Document Controller Salary at Rfco Inc BETA

Got Questions? Email us: CSI-IS-141@CYNETSYSTEMS.COM Job Title: Senior Technical Writer (QMS) Job Location: Sunnyvale, CA Job Type: Contract Job Description: The Technical Writer ensures that the development and delivery of process documentation standard operating procedures (SOPs) are consistent and compliant with company and regulated guidelines. The Technical Writer writes, edits, and maintains usable, accurate, clearly presented, and consistent internal process documentation. The Technical Writer requires general guidance on new assignments and processes but is expected to complete day-to-day work with little instruction. This is a self-directed role requiring exceptional time management and communication skills. Requirements: 3-5+ years of writing or editing experience in a regulated environment focusing on internal process documentation SOPs. Bachelor’s degree in communications, professional writing, biological/medical/engineering sciences, or equivalent. Strong writing and gramm

Position: Document Control Specialist Location: San Jose, CA Position Summary: Our client is seeking a Document Control Specialist to support our Project Management team. This role requires a highly organized and detail-oriented professional who can efficiently manage document flow, support administrative tasks, and assist with clerical duties across departments. The ideal candidate is proactive, flexible with changing priorities, and able to multitask effectively in a fast-paced construction environment Key Responsibilities: Document Control (Primary – Project Management Support) Oversee printing, scanning, duplicating, and filing of project documents and drawings. Manage and track incoming and outgoing project documentation. Maintain electronic and hard copy files, ensuring proper labeling and organization. Control the distribution of electronic documentation across teams. Manage the processing of change notices and new releases. Store, log, track, and update documents, including dra

Job Description Job Description SpecCoat (Specialized Coating Services) is a well-established and growing manufacturing company located in Fremont. SpecCoat specializes in the conformal coating and encapsulation (potting) of printed circuit board assemblies. To support this growth, the position of Documentation Manager is now open. Job Description · Develop and implement document control processes and procedures to ensure the accurate and efficient management of company documents. · Manage the creation, revision, and distribution of controlled documents, including policies, procedures, specifications, and technical documents. · Ensure that all documents are categorized, indexed, and stored in a systematic and accessible manner. · Maintain document databases and control logs to track document history, status, and revisions. · Coordinate document reviews and approvals with relevant stakeholders to ensure accuracy and compliance. · Monitor document changes and updates, and communicate rev

Summary The Document Control Analyst will support product programs by managing Standard Operating Procedures (SOPs), Work Instructions, Forms, and Records throughout the product lifecycle-from concept to obsolescence. This role requires experience working in regulated environments (e.g., ISO 13485) and the ability to operate with minimal supervision. The ideal candidate is flexible, detail-oriented, hands-on, and able to manage competing demands effectively. Responsibilities Maintain and manage the Labs' Quality Management System (QMS) documentation and records throughout the product lifecycle. Create and release documents based on input from quality and compliance teams to support new product introductions, production releases, clinical trials, and FDA submissions. Ensure documentation and data related to Quality System requirements are controlled for integrity and accessibility. Oversee document control activities such as version control, distribution, and reporting to ensure regulat

Job Description Job Description Responsibilities: -Prepare work packages & submit to customer's portal -Review as-built documentation & follow format guidelines -Support project management & improve processes -Report on QC standards to management & document close-outs -Remove roadblocks & communicate with PM team Qualifications: -Strong verbal, written skills; attention to detail -Project Management and/or construction industry experience -Skilled in MS Office; Project Management software preferred

Job Description Saylor Consulting Group (SCG) has an opportunity for an Office Engineer/Document Control Specialist to join our team to support an ongoing contract with our client, Caltrain, for a planned reconstruction effort. Must be willing to work as a W2 employee full-time hours, on-site in San Jose, CA. The Office Engineer will be responsible for managing the internal flow of information among the team members and ensuring documents are correctly filed and saved for future retrieval. The Office Engineer will request outstanding documents from project team members for the project file. It is the responsibility of the Office Engineer to ensure submittals are received per the Contractor's reviewed Submittal Register and that the documents are transmitted per the distribution list. They will maintain databases for transmittals, correspondence, weekly meetings, material testing, Submittals, RFIs, COs, PCOs, Non-compliance Reports, progress payments, material weight tickets/tags and pu

Job title:- Technical Writer - USA Location: Mountain View, CA Duration:- 4+ Months Pay rate: $50/hr This is an onsite position. Description: As the Engineering Services Analyst, you will be responsible for developing and maintaining document transmittals, records, and systems for Client's products. You will ensure all involved parties across Client and Client's supply chain partners receive accurate and timely product documents and change notifications. Roles & Responsibilities •Manage the distribution and tracking of Client product documentation •Partner cross functionally on change order generation, completeness, accuracy validation and distribution to affected parties. Collaborate with users to correct issues before routing for approvals •Manage the change order processing life cycle stages including approval workflow, approval list, approval turnaround time, distribution matrix and implementation at supplier organizations •Organize and drive change control board review (CCB) for c

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing's syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. This position reports to the Sr. Manager of Document Control and Training and is responsible for supporting