Procurement Talents (All Levels) Semiconductor Job at Randstad (Kuala Lumpur)

Procurement Talents (All Levels) Semiconductor

Our client is a global powerhouse within the Semiconductor industry, driving inn...

Location

Malaysia , Kuala Lumpur

Salary:

6000.00 RM / Month

Randstad

Expiration Date

July 10, 2026

Requirements

Bachelor's Degree in Supply Chain, Business, Engineering, or a related field
Open to all levels (1–3 years for Junior, 5+ years for Senior, 10+ years for Management roles)
Experience in Semiconductor, Electronics, or high-volume Manufacturing is highly preferred
Strong analytical mind, resilient under pressure, and excellent negotiation skills

Job Responsibility

Manage local and global sourcing for Direct Materials (wafers, lead frames, chemicals) or Indirect Materials (CAPEX, MRO, facilities)
Monitor and evaluate vendor performance, ensuring strict adherence to quality and Just-in-Time delivery schedules
Execute cost-saving initiatives and Value Engineering projects to maintain competitiveness in the semiconductor market
Mitigate supply chain disruptions by developing alternative sourcing strategies and maintaining strong buffer stocks
Ensure all procurement activities align with international electronics industry standards and RBA (Responsible Business Alliance) guidelines

New

Manager Packaging Engineering

WHAT YOU DO AT AMD CHANGES EVERYTHING At AMD, our mission is to build great pro...

Location

Taiwan , Hsinchu

Salary:

Not provided

AMD

Expiration Date

Until further notice

Requirements

Minimum 15 years of experience in InFO or 2.5D/3D bump/TSV/packaging, Flip Chip BGA/LGA, or WLFO process engineering, with strong hands-on experience in assembly manufacturing operations
Deep knowledge of InFO, chiplet packaging, 2.5D/3D TSV/packaging, Flip Chip BGA/LGA processes, and chip-package interaction
Demonstrated experience leading and scaling engineering teams, including coaching, performance management, succession planning, and development of technical talent
Minimum 5 years of experience in supplier management, including performance management, issue escalation, and stakeholder engagement
Familiarity with DOE, JMP, and data-driven problem-solving methodologies
MS degree in Mechanical, Materials, Chemical Engineering, or a related field is preferred
Highly motivated leader with the ability to balance strategic direction and operational execution, drive solutions, and lead teams effectively in a fast-paced, multi-tasking environment
Strong experience preparing reports and executive presentations, and communicating root cause, resolution, and program status effectively to all levels of the organization
Strong leadership presence with the ability to coach, motivate, and develop engineers while maintaining high standards of technical execution
Excellent interpersonal, communication, analytical, project management, and prioritization skills

Job Responsibility

Provide leadership for a team of engineers responsible for InFO, EFB/CoWoS-L, CoWoS-S, WLFO, FCBGA, LGA, and chiplet package manufacturing readiness for new product bring-up at manufacturing sites
Own team execution for packaging yield, quality, cost, and operational productivity improvement and sustaining activities
Define technical direction and drive assembly process baseline standardization and continuous improvement across supported manufacturing sites and suppliers
Oversee packaging interaction activities across assembly, bump, 3D IC, HBM, wafer fab, wafer sort, functional test, and mark/pack to ensure aligned execution and issue resolution
Partner with assembly manufacturers to enhance process, equipment, and material capability for future-generation technology products
Work closely with Packaging BU and cross-functional stakeholders to ensure NPI and ramp readiness at manufacturing sites, with disciplined follow-up on team deliverables and timely status reporting
Manage team performance in driving assembly manufacturing site and supplier performance related to yield, quality, out-of-control lot disposition, and outlier management, with clear closed-loop reporting
Lead engagement with internal engineering counterparts and broader package engineering, procurement, supply chain, reliability, and other organizations to deliver programs with accurate and timely status updates throughout the product life cycle
Own strategic supplier management, including relationship management, performance reviews, issue escalation, and alignment to business and technology objectives
Lead planning and execution of change management initiatives driven by internal or external stakeholders

Fulltime

New

Sr Associate Plant QA

If you feel like you’re part of something bigger, it’s because you are. At Amgen...

Location

Netherlands , Breda

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience
Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations
Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases
Manufacturing and/or Quality analytical processes and operations
Fluent in the English language

Job Responsibility

Provide daily guidance and support to Production staff regarding compliance with Standard Operating Procedures and Work Instructions
Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations
Review and approve batch production record data entries before production activities take place
Perform finished product checks during (commercial) production runs
Compile and review batch records for lots assembled, packaged, and labeled at ABR and contract manufacturers in preparation for disposition by QP
Review and approve Deviation records

What we offer

Competitive salary
Bonus structure
Fixed 13th month
Holiday allowance
Collective health insurance
On-site gym
Vitality program
Restaurant with healthy food

Fulltime

New

Technical Lead - Value Engineering

Being an Engineer at Baxter means you play a critical role in helping us achieve...

Location

United States of America , Aibonito

Salary:

80000.00 - 100000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

5-8+ years experience with Bachelor’s degree in Mechanical, Materials, Plastics, Chemicals, Packaging, or Manufacturing engineering or related field
Proven experience delivering multi-million dollar value engineering savings
Proven experience leading cross-functional projects end-to-end using structured project management methods
Working knowledge of GMP, change control, deviation/CAPA concepts, and validation/qualification principles
Strong analytical capability
Strong communication skills and cross-functional influence skills
Travel required, 10-20%
Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Job Responsibility

Identify and evaluate total cost optimization opportunities across materials, components, and processes across ITP sites with specific focus on insourcing, alternate sourcing and process & product value engineering
Ensure alignment to site and partner with Manufacturing Strategy to align to designed future state
Perform structured should-cost, clean-sheet, and teardown analyses
Support category strategies with fact-based cost drivers and benchmarks
Facilitate cross functional Continuous Improvement, Kaizen and Cost Optimization events to generate and prioritize ideas
Lead a cross functional technical team through the planning and execution of projects using various engineering and scientific techniques, procedures and criteria
This includes constructing detailed, accurate schedules, driving and collaborating with a core team, and guiding technical support groups
Lead or support technical change execution including specification and material substitution
Coordinate sample builds, trials, and testing
Support change control processes, validation, and implementation (e.g., cut-in planning)

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

New

Specialist Quality Assurance – Drug Substance Deviations

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master's degree and 2 years of Quality Assurance experience
OR Bachelor's degree and 4 years of Quality Assurance experience
OR Associate's degree and 8 years of Quality Assurance experience
OR High school diploma / GED and 10 years of Quality Assurance experience

Job Responsibility

Provide Quality oversight to ensure clinical and commercial pharmaceutical products are manufactured, tested, stored, and distributed in compliance with cGMP and applicable regulations
Provides an additional QA oversight by critically reviewing and challenging deviation designations made at the shop floor to ensure accurate, consistent, and compliant classification
Collaborates with Manufacturing and cross-functional stakeholders to reassess impact, drive alignment, and support sound decision-making
Provides QA oversight by critically reviewing and challenging initial deviation write-ups to ensure accurate reflection of the event
Partners with deviation owners to strengthen event descriptions and ensure a clear, compliant initial resolution
Ensures that required sections, including further processing and continued operations, are completed accurately and within established timelines
Serve as Deviation QA Contact and decision-maker for deviations, maintaining accountability for investigation quality, timelines, documentation, and closure
Actively participate in deviation and RCA meetings, managing multiple concurrent deviations and driving effective resolution
Conduct thorough root cause investigations, including floor presence, process observation, and personnel interviews across shifts, including nights when required
Review, approve, and track cGMP documentation, including Deviations, CAPAs, CAPA Effectiveness Verification (EV), Change Controls, validations, and associated records

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
comprehensive employee benefits package including a Retirement and Savings Plan with generous company contributions
group medical, dental & vision coverage
life & disability insurance
discretionary annual bonus program
stock-based long-term incentives
award-winning time-off plans

Fulltime

New

Product Technical Specialist - Harvesting

Location

United States , Ames; Grand Island; New Holland; Racine

Salary:

86625.00 - 132825.00 USD / Year

CNH Industrial

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Agricultural, Mechanical or Electrical Engineering
5+ Years experience in Quality, Service or Engineering related role
Strong analytical skills (preferably with knowledge of statistical tools)
Logical and rigorous problem-solving approach and experience with problem solving tools
Organizational and project management skills with the ability to participate in and lead cross-functional teams
High level of autonomy / self-starter with ability to drive results

Job Responsibility

Serve as the primary owner for complex, unresolved technical issues beyond Level-1 and Level-2 support
Lead technical diagnosis and troubleshooting for high-impact customer issues requiring engineering involvement
Own the resolution of technical inquiries by responding through established support channels and publishing clear guidance via Issue Master, Service Bulletins, Service News Updates, and Knowledge Articles to contain and resolve issues
Interface between field issues and engineering, ensuring issues are well-defined, reproducible, and actionable
Represent the customer perspective in cross-functional discussions related to quality, reliability, and product improvement
Proactively analyze field, dealer, and system data to identify emerging issues early, enabling timely containment actions before issues escalate to widespread customer impact
Use field and dealer feedback to help identify emerging issues and systemic trends
Support containment strategies that minimize customer impact while permanent fixes are developed

What we offer

Comprehensive benefits program designed to support your health, well-being, and long-term success
Competitive compensation
Flexible work arrangements
Opportunities for continuous development

Fulltime

New

Sr. Associate Quality Complaints

Amgen is seeking a Sr Associate Quality Complaints owner and member of the Produ...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree
OR Bachelor’s degree and 2 years of Quality experience
OR Associate’s degree and 6 years of Quality experience
OR High school diploma / GED and 8 years of Quality experience
Fluency in verbal and written English to be able to understand & articulate technical concepts

Job Responsibility

Conducts low to medium complexity complaint investigations and determines if complaint investigations require escalation for further investigation
Evaluates and ensures triaged product complaint records comply with applicable procedures
Evaluates and owns complaint records with basic investigations
Ensures quality of complaint records
Completes assigned assessments per applicable procedures
Applies analytical skills to evaluate complex situations using multiple sources of information
Executes the complaint process per SOP requirements
Owns or manages the review/approval process flow in CDOCS of controlled documents
while adhering to format, content, and style guidelines, considering usability, and ensuring accuracy, consistency, and quality according to templates and style guide
Supports management of assigned projects or project tasks to achieve agreed deliverables within time and with expected quality, including (but not limited to) proactive written / in person communication, status updates, tracker & tool maintenance

Fulltime

New

Attorney (LATAM)

Why Valvoline Global Operations? At Valvoline Global Operations, we’re proud to...

Location

Mexico , Guadalajara

Salary:

Not provided

Valvoline Global

Expiration Date

Until further notice

Requirements

Bachelor's degree with a focus in law, paralegal studies, or related field
Minimum of 5 years' work experience with responsibilities that cover the tasks of a paralegal or a legal assistant
Proven track record of working in positions where accuracy, structured and documented work, and prioritizing have been key
Understanding of applicable law, guidelines, regulations, and legal processes in one or more specialized areas
Understanding of the US Foreign Corrupt Practices Act, Trade Regulations, and antitrust & anti-competition laws
Excellent communication, both written and oral, drafting and negotiation skills
Drive for Results: Create high-performance work systems and processes built on best practices to deliver business goals
Ability to establish and maintain harmonious working relationships with team members, staff, and external stakeholders, and to work effectively in a professional team environment
Strong organizational and planning skills in a fast-paced environment, able to set priorities and meet deadlines
Hands-on, proactive, and problem-solving mentality

Job Responsibility

Supporting LCL and HR Business Partner with ongoing labor law compliance and problem-solving, including but not limited to employment agreements, benefits, unions, and subcontracting
Supporting the LATAM Credit team with ongoing credit securities in Mexico, including pagares and mortgages on real property. Duties include collecting required documentation, drafting pagare/mortgage documents, and arranging notary services for signature
Assisting LCL in completing the ongoing review of importation and labeling requirements in Mexico to update the supply chain team on compliance obligations
Drafting agreements covering distributors, resellers, annexes, processing of additional relevant changes, implementations or corrections based on business plans, pricelists, agreement request forms, processing of potential changes, additions or adjustments of agreements, GT&C, etc. Reviewing various business contracts, documents per request by LCL
Maintaining an up-to-date file and database of administrative and other corporate-related governance documentation, facilitating the preparation of resolutions and updating corporate documentation in accordance with business needs and legal requirements. Maintaining structure and records of intercompany services, licensure, and other agreements, in consultation with the applicable departments
Monitoring changes in relevant legislation and the regulatory environment and taking action accordingly. Gathering and analyzing legislation, statutes, decisions, and legal articles, codes, documents and other data
Consultation with other resource groups based within and outside EMEA (Legal, Tax, Insurance, Accounting, Treasury, Communications etc.)
Organizing and maintaining documents in a paper or electronic filing system, where applicable

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Procurement Talents (All Levels) Semiconductor

Job Description

Job Responsibility

Requirements

Looking for more opportunities?

Procurement Talents (All Levels) Semiconductor

Procurement Talents (All Levels) Semiconductor

Manager Packaging Engineering

Sr Associate Plant QA

Technical Lead - Value Engineering

Specialist Quality Assurance – Drug Substance Deviations

Product Technical Specialist - Harvesting

Sr. Associate Quality Complaints

Attorney (LATAM)

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