Document Control Specialist: Average Salary in Willow Grove, PA in 2024

This opportunity entails being responsible for performing routine document controls assignments requiring basic knowledge of document controls principles. Our Philadelphia office is looking for a New Grad Document Controls Specialist I to join our Project Controls Group. Administers the document con...

Staples, rubber bands from documents. Organize assigned pages into logical documents and determine appropriate attachments. Efficiently scan documents and complete projects per the job specifications. Physically identifying document types and separating them according to manager instructions. ...

Generate, control and release documentation . Evaluate ECN submissions for accuracy and required content in accordance with ECN process documentation . Determine appropriate approval path, and serve as control to prevent undesired or unauthorized changes . Coordinate with Engineering department to p...

Staples, rubber bands from documents. Organize assigned pages into logical documents and determine appropriate attachments. Efficiently scan documents and complete projects per the job specifications. Physically identifying document types and separating them according to manager instructions. ...

The Senior Quality Control Specialist is responsible for developing and assisting in various operational audits for the OpenSky Credit Card Division. In this role, the Senior Quality Control Specialist will also participate in bank wide audits. Maintain audit schedule for quality control department....

Direct experience supporting staff in an administrative assistant role. ...

Assist the Quality/Training Manager and Assistant Manager with administrative functions, including developing Standard Operating Procedures (SOPs), Quality Standard Definition Document (QSDD), Quality Forms, and coordinating quality recognition programs. As a Temporary Quality Assurance Specialist w...

Assist the Quality/Training Manager and Assistant Manager with administrative functions, including developing Standard Operating Procedures (SOPs), Quality Standard Definition Document (QSDD), Quality Forms, and coordinating quality recognition programs. As a Temporary Quality Assurance Specialist w...

The Quality Control Specialist responsible for the executed test methods review and raw data review for lot release. The role has a good understanding of Quality Control and apply practical knowledge of phase appropriate GMPs and regulatory requirements in the product development life cycle, includi...

The Quality Control Specialist will be responsible for the following:. Perform daily GMP Quality Control laboratory testing activities. Minimum of 2 years experience in the pharmaceutical industry working in a GMP quality control laboratory. GMP Quality Control role; experience with cell therapy pro...

Acts as the Primary Quality Assurance Representative for designated clients. In an inter-departmental team environment, works to facilitate/incorporate effective quality practices for new and existing clients. Interact with MFG management to provide quality perspective on routine operations and supp...

Reporting to the Veeva Quality Assurance Lead, the Veeva Quality Assurance Specialist will review, itemize and migrate all regulatory documentation from the current document management system to the SiteVault platform. The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Qual...

The Administrative Assistant for Stewardship reports to the Director of Stewardship and will provide administrative support to the Stewardship team in the Office of University Advancement. Posting Details (Default Section) Posting Number: 20244150S Position Title: Administrative Assistant II, Stewar...

The Quality Assurance Specialist is responsible for assisting the Quality Assurance Manager in performing data audits, special audits, assisting with external and systems audits, overseeing the maintenance of QC records, certifications, Standard Operating Procedures (SOPs), training records, Demonst...

Clinical Documentation Specialist/Coder. Part-Time Clinical Documentation Specialist/Coder. As a Clinical Documentation Specialist/Coder, you will carry out our Mission of Love by. Our Clinical Documentation Specialist/Coder is responsible for the following:. ...

Are you a passionate person with a strong work ethic and pursuing a career in Human Resources? Invicro is looking for a HR Specialist to support our US HR team! This successful candidate will handle coordinating the efforts around hiring and onboarding new employees, supporting HR processes and proj...

The Quality Control Specialist II, Compliance Investigator will assist the Laboratory Manager in advancing and closing QC related investigations. Basic knowledge of biological drug development with respect to Quality Control. Revise Quality documents in support of deviation mitigation and/or CAPAs. ...

May provide back up to other Administrative job duties. ...

GMP Documentation Specialist - Permanent - Philadelphia, PA. Proclinical is seeking a GMP Documentation Specialist to join an esteemed biotech company in Philadelphia, PA. GMP Documentation Specialist's responsibilities will be:. In this role, you will support documentation processes, including draf...

Iovance is seeking a Specialist, Quality Control, Operations Strategy, who will support the long-term sustainability of the Lean Labs initiative within the Iovance Quality Control Department. Develop and upkeep planning tools to allow for site growth within the quality control organization such as h...

As an Administrative Assistant at Elite Branding, you will play a crucial role in ensuring the smooth operation of our office and supporting our team in various administrative tasks. Proven experience as an administrative assistant or in a similar role. Provide administrative support to the manageme...

TMF Quality Control Specialist will report to TMF Leader. Responsible for processing TMF documentation and performing quality control (QC) review in accordance with standard operating procedures (SOPs), work instructions (WIs), ICH GCP guidelines, TMF reference model and study specific TMF Plans. Pe...

The Specialist I is responsible for day-to-day Quality Assurance Operations activities in accordance with cGMPs, CFRs, ICH guidelines and company policies and procedures. The Specialist I will support Quality Assurance lot release and disposition activities including process observation, batch recor...

Processes bills; proofs billing sheets; reviews and edits Works closely with administrative support staff; proofs documents returned from word processing; ensures that attorney time sheets are provided to appropriate person in a timely Performs legal assistant duties as Performs overload typing, fil...

Lead dialogue to align and collaborate with customers regarding quality agreements. Perform training to Quality department on the tasks associated with this role as required. Leads and Supports departmental and customer projects and/or assignments as indicated by Quality Management including CAPAs a...