your CV to yiling.tan(@)randstad.com.sg. Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    about the companyOur client is a global leading supplier of semi-finished copper and copper alloy products, serving the semiconductor, automotive, datacom, consumer and industrial/factory automation industries. They’re on a look out for a reliable Senior QA/Customer Quality Engineer to join the team during an exciting time in their development.about the jobReporting into the QA Manager, this person will be responsible for:Resolve customer complaints (onsite & off site) for existing and new customer accountsCustomer Field Application Failure Claim resolutionFacilitate Non-conforming Product disposal (EW, EAF, RMA)Liaise with inter-department on Customer Claim issues, i.e. RTV, payment, retain sample.Plans and coordinates with Production on non-conformance product screening.Conduct containment measures and MRB controls.Conduct Specification Review (Product and Corporate)Lead Customer Audit / Visits Review and oversee Improvement Plans, Projects and Technology Roadmaps update.Establish visit programs to customersProvide engineering support to Internal Departments on quality and technical issues.Participate in Internal Quality Audit programDevelop Systems, optimize Work processes for Operational excellenceProcess Change Management (ECN, PCN, PPAP)Training of junior staffjob requirementDegree/Diploma in Material Science/Mechanical/Precision Engineering/Chemical Processing/Quality ManagementMinimum 3 years of relevant experience Experience in metal fabrication, precision engineering, etching or tool & die industry will be an added advantageProficient with MS OfficeGood knowledge or hands on with SAP is an advantageExpert on ISO Standards and ISO Internal AuditingWilling to work in the West (Pioneer/Jurong/Joo Koon)If you are interested in exploring this position, kindly send your CV to yiling.tan(@)randstad.com.sg. Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    • permanent
    • S$5,500 - S$7,000, per month, + AWS + VB
    • full-time
    about the companyOur client is a leading manufacturer of innovative contact lenses and services, with main manufacturing sites in Singapore and other affiliates in other global markets. WIth a strong commitment to industry R&D, this company is now looking for a driven QA manager to lead their QA team.about the jobReporting into the Managing Director directly, you will:Ensure overall compliance adequacy and operational effectiveness of the QA Operations for the contact lens and lens care products manufacturing.Formulate and implement work procedures that meet quality and regulatory requirements.Ensure high level of compliance to ISO 13485, EU MDR 2017/745, MDSAP regulations and other relevant national authorities requirementsSupport the documentation of CVM GDPMD system to ensure its compliance to MY-MDA requirements.Work closely with internal departments to resolve internal and external quality issues; and to improve overall process yield. Leading and participating in quality improvement programs and cross functional projects.Conduct failure analysis for customer complaint returns & manage customers’ complaint Coordinate with supplier(s) on the quality trends, including the corrective and preventive actions through Supplier Management Program.Develop, implement, monitor and maintain ISO 13485 QMS Certification, MDSAP Certification, CE Certification, MOH Certification and other GMP systems.Update and maintain the National and International Regulations Requirements Guidance, Standards and Technical Guides & ensure that gap analysis is performed Act as QMR and PRRC with scope as stated in the Quality Manual and liaise with third party auditors (NB and Regulatory authorities) or inspectors in relation to site audits, desk audits or random inspections.job requirementDegree in Engineering, Life Sciences or equivalent.ISO 13485:2016 lead auditorMinimum 3 years of quality management related experience in the medical device/biotechnology/pharmaceutical industry with minimum 2 years experience in regulatory affairs.Familiar with cGMP and EU MDR 2017/745 requirements.Working knowledge of metrology tools and equipment such as calipers, micrometers and lensmeter.Knowledgeable in Validation/Qualification process..Proficient in Minitab and MS Office applications.If you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    about the companyOur client is a leading manufacturer of innovative contact lenses and services, with main manufacturing sites in Singapore and other affiliates in other global markets. WIth a strong commitment to industry R&D, this company is now looking for a driven QA manager to lead their QA team.about the jobReporting into the Managing Director directly, you will:Ensure overall compliance adequacy and operational effectiveness of the QA Operations for the contact lens and lens care products manufacturing.Formulate and implement work procedures that meet quality and regulatory requirements.Ensure high level of compliance to ISO 13485, EU MDR 2017/745, MDSAP regulations and other relevant national authorities requirementsSupport the documentation of CVM GDPMD system to ensure its compliance to MY-MDA requirements.Work closely with internal departments to resolve internal and external quality issues; and to improve overall process yield. Leading and participating in quality improvement programs and cross functional projects.Conduct failure analysis for customer complaint returns & manage customers’ complaint Coordinate with supplier(s) on the quality trends, including the corrective and preventive actions through Supplier Management Program.Develop, implement, monitor and maintain ISO 13485 QMS Certification, MDSAP Certification, CE Certification, MOH Certification and other GMP systems.Update and maintain the National and International Regulations Requirements Guidance, Standards and Technical Guides & ensure that gap analysis is performed Act as QMR and PRRC with scope as stated in the Quality Manual and liaise with third party auditors (NB and Regulatory authorities) or inspectors in relation to site audits, desk audits or random inspections.job requirementDegree in Engineering, Life Sciences or equivalent.ISO 13485:2016 lead auditorMinimum 3 years of quality management related experience in the medical device/biotechnology/pharmaceutical industry with minimum 2 years experience in regulatory affairs.Familiar with cGMP and EU MDR 2017/745 requirements.Working knowledge of metrology tools and equipment such as calipers, micrometers and lensmeter.Knowledgeable in Validation/Qualification process..Proficient in Minitab and MS Office applications.If you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    • permanent
    • S$5,000 - S$10,000, per month, + AWS + VB
    • full-time
    about the companyOur client is a global leader in providing certification, inspection, and test services for companies across sectors. With an extensive network across ASEAN, this company now has exciting opportunities for a driven Medical/MHS Auditor to join their dynamic team, to support the ASEAN region in performing Audits, inspections and trainings for clients.about the jobPerform Audits/Inspections in ISO 13485 / MDD, J-QMS, CMDCAS, MDSAP / Specific medical device standardsPerform in-house and public training for clients (e.g. ISO 13485 / MDD / Specific Medical Device Standards / QSR)Conduct audits on clients’ medical device quality systems based on regulatory requirements for access into EU, Japan and CanadaAssist Sales by providing technical advice to clients and respond to enquiries Process clients’ queries, Change Notifications, EC certificate extensions and audits effectively Take charge of pre/post audit tasks including calculation of audit duration, quotations, audit registration, preparation of documentations etc.Maintain authorizations for auditing and technical reviews and corresponding objective evidence Develop and review audit methodologies for accreditation complianceUndergo relevant training, qualification, or certification process to be qualified to provide further services. To generate, compile and prepare assessment reports and recommendations for review of certification bodies. job requirementDegree/diploma Minimum 5 years of relevant experience in the medical/pharmaceutical/biotechnology industry, with preferably at least 2 years in Quality Assurance work with manufacturers of medical devicesGood knowledge of medical device directives, ISO 9001 and ISO 13485 standards will be an added advantageGlobal Regulatory Affairs background, including MDD/IVDD is preferredMust be comfortable with extensive traveling (up to 50%) within ASEAN (largely Thailand and Malaysia, occasional travel to USA and Europe)If you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    about the companyOur client is a global leader in providing certification, inspection, and test services for companies across sectors. With an extensive network across ASEAN, this company now has exciting opportunities for a driven Medical/MHS Auditor to join their dynamic team, to support the ASEAN region in performing Audits, inspections and trainings for clients.about the jobPerform Audits/Inspections in ISO 13485 / MDD, J-QMS, CMDCAS, MDSAP / Specific medical device standardsPerform in-house and public training for clients (e.g. ISO 13485 / MDD / Specific Medical Device Standards / QSR)Conduct audits on clients’ medical device quality systems based on regulatory requirements for access into EU, Japan and CanadaAssist Sales by providing technical advice to clients and respond to enquiries Process clients’ queries, Change Notifications, EC certificate extensions and audits effectively Take charge of pre/post audit tasks including calculation of audit duration, quotations, audit registration, preparation of documentations etc.Maintain authorizations for auditing and technical reviews and corresponding objective evidence Develop and review audit methodologies for accreditation complianceUndergo relevant training, qualification, or certification process to be qualified to provide further services. To generate, compile and prepare assessment reports and recommendations for review of certification bodies. job requirementDegree/diploma Minimum 5 years of relevant experience in the medical/pharmaceutical/biotechnology industry, with preferably at least 2 years in Quality Assurance work with manufacturers of medical devicesGood knowledge of medical device directives, ISO 9001 and ISO 13485 standards will be an added advantageGlobal Regulatory Affairs background, including MDD/IVDD is preferredMust be comfortable with extensive traveling (up to 50%) within ASEAN (largely Thailand and Malaysia, occasional travel to USA and Europe)If you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    • permanent
    • S$1,800 - S$2,700, per month, +AWS+VB
    • full-time
    about the companyOur client designs, manufactures equipment and materials in the medical devices industry. They have the people and ethos to act with speed, innovation, enterprise and creativity. The scope of the offer, the size of the business, the autonomoy to drive your career forward all adds up to a great place to work.about the jobPerform First Article inspection as per procedure, drawings and BOMEnsure NCR disposition is done correctlyInterpreted technical drawing and translate it into First Article Inspection reportFiling of FAI and FAAS reportsPerform NCR verification for rework parts from supplier on First Article related issueManaged non-conformance reportsSupport QA team to perform in-process/outgoing quality inspection when requiredPart quality inspectionPerform and verify root cause analysis of returned instrumentsskills & experience requiredDiploma / Higher NITEC / NITEC in mechanical / mechatronics / quality engineering or equivalentMin 2 years in instrument / equipment manufacturing environment Operate accurate measurement instrument (Smart scope / CMM / Profile projector) Hands on with basic measuring instrument (example: caliper, micrometer, and height gauge)Able to read mechanical drawing and use of CMM MachineAble to commence within a short notice / immediately will be a plusIf you are interested in the position , kindly send your CVs in to yitwei.kwan(@)randstad.com.sgPlease include your availability, expected salary and reason for leaving current job.We regret that only shortlisted candidates will be contactedEA: 94C3609 / Reg: R1325913. Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.
    about the companyOur client designs, manufactures equipment and materials in the medical devices industry. They have the people and ethos to act with speed, innovation, enterprise and creativity. The scope of the offer, the size of the business, the autonomoy to drive your career forward all adds up to a great place to work.about the jobPerform First Article inspection as per procedure, drawings and BOMEnsure NCR disposition is done correctlyInterpreted technical drawing and translate it into First Article Inspection reportFiling of FAI and FAAS reportsPerform NCR verification for rework parts from supplier on First Article related issueManaged non-conformance reportsSupport QA team to perform in-process/outgoing quality inspection when requiredPart quality inspectionPerform and verify root cause analysis of returned instrumentsskills & experience requiredDiploma / Higher NITEC / NITEC in mechanical / mechatronics / quality engineering or equivalentMin 2 years in instrument / equipment manufacturing environment Operate accurate measurement instrument (Smart scope / CMM / Profile projector) Hands on with basic measuring instrument (example: caliper, micrometer, and height gauge)Able to read mechanical drawing and use of CMM MachineAble to commence within a short notice / immediately will be a plusIf you are interested in the position , kindly send your CVs in to yitwei.kwan(@)randstad.com.sgPlease include your availability, expected salary and reason for leaving current job.We regret that only shortlisted candidates will be contactedEA: 94C3609 / Reg: R1325913. Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.
    • permanent
    • S$2,800 - S$3,200, per month, + AWS + VB
    • full-time
    about the companyOur client is a molecular diagnostic biotechnology company with lab operations globally in Singapore, USA, China and Japan. They specialize in the manufacturing and provider of diagnostic tests and services and are now on a look out for a QA Executive to join their team during this exciting time in their development. about the jobImprovement / enhancements to existing processesCross functional collaboration to ensure successful implementation / revision of processesDocument control, drafting and reviewAssist in internal audits, conduct/facilitate 2nd and 3rd party auditsFacilitate/assist in process validationUpkeep of PD, NC, CAPAFacilitation of customer feedback and complaints with respect to the quality of the productFacilitate and assist in design/technology transferMonitoring of QMS processes to ensure compliance to standardsConduct training on general QMS processes.Monitor and control of artworkVerification of actions resulting from quality eventsFacilitate in risk management activitiesMonitoring of vigilance/post market surveillance activitiesVendor evaluation/re-evaluationInfrastructure and working environment monitoringjob requirementDegree/Diploma in a related Science or Engineering disciplineMinimum 1 to 3 years of QA Experience would be preferred.Willing to work in the West (Boon Lay/Pioneer/Jurong)If you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    about the companyOur client is a molecular diagnostic biotechnology company with lab operations globally in Singapore, USA, China and Japan. They specialize in the manufacturing and provider of diagnostic tests and services and are now on a look out for a QA Executive to join their team during this exciting time in their development. about the jobImprovement / enhancements to existing processesCross functional collaboration to ensure successful implementation / revision of processesDocument control, drafting and reviewAssist in internal audits, conduct/facilitate 2nd and 3rd party auditsFacilitate/assist in process validationUpkeep of PD, NC, CAPAFacilitation of customer feedback and complaints with respect to the quality of the productFacilitate and assist in design/technology transferMonitoring of QMS processes to ensure compliance to standardsConduct training on general QMS processes.Monitor and control of artworkVerification of actions resulting from quality eventsFacilitate in risk management activitiesMonitoring of vigilance/post market surveillance activitiesVendor evaluation/re-evaluationInfrastructure and working environment monitoringjob requirementDegree/Diploma in a related Science or Engineering disciplineMinimum 1 to 3 years of QA Experience would be preferred.Willing to work in the West (Boon Lay/Pioneer/Jurong)If you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    • permanent
    • S$4,500 - S$6,000, per month, + VB + transport allowance
    • full-time
    about the companyOur client is a global leading supplier of semi-finished copper and copper alloy products, serving the semiconductor, automotive, datacom, consumer and industrial/factory automation industries. They’re on a look out for a reliable Senior/Principal QA/Customer Quality Engineer to join the team during an exciting time in their development.about the jobReporting into the QA Manager, this person will be responsible for:Resolve customer complaints (onsite & off site) for existing and new customer accountsCustomer Field Application Failure Claim resolutionFacilitate Non-conforming Product disposal (EW, EAF, RMA)Liaise with inter-department on Customer Claim issues, i.e. RTV, payment, retain sample.Plans and coordinates with Production on non-conformance product screening.Conduct containment measures and MRB controls.Conduct Specification Review (Product and Corporate)Lead Customer Audit / Visits Review and oversee Improvement Plans, Projects and Technology Roadmaps update.Establish visit programs to customersProvide engineering support to Internal Departments on quality and technical issues.Participate in Internal Quality Audit programDevelop Systems, optimize Work processes for Operational excellenceProcess Change Management (ECN, PCN, PPAP)Training of junior staffjob requirementDegree/Diploma in Material Science/Mechanical/Precision Engineering/Chemical Processing/Quality ManagementMinimum 3 years of relevant experience Experience in metal fabrication, precision engineering, etching or tool & die industry will be an added advantageProficient with MS OfficeGood knowledge or hands on with SAP is an advantageExpert on ISO Standards and ISO Internal AuditingWilling to work in the West (Pioneer/Jurong/Joo Koon)If you are interested in exploring this position, kindly send your CV to yiling.tan(@)randstad.com.sg. Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    about the companyOur client is a global leading supplier of semi-finished copper and copper alloy products, serving the semiconductor, automotive, datacom, consumer and industrial/factory automation industries. They’re on a look out for a reliable Senior/Principal QA/Customer Quality Engineer to join the team during an exciting time in their development.about the jobReporting into the QA Manager, this person will be responsible for:Resolve customer complaints (onsite & off site) for existing and new customer accountsCustomer Field Application Failure Claim resolutionFacilitate Non-conforming Product disposal (EW, EAF, RMA)Liaise with inter-department on Customer Claim issues, i.e. RTV, payment, retain sample.Plans and coordinates with Production on non-conformance product screening.Conduct containment measures and MRB controls.Conduct Specification Review (Product and Corporate)Lead Customer Audit / Visits Review and oversee Improvement Plans, Projects and Technology Roadmaps update.Establish visit programs to customersProvide engineering support to Internal Departments on quality and technical issues.Participate in Internal Quality Audit programDevelop Systems, optimize Work processes for Operational excellenceProcess Change Management (ECN, PCN, PPAP)Training of junior staffjob requirementDegree/Diploma in Material Science/Mechanical/Precision Engineering/Chemical Processing/Quality ManagementMinimum 3 years of relevant experience Experience in metal fabrication, precision engineering, etching or tool & die industry will be an added advantageProficient with MS OfficeGood knowledge or hands on with SAP is an advantageExpert on ISO Standards and ISO Internal AuditingWilling to work in the West (Pioneer/Jurong/Joo Koon)If you are interested in exploring this position, kindly send your CV to yiling.tan(@)randstad.com.sg. Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contacted.Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    • permanent
    • S$7,000 - S$8,000, per month, + VB
    • full-time
    about the companyOur client is a bespoke, collaborative perfumery house for the luxury-lifestyle generation. They are on a lookout for innovative talents with an entrepreneurial spirit to join their dynamic team to make the world of Personalized Perfumery accessible to all. If you’re an agile QC Manager, now is the best time to seize this opportunity!about the jobReporting into the Head of Operations, the QC Manager will be responsible for checking the quality of incoming/outgoing products for the company and the production procedures. These include:Perform quality control checks and outgoing materials/ordersPerform regular and timely quality assessments on all incoming materials (e.g. scent concentrates, raw and packaging materials) from vendors – visual, feel and olfactory checksReject all products that fail to meet quality expectations and ensure proper part segregationRead and develop blueprints, plans, and specifications to understand the requirements of products and ordersDocument inspection outcomes by completing detailed reports and performance records.Process non-conformance report for products found to be out of specifications.Resolve quality-related issues with relevant teams in a timely mannerRecommend improvements to the receiving, production and outbound process to ensure quality control.job requirementDiploma/degree in Engineering/Manufacturing/Supply Chain or equivalent Minimum 4 to 5 years of experience in a similar QA/QC position with a pharmaceutical backgroundStrong understanding of quality control standards and testing techniquesCertification in quality control techniques is preferredFamiliar with root cause analysisGood knowledge of ISO 9001 or ISO 22716 will be an added advantageExcellent knowledge of MS OfficeIf you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contactedApplicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172
    about the companyOur client is a bespoke, collaborative perfumery house for the luxury-lifestyle generation. They are on a lookout for innovative talents with an entrepreneurial spirit to join their dynamic team to make the world of Personalized Perfumery accessible to all. If you’re an agile QC Manager, now is the best time to seize this opportunity!about the jobReporting into the Head of Operations, the QC Manager will be responsible for checking the quality of incoming/outgoing products for the company and the production procedures. These include:Perform quality control checks and outgoing materials/ordersPerform regular and timely quality assessments on all incoming materials (e.g. scent concentrates, raw and packaging materials) from vendors – visual, feel and olfactory checksReject all products that fail to meet quality expectations and ensure proper part segregationRead and develop blueprints, plans, and specifications to understand the requirements of products and ordersDocument inspection outcomes by completing detailed reports and performance records.Process non-conformance report for products found to be out of specifications.Resolve quality-related issues with relevant teams in a timely mannerRecommend improvements to the receiving, production and outbound process to ensure quality control.job requirementDiploma/degree in Engineering/Manufacturing/Supply Chain or equivalent Minimum 4 to 5 years of experience in a similar QA/QC position with a pharmaceutical backgroundStrong understanding of quality control standards and testing techniquesCertification in quality control techniques is preferredFamiliar with root cause analysisGood knowledge of ISO 9001 or ISO 22716 will be an added advantageExcellent knowledge of MS OfficeIf you are interested in the position, kindly send your CVs to yiling.tan(@)randstad.com.sg.Please include your availability, expected salary and reason for leaving your current job.We regret that only shortlisted candidates will be contactedApplicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents.EA: 94C3609 / Reg: R21103172

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