Total 41 qc engineer job vacancies in Quality Assurance / Control category in D14 Geylang, Eunos

• Inspecting Materials: Perform thorough inspections of incoming raw materials, such as wood, hardware, and finishing materials, to ensure they meet quality standards and specifications.
• Quality Checks: Conduct visual inspections and measurements on finished carpentry products, including furniture, cabinets, doors, and other woodwork, to verify conformance with quality standards and customer requirements.
• Testing: Assist in conducting tests and evaluations on carpentry products, including strength tests, durability tests, and other quality control procedures to identify any defects or deficiencies.
• Documentation: Maintain accurate records of inspection results, test data, and quality control documentation. Prepare reports summarizing findings and recommendations for improvement.
• Problem Identification: Identify and report any quality issues, defects, or non-conformities to supervisors or management promptly. Collaborate with production teams to address and resolve quality concerns.
• Equipment Maintenance: Maintain and calibrate inspection equipment and tools regularly to ensure accuracy and reliability.

Requirements

· Min ‘O’ Levels with at least 1-2 years of relevant experience in related field.

· Strong management skills and leadership qualities.

· Experience in manufacturing setting preferred

Overview:

The QC Specialist is responsible for timely review, confirmation, disposition, and resolution of nonconforming materials in accordance to established NC process to meet quality targets. You will investigate instrument complaints, pursue containment action, root cause identification and corrective actions. You will also execute continual improvement initiatives to meet organization objectives, support IQC process and participate in Supplier Improvement Initiative and will also support and execute installation qualification and maintenance of QC ancillary equipment.

How You’ll Make an Impact:

• Responsible to verify and confirm supplier material defects in daily walk-the-line. Ensure defects are adequately investigated with supporting reports.
• Drive cross functional teams in nonconformance investigation. Review Quality Notification activities for timely defect disposition. Responsible to ensure all QN tasks are adequately completed before closure.
• Investigate instrument complaint, established immediate containment, identify root cause and implement correct action.
• Engage cross functional team to improve QC test First Pass Yield. Participate in continuous improvement initiatives.
• Support IQC process with specification review and Quality Inspection Plan set up.
• Support QC Lab equipment validation, calibration, and preventive maintenance.
• Generate weekly, monthly QN reports for trend analysis and presentation in scheduled Management Review meeting. Drive QN closure to meet aging and defect cost targets
• Participate in Product Transfer Initiative – New or existing products from other sites. Review QC test procedure for adequacy

What You Bring:

• Bachelor’s degree in Mechanical or Electrical Engineering or Diploma in Mechanical or Electrical Engineering with minimum 5 years of Quality Engineering experience or demonstrated competency.
• 1 - 3 years of manufacturing quality assurance / control /engineering experience in a regulated environment preferred
• Knowledge of ISO 13485 MDSAP requirements. Lead Auditor preferred
• Experience in Process Validation, Non-conforming Process, Customer Complaint investigation.
• Possesses excellent problem-solving, interpersonal, communication and leadership skills.
• Must be self-motivated, result oriented with minimal supervision.
• Hand-on experience of statistical tools application. Lean/ Six Sigma Green Belt preferred.
• Experience with ERP systems a plus, SAP preferred.
• While this list of qualifications may help an employee to succeed in this position, capable candidates may have a wide range of backgrounds or skills. If you have experience that aligns with the responsibilities of this role, we encourage you to apply.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.

Benefits: Bio-Rad's biggest asset is our people, and this is the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee’s work and life cycle. We’re proud to offer comprehensive medical plans and insurance, flexible benefits, wellness programs, extensive learning and development opportunities and more.

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply.

Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

JOB DESCRIPTION:

• Provide Quality Operation support on the production floor.
• Participate/Perform discrepant material disposition.
• Manage a team of Quality Inspectors.
• Participate in problem solving and root cause analysis using standardized investigation tools.
• Liaise with interplant associates to resolve quality issues.
• Review and analyze Quality Indicators and collaborate with manufacturing department to proactively resolve non conformances and operational issues.
• Participate in lean activities.

REQUIREMENTS:

• Diploma/Bachelor degree in Precision Engineering, Mechanical Quality, Engineering or equivalent.
• Minimum 5 years of Quality Assurance experience.
• Strong knowledge and skill in CMM programming.
• Great Interpersonal skills and customer oriented.
• Good initiative and a fast learner with good orginizing skills.
• Good communication skills and able to work as a team.

Job Description:

• Assist in full spectrum of QAQC tasks and internal audit exercise from design stage, construction stage and Conquas/ Quality Mark preparation stage.
• Assist in maintaining the Project Quality System in accordance with and company’s policy.
• Assist in verifying that Project Quality System established is being properly followed and that the construction works satisfy the contract / customer quality requirements.
• Establish inspection and test plans based on the contract.
• Coordinate the quality control aspect of the project.
• Report on operational procedures which affect quality and propose improvements to the project quality system.
• Prepare reports on Authority inspections (RI inspection, BCA TOP inspection etc.)
• Organize and conduct handling over punch walks with client and consultant team.
• Ensure all site inspection records, QAQC documents and TC records are up to date.
• Check, evaluate and confirm work done and material supply quantity status for the purpose of rectification works progress claims.
• Responsible for the compliance to safety & occupational health practices to be implemented at QAQC Section
• Attend internal and external meeting if required.
• Assist in all CONQUAS and QM assessments.
• Any other ad-hoc duties as assigned.

Job Requirements:

• Bachelor Degree in Civil Engineering or its equivalent
• Certified QM/ Conquas Manager will be added an advantages
• Familiar with local regulations pertaining to Builder’s Licence, Work Head Registration or other related requirements.
• For experience QA / QC personnel will be considered for the Assistant Manager / Manager position.
• Ability to analyze and synthesize complex issues quickly and propose counter measures to settle the issues.
• Good knowledge of documentation procedures
• Good verbal and written communication skills
• Able to communicate in English and Madarin

As a Lead Test Automation Engineer, your unique blend of software engineering and test expertise will drive high-quality deliverables and optimize development processes. One of your key projects will be constructing a centralized dashboard that aggregates end-to-end test results from various CI/CD deployments, enhancing visibility and efficiency across teams. Other key items include the development of data generation utilities, and accessibility testing tools, which will foster comprehensive and inclusive testing.

Your responsibilities will include:

• Champion and drive product quality and test automation practices.
• Lead a team of Test Automation Engineers to produce robust automated test suites for web and mobile applications, fostering an environment of reliability.
• Architect, develop, and maintain a centralized dashboard that consolidates E2E test results from various CI/CD pipelines, enhancing transparency and decisionmaking across teams.
• Design and implement sophisticated data generation utilities, enabling the creation of realistic and extensive test data sets for more effective testing scenarios.
• Develop comprehensive accessibility testing tools to ensure our applications adhere to accessibility standards and provide an inclusive user experience.

What we’re looking for:

• A degree in Computer Science, Computer or Electronics Engineering, Information Technology or related disciplines.
• A minimum of five years of work experience in test automation.
• A minimum of two years of leading test automation teams.
• Proficient with Javascript/ Typescript.
• Experience in continuous integration is preferred.
• Experience in test automation such as open source automated testing frameworks, like Selenium with Cucumber, Appium, Robot etc.
• Experience in web development (e.g. NodeJS, ReactJS) with their respective debugging tools.
• Great interpersonal skills and ability to deliver news or direction with tact, and to persuade.

BIOTRONIK is a leading Medical Device company dedicated to revolutionizing patient care through innovative medical device software solutions. With a commitment to cutting-edge technology and a passion for improving healthcare outcomes, we are at the forefront of transforming the industry.

We are seeking a skilled and motivated Cloud Test Engineer to join our team. In this role, you will play a crucial part in ensuring the quality and reliability of our cloud-based software solutions for medical devices product.

If you are passionate about leveraging cloud technology to make a positive impact on medical device product, we want to hear from you.

Your Responsibilities

• Develop and execute test plans, test cases, and test scripts for Cloud-based software solutions, ensuring thorough testing coverage.
• Collaborate with cross-functional teams, including software developers, product managers, and quality assurance professionals, to identify and address software defects.
• Design, implement, and maintain automated testing frameworks for cloud-based applications to enhance testing efficiency and scalability.
• Conduct performance testing, load testing, and stress testing of Cloud-based software systems to ensure optimal performance under various conditions.
• Work closely with regulatory affairs and compliance teams to ensure testing proceccess align with industry standards and regulations.

Your Profile

• Bachelor’s Degree in Computer Science, Software Engineering, or a related field; advanced degree preferred.
• Proven experience as a Test Engineer is preferable.
• Experience with automated testing frameworks such as Selenium, Junit and Gherkin.
• Familiarity with cloud platforms such as AWS, Azure, or Google Cloud Platform.
• Strong analytical skills and attention to detail.
• Excellent communication skills and the ability to collaborate effectively in a team environment.
• Prior experience from the healthcare or medical device industry would be an added advantage.

What we offer

• being encouraged to think and act entrepreneurially
• working in global teams and projects
• developing yourself professionally

The Compliance Engineer will be part of a manufacturing functional team. The team plays a leading role as change agents in supporting the site towards the zero defects goal. The team will focus on discrepancy (unplanned events) management, identify and implement remediation and proactive continuous improvement across the organization representing all functions. The position requires proficiency in facilitation of investigations, analytical thinking toward identifying root cause, teamwork, collaboration to identify and implement solutions, technical writing capabilities to write clear and concise quality records. The position requires skill and knowledge in Technical Writing, Quality Systems, RCA Methodologies, Risk Management, Continuous Improvement Methodologies, Project Management and presentation to Health Authorities/ audits.

Responsibilities:

● Manage the investigation Unplanned Events (iUPE) end-to-end process as Owner in accordance with procedures, performance measures, and standard lead times.

● Notify Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.

● Effectively facilitate cross-functional discussions associated with investigation’s cause, remediation and impact analysis.

● Collaborate with cross-functional groups to identify, design and implement process and system improvements and initiatives.

● Lead trending analysis to identify systemic issues and facilitate resolution to prevent trends/ issues.

● Drive continuous improvement to develop and implement initiatives in cross-functional collaboration to reduce defects in identified problem areas.

● Manage the remediation as Owner (if necessary), working collaboratively across several functions to achieve timely closure.

● Manage assignments that are complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations.

● Support and participate in site inspection readiness initiatives, audits, and regulatory inspections.

● Manage work and competing priorities to achieve department objectives and company goals.

● Own the development of personal performance goals and departmental objectives.

● Identify and solve the problems proactively.

● Collaborate with necessary stakeholders to establish processes to meet targets and timelines for UPE management and continuous improvement initiatives.

About You:

● At least a degree in a relevant science/engineering discipline.

● At least 5-7 years of relevant experience in the pharmaceutical industry.

● Exhibits good knowledge of international cGMP and compliance requirements.

● Proficiency of the technical process and workflow of discrepancy/ Unplanned Events Process.

● Strong technical writing skills.

● Display a good level of problem solving ability and provide suggestion/alternative solutions on complex issues resolution.

● Displays strong interpersonal, exceptional teamwork and collaboration skills.

● Highly motivated, well organized and able to develop alternate solutions to issues.

● Ability to communicate clearly and professionally in both writing and verbally.

● Experience with mammalian/bacterial biopharmaceutical production strongly preferred.

Position Summary:

This is a 12-month contractual position. This position is responsible for supporting the Regional Operations and Lam Quality Program in the region and primarily working on generating and analyzing first level data, report compilation and administrative support.

Job Responsibilities:

Support Quality Management Program

1. Build customer trust through consistent communication and reporting.
2. Contribute to the Quality Community & collaborate with all regional QPLs.
3. Admin and support role in the Lam Quality Management through the IQMS (Integrated Quality Management System):

- IRF (Investigation Request Form) submission review & approval

- GQ (Global Quality) report Update requested information (E.g. damage code)

- GQ report NCe (Non-Conformity external) with Inv Group - Field Service

- Reverse logistic report

- GQ report Needing Action (FQM (Functional Quality Manager)/ QPL (Quality Program Lead)) Report

• ETS (Event Tracking System) tickets follow up
• NCe audits

Regional Operations Support

• Compilation of CADO (Cost Allocation Distribution Options), mandatory retrofit and tool in install reports and follow up with end users for closure.

Job Requirements:

• Professional certificates or tertiary education equivalent (A levels, Diploma, Nitec)
• Possesses strong inter-personal, negotiation and communications skills.
• Possesses strong Microsoft Office application skills
• Strong analytical skills and experience in MS PowerBI/ Qlik Sense application will be advantageous

Activate Interactive Pte Ltd (“Activate”) is a leading technology consultancy headquartered in Singapore with a presence in Malaysia and Indonesia. Our clients are empowered with quality, cost-effective, and impactful end-to-end application development, like mobile and web applications, and cloud technology that remove technology roadblocks and increase their business efficiency.

We believe in positively impacting the lives of people around us and the environment we live in through the use of technology. Hence, we are committed to providing a conducive environment for all employees to realise their full potential, who in turn have the opportunity to continuously drive innovation.

We are searching for our next team members to join our growing team.

If you love the idea of being part of a growing company with exciting prospects in mobile and web technologies that create positive impact on people’s lives, then we would love to hear from you.

Co-Development Business Unit is looking for Quality Engineer (Software)

Internal Code: A24007

What will you do?

• Create and maintain automated test cases, test plans and test framework ensuring that they are up to date with requirements and policy changes.
• Co-create user story acceptance criteria.
• Create, maintain, and improve the automated test framework and test environments.
• Conduct testing on new features and file defects.
• Perform various tests such as manual/functional/performance/exploratory tests support UATs.
• Assist in resolving production cases.
• Participate in all agile ceremonies.

What are we looking for?

• Degree in software engineering, computer engineering, electrical engineering or infocomm-related discipline
• At least 3 years of professional software quality testing experience with hands-on automation
• Strong understanding of testing techniques, risk analysis
• Strong understanding of test-driven development,
• Experience with continuous integration and continuous delivery (using Gitlab will be an added advantage)
• Experience with automation scripting (i.e. Java)
• Experience with open-source automated testing frameworks (i.e. Selenium Webdriver, Cucumber)
• Experience with open-source performance testing tools (i.e. JMeter, Gatling, Locust) or enterprise level testing tools (HP LoadRunner)
• Experience with open-source penetration testing tools (ZAP, Burp Suite, SQL Map) or enterprise level penetration testing tools (HP WebInspect, Nessus, CheckMarx)
• Working experience in Agile environment will be an added advantage
• Excellent verbal communication and listening skills

What do we offer in return?

• Fun working environment
• Employee Wellness Program

Does it sound like something you are interested in exploring further? Please be in touch with our team for an initial chat at chi@activate.sg

Activate Interactive Singapore is an equal opportunity employer. Employment decisions will be based on merit, qualifications and abilities. Activate Interactive Pte Ltd does not discriminate in employment opportunities or practices on the basis of race, colour, religion, gender, sexuality, national origin, age, disability, marital status or any other characteristics protected by law.

Protecting your privacy and the security of your data are longstanding top priorities for Activate Interactive Pte Ltd.

Your personal data will be processed for the purposes of managing Activate Interactive Pte Ltd’s recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results, and as is otherwise needed in the recruitment and hiring processes.

Please consult our Privacy Notice (https://www.activate.sg/privacy-policy) to know more about how we collect, use, and transfer the personal data of our candidates. Here you can find how you can request for access, correction and/or withdrawal of your Personal Data.

Apply for this job

1. Job Responsibilities:Test and document the functionality, performance, and stability of the app.
   Identify and report bugs, including detailed reproduction steps and screenshots.
   Participate in the writing and updating of test documents.
   Work closely with the development team to ensure bug fixes and feature improvements.
   
2. Qualifications:Have basic experience in mobile application testing, familiar with testing processes and methods.
   Familiar with common mobile operating systems (such as iOS and Android) and devices.
   Have good communication skills and a spirit of teamwork.
   Ability to think independently, solve problems, and have strong learning ability.
   Candidates with programming background or experience in automated testing are preferred.
   

Overview:

The QC Specialist is responsible for timely review, confirmation, disposition, and resolution of nonconforming materials in accordance to established NC process to meet quality targets. You will investigate instrument complaints, pursue containment action, root cause identification and corrective actions. You will also execute continual improvement initiatives to meet organization objectives, support IQC process and participate in Supplier Improvement Initiative and will also support and execute installation qualification and maintenance of QC ancillary equipment.

How You’ll Make an Impact:

• Responsible to verify and confirm supplier material defects in daily walk-the-line. Ensure defects are adequately investigated with supporting reports.
• Drive cross functional teams in nonconformance investigation. Review Quality Notification activities for timely defect disposition. Responsible to ensure all QN tasks are adequately completed before closure.
• Investigate instrument complaint, established immediate containment, identify root cause and implement correct action.
• Engage cross functional team to improve QC test First Pass Yield. Participate in continuous improvement initiatives.
• Support IQC process with specification review and Quality Inspection Plan set up.
• Support QC Lab equipment validation, calibration, and preventive maintenance.
• Generate weekly, monthly QN reports for trend analysis and presentation in scheduled Management Review meeting. Drive QN closure to meet aging and defect cost targets
• Participate in Product Transfer Initiative – New or existing products from other sites. Review QC test procedure for adequacy

What You Bring:

• Bachelor’s degree in Mechanical or Electrical Engineering or Diploma in Mechanical or Electrical Engineering with minimum 5 years of Quality Engineering experience or demonstrated competency.
• 1 - 3 years of manufacturing quality assurance / control /engineering experience in a regulated environment preferred
• Knowledge of ISO 13485 MDSAP requirements. Lead Auditor preferred
• Experience in Process Validation, Non-conforming Process, Customer Complaint investigation.
• Possesses excellent problem-solving, interpersonal, communication and leadership skills.
• Must be self-motivated, result oriented with minimal supervision.
• Hand-on experience of statistical tools application. Lean/ Six Sigma Green Belt preferred.
• Experience with ERP systems a plus, SAP preferred.
• While this list of qualifications may help an employee to succeed in this position, capable candidates may have a wide range of backgrounds or skills. If you have experience that aligns with the responsibilities of this role, we encourage you to apply.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.

Benefits: Bio-Rad's biggest asset is our people, and this is the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee’s work and life cycle. We’re proud to offer comprehensive medical plans and insurance, flexible benefits, wellness programs, extensive learning and development opportunities and more.

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply.

Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

Qualifications & Requirements:

• Tertiary qualification in Information Technology or Engineering

• At least 3 years’ relevant experience in executing testing and developing test automation solutions involving devices (UI-based or embedded) and/or back-office systems with familiarity on the full system development lifecycle from requirement, development, to testing and deployment;

• Good written and verbal communication skills;

• Able to work well both independently as well as in a team;

• Certification in software testing preferred;

• Experience in Micro-payments/Automatic Fare Collection systems using Smart Cards and in diverse test execution phases (System Integration Testing, User Acceptance Testing, Performance testing) would be an advantage

Responsibilities:

• Preparing the test environment, designing, and developing the test cases.

• Preparing the test environment, executing the test procedures.

• Automating the test solution based on the system design using scripting or programming languages as well as performance tuning.

• Create traceability to requirements, analyze gaps and address them.

• Logging and tracking defects to closure

• Conducting test reviews with internal and external stakeholders.

• Perform root cause analysis for production and user acceptance defects, address test gaps to ensure test efficiency

• Develop design documents and user manuals which would effectively describe and provide clear instructions on the test automation solution to the end users who include testers and stakeholders.

The Compliance Engineer will be part of a manufacturing functional team. The team plays a leading role as change agents in supporting the site towards the zero defects goal. The team will focus on discrepancy (unplanned events) management, identify and implement remediation and proactive continuous improvement across the organization representing all functions. The position requires proficiency in facilitation of investigations, analytical thinking toward identifying root cause, teamwork, collaboration to identify and implement solutions, technical writing capabilities to write clear and concise quality records. The position requires skill and knowledge in Technical Writing, Quality Systems, RCA Methodologies, Risk Management, Continuous Improvement Methodologies, Project Management and presentation to Health Authorities/ audits.

Responsibilities:

● Manage the investigation Unplanned Events (iUPE) end-to-end process as Owner in accordance with procedures, performance measures, and standard lead times.

● Notify Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.

● Effectively facilitate cross-functional discussions associated with investigation’s cause, remediation and impact analysis.

● Collaborate with cross-functional groups to identify, design and implement process and system improvements and initiatives.

● Lead trending analysis to identify systemic issues and facilitate resolution to prevent trends/ issues.

● Drive continuous improvement to develop and implement initiatives in cross-functional collaboration to reduce defects in identified problem areas.

● Manage the remediation as Owner (if necessary), working collaboratively across several functions to achieve timely closure.

● Manage assignments that are complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations.

● Support and participate in site inspection readiness initiatives, audits, and regulatory inspections.

● Manage work and competing priorities to achieve department objectives and company goals.

● Own the development of personal performance goals and departmental objectives.

● Identify and solve the problems proactively.

● Collaborate with necessary stakeholders to establish processes to meet targets and timelines for UPE management and continuous improvement initiatives.

About You:

● At least a degree in a relevant science/engineering discipline.

● At least 5-7 years of relevant experience in the pharmaceutical industry.

● Exhibits good knowledge of international cGMP and compliance requirements.

● Proficiency of the technical process and workflow of discrepancy/ Unplanned Events Process.

● Strong technical writing skills.

● Display a good level of problem solving ability and provide suggestion/alternative solutions on complex issues resolution.

● Displays strong interpersonal, exceptional teamwork and collaboration skills.

● Highly motivated, well organized and able to develop alternate solutions to issues.

● Ability to communicate clearly and professionally in both writing and verbally.

● Experience with mammalian/bacterial biopharmaceutical production strongly preferred.

Description

• Inspection of Parts & Tooling using QC equipment
• CMM inspection
• Incoming & Outgoing Inspection
• Maintain QC instruments
• Prepare QC reports and ensure all quality inspection are maintained in accordance to AS9100
• Coordinate with production on quality issues
• Develop methods and checklist for inspection
• Assist in design of various fixtures and tooling for in house inspection

Requirement

• Minimum diploma in Mechanical / Precision Engineering
• Able to interpret drawings & GDT
• Experienced in CMM inspection
• Minimum 3 year in similar working environment

Working Hours :

• Monday to Friday 8.30am - 5.30pm
• Saturday : 8.30am - 12.30pm
• Shift work included