This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labelling commensurate with the available data. Accountable to the asset GRL ...
The Regulatory Affairs Specialist is responsible for ensuring that the company aligns with all of the regulations and laws pertaining to our business; working with federal, state, and local regulatory agencies on specific issues affecting our business; and advises the company on the regulatory aspec...
This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labelling commensurate with the available data. Accountable to the asset GRL ...
The Federal Regulatory Affairs Manager directs US Federal regulatory package/dossier development, product registration, and lifecycle management of all Certis Biologicals products. The Regulatory Affairs team is responsible for obtaining and maintaining regulatory approvals for Certis Biologicals li...
This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labelling commensurate with the available data. Accountable to the asset GRL ...
Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams, and Operations brand teams for assigned projects negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions. ...
This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labelling commensurate with the available data. Accountable to the asset GRL ...
Title: Food Regulatory Affairs Analyst Location: Baltimore, MD - Hybrid 2-3 days a week on-site Schedule: M-F 8am-5pm Type: 6-month contract extendable with a potential for hire Pay: $20-25 per hour Start date: Immediate Overview: Savor the flavor of a unique opportunity within our client's Regulat...
This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labelling commensurate with the available data. Accountable to the asset GRL ...
Savor the flavor of a unique opportunity within our client's Regulatory Affairs group! They are seeking an entry-level Regulatory Affairs Analyst. If you've got a zest for detail and a taste for advancing your career in regulatory affairs, apply now!. Experience in Regulatory Affairs or related func...
Develops regulatory strategies for moderately to highly complex submissions to FDA and other regulatory agencies. Provides risk assessments of strategies and regulatory options to business teams and to product development/support teams. Represents the business in interactions with regulatory authori...
The Director of Regulatory Affairs is responsible for planning, organizing, implementing and evaluating regulatory compliance initiatives to support patient safety and quality and ensure continuous compliance with Federal, State and local regulatory requirements. This position involves interpreting ...
Reporting to the Director of Regulatory Affairs, responsible and accountable for developing and implementing sound strategies for complex regulatory submissions for functional unit. Assesses regulatory pathways for new product platforms and product modifications; develops regulatory strategies and t...
Soliant is seeking a qualified pharmacist with long-term care (LTC) experience to join our team in Columbia, MD. As a pharmacist with Soliant, you'll enjoy excellent support and flexible scheduling options. ...
Primary responsibilities of the Technical Writer are as follows:. Research highly technical subject matter, organizes information from multiples sources, and express technical information in written form that is comprehensible to a wide audience of readers. Apply concepts for technical writing based...
As a Data Analysis & Automation Team Technical Writer, you will support End user Services Architecture, Integration and Unified Communications teams including Program Managers, Technical Leads, Mission Leads, and Systems Engineers. Peraton is hiring a Data Analysis & Automation Team Technical Writer...
Womble Bond Dickinson (US) LLP is seeking an experienced Real Estate, Design & Construction Project Manager for all current and new offices. This person would be responsible for planning and delivering workspace projects, instrumental in day-to-day operations, and ultimately building of repeatable a...
The primary focus of this position is to serve as the Project Manager/Lead on the engineering development and design of bridge projects within the Bridge/Structures Design Division. Project Manager - Bridges/Structures. Actively manage and oversee the work of Project / Design Engineers and Engineeri...
Coordinate the day-to-day administrative activities of the clinical research trials program, including mentoring Research Regulatory Specialists with a focus on study activation. Lead a team of Research Regulatory Specialists and/pr Coordinators. Prepare and/or provide guidance to Regulatory Special...
Collaborate with collection architecture developers, signals analysts, network analysts, computer scientists, and external agencies to acquire, maintain and maximize access to global communications. The role of Analyst includes Identify policies and authorizations necessary to provide compliant targ...
Job Title: Technical Writer (TW1) - Skill Level 1Responsibilities:. Two (2) years of experience as a Technical Writer in programs and contracts of similar scope, type, and complexity required. An additional two (2) years of Technical Writer experience may substitute for an Associate’s degree. ...
The technical writer should have the ability to design and layout graphical product overviews and related marketing material. Candidate should have a foundation in writing technical documentation, briefings, and manuals and be comfortable interacting with software engineers, development teams, custo...
Join RPh on the Go for an exciting travel opportunity as an Emergency Room Pharmacist in Arizona. ...
Provides educational services including professional development and training to pharmacists, pharmacy students, pharmacy residents, pharmacy technicians, nurses, physicians, other health care professionals. ...