For the Support Services department, works with various word processing and other software applications in order to produce documents for attorneys and staff according to established policies and procedures: e. Operates a computer with multiple software applications in order to transcribe digital di...
The Quality Assurance Document Control Specialist (QADC) I is located at Iovance’s Cell Therapy Center (iCTC) in Philadelphia PA. Independently manage and monitor the processing, review, and approval of the archived documents in the Electronic Document Management System (eDMS). Maintain master docum...
For the Support Services department, works with various word processing and other software applications in order to produce documents for attorneys and staff according to established policies and procedures: e. Operates a computer with multiple software applications in order to transcribe digital di...
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. ...
This opportunity entails being responsible for performing routine document controls assignments requiring basic knowledge of document controls principles. Administers the document lifecycle for engineering and construction documents. Defines standards and workflows for document management as well as...
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. ...
Iovance is seeking a Quality Control (QC) Laboratory Support Analyst I who will assist the QC Laboratory Support Manager with the day-to-day upkeep of the QC investigations and supporting documentation. Review and approve GMP quality control laboratory testing documentation at the iCTC facility with...
Document Cloud Sales Specialist (Digital Media) focuses on selling, growing, and renewing customers in Adobe’s Document Cloud corporate business organization which boasts outstanding software solutions within a named book of business. Articulate the Document Cloud solutions and benefits to director-...
Harmony Biosciences is recruiting for an Administrative Assistant, Technical Operations in our Plymouth Meeting, PA location. In this role you will provide general administrative and project-specific support to Tech Ops department members including scheduling meetings, conference calls, travel arran...
Specialist, Quality Control, Operations Strategy. Develop and upkeep planning tools to allow for site growth within the quality control organization such as headcount capacity models for increased manufacturing capabilities and onboarding of new quality control assays, tests, and processes that cont...
The Quality Assurance Specialist will organize and execute aspects of GMP implementation at the East Norriton manufacturing facility. Maintain a presence of Quality Assurance on the manufacturing floor during GMP runs to ensure compliance to GMPs. QA Specialist – East Norriton, PA. The successful ca...
The Quality Release Specialist will support review of documentation and support releasing of materials and products. Interface with functional groups, such as Manufacturing, Quality Control, and Document Control, to determine events (errors, deficiencies, discrepancies, deviations and other observat...
This is your opportunity to start a lifelong career with unlimited opportunity.Discover the flexibility youve been searching for by taking a minute to finish our online application.No experience, Willing to train.Ability to work within recognized turnaround times.Must have exceptional social skills ...
This work-from-home position is ideal for anyone with a diverse professional background, including administrative assistants, data entry clerks and typists, customer service reps or drivers. Roles include data entry clerk, customer service agent, nurse or medical assistant - just choose what suits y...
Previous data entry experience is an advantage. Proven ability to enter data quickly and accurately. ...
Data Entry Clerk Work From Home - Part Time Remote Focus Group Panelists. Data entry clerk experience is not necessary. If you are a data entry clerk or someone just looking for a flexible part time remote work from home job, this is a great way to supplement your income. No Data Entry experience ne...
A paid Product Tester position is perfect for those looking for an entry-level opportunity, flexible or seasonal work, temporary work or part-time work. ...
ESSENTIAL DUTIES AND RESPONSIBILITIES:May perform one or more of the following duties as determined by manager or business needs:Responsible for ensuring timely and accurate processing and quality control (not limited to):* Review electronic data base (receive and accurately distribute incoming mail...
Up to $55 per hour / Flexible hours / Technology and tools provided - As a Data Entry Clerk you'll: Accurately enter data into various databases and systems from source documents while adhering to deadlines; Review and correct any errors or inconsistencies in the data; Verify data by comparing it to...
We are seeking a detail-oriented and reliable Data Entry Clerk to join our growing team. Accurately input and update data in our databases and systems. High school diploma or equivalent; additional certification in data entry or related fields is a plus. Proficiency in Microsoft Office Suite (Excel,...
Primary Quality Assurance Representative for designated clients. Interact with MFG management to provide quality perspective on routine operations and support systems. Participate in quality and process improvement initiatives, and project teams. ...
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...
Job Title: Administrative Assistant. This Senior Management Assistant will work closely with the Executives Assistants in supporting 4-5 members of the U. They will offer administrative support when needed and must be able to balance various administrative tasks efficiently. ...
A Specialist role to provide Quality oversight in manufacturing operations at the site and monitor processes for adherence to established procedures/regulatory compliance. High level job accountabilities included activities related to sterility assurance, manufacturing oversight, quality system and ...
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...