Review and update documents for maintenance and quality control. Proven work experience as a Document Controller or similar role. Print and distribute documents as needed. Scan and upload documents according to company procedure. ...
The Document Control Specialist is responsible for administering and maintaining the departmental controlled documents, records, and the documents control system in accordance with company business requirements. This position also support all documentation activities including review and update chan...
As the Document Control Specialist, you will be responsible for developing and maintaining document transmittals, records, and systems for our client's first commercial scale projects. Perform project document control activities such as ECN (Engineering Change Notice), managing the distribution matr...
Review and update documents for maintenance and quality control. Proven work experience as a Document Controller or similar role. Print and distribute documents as needed. Scan and upload documents according to company procedure. ...
What you’ll do: Craft and implement robust quality assurance protocols for Wi-Fi HaLow ICs Collaborate with cross-functional teams to proactively address quality-related issues and to ensure seamless alignment in quality control processes Oversee comprehensive testing and validation procedures...
AS or equivalent experience in engineering/technical documentation and change control. Strong understanding of engineering change control, experience working with/chair CCB (Change Control Board). Provide training for Document Control procedures and tools: Arena, Jira, NetSuite . Process all Ch...
The Document Control Specialist is responsible for administering and maintaining the departmental controlled documents, records, and the documents control system in accordance with company business requirements. This position also support all documentation activities including review and update chan...
The Document Control Specialist or ECO Analyst is responsible for overseeing and maintaining accuracy within the change management system. ...
Perform Document controller activities in Veeva for all GMP controlled documentation, including policies, SOPs, and protocols, in alignment with established procedures. Handle control, issuance, reconciliation, and archiving of GMP manufacturing and testing documentation, including batch manufacturi...
The Quality Assurance Specialist II is an intermediate level position with hands-on QA experience. The individual will also assist in the quality operations area, such as batch record and quality control data review, line clearances, AQL inspection, and will interact with cross-functional groups suc...
Bachelor’s degree in Life Sciences, Quality Assurance, or related field. Minimum of 3 years in a GMP environment, with experience in quality assurance for small and/or large molecules. This role involves technical writing, conducting thorough investigations, and monitoring quality system records to ...
Document Control Coordinator I. Working knowledge and understanding of document control and quality systems based on ISO 9001 or AS9100 standards. Maintains the current revisions of documents and prevents the unintended use of obsolete documents. Ability to revise documents and generate change notic...
Manages and audits document control process and systems to ensure control and availability of documentations to appropriate personnel. Scan hard copy documents into digital format and save the scanned documents in appropriate digital folder. Oversee the creation, organization, distribution, and stor...
Excellent employment opportunity for a Documentation Specialist I in the Fremont, CA area. Collaborates within Manufacturing to resolve batch record discrepancies or errors as it relates to Good Documentation Practices or Manufacturing Execution System (MES) inventory. Required skills: BATCH RECORD ...
Quality Assurance (QA) Specialist, External Manufacturing will play a pivotal role in ensuring that all external batch records adhere to Vaxcyte’s quality standards and regulatory requirements. Minimum of 5+ years of experience in quality assurance, batch record review, manufacture, or quality syste...
As a Senior Quality Control Specialist, you are an excellent communicator who can work closely with Producers, Design Supervisors, Production Designers, Studio Artists and Technical artists to ensure assets are successfully delivered without errors. Working closely with our content creation departme...
Join the #1 beer distributor in the United States! .Medical, Dental, Vision, Vacation Pay and Paid Holidays.Certified Great Place to Work 2024 - for the 4th Consecutive Year.First point of contact for visitors.Position Responsibilities may include, but not limited to:.Answer and direct all incoming ...
Minimum 2 years of experience in software quality assurance (Web development experience is a plus). As an Intermediate QA Specialist, you will report to the QA Lead. You will execute on QA tasks with speed and great quality for the overall agility of the QA team. Is co-responsible for the quality of...
Minimum 2 years of experience in software quality assurance. He/She Provides execution of QA tasks with speed and great quality for the overall agility of the QA team. Be responsible for the quality of projects based on the requirements and design specifications. ...
The ideal Administrative Assistant to the Top Seller is motivated, results oriented and committed to providing outstanding customer service every day. ...
Thermo Fisher Scientific is seeking a Senior Administrative Assistant for the Chromatography and Mass Spectrometry R&D organization. Work effectively with management at various levels and provide administrative support. This may include crafting and updating spreadsheets, databases, and other ad...
The ideal candidate will be responsible for improving the current processes and bringing in new systems for process improvement as a part of the Quality Assurance team. Quality Assurance; or experience working in a cGMP regulated environment with positions of progressive responsibility. Overall unde...
Administrative Assistant / Receptionist. The Administrative Assistant / Receptionist will be responsible for being the face of Hammon Plating, Palo Alto. Respond professionally and amiably to requests for administrative support or assistance. Assist other staff in administrative tasks, as requested....
The Senior Quality Control NGS Specialist will join our Quality team as a Next-Generation Sequencing (NGS) subject matter expert in Quality to be a key player in all scientific and documentation aspects of product development, release, stability, and investigations in support of maintaining and impr...
Takes the initiative to resolve issues within specified policies and guidelines and provides mentoring to administrative community members on problem solving. ...