588 Engineering jobs

Salary Range :  15,000.00 - 18,000.00

Salary Range : 6,000.00 - 8,000.00

Key Responsibilities/Accountabilities: Perform field walk downs/inspections to review the work for conformance with the design drawings, specifications, applicable codes/standards, and company policies/procedures Coordinates the walk-down at the time of Turnover Package Release from Construction to Commissioning and then again just prior to the Turnover from Commissioning to the Client Assists in the identification of exceptions to the Turnover Package Assembles the required documentation into Turnover Packages that are transmitted to the Client for acceptance Turnover Coordinators will be involved with the assembly of Turnover Packages Must be knowledgeable to manage schedule and document all Preventive Maintenance activities To manage System Turnover Package Construction Completion Paperwork Coordinates and manages system punch list Leads a System Turnover Meeting with Construction Personnel to identify upcoming construction completion needs and status progress Review/interpret engineering drawings, specifications, and other design documents

Job Description: Product drawing review and provide DFM input Define production process flow and tooling list Engineering evaluation (Customer & Internal) Lead and publish process FMEA Perform Failure Analysis and provide corrective action Process / Yield monitoring and Improvement Lead the FA audit / new program process audit to meet customer requirement Liaise with group of companies and customer about new program transfer

Responsibilities: To carry out processing work according to ISO 9002 procedures To identify all raw material used in for all the process To ensure quality product produced and cleanliness of working place To ensure the quality finished product during flaking eg. Size and colour of theproduct To ensure the packing label according to the sales order acceptance

Position Title : Senior SQE Engineer - Mechanical Commodity Technical Skills :  SQE with PCB experience Salary Range : 3,500.00 - 6,700.00 Job Responsibility Review the mechanical parts (Catalog and Build To Print) 2D drawing and establish effective Incoming Inspection Instruction and critical to function dimension measurement. include train the incoming inspectors to Train and ensure Incoming inspector understand and execute the inspection plan with competence. Analyse and resolve problems related to material quality affecting production line and drive suppliers on root-cause and corrective action. (SCAR) Perform supplier performance audit, process verification, audit effectiveness of corrective and preventive action. Work with supplier and material buyer/internal CFT team to dispose the materials inventory in MRB and RTV areas. Define supplier STS/Skip Lot inspection program/process. Conduct periodic key supplier performance monitoring and review, proactively follow-up and work with supplier for timely and effective issues closure to achieve respective customer accounts Key Suppliers' DPPM Quality Targets. Work in conjunction with Regional CM/GCE from time-to-time for new supplier survey, qualification and bring-up based on business localization needs, with main focus on PCB, mechanical and packaging suppliers

Maintain injection machine and auxiliary equipment for  production use. Verified & execute all checklist. Ensure 5S to meet requirement. Offer salary : RM3,800 – RM4,500. Working Pattern: 5 days (8:00am – 6:00pm) Location: Larkin

JD for Validation Deputy Lead Sl. No. Job Responsibilities 1 Overall responsible for review and approval of protocols, ensuring process validations, cleaning validations, hold time studies, transport validations and product related validations are planned, executed as per laid down procedures and schedules, review and approval of reports, implementation of recommendations. 2 Strategic planning and scheduling of activities within team members of Quality Assurance and coordination with cross functional teams to ensure smooth, cGMP and quality compliant manufacturing process. 3 Responsible for timely closure of summary reports 4 Responsible for Review of Validation Master plan. 5 Responsible for continuous process validation 6 Responsible to lead internal and external audits. The coordination involves liaising with all Head of the Departments during the audits for furnishing the requirements as requested by the auditor(s), to be with the auditor during the audit rounds and meeting, document review as deemed necessary and intimated by reporting authority. Responsible to provide appropriate technical responses during the audit. This also includes convening internal meetings periodically before the audit to review the preparedness as well as meetings during the audit days to understand the possible issues raised during the audit in order to identify and implement appropriate action plan to be presented to the auditor. Identifying, monitoring compliance to CAPA identified as an outcome of audit observations. 7 Responsible to nurture a well-trained and motivated team as well as establish and maintain a positive community relationship with the peers, superiors and subordinates. 8 Responsible for allocating key performance areas / quality goals for the team members in validation department for continuous quality improvement. 9 Involve in continuous improvement plans by effective quality gap analysis programs, from the learnings obtained as part of internal and external audits as well as with changes in the regulatory expectations. 10 To actively participate QMS meetings with peers and superiors. Update and discuss issues, if any with the higher management in order to find an effective solution keeping product quality, safety and efficacy as the top priority. 11 To approve the documents and records prepared for the applicable section as and when required. 12 Trouble shooting and root cause analysis with providing effective corrective actions and preventive actions for all non-conformances / out of specifications / out of trends / complaints / product recalls, etc. 13 Coordinate with India team for harmonized Quality Assurance Procedures 14 Ensure that Validation activities are carried out using approved materials and procedures, trained / qualified / certified people, calibrated instruments, facility etc. 15 Ensure that CPP and CQAs are trended and if any out of trend is investigated as per the approved procedures.

Job Description: 1. Study insert / electrode drawing together with mould maker if necessary. 2. Do a rough check on the length, width and height. 3. Set work piece onto the machine. Use vice or clamp for metal insert. Use Erowa System for electrode. 4. Set cutter according to the CNC & EDM Electrode Setup Sheet provided by programmer. 5. Transfer NC program created by programmer into machine. 6. Perform CNC Milling process. 7. Perform measurement using dial test indicator / micrometer or vernier caliper on a few critical dimension. 8. Place the completed work piece on the outgoing rack.

Job Description: 1. Study inserts drawing and discuss with mold maker if necessary. 2. Study the CNC & EDM Electrode Setup Sheet to determine the electrode used. 3. Ensure that the work piece nos. is tally with the insert drawing and CNC & EDM Electrode Setup Sheet. 4. Set work piece onto machine. 5. Check electrode using the Erowa Pre-setter. 6. Transfer EDM data to machine. 7. Set machine condition and do a dry run. 8. Perform EDM operation. 9. Perform measurement using dial test indicator / micrometer or vernier caliper on a few critical dimension. 10. Place the completed work piece on the outgoing rack.

• Liaise with customer and internal team on quality issues. • Able to read and write in Chinese. • Set up interdepartmental standard to allow smooth operation. • Perform root Cause analysis on quality issues. • Involved on DFM & APQP during project development stage. • Good knowledge in 8D Analysis. • Offer salary : RM4,500 – RM6,500. • Working Pattern: 5 days (8:00am – 6:00pm) • Location: Larkin

RESPONSIBILITY Responsible for Surface Treatment/ washing line operation, quality monitoring, Electroplating Chemicals, Production Planning & Preventive Maintenance/ Breakdown Analysis. Implement and oversee performance metrics, including productivity, efficiency and utilization. Initiate, implement, and report on cost reduction strategies and productivity improvement projects. Manages department priorities and ensures that work procedures, quality standards and on time delivery schedules are met. Evaluates production related issues, facilitates root cause analysis and provides effective solutions and standardization to increase productivity to help meet Oversees employee scheduling and overtime requirements based on customer, business and production needs. Manages overall attendance and performance standards for assigned employees. Develops and implements operating methods and training procedures designed to eliminate operating problems and improve product quality. Working Hours: Working Schedule i. Under Probation       - 5.5 working days    Mon~Fri : 8.15am to 5.30pm                                                                       Sat           : 8.00am to 12.00pm i. After Confirmation - 5 working days    Mon~Fri : 8.15am to 6.00pm 

Job Description: Study insert / electrode drawing together with mould maker if necessary. Ensure that the work piece nos. is tally with the insert drawing. Create a program as according to drawing. Set work piece / electrode onto machine. Perform wire cut operation. Perform measurement using dial test indicator / micrometer or vernier caliper on a few critical dimension. Place the completed work piece on the outgoing rack.  

RESPONSIBILITIES : Designing new motor / IO / Interface boards, PCB integration and schematics Electrical hardware design of application and development projects (schematics, panel layouts, cable run outs, network topologies, cable designations, I/O overviews, terminal references etc.) Motor regulations, power/electrical & pneumatics management system and provide technical solutions.For new products, identify requirements and technical constraints, source for material, test, characterise and optimise their performance.Identify EOL hardware products, source for replacement, test, characterize and optimize performance.

Job Responsibility • Lead on engineering for Cardiac Science Medical (AED) & Hitachi Healthcare (Ultrasound) projects • Utilize customer package and create the process flow, documented in (Work Instruction) and apply the process to production manufacturing. • Lead to perform NPI and FA Report for new models or products. • Design/ improve stencil and wave pallet for production. • Design/ improve jigs and fixtures for production. Cycle time & line balancing study to improve production output & productivity. • Control and maintain BOM, ECO, AVL and MPN in system (ODC, Citrix, Matrix & ETQ). • Process control for SMT PCBA assembly for medical equipment/ product. • Provide DFM (Design for Manufacturability) inputs to Design Team during NPIs. • Continuous communication with customer to get better understanding on their requirements. • Transfer necessary Product Knowledge from customer to internal parties i.e. Trainers, Process Engineers, etc. • Lead in equipment validation protocol & reports (IQ, OQ and PQ) for new line setup & new product validation. • Involvement in kaizen & lean six sigma activities to re-layout box build line by separating sub assy line from main assy process. Using the same operator for both sub & main assy line. Re-train the operators & reduce headcount. • Lead engineering activities to establish containment action and root-cause in the event of Product Quality Issues, Low Yields, Quality Reject, Product failures, etc. • Trouble-shoot, analyze and resolve Process & Product related failures

JD for IPQA Deputy Lead Sl. No. Job Responsibilities 1 Responsible for In process – QA and lead a team of IPQA professionals for ensuring total compliance of quality assurance functions of Drug Product Manufacturing Block as follows. 2 Responsible for issuance, control, review, reconciliation and retrieval of GMP documents like Batch Manufacturing, Packing, Dispatch Records, Formats, and Logs. 3 Responsible for monitoring quality assurance of manufacturing operations to ensure that those are carried out as per laid down instructions in batch documents, Standard Operating Procedures and related GMP documents. Responsible to ensure that highest quality and cGMP standards, data integrity requirements are followed. Should have prior experience in working with sterile aseptic formulation. 4 Strategic planning and scheduling of activities within team members of In process Quality Assurance and coordination with cross functional teams to ensure smooth, cGMP and quality compliant manufacturing process at shop floor. 5 Responsible for batch document and associated documents review, batch release 6 Allocating job responsibilities to the IPQA team members, ensuring effective training, mentoring, work delegation, monitoring team members to execute effective QA function. 7 Responsible to lead internal and external audits. 8 Responsible to nurture a well-trained and motivated team as well as establish and maintain a positive community relationship with the peers, superiors and subordinates. 9 Responsible for allocating key performance areas / quality goals for the team members for continuous quality improvement and training the IPQA team. 10 Involve in continuous improvement plans by effective quality gap analysis programs, from the learnings obtained as part of internal and external audits as well as with changes in the regulatory expectations. 11 Responsible for ensuring GMP rounds and reporting observations as per procedure. Inculcating quality culture within team and area of work in cross functional team.Responsible for ensuring timely reporting deviations, approve immediate action plan, assess impact, complete investigations and approve, monitor CAPA. 12 To approve the documents and records prepared for the applicable section as and when required. 13 Change Management and Deviation Management Panels which involves assessing the changes and deviations with the panel members, responsible for assessing the impact of the change and deviation as well as draw out an effective action plan for change managements and corrective action preventive action plans to prevent the recurrence of deviations. 14 Responsible for trending and compilation and approval of Annual Product Reviews as per defined procedures and ensure that media fill is carried out as per the schedule. 15 Ensure that manufacturing operations are executed using approved materials and procedures, trained / qualified / certified people, validated processes, calibrated instruments, qualified and validated equipment’s, facility.

Design the Analog circuit in power management products. Design includes low & high voltage CMOS circuit, SPICE simulation, IC design and evaluation. Perform system level and block level IC design activities including circuit architecture definition, circuit design, schematic capture, circuit and sub-system simulation, chip floor-planning, and layout planning. Create clear documentation of design and product development activities to ensure high quality designs and to support dissemination of important design information to cross-functional teams Expect to do measurement on IC in the lab, conducts experimental test and evaluates results.

Job Description Support the E RP system   for day-to-day operations and new requirements. To test and deploy ERP system for various companies within the Group. To support end users on technical issues & requests. Ensure any new operational requirements are adopted and run efficiently.

Job Scope & responsibilities implement and control the production schedule according to production plan obtain optimum production and utilization of human resources, machines, and equipment. recruit employees, assign, direct, and evaluate their work, provide training and oversee the development and maintenance of staff competence, discharge staff, and resolve personnel grievances coach, counsel and discipline employees as necessary, including performance management. Develop, motivate and coach team members; act as an employee advocate and interview potential new hires. interpret company policies to workers and enforces safety and environmental regulations communicate and demonstrate the production best practices, ethics, values and philosophy such that these cultural attributes are incorporated throughout the organization work out and implement standard operating procedures for production operations and ensure that standard operating procedures are adhered to ensure implementation and adherence to health and safety procedures monitor quality standards of products, implement and enforce quality control and tracking programs to meet quality objectives analyse production and quality control to detect and correct problems. Keep management abreast of progress, developments pending problems good understanding of CNC Manufacturing Methods & cutting tools, very good knowledge of engineering drawing to manufacturing engineering drawing interpretation. good knowledge of GD&T interpretation & self-review capability very good inspection methods & gauging concepts selection and usage determine and implement improvements to the production process maintain all IATF16949 requirements that relate to CNC machining/processing. perform special projects as required.

Salary Range 14,000.00 - 20,000.00 For job description, click the following link: /kcfinder/upload/files/PAD.pdf