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100+ Validation Engineer Jobs - September 2026 - Urgent Hiring
Paparan 179 hasil carian kerja kosong untuk
"validation engineer"
Jangan lepaskan peluang untuk kerja Validation Engineer terkini!
Urus Pemberitahuan
Undisclosed
Singapore
- Develop risk assessment, system impact assessments, validation plans, protocols and reports that support the qualification and validation of systems.
- Develop and execute Commissioning and validation Protocols for Bioprocess Equipment’s.
- Develop and execute Commissioning and validation of Clean Rooms, HVAC systems, EMS and BMS Systems, Clean utilities and black utilities system. ...
Posted
24 days ago
Undisclosed
KL City
- Develop risk assessment, system impact assessments, validation plans, protocols and reports that support the qualification and validation of systems.
- Develop and execute Commissioning and validation Protocols for Bioprocess Equipment’s.
- Develop and execute Commissioning and validation of Clean Rooms, HVAC systems, EMS and BMS Systems, Clean utilities and black utilities system. ...
Posted
24 days ago
Undisclosed
Tuas
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance. ...
Posted
25 days ago
Undisclosed
Singapore
- Lead transfer of wafer sort (CP), burn-in, and final test (FT) solutions from R&D into manufacturing.
- Debug, qualify, release and sustain ATE test programs for volume production.
- Support silicon bring-up, characterization, correlation, and production validation. ...
Posted
a month ago
Undisclosed
Singapore
- IC Test Development & Manufacturing Release
- Lead transfer of wafer sort (CP), burn-in, and final test (FT) solutions from R&D into manufacturing.
- Debug, qualify, release and sustain ATE test programs for volume production. ...
Posted
a month ago
SGD5,000 - SGD7,000 Sebulan
Singapore
- Plan, execute, and manage commissioning, qualification, and validation (CQV) activities for pharmaceutical/biotech manufacturing facilities, utilities, and process equipment.
- Develop and review CQV protocols (IQ/OQ/PQ) and reports in compliance with GMP, GAMP 5, and company procedures.
- Coordinate with engineering, project, and quality teams to ensure timely CQV execution. ...
Posted
a month ago
Undisclosed
Singapore
- Develop and optimize capillary underfill and advanced dispensing processes for semiconductor packages.
- Establish process windows for underfill dispense, flow, cure, and post-cure operations.
- Evaluate new underfill materials and dispensing technologies. ...
Posted
a month ago
Undisclosed
Ang Mo Kio
- Develop and optimize capillary underfill and advanced dispensing processes for semiconductor packages.
- Establish process windows for underfill dispense, flow, cure, and post-cure operations.
- Evaluate new underfill materials and dispensing technologies. ...
Posted
a month ago
SGD5,000 - SGD6,500 Sebulan
Singapore
- Lab Test Engineer - European MNC 1 year contract renewable with benefits Salary: $6500 max 5 days work week (Mon-Fri) Location: Gul
- Job Scope: Engineer - The Test Engineer is responsible for planning, coordinating, and executing laboratory testing activities to verify material performance, quality and compliance with applicable standards and customer requirements. The role oversees test preparation, test execution, data analysis, and reporting while ensuring adherence to safety, quality, and regulatory requirements.
- Key Responsibilities for both positions: ...
Posted
a month ago
KINGSFORCE MANAGEMENT SERVICES PTE LTD
SGD7,000 - SGD9,000 Sebulan
Bukit Merah
- Plan, execute and manage DeltaV Computer System Validation (CSV) lifecycle activities.
- Prepare, review and execute validation documentation including URS, FS, DS, Risk Assessments, Traceability Matrix, IQ, OQ, PQ protocols and Validation Reports.
- Perform qualification of DeltaV hardware infrastructure, including Professional Plus, Application & Operator Stations, M-Series/S-Series/PK Controllers, CIOCs, I/O systems, network components and virtual environments. ...
Posted
a month ago
Undisclosed
Singapore
- CQV Engineer
- Pharmaceutical & Biopharmaceutical Projects
- Singapore ...
Posted
a month ago
SGD4,000 - SGD6,000 Sebulan
Downtown Core
- Responsible for developing, testing, and improving premium connections and OCTG products during the development phase, ensuring they meet rigorous industry standards.
- Coordinating with customers and providing technical advice/training on the range of OCTG products, often involving rig field services.
- Executing validation tests (often in specialized, high-pressure, or high-temperature environments) to verify the integrity and performance of new designs. ...
Posted
a month ago
Undisclosed
- Collaborates with Customers throughout all stages of validation projects to establish cycle process parameters in compliance with ISO 11135. Coordinates validation cycles and reviews and approves validation protocols, reports, and CSPs within agreed timelines.
- Liaises with quality, operations, planning, laboratory, and customer service teams to coordinate and complete customer validation projects.
- Prepares for, supports, and facilitates internal and external audits by Customers, notified bodies, and Regulatory Agencies. Implements corrective actions for assigned audit findings. ...
Posted
3 months ago
Undisclosed
KL City
- Ensure continuous, compliant operation of GxP-relevant computer systems under Managed Services.
- Lead and coordinate validation and re-validation efforts, maintaining audit-ready lifecycle documentation.
- Support change management, upgrades, migrations, and decommissioning while preserving validation state. ...
Posted
5 days ago
Undisclosed
Malaysia
- Execute system-level validation and regression testing for post-silicon platforms
- Validate system configurations and ensure stability from firmware/BIOS to OS levels
- Perform manual and automated regression testing ...
Posted
5 days ago
Undisclosed
Singapore
- Verification of the solution to confirm the system’s compliance to the Functional Baseline requirements
- Validation of the solution to confirm the system’s fitness for purpose in accordance with the Operational Concepts.
- Contribute in System Requirement Analysis activities to confirm requirements are testable and allocate a Verification Method(s) and Verification Phase(s), documented in the Verification Cross Reference Matrix (VCRM). ...
Posted
6 days ago
Undisclosed
- Responsibilities
- Lead cross-functional strategic initiatives focused on cost reduction, yield improvement, quality enhancement, and operational excellence.
- Qualifications ...
Posted
7 days ago
Undisclosed
Singapore
- Work closely with the client's site CSV Lead and RoviSys project teams to generate CSV deliverables for product software and IT infrastructure during automation project execution, for systems supported by RoviSys.
- Collaborate with client IT/OT, Quality, MSAT/Automation, Manufacturing, and Quality Control teams on assessments such as System Impact Assessment, Criticality Assessment, Data Integrity Assessment, and Audit Trail Assessment.
- Manage and maintain lifecycle documentation for validated systems. ...
Posted
7 days ago
Undisclosed
- Focused on memory sub-system validation
- Provide DDR technical leadership in the development of new test & validation
- Develop and execute system level memory sub-system validation test plans across products ...
Posted
7 days ago
BST CONSULTANTS PTE. LTD.
SGD3,700 - SGD3,700 Sebulan
Singapore
- A motivated and detail-oriented Entry-Level Project Engineer to join our team in Singapore. In this role, you will have the unique opportunity to be trained and mentored in the end-to-end process of UNECE R155 (Cybersecurity) and R156 (Software Update) vehicle type approval projects. This is an excellent entry point into the high-growth field of automotive cybersecurity compliance.
Posted
9 days ago
RRECRUITER PTE. LTD.
Hyde Engineering + Consulting
Undisclosed
Tuas
- Position: CIP Engineer (Clean-in-Place) - Engineering & CQV Location: Singapore The CIP Engineer will be responsible for the design review, commissioning, qualification, validation, optimization, and lifecycle management of Clean-in-Place (CIP) systems within pharmaceutical, biopharmaceutical, vaccine, API, and sterile manufacturing facilities. The role requires a combination of engineering expertise and CQV experience to ensure that CIP systems are designed, installed, tested, and operated in compliance with cGMP, FDA, EU GMP Annex 1, ISPE, and company quality standards. The successful candidate will support project execution from Concept Design through Operational Qualification (OQ), Performance Qualification (PQ), and Continued Process Verification (CPV) Responsibilities Engineering Responsibilities • Review and support the design of CIP systems for pharmaceutical and biopharmaceutical manufacturing facilities. • Evaluate P&IDs, process flow diagrams, equipment layouts, and automation sequences related to CIP systems. • Verify CIP system design against process requirements, product contact surfaces, cleanability, and regulatory expectations. • Support FAT, SAT, and vendor package reviews. • Conduct engineering assessments for: ? CIP skids ? Process vessels and tanks ? Bioreactors and fermenters ? Transfer lines and manifolds ? Fill-finish equipment ? WFI and purified water interfaces • Perform hydraulic and process evaluations to ensure adequate flow, velocity, turbulence, and coverage. • Identify opportunities for CIP cycle optimization to reduce water, chemical consumption, and cycle times. • Support troubleshooting of CIP failures and cleaning effectiveness issues. CQV Responsibilities • Develop and execute Commissioning and Qualification activities for CIP systems. • Prepare and execute: ? Commissioning Test Plans (CTPs) ? Installation Qualification (IQ) ? Operational Qualification (OQ) ? Performance Qualification (PQ) ? Validation Protocols ? Validation Summary Reports (VSRs) • Support traceability matrix development and management. • Coordinate punch-list resolution and CQV documentation closure. Cleaning Validation Responsibilities • Support cleaning validation strategy development. • Define worst-case product selection and cleaning validation matrices. • Coordinate sampling activities including: ? Swab sampling ? Rinse sampling • Analyze cleaning validation data and support final reports. • Collaborate with Manufacturing, QA, QC, and Validation teams during execution. Automation & Controls Support • Review CIP automation logic and sequence of operations. Qualifications and other requirements Education • Bachelor's Degree in: ? Chemical Engineering ? Mechanical Engineering ? Bioprocess Engineering ? Process Engineering ? Pharmaceutical Engineering ? Related Engineering Discipline Experience • 5-10 years of experience in pharmaceutical or biopharmaceutical engineering and CQV. • Minimum 3 years of direct CIP engineering and qualification experience. • Experience supporting GMP regulated facilities including: ? Biologics ? Vaccines ? Sterile Manufacturing ? OSD ? API Facilities • Proven experience executing CQV protocols and validation documentation. Technical Skills • CIP system design and operation • Cleaning validation principles • Commissioning and Qualification • GMP regulations • P&ID review • FAT/SAT execution • Technical report writing Key Competencies • Technical Leadership • Problem Solving • Project Execution • Cross-Functional Collaboration • Risk Assessment • Documentation Excellence • Communication and Stakeholder Management • Attention to Detail • Continuous Improvement Mindset Success Measures • The CIP Engineer will be considered successful when: ? CIP systems are delivered, commissioned, and qualified on schedule. ? Cleaning validation programs pass regulatory and internal quality audits. ? CQV documentation is completed error-free and on time. • CIP cycle performance meets defined operational and process requirements
Posted
13 days ago
Undisclosed
Singapore
- Own PCIe PHY validation strategy, plans, coverage, and execution from pre-silicon through production.
- Lead hands-on electrical characterization of TX/RX, reference clock, reset, equalization, lane margining, jitter, and channel performance.
- Perform PCIe bring-up and debug using LTSSM analysis, register dumps, firmware logs, protocol traces, and electrical measurements. ...
Posted
19 days ago
Undisclosed
Singapore
- Be eligible for Security Clearance from the Singapore Ministry of Home Affairs (CAT2)
Posted
8 days ago
Undisclosed
Singapore
- Design and maintain offline evaluation suites (golden sets, regression packs, adversarial/safety probes) and the continuous-evaluation scoring pipeline across archetypes.
- Conduct operability gate reviews: assess evidence packs, reproduce evaluation results, and recommend go/no-go with documented findings.
- Own the model-update regression pack methodology and adjudicate regression runs against archived baselines with AIML Operations team. ...
Posted
21 days ago
GOAL SETTERZ BUSINESS SOLUTIONS PTE. LTD.
SGD3,000 - SGD3,000 Sebulan
Singapore
- Assist in characterising new semiconductor products across different temperature conditions.
- Support engineers in verifying whether product parameters meet the required specifications.
- Assist with feasibility studies and the preparation of test plans for Wafer Sort and Final Test. ...
Posted
22 days ago
Undisclosed
Singapore
- Develops fixed equipment & piping inspection strategy using either industry best practice such as Times Based Inspection as per API code requirement or Risk Based Inspection (RBI) or Chevron methodology such as Fixed Equipment Asset Strategy (FEAS). Perform fixed equipment & piping inspection onsite when required.
- Contributes as fixed equipment & piping SME to determine integrity of plant equipment for safe operation and perform engineering review & evaluation (i.e fitness for service) when needed
- Act as owner of various inspection program (piping, tanks, vessels, pressure relief device (PRD) & others) and responsible for the overall program health, effectiveness, optimization and ensure compliance to code/regulation. ...
Posted
23 days ago
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Cari Kerja "validation engineer" Berdasarkan:
Cari Kerja "validation engineer" Berdasarkan: