Search Results: 4,868 vacancies
Title:Document Specialist
Location: Cranbury, NJ
Schedule: M-F Full Time
Type: Direct Hire
Responsibilities
The Document Specialist... ...with knowledge of SQF and GMP’s preferred, Strong GMP and regulatory experience required
Proficient in Microsoft Office- Word...
Suggested
Full time
Title: Document Specialist
Location: Cranbury, NJ
Schedule: M-F Full Time
Type: Direct Hire
Responsibilities
The Document Specialist is responsible for maintaining all production and quality related documents according to the SQF & FDA requirements. The Document Specialist...
Suggested
Full time
...Title - Documentation Specialist
Duration - 6 months
Location: Branchburg, NJ 08876
Description:
Anywhere b/w 6:30am -8:00pm M-F (onsite)
OT as needed - Depends on business needs
Responsibilities:
Creation of PI sheets in the ERP system and obtaining...
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Work experience placement
...of Science, the nation’s largest single supporter of basic research in the physical sciences.
We are seeking to fill a Document Management Specialist position!
This position serves a key role in facilitating processes and programs supported by the Planning, Assurance,...
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Full time
Contract work
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Remote job
Work visa
Flexible hours
Shift work
Afternoon shift
...to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day.
Document Control Specialist
Onsite: Hamilton, NJ
Pay rate: $16/hr.
* Performs business support or technical work, using data organizing and coordination...
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...to support the ever-growing business.
This position is onsite based in our Dayton, NJ Office.
The Opportunity:
The Regulatory Compliance Specialist will contribute to our organization success by ensuring the organization adheres to legal and relevant regulatory requirements...
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Permanent employment
Internship
Local area
Worldwide
...Document Scanning & Indexing Specialist
Up to $18.50/hour - Part time
Mercer County, NJ
What We Need:
Our Arc Mercer Business Enterprise needs a Document Scanning & Indexing Specialist. The Document Scanning & Indexing Specialist is responsible for complete...
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Part time
...experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization. In this role, you will be primarily... ....
Participate in the development and review of submission documentation to support successful INDs/CTAs as well as marketing...
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Fixed term contract
Remote job
...Job Description
Job Description Job Title: Document Coordinator II
Pay Range: $20-$22/hr
Contract: 6-month W2 contract (potential to extend)
Work Location: Branchburg, NJ 08876
Work Schedule: 6:30am-8pm (Mondays to Friday, OT as needed - Depends on business...
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Monday to Friday
...proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
The Role
The Director, Regulatory Advertising & Promotion is responsible for ensuring that all promotional materials and activities comply with the applicable laws...
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Fixed term contract
Remote job
...Job Description
Job Description Coding and Documentation Specialist - Population Health
Be a part of our talented and growing team!
Are you looking for a Full-Time Coding and Documentation Specialist - Population Health position in an office setting? At Princeton...
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Full time
Private practice
Local area
Relocation bonus
Monday to Friday
...of information from Tissue Transplant Return Cards (TTR) and Data Registry Cards. Working with other departmental personnel, the document coordinator will maintain and file records, as well as maintain the file room. This position will prepare, process, and sustain storage...
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Remote job
Contract work
Local area
Job Description
Job Description Description: Gentell is one of the largest vertically integrated wound care companies in the world. Based in Yardley, PA and with offices, distribution centers and manufacturing plants around the world, our purpose is to make a positive...
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The Regulatory Affairs Manager will create, evaluate and execute domestic and/or international... ..., Technical Files and other regulatory documentation) for product approvals/clearances... ...5 to 10 team members at the Associate, Specialist or Manager levels.
EDUCATIONBachelor's...
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Worldwide
...into a pivotal role in the world of US regulatory affairs? We're seeking a dynamic individual... ...devices.
As a Regulatory Affairs Specialist at Guerbet, you will collaborate closely... ...timely submission of all Guerbet regulatory documents. You will stay at the forefront of US...
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Local area
...work every day is important to us.
The Senior Manager, Regulatory Affairs will handle publishing and coordinating tasks for... ....
Validate and QC of incoming and outgoing regulatory data/documents.
Archival of other necessary submissions and/or documents....
Temporary work
Local area
Immediate start
Flexible hours
...Senior Director, Global Regulatory Affairs Strategy
The position will provide regulatory affairs strategic leadership for the company... ...programs
Ability to author clear and concise regulatory documents with oversight of all documents for regulatory submissions and...
Local area
SUMMARY OF POSITION Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated... ...highest quality standards are met. 24. Critically reviews documentation intended for submission to the FDA for internal consistency,...
...you.
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Assistant Director Regulatory Affairs
at
Scientific Search .
Assistant Director of... ...Engaging with and contributing to the compilation of critical documentation and information from clients and stakeholders.
About You
Hold...
Permanent employment
Full time
Worldwide
...Responsibilities:
Provides strategic global regulatory guidance to cross-functional project teams responsible for product development... ...and guidelines.
Reviews and approves (when necessary) documents used in regulatory submissions.
Participates in preparing...
Contract work
For contractors
