539 Product Testing jobs in Malaysia

Develop test programs on RF tester platforms.

Job Description

In your new role you will:

1. Develop test programs on RF tester platforms.
2. Develop, modify, optimize, and buy-off Automatic Test Equipment, Load/DUT boards, adapters & sockets, handlers, and temperature conditioning systems. Resolve related issues.
3. Develop new methods and processes to optimize quality, efficiency, and effectiveness of reliability qualification of products, technology, materials, and process changes.
4. Implement equipment and process adaptations according to new requirements from roadmaps. Be a work package member for the project team and deliver know-how to the Engineering sustaining team.
5. Plan and manage technical feasibility checks on new reliability projects and provide feedback to clients and lab logistics planners.
6. Coordinate internally with Operation and Engineering sustaining teams to prioritize and achieve timelines, including milestones and deadlines for reliability.
7. Plan, carry out, and liaise internally with Operation and Engineering sustaining teams on test package releases, assignments, and test-related issues.
8. Establish documentation for new equipment and processes, such as work instructions, machine operating instructions (MOI), specifications, and OJTI.
9. Participate in continuous improvement projects, productivity initiatives, problem solving using 8D methodology, workshops, paper presentations, and departmental events.

Your Profile

You are best equipped for this task if you have:

1. Bachelor’s Degree in Engineering (Electrical/Electronics or equivalent). Minimum 3 years of related experience in semiconductor electrical testing is preferred (experience in electrical testing, working principles of electrical test equipment, or stress equipment is an advantage).
2. Knowledge of electrical testers or handlers for RF products.
3. Knowledge of automatic data transfer from testers to databases, tester data file formats, and drift analysis.
4. Knowledge of working principles, troubleshooting, diagnostic/test program debugging, interpretation of schematics/electronic circuitry, and basic repair of automatic test equipment.
5. Programming skills in C++, Visual Studio, Arduino, and embedded systems.
6. Good analytical and problem-solving skills.
7. Good communication and interpersonal skills.

#WeAreIn for driving decarbonization and digitalization.

As a global leader in semiconductor solutions for power systems and IoT, Infineon enables solutions for green energy, mobility, and smart IoT. We drive innovation and customer success, caring for our people and empowering them to reach goals. Join us in making life easier, safer, and greener.

We embrace diversity and inclusion, welcoming everyone for who they are. Our environment is based on trust, openness, respect, and tolerance. We are committed to providing equal opportunities, basing recruiting decisions on experience and skills.

Job responsibilities:

Responsible for the operational aspects of all analytical testing within the QC Laboratory.

• Lead, coach and develop QC personnel (analysts and scientists) to ensuring that analytical testing (chemical, physical and microbiological) and data review is performed in a reliable and timely manner to support production operations with adherence to Standard Operating Procedures (SOP).
• Ensure that the quality systems and practices in the laboratory comply with Good Laboratory Practices (GLP), Good Documentation Practices (GDP), current Good Manufacturing Practices (cGMP) and Quality Management Standards (QMS).
• Develop, optimize, implement analytical methods and working procedures for characterization, release, and stability testing of viral vector gene therapy products.
• Develop the organisation's quality testing policy in alignment with regulatory standards.
• Lead and perform lab method validation, transfers of analytical methods from other collaborators/clients, protocol harmonization and optimization from R&D to Production.
• Lead development and qualification of new and/or improved assays and characterization of viral vector products using molecular, biophysical, and other analytical assays.
• Conduct, review or approve laboratory investigations and ensure all follow up actions are completed. Make decisions based on scientific and logical reasoning.
• Compile data, generate reports and perform computations using data analysis software, spreadsheets, graphing, and curve fitting software.
• Align with MSAT, Quality and Production teams on phase appropriate analytical methods and strategies for in-process and QC release testing.
• Collaborate with team members to identify and evaluate assay improvements with the goal of optimizing the current rAAV production process.
• Train fellow colleagues on written procedures pertaining to equipment operation, test methods and general laboratory operations.
• Draft and edit lab protocols, standard operating procedures, sampling plans, technical documents, and release testing records for regulatory or tech transfer purposes.
• Ensure real time documentation, maintain data integrity and appropriate traceability as per quality system.

Qualifications:

• PhD in Cell and Molecular Biology, Immunology, Biotechnology, Biochemistry, Microbiology or related fields with 6+ years of relevant experience, or Master/Bachelor’s degree with a minimum of 8+ years of relevant industry experience in a cGMP setup.
• Prior experience performing viral genome titre, infectivity, potency, host cell protein, and host cell DNA assays are required.
• Extensive hands-on experience with development of analytical techniques for characterization and analysis of viral vectors is desired, including: Flow cytometry, qPCR, dPCR, ELISA, SDS-PAGE, Western blot, mycoplasma, sterility, endotoxins.
• Experience in the design and optimization of cell-based potency and infectivity assays.
• Must have experience facing regulatory, Client & external cGMP audits.
• Must have the knowledge of contract testing labs management and its certification.
• Strong knowledge of Regulatory and Pharmacopeia requirements for viral vector gene therapy products.
• Experience with processes involved in viral vector GMP manufacturing, characterization and QC release testing.
• A highly motivated team player with an ability to be productive and a willingness to lead and learn in a fluid, fast-paced and environment are essential.
• Excellent organizational and collaborative skills.

Direct message the job poster from ASSB Toyota Malaysia (Assembly Services Sdn Bhd)

Job Summary:

To coordinate activities for process compliance at manufacturing.

Operational:

• Prepare the ASSB plant for COP audits by ensuring all documentation, processes, and facilities meet compliance standards.
• Facilitate the deployment of COP-related information and updates to relevant departments to ensure alignment and awareness.
• Develop, review, and maintain internal procedures related to ASSB operations to support continuous compliance and improvement.
• Collaborate with cross-functional teams to address audit findings and implement corrective actions.
• Monitor ongoing compliance activities and ensure adherence to regulatory and company standards.
• Provide training and guidance to staff on internal procedures and audit requirements.

Job Requirements:

• Minimum of a Bachelor's Degree in Engineering or Manufacturing-related field, with a CGPA of 3.5 or above.
• Excellent proficiency in English communication, both written and verbal.
• Demonstrated experience in Process Auditing, with strong analytical thinking and problem-solving abilities.
• Proficiency in interpreting technical documents and preparing comprehensive reports.
• Effective communication skills to liaise with cross-functional teams and stakeholders.
• A minimum of 1 year of relevant experience in manufacturing or auditing environments.

• Seniority level Executive

• Employment type Contract

• Job function Quality Assurance and Manufacturing
• Industries Manufacturing

Referrals increase your chances of interviewing at ASSB Toyota Malaysia (Assembly Services Sdn Bhd) by 2x

Petaling Jaya, Selangor, Malaysia 1 day ago

Federal Territory of Kuala Lumpur, Malaysia 3 weeks ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 4 hours ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 month ago

Bukit Jalil, Federal Territory of Kuala Lumpur, Malaysia 2 months ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 week ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 week ago

Petaling Jaya, Selangor, Malaysia 3 days ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 2 weeks ago

Bukit Jalil, Federal Territory of Kuala Lumpur, Malaysia 1 month ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 month ago

WP. Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 week ago

Petaling Jaya, Selangor, Malaysia 1 day ago

Federal Territory of Kuala Lumpur, Malaysia 2 days ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 6 months ago

Petaling Jaya, Selangor, Malaysia 1 month ago

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia MYR2,800.00-MYR4,500.00 1 week ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable, and more connected world.

Supervise and control all incoming material, process, outgoing product quality, and drive continuous quality improvement.

People Management

Lead the quality control and quality assurance department, including failure analysis, SI testing, allocating and balancing work across direct reports; reviewing and providing timely performance feedback; mentoring, developing, and motivating team members; resolving tough people/functional issues; submitting manpower applications; interviewing candidates; and providing feedback to achieve performance targets, retain, and develop key talent. Ensure compliance with requirements and optimize process capabilities to ensure product quality, customer service, and cost-effectiveness. Lead initiatives to reduce DPPM, customer complaints, returned values, and quality costs.

Procedure & Policy

Check department policies, initiate policy changes, prepare related materials, and monitor policy execution to ensure compliance with corporate standards.

Budgeting

Coordinate with functional teams to prepare annual department budgets and work plans, compare expenses monthly, analyze results, and report to the department director. Develop quality plans with management to set annual goals, build implementation strategies, and monitor progress. Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.

Quality Control

Lead incoming material and supplier management, facilitate quality improvements, monitor operations for compliance with instructions, identify risks, and ensure proper resource allocation. Oversee outgoing product quality control, monitor training, and ensure effective application of quality tools.

Customer Complaint Management

Analyze customer complaints, organize monthly quality review meetings, negotiate with customers, conduct site visits, and monitor follow-up actions to resolve issues cost-effectively and improve satisfaction.

Quality Issue Resolution

Guide engineers to resolve on-site quality issues, assist in cross-functional problem-solving, and lead supplier-related defect resolution and improvement initiatives.

Quality Improvement

Initiate and monitor monthly cross-audits, review Six Sigma improvements, and oversee daily quality improvement activities to ensure continuous enhancement of quality standards.

Reporting

Prepare operational performance reports, analyze quality data, and report findings to management and relevant stakeholders.

• Bachelor's degree in process engineering or quality-related field
• 8-10 years of experience in quality management, including 5 years in people management

Location: Prai, Penang, MY, 13600

Travel: 10% to 25%

Requisition ID: 138724

Function: Quality

Job Segment: Supply Chain Manager, Quality Manager, Operations, Customer Service

Company Overview

Working at GE Aerospace means you are bringing your unique perspective, innovative spirit, drive, and curiosity to a collaborative and diverse team working to advance aerospace for future generations. If you have ideas, we will listen. Join us and see your ideas take flight!

Site Overview:

GE Aerospace Engine Services Malaysia (GEESM) in Subang plays a vital role in ensuring the safety and performance of aviation fleets every day. Established in 1997 as a Center of Excellence for CFM56 engines, GEESM has grown into a key hub of our global operations. It now services commercial aircraft engines, components, and accessories.

Employing more than 700 highly skilled local professionals and providing MRO services to more than 50 airlines worldwide, GEESM continues to exceed our customers’ expectations. With our technical expertise and pioneering spirit, we elevate the flying experience to new heights.

Role Overview:

• Lead & coordinate investigations on customer escapes, closing the communication loop with relevant customer contacts to update on Containment Actions, Root Cause Analysis, and Corrective and Preventive action plans, by providing a full Investigation Report.

• Coordinate with Quality team and relevant functional leaders to finalize/review Root Cause Analysis and Corrective and Preventive action plans. Monitor and drive closure of outstanding actions arising from various investigations & surveillance activities.

• Cell Quality focal for operational issues surrounding Cost of Quality, process FTY or process failures. Provide Quality guidance to approved personnel, shop processes and operations in assigned Cells.

• Conduct Competency Assessment for qualified candidates to be established as Certifying Staff or Approved Mechanic.

• Perform general and scheduled Surveillance of operations areas and processes.

• Lead process observations and improvement action. Initiate and coordinate pFMEA events and follow through with various stake holders on risks mitigation actions. Finalize process changes or improvement through a FAI event.

• Conduct Quality Trainings / Flow downs / Briefing as scheduled or arising from any Quality event.

• Review Regulatory Airworthiness Directives received from Technical Publication and attend or support AD Review Board. Update AD check list for Certifying Staff.

The Ideal Candidate:

• The ideal candidate is someone who is detail-oriented and committed to maintaining high-quality standards in their work. They should consistently meet deadlines and deliver results efficiently, even under pressure. Excellent communication and interpersonal skills are advantageous, along with a proven ability to lead and drive strategic initiatives.

Required Qualifications:

• Degree in Engineering/Operations Management or other related technical fields.

• Minimum 7 years’ experience in Quality or Engineering role in aviation, automotive, manufacturing or other relevant field.

• Trained/Certified or practical knowledge of RCCA, PFMEA/FAI procedures and discipline.

• In-depth technical knowledge of Aviation Regulations and quality practices.

• To be able to support Night Shift rotation as needed.

Preferred Qualifications:

• Green Belt Certified and practical knowledge of MSA/CpK

• Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan and execute programs. Established project management skills.

• Able to work independently and able to provide technical and quality guidance to Quality team members.

• Basic knowledge of MRO Operations and MRO SAP.

• Able to work independently with minimum supervision.

Whether we are manufacturing components for our engines, driving innovation in fuel and noise reduction, or unlocking new opportunities to grow and deliver more productivity, our GE Aerospace teams are dedicated and making a global impact. Join us and help move the aerospace industry forward.

Relocation Assistance Provided: No

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our diverse community of people, customers, patients, and the planet. We are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role:

The Quality Control (QC) Specialist promotes and integrates quality into every aspect of our BioReliance biologics safety testing business in Singapore. Your duties include supporting QC operations (environmental monitoring and release of critical raw materials), ensuring data integrity, and managing systems to ensure laboratory testing operations comply with scientific standards, GxP, and SOPs. You will ensure quarantine materials are received and released according to quality procedures. Developing and maintaining effective relationships with operational, support, and quality assurance teams is crucial for success in this role.

Who You Are:

• Graduate degree in life sciences, microbiology, or a related field
• At least 2-3 years of relevant experience
• Strong scientific expertise in microbiology
• Experience working in a QC materials release environment
• Pharmaceutical experience is preferred; other industry backgrounds will be considered
• Experience in a GLP/GMP regulated environment is highly desirable
• Focused on quality and safety with excellent planning and organizational skills
• Good communication and interpersonal skills, highly self-motivated, with initiative and drive

What We Offer: We value diverse backgrounds, perspectives, and experiences, which drive our innovation and excellence. We are committed to providing access and opportunities for growth at your own pace. Join us in fostering a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and join a team dedicated to Sparking Discovery and Elevating Humanity!

Join to apply for the Quality Control Executive role at Alpro Pharmacy Sdn Bhd

Join to apply for the Quality Control Executive role at Alpro Pharmacy Sdn Bhd

This range is provided by Alpro Pharmacy Sdn Bhd. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Job Responsibility

• Conduct routine quality control tests on raw materials, in-process samples, and finished milk powder products using approved methodologies and equipment.
• Perform regular inspections of production lines, ensuring adherence to quality standards and taking representative samples for analysis.
• Oversee the calibration and maintenance of quality control equipment to ensure accurate and reliable test results.
• Responsible for in-going and out-going inspection process.
• To monitor all non-conformance products, matter and liaise with related department for corrective action and preventive action.
• Implement quality control policies, procedures, and standards for inspection, assist in updating QC Manual.
• Troubleshoot manufacturing quality issues.
• To involve in performing internal and external audits to determine compliance to Food Safety / HACCP / GMP and identify areas for improvement.
• Record and maintain accurate data related to quality control tests and inspections.
• Analyze the data to identify trends or deviations that require attention.
• Adherence to hygiene and safety protocols in the quality control laboratory and during sampling procedures.
• Responsible for the Food Safety issues.
• Support ad-hoc tasks as and when required.
  
  

• A bachelor's degree in Food Science, Food Technology, Chemistry, or a related field is typically required.
• Must fluent in Mandarin as requires dealing with Mandarin speaking internal.
• Fresh graduates are welcome to apply
• Preferably good knowledge in GMP / HACCP / HALAL.
• Prior experience in quality control within the food or dairy industry, knowledge in milk powder manufacturing, is a plus.
• Ability to identify and address quality issues, investigate root causes, and implement corrective actions.
• Familiarity with laboratory equipment and techniques used in quality control testing.
  
  

• Career Development
• Medical
• Staff Meal
• Badminton Club

• Seniority level Entry level

• Employment type Full-time

• Job function Other
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Alpro Pharmacy Sdn Bhd by 2x

Get notified about new Quality Control Executive jobs in Seremban, Negri Sembilan, Malaysia .

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

JOB DESCRIPTION

• Ensure compliance with major international quality programs like ISO 9001, API 15LR & 15HR, and various certification societies (DNV, Lloyds, ABS, BV, NSF, FM, etc.)
• Conduct and manage Internal and External Audits.
• Oversee customer inspection activities and maintain good relationships with clients.
• Establish procedures for quality control and perform daily quality inspections to identify defective products, preventing their shipment to customers.
• Ensure the quality system complies with all relevant standards and customer specifications.
• Develop and maintain the quality system in accordance with the requirements of each certification body, serving as an important tool for marketing and bid submissions.

JOB REQUIREMENTS

• Bachelor's degree in engineering or equivalent.
• Knowledge of ISO 9001 standards.
• Preferably 1 to 2 years of experience in QA and QC.
• Fresh graduates or candidates with no prior work experience are encouraged to apply.