Total 387 qa engineer jobs in selangor

Duties & Responsibilities 

• Design and analyse experiments and success metrics to identify causal links between data quality measures and business outcomes.
• Establish & maintain Data Quality Scorecards to proactively monitor and report on data quality to relevant stakeholders;
• In charge of converting raw data into usable information for analytics and business decision-making.
• Analyzes complex data elements, systems, data flows, dependencies, and relationships to contribute to conceptual, physical, and logical data models.
• Analyzes data-related system integration challenges and proposes appropriate solutions.
• Collaborate and work across functional and multidisciplinary teams in a dynamic environment to develop an understanding of evolving/agile business needs.
• Track and resolve risks, issues, and action items throughout the project lifecycle.
• Ability to optimise the code to ensure processes perform optimally.
• Provide data-driven guidance and recommendations on strategic questions or improvements around data quality.
• Undertake data profiling and source system analysis and present clear insights to colleagues to support the end-use of the data.
• Design, implement, test, deploy, and maintain stable, secure, and scalable data engineering solutions and pipelines in support of data and analytics projects, including integrating new sources of data into the central databases.

Qualifications 

• BS/MS in Computer / Data Science, Mathematics, Applied Science, Statistics, AI, or other quantitative Science / Engineering field.

Perks & Benefits

• Employee equity
• Regular team activities
• Personal leave
• Open culture
• Personal development opportunities

Key Responsibilities:

• Liaise with team to solve quality issue and provide countermeasure report
• Liaise with customers and suppliers on quality issue
• Responsible for Quarantine Area
• Monitor calibration and verification of equipment and jigs
• Verify raw material mill cert and sub-parts compliance
• Responsible and assist in quality improvement (Kaizen)
• Prepare quality checking document (First Article, PIS, Outgoing Data Sheet)
• Assist in preparing visual management to operator
• Ensure subordinate is properly train for inspection and knowledge on product quality
• Assist HOD from time to time
• Meet KPI given

Job Requirements:

• Bachelor’s Degree in Engineering (Mechanical, Manufacturing or equivalent)
• Minimum 1 year of experiences in quality
• Fresh graduate is encouraged to apply.
• Able to work and communicate effectively with all levels and proactive.
• Able to travel around Klang Valley
• Good attendance, willingness to learn, meticulous, diligent, honest and self-discipline.

Perks & Benefits

• Company trips
• Medical insurance

Job Responsibilities

• To manage and oversee all activities related to Quality Assurance. 
• As Quality Management Representative/ Facility Quality Representative.
• Establish and maintain Quality Management System & coordinate of conducting context review meeting, risk and opportunities assessment, Internal Audit &  Management Review.
• Reviewing the performance of the QMS, including needs for improvement.
• Promoting awareness of customer’s requirements throughout the organization & liaise with external parties on matter relating to the QMS.
• Responsible all quality assurance activities 
• Entrusted by the Quality Assurance Representative and is responsible for deploying the latest version of SQM issued by Customer and putting it into practice at all departments concerned of the facility.
• In-charge of Document Control Center (DCC)- ensuring changes in manual, procedures and forms all well updated and distributed & proper upkeep the ISO documents according to retention periods.
• Respond to customer complaint and lead team in problem solving and quality improvement plan between project management, Production & Warehouse and customer.
• Review and support of sample Inspection and perform QA job periodically at customer location to ensure good quality control.
• Perform analysis on products and identify root cause, suggest solutions, investigate product quality in order to make improvements to achieve better customer satisfaction.
• Plan, create and manage the overall Quality Planning strategy.
• Collaborate with the Project Development team to ensure consistent project execution.
• Identify quality assurance process bottleneck and suggest actions for improvement.
• Oversee continuous improvement projects.
• Identify key KPIs for product quality.
• Prepare and present reports and metrics to Management.
• Prepare monthly quality report on the ongoing projects.
• Attend to ad-hoc task and be a team player.

Perks & Benefits

• Bonus
• Allowance (travel stipends, transportation, etc.)

Job Responsibilities

• To manage and oversee all activities related to Quality Assurance. 
• As Quality Management Representative/ Facility Quality Representative.
• Establish and maintain Quality Management System & coordinate of conducting context review meeting, risk and opportunities assessment, Internal Audit &  Management Review.
• Reviewing the performance of the QMS, including needs for improvement.
• Promoting awareness of customer’s requirements throughout the organization & liaise with external parties on matter relating to the QMS.
• Responsible all quality assurance activities 
• Entrusted by the Quality Assurance Representative and is responsible for deploying the latest version of SQM issued by Customer and putting it into practice at all departments concerned of the facility.
• In-charge of Document Control Center (DCC)- ensuring changes in manual, procedures and forms all well updated and distributed & proper upkeep the ISO documents according to retention periods.
• Respond to customer complaint and lead team in problem solving and quality improvement plan between project management, Production & Warehouse and customer.
• Review and support of sample Inspection and perform QA job periodically at customer location to ensure good quality control.
• Perform analysis on products and identify root cause, suggest solutions, investigate product quality in order to make improvements to achieve better customer satisfaction.
• Plan, create and manage the overall Quality Planning strategy.
• Collaborate with the Project Development team to ensure consistent project execution.
• Identify quality assurance process bottleneck and suggest actions for improvement.
• Oversee continuous improvement projects.
• Identify key KPIs for product quality.
• Prepare and present reports and metrics to Management.
• Prepare monthly quality report on the ongoing projects.
• Attend to ad-hoc task and be a team player.

Perks & Benefits

• Annual leave
• Medical

Requirements & Responsibilities

• Possess at least a Bachelor Degree or Professional Degree in Science or Food Technology or equivalent.
• Preferably with understanding on GMP, FSSC 22000, ISO 9000, HACCP & HAS
• Understanding in Quality Assurance System in beverage manufacturing plant is preferable
• Computer literate and can communicate well with all level is essential
• This position requires candidate to possess strong leadership qualities, willing to work independently and ready to take challenges 
• Good Management skills and acquire problems solving and decision making skills
• Fresh Graduates are encourage to apply

Perks & Benefits

• Contractual bonus
• Performance Bonus
• Travelling Allowance 
• Company Trips & Dinner
• Medical insurance
• Free Personal Accident insurance
• Various Leaves
• Personal development opportunities
• Free company products
• Monthly staff purchase

JOB DESCRIPTION

• Ensures the compliance to ISO 9001, ISO 13485, Good Distribution Practice for Medical Device (GDPMD) standards and any other relevant regulatory standards at all times.
• In charge of prepare, review, implement, and maintain the ISO 9001 and ISO 13485 quality management system, as well as the GDPMD regulatory compliance system.
• Part of Risk Management Team & Post Marketing Surveillance Team.
• Evaluates audit findings and implements appropriate corrective actions. Investigates, plans and monitors the corrective and preventive action plan.
• Handles all internal audit and external audits, customer and regulatory audit needed by Company.
• Ensures ongoing compliance and up-to-date with quality standards and industry regulatory requirements.
• Performs random testing and inspection for incoming stocksand finished products. Collects, compiles, and analyses statistical quality data.
• Liaises with the external parties including government body and certification body on matters relating to the Malaysian medical device regulatory requirements.
• Assists superior to ensures validity and on-time renewal of ISO certifications, GDPMD certifications and CE marking with the relevant Authorities.
• Prepares reports to communicate outcomes of quality activities. Investigates customer complaints and internal non-conformances of materials and finished products.
• Assists superior in identifying and planning necessary trainings for the personnel involved in the supply chain activities/operations and period the training to satisfy these needs.
• Carries out other tasks or projects being assigned by the Management from time to time.

JOB REQUIREMENT

• Preferably a Bachelor’s Degree / Post Graduate in Pharmacy, Biomedical Science, Medical Science, Engineering or any other related studies.
• Working experience in QA/QC is an added advantage.
• Knowledgeable in ISO 9001, ISO 13485 and GDPMD is an added advantage.
• Good command in English and Bahasa Malaysia both in written and spoken.
• Positive working attitude and result-oriented person.
• Team player and also able to work independently with minimum supervision.
• Healthy and self-motivated person.

Benefits & Others

• Medical
• Bonus
• Miscellaneous Allowance

Requirements & Responsibilities

• Diploma or equivalent.
• At least 1-2 years of working experience in the related field.
• Familiar with microbiological and physical testing.
• Knowledge in the food industry will be an added advantage.
• Good command in written and spoken in English & Bahasa Malaysia.
• Good communication, analytical and organizational skills.
• Good working attitudes and attendance.
• Able to work on shifts.
• Willing to be work in Semenyih. 
• Product rejection inspection
• Raw Material inspection and Lab testing
• Document controller (audit)
• General office tasks
• Ensures compliance to all laboratory procedures and work instructions.
• Responsible to manage documentation and filing of laboratory documents.
• Any other duties as required and assigned by the Management.

Perks & Benefits

• Annual leave
• Medical

Job Scope:

• Assist in Halal Certification registration (MyeHalal).
• Ensure renewal of product certification.
• To ensure continuous maintenance and implementation of Halal Assurance System.
• Regularly plan and conduct Halal internal audit and Halal Awareness training for staff.
• Responsible for all halal related matters and handle Halal Certification for required products
• Assist in training related companies for Halal Certification matter.
• Prepare related documentation when needed.

Requirements:

• Minimum Diploma / Bachelor Degree in related studies/ profession.
• Possess Halal Executive Certificate from certified trainer by HPB JAKIM.
• Have a minimum 1-year experience in Halal field/industry.
• Knowledge in Halal, MESTI, GMP, HACCP, ISO 22000.
• Well verse in Mandarin, English & Bahasa Malaysia (speaking & writing).
• Willing to travel (if needed).
• Able to work independently.
• Willing to learn and have good communication skills.
• Able to start immediately.

Perks & Benefits

• Open culture
• Personal development opportunities

Job Responsibilities

• Having enough knowledge in Product Quality Assurance
• Having enough knowledge and skill to operate all the QA equipments.
• Having enough knowledge regarding each products's specifications.
• Having reasonable knowledge and skills on computer
• Having more than basic knowledge regarding ISO 9001 and ISO 14001
• Trained for ISO Internal Auditor

Job Requirements

• Required language(s): Mandarin, English
• 3 year working in QA.
• ISO certificates

Perks & Benefits

• Employee equity
• Personal leave
• Sabbatical leave
• Open culture
• Personal development opportunities

Job Descriptions: 

• Conduct and review local and oversea relevant GMP procedures.
• Responsible for relevant regulatory affairs and monitoring the regulation trend of oversea, to ensure that the product are compliance to regulatory.
• Monitor and disseminate information to relevant department on the changes of 
  local and oversea laws and regulations that might affect registration, 
  manufacture and distribution of products.
• Compile and maintain systematic filling of product registration dossier etc. 

Requirements: 

• Bachelor Science / STPM (Science/Bio.) fresh graduates or similar qualification is encourage to apply 

Interested candidates are invited to write-in or email the application stating 
comprehensive details of qualification, expected salary, contact telephone number. 

GLADRON CHEMICALS SDN BHD (93253-W) 
No. 7, Jalan TP 7, UEP Industrial Park, 
40400 Shah Alam, Selangor, Malaysia. 
Tel : 03 5191 8989 
Email : howard@gladron.com 

Perks & Benefits

• Annual leave
• Medical

Responsibilities:

• Review the existing laboratory quality procedures and methods for improvement.
• Maintaining material incoming inspection list and material standard.
• Verify supplies COA, COC, test results etc.
• Maintenance of standard colour sample.
• Issuance of certificate of analysis to customer upon request.
• Control product specification.
• Issuance of chemical safety data sheet to customer upon request.
• Control, maintenance and calibration of measuring and monitoring equipment.
• Perform incoming test for pre-shipment sample.
• Perform incoming test for the actual raw material arrival stock.
• Verify Certificate of Analysis from supplier against the new arrival stock.
• Conduct inspection and test onto all the products produced by the manufacturing processes and to be delivered to the customer.
• Determine and locate the root causes for the KIV or RP products and proposed effective corrective action to the management.
• Process monitoring and process check for the KIV or RP products.
• Prepare Certificate of Analysis for our product if necessary.
• Assist in the improvement of production work flow, which focus on consistency of quality.
• Assist in the process monitoring and process check for "first formulation" if necessary.

Requirements:

• Proven working experience as a labouratory assistant.
• Familiarity with automated labouratory equipment.
• Computer literacy and experience with labouratory Information Systems.
• Accuracy and close attention to detail.
• Excellent analytical judgement.
• Current licence or relevant certification.

Perks & Benefits

• Employee equity
• Personal leave
• Personal development opportunities

Job Descriptions: 

• Conduct and review local and oversea relevant GMP procedures.
• Responsible for relevant regulatory affairs and monitoring the regulation trend of oversea, to ensure that the product are compliance to regulatory.
• Monitor and disseminate information to relevant department on the changes of 
  local and oversea laws and regulations that might affect registration, 
  manufacture and distribution of products.
• Compile and maintain systematic filling of product registration dossier etc. 

Requirements: 

• Bachelor Science / STPM (Science/Bio.) fresh graduates or similar qualification is encourage to apply 

Interested candidates are invited to write-in or email the application stating 
comprehensive details of qualification, expected salary, contact telephone number. 

GLADRON CHEMICALS SDN BHD (93253-W) 
No. 7, Jalan TP 7, UEP Industrial Park, 
40400 Shah Alam, Selangor, Malaysia. 
Tel : 03 5191 8989 
Email : howard@gladron.com 

Perks & Benefits

• Annual leave
• Medical

Job Descriptions: 

• Conduct and review local and oversea relevant GMP procedures.
• Responsible for relevant regulatory affairs and monitoring the regulation trend of oversea, to ensure that the product are compliance to regulatory.
• Monitor and disseminate information to relevant department on the changes of 
  local and oversea laws and regulations that might affect registration, 
  manufacture and distribution of products.
• Compile and maintain systematic filling of product registration dossier etc. 

Requirements: 

• Bachelor Science / STPM (Science/Bio.) fresh graduates or similar qualification is encourage to apply 

Interested candidates are invited to write-in or email the application stating 
comprehensive details of qualification, expected salary, contact telephone number. 

GLADRON CHEMICALS SDN BHD (93253-W) 
No. 7, Jalan TP 7, UEP Industrial Park, 
40400 Shah Alam, Selangor, Malaysia. 
Tel : 03 5191 8989 
Email : howard@gladron.com 

Perks & Benefits

• Annual leave
• Medical

JOB RESPONSIBILITIES

• Support the R&D department in all research and development of new products and existing products; food & beverages categories (dairy, juices, food supplements and others).
• Evaluate current and new/alternative raw materials and packaging materials when necessary.
• Involve in conducting sensory evaluation and shelf life determination & stability study toward new product & existing products.
• Responsible in prepare/produce the product samples and maintain the final product samples; OEM’s clients and in-house projects.
• Assist in production trials and first commercial run of new product.
• Record every product data in terms of formulation history and sample availability.
• Record product data analysis and specifications of products.
• Update all R&D documentation and daily analysis records and maintained filed in accordingly.
• Ensure facilities and equipment are organized and well maintained.
• Perform QC such as sensory and visual checks on all finished products (upon requested), new samples prepared, shelf-life samples to observe quality and taste.
• Maintain and organize product samples from spot checks for quality review.
• Maintain the R&D laboratory and ensure cleanliness within the laboratory.
• Assist in the running and maintenance of instruments/equipment’s.
• Provide troubleshooting supports as needed.
• Perform ad hoc tasks assigned by superior from time to time.

JOB REQUIREMENTS

• Preferably male.
• Strong organizational skills and detail orientation.
• Ability to work well as part of a team.
• A positive attitude and professional appearance and manner.
• Good oral and written communication skills (English & BM) (e.g. report writing and presentation).
• Team player mindset with communication & collaboration skills.
• Meticulous and pays attention to details.
• Independent and able to work with minimal supervision.
• Must have valid driver’s license with clean driving record.
• Must be able to travel.
• No work experience required (fresh graduates are welcome), but working experience in food industry before is an advantage.

**Good Remuneration Package (Benefits)
**Yearly Performance Reward & Increment
**Positive working environment

Interested candidates, please submit your latest resume to hr.psfood@gmail.com 
@ Call 011-26725003. Only shortlisted candidates will be notified. 

Perks & Benefits

• Annual leave
• Medical

JOB DESCRIPTION

• Ensures the compliance to ISO 9001, ISO 13485, Good Distribution Practice for Medical Device (GDPMD) standards and any other relevant regulatory standards at all times.
• In charge of prepare, review, implement, and maintain the ISO 9001 and ISO 13485 quality management system, as well as the GDPMD regulatory compliance system.
• Part of Risk Management Team & Post Marketing Surveillance Team.
• Evaluates audit findings and implements appropriate corrective actions. Investigates, plans and monitors the corrective and preventive action plan.
• Handles all internal audit and external audits, customer and regulatory audit needed by Company.
• Ensures ongoing compliance and up-to-date with quality standards and industry regulatory requirements.
• Performs random testing and inspection for incoming stocksand finished products. Collects, compiles, and analyses statistical quality data.
• Liaises with the external parties including government body and certification body on matters relating to the Malaysian medical device regulatory requirements.
• Assists superior to ensures validity and on-time renewal of ISO certifications, GDPMD certifications and CE marking with the relevant Authorities.
• Prepares reports to communicate outcomes of quality activities. Investigates customer complaints and internal non-conformances of materials and finished products.
• Assists superior in identifying and planning necessary trainings for the personnel involved in the supply chain activities/operations and period the training to satisfy these needs.
• Carries out other tasks or projects being assigned by the Management from time to time.

JOB REQUIREMENT

• Preferably a Bachelor’s Degree / Post Graduate in Pharmacy, Biomedical Science, Medical Science, Engineering or any other related studies.
• Working experience in QA/QC is an added advantage.
• Knowledgeable in ISO 9001, ISO 13485 and GDPMD is an added advantage.
• Good command in English and Bahasa Malaysia both in written and spoken.
• Positive working attitude and result-oriented person.
• Team player and also able to work independently with minimum supervision.
• Healthy and self-motivated person.

Benefits & Others

• Medical
• Bonus
• Miscellaneous Allowance