SR Quality systems specialist

Planet Innovation (PI) is a globally recognised Healthtech Innovation and Manufacturing company. PI offers the full spectrum of product design, engineering and manufacturing services for its customers in the diagnostics, life sciences and healthcare industries. Our clients include many of the world's top medical device companies, as well as some of the...

Position: Sr. Quality Engineer, Req#: 7020-1 Location: Irvine, CA  (100% onsite) Duration: 6+ Months Contract   Job Description: This Quality Engineer will support the Pilot Quality Engineering team for the Pilot Operations as part of the client’s Global Supply Chain. This cross-functional partner will (1) interact with various functional...

**Job Summary** The Document Control Specialist/ Document Control Specialist II / Sr. Document Control Specialist is responsible for administering and maintaining the company’s controlled documents, records, and the document control system in accordance with company requirements. This position is a key role to ensure product and quality system...

Summary:As a Quality Systems Analyst, you'll be at the forefront of transforming clients procedures to establish Critical Care Quality Management System.Key Responsibilities:You will be collaborating with cross functional stakeholders to understand business needs and develop requirements, processes and workflows.You will be supporting setting up and training...

Summary:As a Quality Systems Analyst, you'll be at the forefront of transforming clients procedures to establish Critical Care Quality Management System.Key Responsibilities:You will be collaborating with cross functional stakeholders to understand business needs and develop requirements, processes and workflows.You will be supporting setting up and training...

Summary:As a Quality Systems Analyst, you'll be at the forefront of transforming clients procedures to establish Critical Care Quality Management System.Key Responsibilities:You will be collaborating with cross functional stakeholders to understand business needs and develop requirements, processes and workflows.You will be supporting setting up and training...

Job DescriptionJob Summary The Document Control Specialist/ Document Control Specialist II / Sr. Document Control Specialist is responsible for administering and maintaining the company's controlled documents, records, and the document control system in accordance with company requirements. This position is a key role to ensure product and quality system...

Position: Sr. Quality Engineer,Req#: 6948-1 Location: Irvine, CA (100% onsite) Duration: 9+ Months ContractJob Description: The main function of a quality engineer is to apply engineering theory and principles to problems of industrial layout or manufacturing production. A typical quality engineer can make engineering drawings, write risk analysis documents...

Job DescriptionJob Description10436 – Sr Business Systems Analyst PurposeThe Sr. Business Systems Analyst will analyze business issues, define requirements, design computer programs, and recommend automated system controls and protocols to solve organizational information issues. Determine operational objectives, gather information, and evaluate output...

Job DescriptionJob Description10436 – Sr Business Systems Analyst PurposeThe Sr. Business Systems Analyst will analyze business issues, define requirements, design computer programs, and recommend automated system controls and protocols to solve organizational information issues. Determine operational objectives, gather information, and evaluate output...

Job DescriptionJob Description10436 – Sr Business Systems Analyst PurposeThe Sr. Business Systems Analyst will analyze business issues, define requirements, design computer programs, and recommend automated system controls and protocols to solve organizational information issues. Determine operational objectives, gather information, and evaluate output...

Quality Assurance SpecialistLocation: Irvine, CAHours: 7:00 AM - 3:30 PM, OnsitePay Rate: $27/hr.9 month contract (Great potential to extend or convert)On behalf of our client a pharmaceutical company focused on the development of medical devices for the life science industry. We are seeking an Entry-Level Documentation Specialist to join their team in...

Quality Assurance SpecialistLocation: Irvine, CAHours: 7:00 AM - 3:30 PM, OnsitePay Rate: $27/hr.9 month contract (Great potential to extend or convert)On behalf of our client a pharmaceutical company focused on the development of medical devices for the life science industry. We are seeking an Entry-Level Documentation Specialist to join their team in...

Quality Assurance SpecialistLocation: Irvine, CAHours: 7:00 AM - 3:30 PM, OnsitePay Rate: $27/hr.9 month contract (Great potential to extend or convert)On behalf of our client a pharmaceutical company focused on the development of medical devices for the life science industry. We are seeking an Entry-Level Documentation Specialist to join their team in...

Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: * Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone...

Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: * Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone...

Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: * Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone...

Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: * Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone...

About The Role The Sr. Control System Engineer will develop a cutting-edge Boron Neutron Capture Therapy (BNCT) System for cancer treatment. The Sr. Control System Engineer will design, engineer, program and implement National Instruments (NI) systems associated with distributed control, real time control, automation, testing, and data acquisition systems....

Must Have: 1st Line Support • Ability to use statistical techniques to analyze data DQ IQ OQ PQ ERP / MRP system experience, preferably in QAD Manufacturing Procedures Test Method Validation HM's Top Needs: Process Validations (PQ, OQ, Process Characterization, DOE) Statistical Analysis (Tolerance Interval, ANOVA, Sampling), Heavy experience with Minitab...