Search Results: 3,558 vacancies
...Iron Mountain
Help us convert hard copies to electronic images. We will train!
At Iron Mountain, our Imaging Specialists are responsible for document preparation and scanning. You will be part of a dedicated workforce in a global company that celebrates the skills...
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...personal health monitoring.
JOB SUMMARY:
The Engineering Documentation Specialist is responsible for taking complex technical information... ...and other documentation as required to meet internal and regulatory requirements. The Engineering Documentation Specialist...
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...Job Description
I have a client located in the Eagleville, PA area that has an opportunity for a Document Control Specialist. If you or any of your colleagues are interested in discussing the role please click Apply Now.
In this role you will be working...
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Title: Document Control Specialist Location: Eagleville, PA Type: Contract to Hire Schedule: On-Site M-F 8-5 Overview: Our client a medical device manufacturer in Eagleville, PA is looking to add a Document Control Specialist to their team If you are experienced with updating...
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...surgery so patients can resume their lives as quickly as possible.
Position Summary :
Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements....
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...programs.
Position Summary:
to the Sr. Manager, Global Regulatory Affairs, the job holder will be a current college graduate with... ...:
Support chemical regulatory activities related to documentation including updating raw material information, communicating changes...
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...Kelly Science is seeking a Documentation Specialist for a growing medical device manufacturer located near Warminster, PA.
Salary: $28-35/hour depending on experience
Shift: Monday- Friday 8am-4:30pm
Employment Type: Full Time; Direct Hire
Summary:
As the...
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...the United Kingdom.
The Corporate Information Services Department is seeking a dynamic and talented Senior Clinical Informatics Specialist.
The Senior Clinical Informatics Specialist provides guidance in identifying, developing, implementing, and maintaining an...
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...guidelines and regulations. Coordinates, compiles, and tracks product applications to regulatory agencies.
Essential Duties And Responsibilities:
* Review clinical site regulatory documents to provide Regulatory approval to ship investigational product.
* Regulatory...
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Regulatory Affairs Specialistreq38824Employment Type:
RegularLocation: HORSHAM,PAHave you... ...Position Summary:
The Regulatory Affairs Specialist is responsible for preparing... ...guidelines.Verifies product claims with proper documentation and FDA required record-keeping.Maintains...
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...bringing to market biotherapies used to treat serious and often rare conditions.
Could you be our next CSL Plasma Lead for Global Regulatory Affairs, Plasma? This position is located in our King of Prussia PA, Holly Springs NC, Waltham MA, or Boca Raton office. It is a...
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...as possible.
Position Summary :
The Group Manager, US Regulatory, is responsible for preparing, filing and gaining approval of... ...products under review and of relevant regulations and guidance documents. This individual must be enthusiastic, positive, even-tempered...
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...Asset Plan (IAP)? If so, this role could be an exciting opportunity to explore.
Accountable to the asset GRL and/or the Global Regulatory TG Head for development and delivery of appropriate regulatory strategy(ies) according to plans. In conducting role, planning...
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...biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions.
Could you be our next Regulatory Manager, Advertising and Promotion? This position is located in our King of Prussia PA. It is a Hybrid role. You will report to...
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...Kelly has an amazing opportunity for a Senior Program Document Specialist to join a leading Government Consulting company focused on the National Public Health . This is a Temp-to-Hire opportunity with a starting salary of $75,000 - $80,000and an approximately...
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...surgery so patients can resume their lives as quickly as possible.
Position Summary :
The Lead Regulatory Affairs Specialist leads the preparation of document packages for regulatory submissions for new and sustaining enhanced technologies, software enabling and...
Local area
...Job Description
Job Description Salary: $90,000+
Purpose:
The Regulatory Affairs Manager is responsible for managing the regulatory affairs department and functions to ensure regulatory compliance of quality management system.
Duties & Responsibilities...
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The Corporate Information Services Department is seeking a dynamic and talented Associate Application Analyst - Clinical Documentation.
The Associate Application Analyst - Clinical Documentation supports the implementation of UHS Clinical applications in a Multi...
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...Title: Safety & Regulatory QC
Location: Collegeville, PA
Schedule: Hybrid 2 days/week on site: 3 days/week remote
Start date... ...Collegeville, PA. The ideal candidate will have experience in quality document control, comparison of artwork versus editor's copy and...
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...high-quality menu of services, highest regulatory standards (797 compound compliance),... ...industry.
Come join our team of infusion specialists and ‘be the change’ for our members/... ...and/or telehealth modalities
Documentation:
Maintain accurate and detailed records...
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