- Medical Technology
- Equipment Qualification
- Patient Safety
- Quality System
- Cross-functional Collaborations
- Laboratory Equipment
- Quality Assurance
- Quality Management System
- Root Cause Analysis
- Documentation Practices
- Quality Control
- Continuous Improvement
- Stakeholder Management
- Complaint Investigations
- Data Integrity
Job Details: Job Description: The Role & Your Impact Join Altera’s post-silicon validation team in Bayan Lepas, driving the validation of timing and static/dynamic power models for our advanced Multi-Chip Package (MCP) FPGAs. In this role, you will
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market-leader in implantable hearing devices, more people choose a Cochlear-branded cochlear
Laboratory Quality & Accreditation Support Assist in ISO/IEC 17025 scope extension activities for Pour Cloud CFPP analysis. Support preparation, review, and verification of accreditation-related documents, records, and technical data. Assist with method validation activities and technical data management
Key Responsibilities Demonstrate a primary commitment to patient safety and product quality. Understand and comply with all the regulations governing the quality systems (including ISO 17025). Conduct testing according to written procedures. Responsible for reviewing all
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It Possible. We are seeking a highly analytical and proactive Demand Planning Manager to join
POSITION OVERVIEW: In this role as a BE Process Engineering Engineer, develops new or modified process formulations, defines processing or handling equipment requirements and specifications, and reviews processing techniques and methods applied in the equipment/manufacture, fabrication and
WHY JOIN US? We practice a vibrant & energetic office culture. We provide opportunities for career advancement within the company. Good performance is always rewarded accordingly. “Its our people that make Astro Malaysia’s leading entertainment company.
Company Description Sandisk understands how people and businesses consume data and we relentlessly innovate to deliver solutions that enable today’s needs and tomorrow’s next big ideas. With a rich history of groundbreaking innovations in Flash and
Expected Travel: None Requisition ID: 14172 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become
POSITION SUMMARY: Support SQE Engineers in New Product Introduction (NPI) activities by performing technical quality support, component verification, inspection and measurement support, supplier quality documentation, issue tracking and coordination activities to ensure successful product qualification and
Before you apply to a job, select your language preference from the options available at the top right of this page. Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our
When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer
The QC Manager is responsible for leading all Quality Control activities across manufacturing operations within the Unity (MYU) Business Unit, supporting metal machining, plastic machining, electropolishing (EP), and valve assembly processes. The role ensures products consistently
Key Responsibilities Demonstrate a primary commitment to patient safety and product quality. Understand and comply with all the regulations governing the quality systems (including ISO 17025). Conduct testing according to written procedures. Responsible for reviewing all
Key Responsibilities Ensures all direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.
Key Responsibilities Demonstrate a primary commitment to patient safety and product quality. Understand and comply with all the regulations governing the quality systems (including ISO 17025 for accredited laboratory) and ensure all training is completed as
Key Responsibilities Identifies and resolves complex exceptions to work assignments. Summarizes, analyses, draws conclusions and makes appropriate decisions from test results or other process related findings. Read and interpret technical drawings, procedures, and protocols. Identify Manufacturing
Purpose Statement: The purpose of the Chemist II role is to conduct analytical testing on commercial, stability and non-routine samples, in addition to participate in the test method development, validation and technical transfers as required. They are responsible for
Key Responsibilities Identifies and resolves complex exceptions to work assignments. Summarizes, analyses, draws conclusions and makes appropriate decisions from test results or other process related findings. Read and interpret technical drawings, procedures, and protocols. Identify Manufacturing