Medical Device Document Control Specialist - QA
huMannity Medtec
huMannity Medtec is seeking a detail-oriented Document Control Specialist to join our Quality Assurance team in Santa Clarita, CA. You will administer and maintain controlled documents, training records, and document control systems to meet quality standards. The role requires 3+ years in a regulated environment, strong editing skills, and experience with eDMS and ERP systems. You will collaborate with Engineering, Manufacturing, and R&D to ensure timely document changes and CGMB participation. #J-18808-Ljbffr huMannity Medtec
$25 - $27 per hour
...Document Control Specialist Adecco is currently assisting one of our clients in Valencia with a Document Control Specialist for a medical device manufacturing company. The Document Control individual... ...retention policy. Perform other QA activities as needed and as...Medical deviceHourly payWeekly payTemporary workTraineeshipWork at officeLocal areaMonday to Friday- huMannity Medtec in Santa Clarita, CA is seeking a Document Control Specialist to join our Quality Assurance team. You will administer and maintain controlled documents, records, training documentation, and document control systems in compliance with company requirements...Suggested
$35 - $38 per hour
...an accommodation or an alternative application process. Document Control Specialist Santa Clarita, CA, US 2 days ago Requisition ID: 1053... ...control, quality systems, or a related role within the medical device industry or another regulated environment. Strong attention...Medical deviceHourly payWork at officeWeekend work- AppleOne Employment Services is seeking a detail-oriented Document Control Clerk for a leading manufacturing company. You will support document management, process change orders, and maintain records to ensure quality compliance. Ideal candidates have 2+ years in document...Suggested
- Are you detail-oriented with experience in a manufacturing environment? We are seeking a Document Control Clerk to support document management, change orders, record maintenance, and quality processes for a leading manufacturing company. 2+ years of Document Control experience...SuggestedWork at office
- Boston Scientific is seeking a Senior Design Quality Assurance Engineer to lead quality oversight across design controls for neuromodulation medical-device systems, including implantable leads and surgical tools. This defined-term, hybrid role focuses on risk management...Medical device
- SetPoint Medical's Technical Writer will support the Manufacturing Engineering... ..., and improving manufacturing documentation for the company's commercial medical device products. The Technical Writer... ..., and compliant with document control and Quality Management System requirements...Medical deviceHourly payContract work
- The Alfred E Mann Foundation for Scientific R is seeking a Senior Medical Device Assembler to support the assembly, testing, inspection, troubleshooting, and documentation of implantable and other medical device components in a regulated laboratory and cleanroom environment...Medical deviceFull time
- ...Specific Duties: 1. Performs assigned preventive maintenance on medical and laboratory devices in a timely manner. 2. Performs repairs on medical and... ...to problem calls from the customers. 6. Properly documents equipment preventive maintenance Licensure and Certification...Medical device
$34 - $37 per hour
...accommodation or an alternative application process. Senior Medical Device Assembler Santa Clarita, CA, US 8 days ago Requisition ID:... ...support the assembly, testing, inspection, troubleshooting, and documentation of implantable and other advanced medical device components...Medical deviceHourly payFull timeWeekend work- ...fabrication technician to join the production team fabricating quality medical device parts. The role requires adherence to ISO 9001 standards and... ...assigned area. Training covers safety, chemical handling, and controlled-environment procedures. #J-18808-Ljbffr Boston ScientificMedical device
- ...team. The candidate should have a Bachelor's degree in Engineering and at least 8 years of relevant experience, particularly in Class III medical devices. Extensive knowledge of regulatory standards and strong analytical skills are required. #J-18808-Ljbffr Sonova GroupMedical device
- A medical device company in Santa Clarita is seeking a Quality Technician for an onsite role. The technician will ensure timely processing of product complaints, troubleshoot electronic and mechanical failures, and maintain lab equipment. Candidates should have an AA degree...Medical device
- ...verification and manufacturing, while mentoring engineers and coordinating with suppliers and medical stakeholders. You will drive requirements, create CAD models and drawings, and ensure outputs meet FDA/ISO design controls and quality standards. #J-18808-Ljbffr Sonova GroupMedical device
$27 - $35 per hour
...Airlines and Aviation Referrals increase your chances of interviewing at Round-Peg Solutions (RPS) by 2x Quality Inspector - Mechanical - Level 2 Santa Clarita, CA Quality Engineer II — Medical Device (Onsite — Valencia, CA) Contract #J-18808-Ljbffr Round-Peg Solutions (RPS)Medical devicePermanent employmentContract workTemporary work- A medical technology company in Santa Clarita is seeking a Principal Electrical Engineer to lead product development in active medical... ...in Electrical Engineering and significant experience in medical devices are required. This full-time position offers a competitive...Medical deviceFull time
$36 - $40 per hour
...requirements, clean room protocols, safety regulations, and documented manufacturing procedures, including support for CAPA and root... ...years of manufacturing experience, preferably in aerospace or medical device industry.Minimum of five (5) years of progressive supervisory...Medical deviceHourly payContract workShift workNight shiftAfternoon shift- ...been advancing life-enhancing medical technologies that address... ...Senior Quality Systems Specialist to support and continuously... ...forms, templates, and other controlled documents. Review and approve quality... ...within the medical device industry. Hands-on experience...Medical deviceWork at officeWeekend work
- ...staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and... ...drawings, GD&T, design validation, and engineering documentation is required. Medical device or biopharmaceutical industry experience...Medical device
- ...been advancing life-enhancing medical technologies that address... ...production of implantable medical devices and systems. This role works... ...and maintain manufacturing documentation including SOPs, work instructions... ...in risk management, process control, and quality improvement...Medical deviceContract workInternshipWork at officeRemote workWeekend work
$20 - $21.5 per hour
...Medical Device Assembler Volt is immediately hiring a Medical Device Assembler in Sylmar, CA 91342. As a Medical Device Assembler... ...tools. Packages devices ensuring all parts are accurate and documentation is complete. Performs routine assignments according to...Medical deviceHourly payTemporary workWork experience placementImmediate startMonday to FridayDay shift- ...superintendents, and office staff while ensuring documentation, scheduling, and project records are... ...accurate project files and document control systems. Assist with bid packages,... ...expression, marital status, disability, medical condition, genetic information, pregnancy...For subcontractorWork at officeLocal area
- ...experience. Minimum 1 year of experience in Quality, Manufacturing, Laboratory Operations, Medical Devices, or a related field. Strong troubleshooting, technical documentation, and organizational skills. Ability to work independently in a regulated environment....Medical device
- ...modification of an embedded software code base of a class III medical device. May interface with cross-functional teams to define system... ...modifies, tests embedded software code in C / C++ and Python.Documents software development and/or test development by writing documents...Medical device
- Our client is a global medical technology company seeking a Principal... ...and wearable medical devices. This individual will guide products... ...with FDA, ISO, and design control requirements.Mentor engineers... ...device innovation.EOE Statement: Specialist Staffing Group is an equal...Medical device
$79k - $95k
...oversee product assemblers for a micro-controller medical device manufacturer. Here's your day-to-... .... Ensure all work is performed per documented procedures, quality and compliance standards... ...with engineering, planning, QA and R&D. Perform capacity analysis...Medical device- ...Engineer to provide hands-on sustaining quality support for medical devices in a regulated environment. This role centers on product quality... ...with cross-functional partners to maintain design control compliance throughout the product lifecycle. #J-18808-Ljbffr...Medical device
- SetPoint Medical is seeking a Buyer I/II to manage high volumes of purchase requests, issue POs, obtain quotes, and coordinate with cross-functional teams in a fast-paced, startup-style environment. Responsibilities include maintaining supplier records, ensuring quality...Medical device
- ...understand and/or write a high level programming language.• Specific knowledge relating to software development for a class III medical devices• Experience using IEC 62304:2006 development process• Experience with client/server models for mobile application• Experience...Medical deviceContract workRemote work
- ...to lead product development and design optimization in medical devices or related fields. The ideal candidate will be proficient... ..., and produce production-ready drawings with rigorous documentation and change control. Collaboration across teams is essential. #J-18808-...Medical device
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