- Exela Pharma Sciences, LLC (Lenoir, NC)
- …possess strong knowledge manufacturing within a regulated industry such as medical device , automotive, or defense.Must be detail-oriented with exceptional ... in process validations, and continues with overseeing risk using statistical quality control during manufacturing. In addition, addressing known issues with a strong… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …experience working in the medical device industry. 2. Knowledge of medical device document control requirements and practices. 3. Experience ... Good Documentation Practices (GDP) requirements. + Maintain paper and electronic training document files to current requirements as defined by the Quality System. +… more
- Danaher Corporation (Minneapolis, MN)
- …+ 5+ years of industry experience in Quality Systems; biotech, pharma, drug product, or medical device document control experience preferred + Experience ... maintaining various aspects of the Quality System, including deviation, CAPA, change control , document control and risk management. In this role, you will… more
- United Therapeutics (Eden Prairie, MN)
- … Device Development is responsible for leading research and development of medical device products and components used in combination products by applying ... cross functionally to define the proposed design, generate appropriate design control documentation, conduct verification and validation testing, and complete risk… more
- Lilly (Indianapolis, IN)
- …work closely with Original Equipment Manufacturers (OEM) to design and build custom medical device assembly machines. These engineers also develop and implement ... life better for people around the world. **Position Brand Description:** Indy Device Manufacturing (IDM) is an external facing team responsible for the manufacturing… more
- Lilly (Durham, NC)
- …result in safety improvements, increased productivity, and variability reduction for device assembly manufacturing lines. This is an exciting opportunity to help ... System from the ground up. **Responsibilities:** As the **Process Automation Engineer - Device Assembly** , you will be supporting and managing the Device … more
- AbbVie (Pleasanton, CA)
- …assist in transfer methods to manufacturing. + Document ECO changes within the Document Control system. + Coordinate design tasks for other team members for ... a range of design concepts. + Prepare, present, and document designs at technical reviews. + Refine and develop...with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international… more
- AbbVie (Irvine, CA)
- …assist in transfer methods to manufacturing. + Document ECO changes within the Document Control system. + Coordinate design tasks for other team members for ... a range of design concepts. + Prepare, present, and document designs at technical reviews. + Refine and develop...with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international… more
- Actalent (Eden Prairie, MN)
- Document Control Specialist Job Description Ensure compliance with regulatory and customer requirements for document control and quality systems. ... + Perform additional tasks as assigned. Essential Skills + Document control + Quality management systems (QMS)... experience within a regulated environment such as Pharmaceuticals, Medical Device , Cosmetics/Personal Care, or Food. +… more
- Medtronic (Newton, MA)
- …user-friendly interfaces that enhance the usability and functionality of our advanced medical devices. The Senior Software Engineer will be a key player in ... components. Experience with regulatory compliance and security protocols specific to medical software (eg, HIPAA, FDA regulations) is preferred but not required.… more
- Amazon (Seattle, WA)
- …by leveraging your platform expertise and supporting your team - Continuously evaluate and document new standards or patterns that emerge from your work - Thrive in ... day in the life As a Senior Design Technologist working on the next generations of device user experiences, no two days are the same. You might start by reviewing a… more
- Kelly Services (Fort Washington, PA)
- …in your career. And we just so happen to be seeking an **Quality Systems Coordinator/ Document Control ** to support a top company in **Fort Washington, PA.** If ... - Hybrid role Must be able to provide own device (ie Laptop, tablet)** **What's a typical day like?...functions to drive completion of outstanding items. + Perform document control activities to ensure GMP documents… more
- BD (Becton, Dickinson and Company) (Tempe, AZ)
- …overtime as needed. + Positive and Professional attitude. + Previous experience in the medical device industry is preferred. + Ability to read documents in rough ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...Excel, and Access. + 2+ years experience in a document control related position, preferably in an… more
- Abbott (Pleasanton, CA)
- …including but not limited to Management Review, Internal Audit, Audit Readiness, CAPA, Document Control , Training, Product Release, and others as needed. + Be ... action and accomplish goals. The Senior Manager, Software Design Control is responsible for managing a team of software...a Quality, Regulatory, or product development role in the medical device industry. + 5+ years' experience… more
- Kelly Services (Atlanta, GA)
- …in pursuing a career in quality control within the biotech, pharmaceutical, or medical device industries and are located in or near the Atlanta, GA area, ... for QC Lab Technician Opportunities - Atlanta, GA Area (Biotech, Pharmaceutical & Medical Device Industries)** We are actively seeking talented individuals for… more
- Kelly Services (Memphis, TN)
- …and compliance always. **Minimum Qualifications:** + Minimum of 1-2 years previous quality control experience in Medical Device or other regulated industry, ... duties as assigned such as RMAs, Production verification support, Document Control , etc., + Know and follow...**Preferred Qualifications:** + Minimum of 1-2 years previous quality control experience in Medical Device … more
- Nestle (Anderson, IN)
- …Practices. Reports also required on all outages and system malfunctions. Document any automation program and system,/ device /instrument configuration changes. + ... enriching you. _This position is not eligible for Visa Sponsorship._ **Electronic Control Technician** Seeking a motivated **Electronics Control Technician** to… more
- ZOLL Medical Corporation (Billerica, MA)
- Acute Care Technology See attached Job Description for Quality Control I At ZOLL, we're passionate about improving patient outcomes and helping save lives. We ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more
- AbbVie (Worcester, MA)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Assurance, Validation of product and processes, Quality Engineering, Quality Control , Training, Regulatory Compliance, Quality Planning, Product Quality and… more
- Upstone Materials (Scottsbluff, NE)
- SIMON | Quality Control Supervisor Subsidiary: Simon Simon is a subsidiary of Colas USA with operations throughout Colorado, Nebraska, South Dakota, and Wyoming. We ... on our international network visit www.colas.com . Job Summary: The Quality Control Supervisor is responsible for daily oversight of activities related to testing… more
