Regulatory Affairs Specialist Jobs in South Plainfield
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Search Results - Regulatory Affairs Specialist Jobs in South Plainfield
Katalyst Healthcares & Life Sciences-South Plainfield
Responsibilities:
The Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs.
Support the IA business units in meeting global registration requirements.
As a regulatory process expert supporting...
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Meditrial Europe Ltd.-New York, 23 mi from South Plainfield
candidate has Regulatory and Clinical Operations experience in the pharmaceutical, medical devices and/or Biotechnologies industries. The role will be responsible for the management and direction of the Clinical Affairs department for the conduct of trials...
allibo.com -
Katalyst Healthcares & Life Sciences-South Plainfield
Responsibilities:
The Regulatory Affairs Specialist II will support the IA business unit in meeting global registration requirements.
As a regulatory process expert supporting global registrations the candidate interprets federal/state...
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Montvale (NJ), 38 mi from South Plainfield
Responsibilities:
Functional Capabilities and Essential job Tasks:
• Understanding, communicating, and general awareness of applicable legislation, regulatory procedures.
• Assist in the creation of regionally compliant Safety Data Sheet’s and Label text.
• Learn...
icims.com -
Katalyst Healthcares & Life Sciences-South Plainfield
M.S. in a technical area is helpful.
Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.)
8 years experience in a regulated industry (e.g. medical devices, pharmaceuticals).
Individuals with "hands-on /authoring...
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Katalyst Healthcares & Life Sciences-South Plainfield
equivalent) in Science, Regulatory Affairs plus 5 years of experience in the offered position or related.
Excellent organizational skills and attention to detail. Strong work ethic with an ability to work independently. an ability to read, understand...
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Katalyst Healthcares & Life Sciences-South Plainfield
and implementation of applicable work processes and instructions. Ensure they are kept up to date and implemented.
Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert...
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Katalyst Healthcares & Life Sciences-Edison (NJ), 5 mi from South Plainfield
Responsibilities:
This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities...
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Katalyst Healthcares & Life Sciences-Raritan (NJ), 12 mi from South Plainfield
Responsibilities and Requirements:
Supporting and Validating Regulatory systems like REMS RIMS
5+ years' experience in Computer System Validation of Regulatory systems like Regulatory Information Management System, REMS, Publishing, eCTD systems...
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Katalyst Healthcares & Life Sciences-Branchville (NJ), 43 mi from South Plainfield
Responsibilities
Implement and maintain the effectiveness of the quality system.
Support day-to-day manufacturing and operations activities related to change control.
Provide consultation and advice to regulatory specialists regarding change...
resume-library.com -
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