Search Results: 15,190 vacancies
...The Opportunity
Description
We're looking for a Documentation Specialist , working in Pharmaceuticals and Medical Products... ...validation master plans, etc.) to ensure compliance with regulatory requirements.
Our Client
Our client is an award...
Suggested
...job, you're making a difference in people's lives.
The Regulatory Specialist supports regulatory compliance for oncology clinical research... ...data, violations, deviations and submission of other study documents to support regulatory compliance and troubleshoots...
Suggested
Work experience placement
Local area
Immediate start
Remote job
...position are to drive improvements in regulatory affairs processes, systems and infrastructure... ...customers.
Regulatory Affairs Specialist work includes:
•Direct submission development... ...and submission of regional technical documentation supporting global registrations across...
Suggested
Work from home
Night shift
2 days per week
1 day per week
...overall quality, completeness, and accuracy of medical record documentation, obtains appropriate clinical documentation through extensive... ...System to ensure industry best practice standards and regulatory compliance related to the CDI and coding functions.
2. Performs...
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Holiday work
Work experience placement
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Flexible hours
Weekend work
...GLAUKOS - ENGINEERING DOCMENTATION SPECIALIST II (BURLINGTON, MA)
How will you make... ...meticulous and detail-oriented Engineering Documentation Specialist to join our team. The ideal... ...role in maintaining quality standards and regulatory compliance within our organization....
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Work experience placement
Local area
...Related duties include participation on design and risk management teams, initiation of regulatory plans for both new products and significant product modifications, documentation of regulatory impact from device modifications, assistance in creating and maintaining Technical...
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Worldwide
...Responsibilities:
Interpret regulatory filings and lead cross-functional teams to comply with new or revised regulations.
Cultivate relationships within Customer Operations, throughout the Company and with external stakeholders. Partner with Corporate Affairs...
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Flexible hours
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...team to support the program.
About This Role:
We are seeking a highly collaborative and passionate Documents & Communications Accessibility Specialist to join us on the ground floor of bringing this important program to life. As a Specialist, you will partner...
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Contract work
Remote job
Monday to Friday
...mail through both internal/external and electronic sources to the Accounts Payable staff, batching, scanning and data entry of AP documents into the electronic file system, supply ordering, records retention and retrieval.
Job Description:
Receive, sort, open and...
Suggested
Shift work
...interface between all functions to ensure the appropriate changes are properly documented and implemented for change order submission and general documentation guidance. The Document Control Specialist I implements changes to change orders including; documentation, bill of...
Suggested
Worldwide
...entry into our operational system
Track and Trace Custom files and reporting
Transfer customs declaration information from documents, or other sources into the customs entry system to allow for the build of a valid customs declaration
Ensure compliance at all...
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Holiday work
...,000 partners, we serve the world’s most sophisticated clients using leading technology and exceptional service.
REGULATORY RISK MANAGEMENT SPECIALIST
Role:
The role supports the EMEA/APAC/NA senior leaders to identify and oversee areas of regulatory change and...
Suggested
Flexible hours
...Job Description
Job Description Shift: 8 am - 5 pm
~ Veeva GxP Documentation and archival
~ Processing, Sorting, Organization, and archival of on-site GxP archives and digital archives
~ Projects related to GxP documentation
~ Assist with the administration...
Suggested
Shift work
...Job Description
Job Description Responsibilities :
~ Veeva GxP Documentation and archival
~ Processing, Sorting, Organization and archival of on-site
~ GxP archives and digital archives
~ Projects related to GxP documentation
~ Assist with the administration...
Suggested
2 days per week
1 day per week
...Job Description
Job Description Job Title: Quality Document Control Specialist
Location: Cambridge, MA
Duration: 6 Months
Job Description:
Duties:
~ Veeva GxP Documentation and archival
~ Processing, Sorting, Organization and archival of on-site Gxp...
Suggested
...May 24 2024
GSK is currently looking for an Associate QA Documentation Specialist in Cambridge, MA. This position provides the opportunity... ...through the process and accurately apply and adapt GSK and regulatory standards.
Helpful to understand the QA function in a start...
Local area
Shift work
...Job Description
Job Description Principal Regulatory Affairs Specialist
Job DescriptionBrioHealth Solutions Inc., Inc. is seeking a skilled... ...for new or changed global regulations and guidance documents and new or revised industry standards, assessing for impact...
...Work Shift:
Rotating (United States of America)The Sr. Regulatory Specialist supports regulatory compliance for clinical research conducted... ...data, violations, deviations and submission of other study documents to support regulatory compliance. Troubleshoot processes...
Full time
Part time
Work experience placement
Local area
Immediate start
Remote job
Flexible hours
Shift work
Rotating shift
$133.2k - $223.2k
...true to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus 2 years...
Full time
Remote job
...consulting firm, is seeking a high energy individual to assist colleagues and clients by applying knowledge of US and international regulatory compliance for product stewardship. Responsibilities include providing regulatory interpretation and guidance, evaluating GHS...
Temporary work
