Total 195 sales support specialist job vacancies in Quality Assurance / Control category in Islandwide

• MNC Company
• Basic $4500 - $6000 + AWS + Variable Bonus
• Excellent Welfare and Benefits + Career progression
• Working location: Jurong Island (Company Transport Provided at Jurong East)
• Working day: Monday to Friday
• Working hours: 8am to 4.30pm

Job Responsibilities:

• Establish, implement, maintain & improve the management systems, namely: ISO 9001, ISO 14001, SS 651
• Establish, implement, review & improve on management systems’ documentations, namely: policy, objectives, manual, procedures, forms, etc.
• Manage all system certification, improvement, and upgrade issues
• Plan, manage and execute all internal and external management system audits to ensure timely closure of issues raised during the audits
• Plan and conduct management reviews
• Develop and oversee the implementation of all QA activities and support in HSE activities
• Follow-up on issues to ensure timely closure of HSEQ-related reports, namely: customer complaint reports, corrective action reports, incident reports, etc.
• Prepare and submit Monthly reports
• Participate as a team member in risk / HSE assessment team
• Participate in external provider audits, where applicable
• Co-ordination of Global QA initiatives and projects
• Knowledge of IATF 16949 Automotive Quality Management System Certification / GMP is preferred
• To perform any other duties or assignments as assigned by superiors

Job Requirements:

• Minimum Diploma or Degree in Chemical Engineering with minimum 5 years of relevant experience in a petrochemical industry

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

THIEN CHING MEI (R2198032)

EA Recruitment Pte Ltd

EA License No: 21C0492

Jobscope

• Provide assistance to internal customers in support of departmental functions.
• Timely escalation of issues or problems identified to direct supervisor. This includes but not limited to; system inefficiencies, the departure of business processes and/or procedures.
• Ensure timely completion of training tasks assigned in training system to be in compliant and aligned with the company's Right to Operate.
• Perform any tasks as requested or assigned by Management to support Quality oversight activities.
• Perform review and format of word documents in preparation for the approval process in Electronic Document Management System.
• Perform issuance and verification of Shop Packet according to the Process Order (PO) schedule.
• Organize for the safekeeping of site records and other documents in an electronic and physical repository;
• Support the day-to-day aspects of records management for various users, and assisting teams with administrative and/or records aspects related to the site;
• File and cross index records in chronological date-order and document number by system or project name in the records repository;
• Provide administrative support during audits and regulatory inspections.

Requirements

• Bachelor Degree in Science / Chemical Engineering or equivalent with relevant pharmaceutical experience.
• Minimum 1-3 relevant years of experience in QA/QC and GMP Compliance
• Familiar with manufacturing operations applications; six sigma and lean principles and process improvement tools.
• Thorough knowledge of GMP compliance regulations, ICH Q7a Guidelines, Good Documentation Practices and other applicable regulations.
• Proven track record of continuous improvement in quality operations or manufacturing.

All qualified applicants, please send in your resume to:

triciagoh@recruitexpress.com.sg

Tricia Celestine Goh (R1981653)

Recruit Express Pte Ltd | Company Reg. No. 199601303W | EA License Number: 99C4599

• MNC Company
• Basic $4500 - $6000 + AWS + Variable Bonus
• Excellent Welfare and Benefits + Career progression
• Working location: Jurong Island (Company Transport Provided at Jurong East)
• Working day: Monday to Friday
• Working hours: 8am to 4.30pm

Job Responsibilities:

• Establish, implement, maintain & improve the management systems, namely: ISO 9001, ISO 14001, SS 651
• Establish, implement, review & improve on management systems’ documentations, namely: policy, objectives, manual, procedures, forms, etc.
• Manage all system certification, improvement, and upgrade issues
• Plan, manage and execute all internal and external management system audits to ensure timely closure of issues raised during the audits
• Plan and conduct management reviews
• Develop and oversee the implementation of all QA activities and support in HSE activities
• Follow-up on issues to ensure timely closure of HSEQ-related reports, namely: customer complaint reports, corrective action reports, incident reports, etc.
• Prepare and submit Monthly reports
• Participate as a team member in risk / HSE assessment team
• Participate in external provider audits, where applicable
• Co-ordination of Global QA initiatives and projects
• Knowledge of IATF 16949 Automotive Quality Management System Certification / GMP is preferred
• To perform any other duties or assignments as assigned by superiors

Job Requirements:

• Minimum Diploma or Degree in Chemical Engineering with minimum 5 years of relevant experience in a petrochemical industry

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

THIEN CHING MEI (R2198032)

EA Recruitment Pte Ltd

EA License No: 21C0492

Quality Assurance (QA) Specialist

Working location: Jurong Island ( Transport pick up : Jurong East )

Work hours: 8 am to 4.30 pm (Mon to Fri)

Salary range: $4500 - $5800

The Quality Assurance (QA) Specialist is responsible for the development, implementation and promotion of QA related activities and compliance in the company. He/ She is also responsible to:

• Establish, implement, maintain & improve the management systems, namely: ISO 9001, ISO 14001, SS 651
• Establish, implement, review & improve on management systems’ documentations, namely: policy, objectives, manual, procedures, forms, etc.
• Manage all system certification, improvement and upgrade issues.
• Plan, manage and execute all internal and external management system audits to ensure timely closure of issues raised during the audits.
• Plan and conduct management reviews.
• Develop and oversee the implementation of all QA activities and support in HSE activities.
• Follow-up on issues to ensure timely closure of HSEQ-related reports, namely: customer complaint reports, corrective action reports, incident reports, etc
• .Prepare and submit Monthly reports.
• Participate as a team member in risk / HSE assessment team.
• Participate in external provider audits, where applicable.
• Co-ordination of Global QA initiatives and projects.
• Knowledge of IATF 16949 Automotive Quality Management System Certification / GMP is preferred.
• To perform any other duties or assignments as assigned by superiors.

Requirements:

• Diploma or Degree in relevant field
• Min 5 years’ experience in a petrochemical industry

If Interest please kindly click on the Apply button

Ong Choon Kiat (James) | Reg No: R22104989

The Supreme HR Advisory Pte Ltd | EA No: 14C7279

• MNC Company
• Basic $4500 - $6000 + AWS + Variable Bonus
• Excellent Welfare and Benefits + Career progression
• Working location: Jurong Island (Company Transport Provided at Jurong East)
• Working day: Monday to Friday
• Working hours: 8am to 4.30pm

Job Responsibilities:

• Establish, implement, maintain & improve the management systems, namely: ISO 9001, ISO 14001, SS 651
• Establish, implement, review & improve on management systems’ documentations, namely: policy, objectives, manual, procedures, forms, etc.
• Manage all system certification, improvement, and upgrade issues
• Plan, manage and execute all internal and external management system audits to ensure timely closure of issues raised during the audits
• Plan and conduct management reviews
• Develop and oversee the implementation of all QA activities and support in HSE activities
• Follow-up on issues to ensure timely closure of HSEQ-related reports, namely: customer complaint reports, corrective action reports, incident reports, etc.
• Prepare and submit Monthly reports
• Participate as a team member in risk / HSE assessment team
• Participate in external provider audits, where applicable
• Co-ordination of Global QA initiatives and projects
• Knowledge of IATF 16949 Automotive Quality Management System Certification / GMP is preferred
• To perform any other duties or assignments as assigned by superiors

Job Requirements:

• Minimum Diploma or Degree in Chemical Engineering with minimum 5 years of relevant experience in a petrochemical industry

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

THIEN CHING MEI (R2198032)

EA Recruitment Pte Ltd

EA License No: 21C0492

Quality Compliance Specialist (Healthcare / North-East / Up to $5000) GDPMDS / ISO13485 / Quality Management System / Auditing / CAPA

Job Description

1. Ensure implementation, monitoring and improving local Quality Management System (QMS) with regulatory compliance across the company in alignment with Healthcare Business Group corporate quality standards and country regulatory requirements
2. Prepare, review, update, track implement and monitor compliance of standard operating procedures
3. Support Quality team in deployment of corporate policy to country local QMS
4. Work closely with cross-functional teams in overseeing and providing regulatory/compliance guidance on operational activities (including customer complaints handling and supplier/subcon management)
5. Support audit(s) activities including internal audit, external audit, supplier audit and regulatory audit
6. Participate in CAPA board meeting to ensure corrective and preventive action is meeting corporate and country regulatory requirements. Ensure timely follow-up, execution, completion of necessary action and review effectiveness of CAPA.
7. Support quality compliance improvement programs/projects
8. Work closely with Management team to improve internal control and governance practices to enhance the effectiveness and efficiency of the operations and process to ensure compliance
9. Serve as the point of the contact in the country on quality compliance matter
10. Conduct and support training activities to cross-functional team in the country in alignment with corporate QMS requirements
11. Support regional Quality Compliance leader to drive and implement any improvement project in country
12. Issue CAPA based on audit findings and follow up through until closure
13. Ensure CAPA effectivenes
14. Conduct and support activity related to Field Corrective Action (FCA). Ensure timely follow-up, execution and completion of necessary action
15. Plan and conduct audit(s) on subcon activity regularly to ensure effectiveness of QMS
16. Identify requirements and establish the process for Issue Review and Escalation to division
17. Leads the Identify and Assess steps within the Issue Review portion of this process. Responsible for documentation and obtaining approvals of the Issue Review Documen
18. Responsible or the investigation in issue review.
19. Other such duties that may be determined by management.

Position Requirements

· Bachelor’s degree in Pharmaceutical, Pharmacy or Science or equivalent

· Has analytical skill, able to interpret information and data for routine operational needs.

· Has good understanding on ISO9001:2015, ISO 13485:2016 or GDP/GDPMD

· Minimum 3-5 years’ experience in Quality function

· Certified ISO 13485 or GDPMD internal auditor is preferred

· Experience with project management is preferred

EA License No. 01C4394 • RCB No. 200007268E •EA Registration No. R22109454 Malcolm Lee Jun Hao

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOLKELLY Singapore Pte Ltd and its affiliates to collect, use and disclose your personal data for the purposes set out in the Privacy Policy available at https://www.persolkelly.com.sg/policies. You acknowledge that you have read, understood, and agree with the Privacy Policy.

• MNC Company
• Basic $4500 - $6000 + AWS + Variable Bonus
• Excellent Welfare and Benefits + Career progression
• Working location: Jurong Island (Company Transport Provided at Jurong East)
• Working day: Monday to Friday
• Working hours: 8am to 4.30pm

Job Responsibilities:

• Establish, implement, maintain & improve the management systems, namely: ISO 9001, ISO 14001, SS 651
• Establish, implement, review & improve on management systems’ documentations, namely: policy, objectives, manual, procedures, forms, etc.
• Manage all system certification, improvement, and upgrade issues
• Plan, manage and execute all internal and external management system audits to ensure timely closure of issues raised during the audits
• Plan and conduct management reviews
• Develop and oversee the implementation of all QA activities and support in HSE activities
• Follow-up on issues to ensure timely closure of HSEQ-related reports, namely: customer complaint reports, corrective action reports, incident reports, etc.
• Prepare and submit Monthly reports
• Participate as a team member in risk / HSE assessment team
• Participate in external provider audits, where applicable
• Co-ordination of Global QA initiatives and projects
• Knowledge of IATF 16949 Automotive Quality Management System Certification / GMP is preferred
• To perform any other duties or assignments as assigned by superiors

Job Requirements:

• Minimum Diploma or Degree in Chemical Engineering with minimum 5 years of relevant experience in a petrochemical industry

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

LIONG ZHAO GUAN (R22107632)

EA Recruitment Pte Ltd

EA License No: 21C0492

Quality Assurance | QA Specialist | Petrochemical Industry | Up to $5800 | Jurong East

Working location: Jurong Island ( Transport pick up : Jurong East )

Work hours: 8 am to 4.30 pm (Mon to Fri)

Salary range: $4500 - $5800

The Quality Assurance (QA) Specialist is responsible for the development, implementation and promotion of QA related activities and compliance in the company. He/ She is also responsible to:

• Establish, implement, maintain & improve the management systems, namely: ISO 9001, ISO 14001, SS 651
• Establish, implement, review & improve on management systems’ documentations, namely: policy, objectives, manual, procedures, forms, etc.
• Manage all system certification, improvement and upgrade issues.
• Plan, manage and execute all internal and external management system audits to ensure timely closure of issues raised during the audits.
• Plan and conduct management reviews.
• Develop and oversee the implementation of all QA activities and support in HSE activities.
• Follow-up on issues to ensure timely closure of HSEQ-related reports, namely: customer complaint reports, corrective action reports, incident reports, etc
• .Prepare and submit Monthly reports.
• Participate as a team member in risk / HSE assessment team.
• Participate in external provider audits, where applicable.
• Co-ordination of Global QA initiatives and projects.
• Knowledge of IATF 16949 Automotive Quality Management System Certification / GMP is preferred.
• To perform any other duties or assignments as assigned by superiors.

Requirements:

• Diploma or Degree in relevant field
• Min 5 years’ experience in a petrochemical industry

The Supreme HR Advisory Pte Ltd | 14C7279

Ong Boon Kiet (Travys) | R22104769

Senior Recruitment Consultant

Quality Operations Specialists must assist site management to oversee the quality system execution on the manufacturing and production areas at all times.

The personnel are required to observe, document, discuss, and report quality adverse events related to the manufacturing of the product and are responsible to ensure highest quality and compliance of released batches.

Responsibilities:

• Ensure that products manufactured meet approved company policies, processes and procedures
• Provide quality oversight of GMP manufacturing and manufacturing support, including technical operations, engineering, QC laboratory and supply chain activities.
• Review completed incoming material inspection packages, Batch Records, Manufacturing Logs, product changeover/line-clearance activities and administration of Quality Logs, e.g., QA Hold, QA tag out.
• Release incoming material, process, and product batches.
• Participate in investigations arising out of non-compliance in incoming materials, QC testing, manufacturing processes, warehousing, and product.
• Participate in change management, including change coordinator and/or QA oversight roles to ensure change plan is managed and complies with applicable policies.
• Perform regular walk-through of manufacturing, engineering, warehouse and QC areas as required to ensure compliance is maintained at all times.
• Participate and support new product introduction, operation excellence projects and other tasks as assigned by management

About You:

• Bachelor Degree in a Natural Sciences (i.e. Biology, Chemistry), Engineering, Pharmacy or other relevant courses
• Prior knowledge of quality / compliance management as well as regulations and standards affecting APIs / Biologics
• Minimum of 2+ years of pharmaceutical, biopharmaceutical experience in Quality and/or Compliance (GxP) environment.
• Experience in SAP, Trackwise are preferred
• Ability to quickly know products and processes in order to assess quality issues
• Committed to quality and maintain a high standard of work at all times
• Demonstrates the highest levels of integrity and a strong work ethic
• Good knowledge of GxP requirements and regulations
• Good planning and scheduling skills
• Good communication and interpersonal skills both verbal and written

Duration : 6 months contract. (Option to renew/convert based on performance)

Job Summary

· We are looking for a Digital Banking Product Manager to lead the digital capabilities deliveries from the business side on our Digital Platforms (primarily on Online Banking, Mobile Banking, Pre-Login Website and Online Real-time Onboarding platform).

· Having keen eye for detail and a good understanding of UX and customer journeys is a big plus.

· Project management skills are also desirable as the selected candidate will be managing multiple streams of digital product deliveries.

· The candidate will ensure that our digital experiences across digital touch points work as intended.

· This is a Direct contract role for 12 months.

Key Responsibilities

Quality Strategy Development: Formulate and execute comprehensive quality assurance strategies aligned with project objectives.
- Test Script Optimization: Review and enhance test scripts to achieve extensive and effective coverage.
- Testing Leadership: Lead and oversee detailed testing activities, including functional, performance, reliability, and regression testing to ensure product quality.
- Quality Assurance Execution: Manage and monitor the performance, reliability, and quality of digital products and services.
- Defect Management: Identify, investigate, and resolve issues within the production process to maintain product integrity.
- Standard Maintenance: Develop, implement, and oversee corrective and preventive actions to uphold quality assurance standards.
- UX Support and Analysis: Analyze user journeys and facilitate User Acceptance Testing (UAT) to ensure exceptional user experiences.
- Project Coordination: Lead multiple projects, ensuring timely delivery and adherence to quality benchmarks.
- Performance Improvement: Develop metrics to assess quality performance and drive continuous improvement initiatives.
- Cross-Functional Collaboration: Collaborate with various teams to align on quality goals and provide training on quality best practices.

Automated Testing Implementation: Design and implement automated testing solutions to improve efficiency and coverage.
- Automation Framework Development: Develop and maintain robust automation frameworks to streamline the testing process.
- Automated Test Scripts: Create and manage automated test scripts for various test scenarios, ensuring thorough validation of product features.
- Continuous Integration: Integrate automated testing processes into continuous integration and continuous deployment (CI/CD) pipelines for seamless development and testing cycles.

Our Ideal Candidate

· 4 plus years experience in Project Management in banking or digital domain.

· Deep understanding of UX principles and their application in digital products.

· Expertise in mobile app technologies and an understanding of their business applications.

· Highly meticulous in identifying and addressing quality issues.

· Excellent analytical and problem-solving skills to tackle complex challenges.

· Ability to perform well in a fast-paced, ever-changing environment and handle evolving project requirements.

· Proficient in using various testing tools and frameworks for manual and automated testing.

· Strong knowledge of automation testing tools and best practices, including experience with scripting and automation frameworks.

· Contract Duration - 12 months

Role Specific Technical competencies

· Project Management

· UX Knowledge

· Communication and Presentation Skills

· Understanding of Mobile App business and tech

· Attention to detail

· Analytical mind and problem-solving aptitude

· Strong organizational skills

About Standard Chartered

We're an international bank, nimble enough to act, big enough for impact. For more than 170 years, we've worked to make a positive difference for our clients, communities, and each other. We question the status quo, love a challenge and enjoy finding new opportunities to grow and do better than before. If you're looking for a career with purpose and you want to work for a bank making a difference, we want to hear from you. You can count on us to celebrate your unique talents and we can't wait to see the talents you can bring us.

Our purpose, to drive commerce and prosperity through our unique diversity, together with our brand promise, to be here for good are achieved by how we each live our valued behaviours. When you work with us, you'll see how we value difference and advocate inclusion.

Together we:

· Do the right thing and are assertive, challenge one another, and live with integrity, while putting the client at the heart of what we do

· Never settle, continuously striving to improve and innovate, keeping things simple and learning from doing well, and not so well

· Are better together, we can be ourselves, be inclusive, see more good in others, and work collectively to build for the long term

What we offer

In line with our Fair Pay Charter, we offer a competitive salary and benefits to support your mental, physical, financial and social wellbeing.

· Core bank funding for retirement savings, medical and life insurance, with flexible and voluntary benefits available in some locations.

· Time-off including annual leave, parental/maternity (20 weeks), sabbatical (12 months maximum) and volunteering leave (3 days), along with minimum global standards for annual and public holiday, which is combined to 30 days minimum.

· Flexible working options based around home and office locations, with flexible working patterns.

· Proactive wellbeing support through Unmind, a market-leading digital wellbeing platform, development courses for resilience and other human skills, global Employee Assistance Programme, sick leave, mental health first-aiders and all sorts of self-help toolkits

· A continuous learning culture to support your growth, with opportunities to reskill and upskill and access to physical, virtual and digital learning.

· Being part of an inclusive and values driven organisation, one that embraces and celebrates our unique diversity, across our teams, business functions and geographies - everyone feels respected and can realise their full potential.

Recruitment Assessments

Some of our roles use assessments to help us understand how suitable you are for the role you've applied to. If you are invited to take an assessment, this is great news. It means your application has progressed to an important stage of our recruitment process.

Visit our careers website www.sc.com/careers

Salary: up to $5.5k

Job Duration: 6 months

Working Days & Hours: 5 Days (8am – 4.30pm)

Location: 5 Days (8am – 4.30pm)

Job Description:

• Able to lead project for Method validation/verification/transfer to introduce new/remediated QC methods for testing existing and new products independently
• Subject matter expert in method validation, verification and transfer; covering wide arrays of methods and complex techniques
• Author of Method validation/verification/transfer Protocols, Reports, Reports, ensuring GMP compliance in ICH Q2(R1), USP <1225>, USP <1226>, EU GMP Chapter 6, and WHO Annex
• Ensure timely release of methods to support commercial production, manufacturing investigations and product investigations
• Ensure RFT in the method introduction process
• Maintain validated status of assays by establishing a control and monitoring strategy to ensure that the method is in the state of control, and the data generated from the method is reliable. Project Management: Analytical Equipment Qualification
• Able to lea project for Analytical Equipment Qualification to qualify/ re-qualify QC equipment for testing existing and new products independently
• Subject matter expert to provide technical advice to Local QC in laboratory related troubleshooting, e.g. lab equipment failure
• Author of equipment qualification documents as indicated in global procedures

Job Requirements: Min Degree in Pharmaceutical Science/Chemistry w 3 years of relevant experience

Interested candidates, please submit your resume to: allylok@recruitexpress.com.sg

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

allylok@recruitexpress.com.sg

Job Description:

• Implement and manage all quality control (QC) procedures, documentation, and record-keeping to ensure compliance with project standards and regulatory requirements.
• Inspect assembly lines and production processes to verify adherence to established standards and procedures. Ensure all components meet the required specifications.
• Conduct daily inspections post-pour and pre-delivery to ensure components are defect-free before shipment. Document and report findings promptly.
• Identify and report non-conformances to the Quality Manager. Facilitate immediate corrective actions to address quality issues.
• Work closely with project planners to develop and refine daily, weekly, and monthly delivery schedules, ensuring timely completion of tasks.
• Oversee subcontractors to ensure they adhere to delivery schedules and quality standards. Address any deviations promptly.
• Arrange appropriate storage for products to prevent damage. Conduct monthly stock takes to maintain accurate inventory records.
• Coordinate the testing of raw materials such as rebar, aggregates, cement, and precision tools to ensure they meet quality standards.
• Lead both internal and external quality assurance (QA) audits, including ISO 9001 audits. Ensure all processes comply with relevant quality standards.
• Collaborate with the design team to address technical issues. Work with subcontractors to resolve quality concerns.
• Prepare monthly reports analyzing quality control data. Provide management with recommendations for improvements and preventive measures.

Job Requirement:

• Degree in Civil and/or Construction Engineering
• At least 3 years of working experience in the civil construction industry
• Experience in all QA/QC functions.
• Able to start work immediately or within short notice.

Interested applicants, please write in through CareersFuture with detailed resume in MS Words format

EA License Number: 23C1730

Please Provide:

1) Availability
2) Current/ Expected salary
3) Reasons for leaving previous employments

We regret that only shortlisted candidates will be notified.

Our client is a healthcare distribution company based in Singapore, they leverage their Regional Distribution Centre (RDC) and pan Asia coverage to provide customized, value-added biologistic solutions for pharmaceutical, clinical trials, medical devices, diagnostics and other related healthcare companies.

Currently they are hiring QA Specialist at their Changi North site under 12 months agency contract.

Working hour: Monday - Friday. 8.30am - 5.30pm

Location: Changi North

Job Scope:

· Check and approve repackaging requirements of products and materials according to Client and regulatory requirement. Full review of batch records to ensure compliance per the repackaging instruction and GMP standards.

· Verify correct execution of repackaging activity against approved / updated repackaging instructions.

· Perform required quality checks and create quality inspection lots in SAP.

· Record Inspection Results and perform Usage Decision and stock posting. Issue necessary documents to facilitate release.

· Authorize to stop any repackaging activities when deviation is observed, when necessary.

· Perform other QA release (e.g. inbound QA release, cold chain temperature release, outbound release) if required.

· Perform back-up and other duties as assigned.

· Perform QA sampling, inspection and release of incoming packaging materials.

· Filing and maintenance of packaging material specifications.

· Updating of logs and trackers as required.

· Ensure general cleanliness and hygienic conditions of each workstation.

· Ensure compliance to ISO procedures, GxP and all regulatory requirements

· Work closely with inter-departments personnel to ensure quality is maintained throughout the organization.

· Conduct internal audits, training and general communication to achieve and sustain a high level of quality performance throughout the organization so as to properly support the business and regulatory (ISO, GMP, GSDP) requirements in the most efficient manner.

· Support QA administrative functions when necessary.

· Participate in any ad hoc projects as assigned by management from time to time.

Requirements:

· Diploma in any related discipline or good knowledge in Quality / Compliance areas in manufacturing can be considered.

· Preferably relevant experience in Quality Control / Quality Assurance works in manufacturing / production / assembly / operation environment.

· Knowledge in ISO, GMP and GSDP preferred.

· Quality-oriented.

· Demonstrate integrity and strong work ethic.

· Good team player with good verbal and written communication skills in English.

· Meticulous with good attention to details.

· Must be able to work in a fast-paced environment.

· Willing to work in cold room environment to perform cold chain QA release.

· Willing to work flexible and extended hours on weekday, weekend and public holidays to support operations and depending on the exigencies of service.

Interested candidates, who wish to apply for the above position, please click the “Apply now” and send your resume via JobDetails (persolkelly.com).

We regret that only shortlisted candidates will be notified.

PERSOLKELLY Singapore Pte Ltd
EA License No: 01C4394
EA Personnel No: R2199890
EA Personnel Name: LEE KIM HOU

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOLKELLY Singapore Pte Ltd and its affiliates to collect, use and disclose your personal data for the purposes set out in the Privacy Policy available at https://www.persolkelly.com.sg/policies. You acknowledge that you have read, understood, and agree with the Privacy Policy.

Job Requirements:

1. Full-time NEA Vector Control Technician License (Required);

2. Class 3 Driving Licence (Manual Company Van Provided);

3. Preferred Candidates: All are welcome, however please note that we do not have S Pass quota.

Key Duties & Responsibilities:

1. To carry out DETAILED INSPECTIONS and to administer appropriate pest management plans to assist with eradicating the pests and provide QUALITY SERVICES to customers’ premises.

2. Able to perform pest control works at RESIDENTIAL, COMMERCIAL, INDUSTRIAL & FOOD ESTABLISHMENTS.

3. MOST of the jobs will be conducted within the F&B premises.

4. 5.5 working days per week.

5. Able and willing to do OTs (OTs will be paid accordingly).

Benefits:

1. High Basic Salary + Allowances + Special bonus + High OT Payout

2. Commission/Incentives and excellent career prospects await the right candidate.

3. Medical benefits and welfare.

Jobscope

• Responsible to review and approve master batch records and subsequent batch records
• Review and approve cleaning records and procedures and ensure compliance with set
• Review and approve GMP documentation Ensure adherence to quality procedures, regulatory requirements and cGMPs.
• Develop and maintain document control process for efficient management and record all documentation
• Ensure proper document classification, sorting, filing and proper archiving
• Performs document quality check in accordance to company ISO document control procedures.
• Review and maintain the accuracy of the records, editing where necessary to ensure they are up to date.
• Undertake various functions related to document control, document archiving, document imaging and maintenance of document register
• Provide administrative support on the area of drafting document control and documentation.

Requirements

• Diploma/ Degree in Biological Science/ Biomedical Science
• Quality Assurance experience is advantageous
• Pharmaceutical GMP / Lifescience environment will be highly preferred

Apply now by sending your resume to tammyyap@recruitexpress.com.sg for more enquiries.

We regret to inform you that only shortlisted candidates will be notified.

Tammy Yap Yong Qi | R24121217 | EA License Number: 99C4599

Recruit Express Pte Ltd Company Reg. No. 199601303W