Johnson & Johnson is immediately hiring multiple Quality Assurance Associates specializing in Document Control to facilitate with production demand and new product development. Review all required documentation prior to release of product. Review all required documentation prior to release of produc...
Clinical Documentation Specialists are responsible and accountable for the day-to-day management and success of the Continuous Documentation Improvement Project to include all modalities, acting as a liaison with specific department staff, speaking, meeting and educating physicians, residents and mi...
Documentation Control Specialist serves as the primary authority, support, and communication hub between stakeholder departments on Change Management (CM) and Product Documentation / Configuration Control. Train new employees on CM and Document Control processes. Change Management of product configu...
TURION) is seeking a CAD Admin & Document Control Specialist to join our team in Irvine, CA. Engineering Document Control . Drawing & Engineering Document Checker . ...
The Document Control Specialist II executes all aspects of documentation control in accordance with ISO 9001. This involves managing the ECO process, reviewing documents, maintaining pertinent documentation, and ensuring that revision control is implemented. This is the opportunity for an ambitious ...
Position DescriptionThe Document Control Specialist II executes all aspects of documentation control in accordance with ISO 9001. This involves managing the ECO process, reviewing documents, maintaining pertinent documentation, and ensuring that revision control is implemented. This is the opportuni...
The Document Control Specialist position provides administrative and operational support to Document Control. This position interacts with multifunctional personnel in the organization, ensuring proper management of controlled documents and quality records. Performs data entries for part updates acc...
Document Control Specialist will be responsible for the release of Engineering deliverables, such as engineering drawings, production work instructions, engineering specifications, documents, and company processes and procedures. Resolve system and user issues or errors with engineering documentatio...
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. Document Control Specialist/ Docume...
The Document Control Specialist II executes all aspects of documentation control in accordance with ISO 9001. This involves managing the ECO process, reviewing documents, maintaining pertinent documentation, and ensuring that revision control is implemented. This is the opportunity for an ambitious ...
The Document Control Specialist is responsible for collecting, maintaining, archiving and retrieving all documents necessary to ensure compliance with the company's Procedures and FDA regulations. The Document Control Specialist monitors production operations to ensure that all users have the l...
Document Control or Quality experience for Document Control Specialist 3 – 5 years of Document Control or Quality experience for Document Control Specialist II. Administration of the document control system to include: Administering and maintaining changes to documents in accordance with company req...
The Trailing Docs Specialist will be responsible for monitoring and forwarding trailing documentation to investors, as well as assisting with scanning and file preparation. Coordinates the tracking, reporting and delivering of trailing documents (deed of trust, title policy, to investors. ...
This opportunity entails administering the document lifecycle for engineering and construction documents. Defines standards and workflows for document management as well as leads the collection, authorization, publication, storage, retrieval, and retention of documents. Establishes (within corporate...
Irvine based Medical Device Company is looking for a Document Control Specialist. Ensuring new documents and records are consistent with company procedures; reviewing all documentation for accuracy, completeness and consistency in content, format, files and approvals. Administration of the document ...
Irvine based Medical Device Company is looking for a Document Control Specialist. Ensuring new documents and records are consistent with company procedures; reviewing all documentation for accuracy, completeness and consistency in content, format, files and approvals. Administration of the document ...
Administrative Program Manager. Minimum 2 years' experience providing administrative support to a manager or director level position. Previous work experience providing administrative support in an academic or healthcare organization preferred. ...
In general, the duties of this position, like those of a Quality Assurance Specialist, are geared toward assisting Quality Assurance Management in administering the company's quality system. Senior Quality Assurance Specialist. Senior Quality Assurance (QA) Specialist. Senior Quality Assurance Speci...
Are you looking for a job and need a second chance to get your career on the move? Staffmark is hiring a Data Entry Clerk in Brea, CA ready to join a positive and collaborative team. Data Entry Clerk tasks include working in the warehouse entering information about the products that are sent for rep...
Years Administrative experience. ...
As we continue to grow, we are seeking a tented Quality Assurance (QA) Specialist to join our team and contribute to the success of our product. As a QA Specialist, you will be responsible for creating and maintaining comprehensive documentation that outlines quality assurance processes, procedures,...
Senior Quality Assurance Specialist. The senior quality assurance specialist will play an instrumental role in supporting our first product launch. Minimum of 2 years of experience working in post market surveillance, complaint handling or adverse event reporting, in quality assurance, or similar ro...
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Investigate moderately complex manufacturing product quality ...
Title: Quality Operations Specialist 1. Familiarity with medical device complaint files and quality records;. Supports quality functions pertaining to manufacturing line support and maintenance, including SAP. Support and coordinate product/process improvements through collaboration with cross-funct...
The Product Quality Engineer is responsible for providing quality engineering support to the manufacturing line, coordinating biocompatibility and sterilization validation activities, and supporting packaging validation and finished goods release for structural heart implant and delivery mechanisms....