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Arkema Inc.
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King Of Prussia, Pennsylvania
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out of King of Prussia, PA, has an opening for a Sr. Product Stewardship and Regulatory Affairs ... compliance activities and be the main point of contact for Thiochemicals, Fluorochemicals, Oxygenated
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Medtronic
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Northridge, California
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earliest possible approvals of clinical trials applications.
Primary Responsibilities ... , you will be responsible for informing both local and global regulatory partners of sustaining changes
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Spacelabs Healthcare, LLC
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Snoqualmie, Washington
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their manager or a member of senior management any quality problems or defects in order for corrective ... activities of the company. This RA Specialist role requires a professional who will work closely with high
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BD (Becton, Dickinson and Company)
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Milpitas, California
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analysis, and ownership of task execution and completion.
Provides support to RA manager and RA ... Job Description Summary
The Senior Regulatory Affairs Specialist is part of the team
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Stryker
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United States
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projects and initiatives from planning through close-out, including the development and maintenance of ... regulatory intelligence to assist in the development of local, regional, and global regulatory strategies
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Stryker
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San Jose, California
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projects and initiatives from planning through close-out, including the development and maintenance of ... regulatory intelligence to assist in the development of local, regional, and global regulatory strategies
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System One
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Pleasanton, California
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experience is preferred.
Experience with Microsoft based applications and general knowledge of PC ... you want to be a part of this exciting work, please apply!
The Regulatory Affairs Specialist
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TELA Bio, Inc.
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Malvern, Pennsylvania
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documentation and procedures, and participating in compliance activities. As a key member of the TELA Bio organization, the individual is expected to establish and maintain a work environment of continuous improvement
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ThermoFisher Scientific
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Asheville, North Carolina
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team member on New Product Development teams, providing regulatory requirements, management of ... billion invested annually in R&D, at Thermo Fisher Scientific you’ll help solve some of the world’s
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System One
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Camden, New Jersey
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preparation of regulatory documents or submissions.
Analyze product complaints and make ... , compliance test requirements, or clarification and follow-up of submissions under review.
Escort
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Henkel
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Bridgewater, New Jersey
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and improve life every day. If you love challenging the status quo, join our community of over 47.000 ... hazard communication for all products in applicable business units and region, including preparation of
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Henkel
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Madison Heights, Michigan
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and improve life every day. If you love challenging the status quo, join our community of over 47.000 ... hazard communication for all products in applicable business units and region, including preparation of
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Henkel
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Rocky Hill, Connecticut
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and improve life every day. If you love challenging the status quo, join our community of over 47.000 ... hazard communication for all products in applicable business units and region, including preparation of
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The University of Texas at Arlington
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Arlington, Texas
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).
GMP Manufacturing:
Assist with the development of manufacturing processes, including ... include in their online resume the following information: 1) Employment history: name of company, period
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System One
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Camden, New Jersey
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preparation of regulatory documents or submissions.
Analyze product complaints and make ... , compliance test requirements, or clarification and follow-up of submissions under review.
Escort
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Danaher Corporation
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Coralville, Iowa
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, development and delivery of solutions that safeguard and improve human health.
This ... .
Experience and understanding of product development process inclusive of Design Control and Risk Management
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Steris
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United States
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the Manager, Regulatory Affairs within the RA Department, the incumbent is responsible for supporting the development and administration of STERIS’s global regulatory responsibilities. This includes, but
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Boston Scientific
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Arden Hills, Minnesota
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approvals including change impact reviews. Your responsibilities will include: Supports the development of domestic and international strategies for regulatory approval of Class I, II and III medical devices
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EUROFINS VRL INC.
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Centennial, Colorado
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responsibilities include, but are not
limited to, the following:
Under the direction of the Manager, Regulatory ... to
ensure organization-wide compliance.
* Assists other departments in the development of SOPs to
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Philips
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San Diego, California
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involvement in the legal and regulatory processes of covered Competent Authorities.
**Your role ... organization to ensure global success of products
Participate in cross-functional project teams and
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Philips
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Pittsburgh, Pennsylvania
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involvement in the legal and regulatory processes of covered Competent Authorities.
**Your role ... organization to ensure global success of products
Participate in cross-functional project teams and
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Philips
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Cambridge, Massachusetts
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the legal and regulatory processes of covered Competent Authorities.
Your role:
Develop ... to ensure global success of products
Participate in cross-functional project teams and provide
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BD (Becton, Dickinson and Company)
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San Diego, California
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, including development of agendas and training/preparation of company personnel attending these meetings ... the department. Is aware of colleague's career goals, suggests development plans and allows others to
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Philips
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Bothell, Washington
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involvement in the legal and regulatory processes of covered Competent Authorities.
**Your role ... organization to ensure global success of products
Participate in cross-functional project teams and
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Philips
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Plymouth, Minnesota
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involvement in the legal and regulatory processes of covered Competent Authorities.
**Your role ... organization to ensure global success of products
Participate in cross-functional project teams and
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Baylor Scott & White Health
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Dallas, Texas
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Members, Investigators and Research Staff. This includes development of presentations regarding regulatory ... Safety Monitoring Board and other people involved in the conduct of research at all Baylor Scott & White
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Catalent Pharma Solutions
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Harmans, Maryland
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oversite authoring, review, and preparation of applications for clinical through commercial submissions ... , and drive the development and evaluation of assigned components of new drug substance and drug product
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Kelly Services
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Irvine, California
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direct Worldwide Regulatory support to lifecycle management and new product development/new product ... partners. Includes the preparation of key market international documents, including Technical Files
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Teleflex
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Morrisville, North Carolina
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assist in mentoring and development of Regulatory Specialists as part of the role.
*Principal ... * :10562
About Teleflex Incorporated
As a global provider of medical technologies
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Unilever
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Carson, California
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. Recognized by Forbes, Fast Company and Time Magazine as one of the most inventive beauty companies, Hourglass ... , Nordstrom, Space NK and more. Hourglass became part of the Unilever Prestige division in 2017. Discover more
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