Senior Regulatory Document Writer

Job DescriptionJob DescriptionAssist in development of the Waste Disposition Alternatives (WDA) decision documents by preparing sections of the Remedial Investigation and Feasibility Study (RI/FS) Scoping/Work Plan, the RI/FS Report, Proposed Plan, and Record of Decision. Support may also be required in the development of DOE Order 435.1 documentation that...

Job DescriptionJob DescriptionUnder direction of senior team members, assist in developing the Remedial Investigation/Feasibility Study Report, Proposed Plan, and Record of Decision for the Environmental Media Decision. Examples of work to be performed include compiling and summarizing information documented in previous reports (e.g., previous investigation...

Job DescriptionJob DescriptionUnder direction of senior team members, assist in developing the Remedial Investigation/Feasibility Study Report, Proposed Plan, and Record of Decision for the Waste Disposition Alternatives Decision. Examples of work to be performed include compiling and summarizing information documented in previous reports (e.g., previous...

Job DescriptionAs a Environmental Regulatory Strategy and Policy Developer at Four Rivers Nuclear Partnership, you will play a crucial role in ensuring regulatory compliance and document development. Your responsibilities will involve working on complex environmental issues related to CERCLA removal and remedial actions and RCRA corrective actions at the...

Job DescriptionJob DescriptionPosition OverviewUnder general supervision, performs environmental regulatory strategy and policy development job functions as assigned by management. Typical job responsibilities assist and support management in regulatory compliance specifically during regulatory document development and implementation. The specific work...

Job DescriptionJob DescriptionPosition OverviewUnder general supervision, performs environmental regulatory strategy and policy development job functions as assigned by management. Typical job responsibilities assist and support management in regulatory compliance specifically during regulatory document development and implementation. The specific work...

About Root Root is a communication and productivity software platform that is uniquely designed to meet the needs of the world's online communities. The Root platform is extensible, allowing third-party developers to create custom experiences with front-end and back-end integrations. Our goal is to empower all the world's communities with technology. Root is...

About Root Root is a communication and productivity software platform that is uniquely designed to meet the needs of the world’s online communities. The Root platform is extensible, allowing third-party developers to create custom experiences with front-end and back-end integrations. Our goal is to empower all the world’s communities with...

About Root Root is a communication and productivity software platform that is uniquely designed to meet the needs of the world’s online communities. The Root platform is extensible, allowing third-party developers to create custom experiences with front-end and back-end integrations. Our goal is to empower all the world’s communities with...

About Root Root is a communication and productivity software platform that is uniquely designed to meet the needs of the world’s online communities. The Root platform is extensible, allowing third-party developers to create custom experiences with front-end and back-end integrations. Our goal is to empower all the world’s communities with...

Job DescriptionJob Description3dB Labs is a growing Defense Contractor focusing on Digital Signal Processing Software and Hardware with a diverse customer base.  We are looking for a Technical Writer to join our production team as we grow and scale our capabilities. The Technical Writer is responsible for taking complex, technical information and...

Job DescriptionJob Description3dB Labs is a growing Defense Contractor focusing on Digital Signal Processing Software and Hardware with a diverse customer base.  We are looking for a Technical Writer to join our production team as we grow and scale our capabilities. The Technical Writer is responsible for taking complex, technical information and...

Job DescriptionJob DescriptionCompany DescriptionBe part of something great!Synchrony Group is an independently owned network of companies, headquartered in West Chester, PA.At Synchrony, we are dedicated to providing the highest quality products and services in the medical communications industry. Our vision is to create the highest value for our clients...

Job DescriptionJob DescriptionLead compilation of new and existing data for the Environmental Media, Waste Disposition Alternatives, and D&D Remedial Investigation and Feasibility Study (RI/FS) processes. Coordinate with site resources to ensure necessary laboratory, data validation and statistical analysis processes are in place for new data collection....

Job DescriptionJob DescriptionLead compilation of new and existing data for the Environmental Media, Waste Disposition Alternatives, and D&D Remedial Investigation and Feasibility Study (RI/FS) processes. Coordinate with site resources to ensure necessary laboratory, data validation and statistical analysis processes are in place for new data collection....

Overview:Cook Research Incorporated (CRI) is a dynamic company that is focused on improving patient care and is staffed with a diverse group of professionals, scientists, and technicians who have expertise in medical products. The highly talented and creative CRI team performs hundreds of in vivo and in vitro tests, manages regulatory submissions globally,...

**About the Department** Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. What we offer you: - Leading pay and annual...

Senior Director, Regulatory Affairs CMCHybrid - West Chester, PAMeet has partnered with a very well-established pharma with hundreds of approved products. They are looking for a Senior Director of Regulatory CMC (biologics) to join their team. This position will be working across the company's mid-stage, new development pipeline and will be reporting into...

Senior Director, Regulatory Affairs CMC Hybrid - West Chester, PA Meet has partnered with a very well-established pharma with hundreds of approved products. They are looking for a Senior Director of Regulatory CMC (biologics) to join their team. This position will be working across the companys mid-stage, new development pipeline and will be reporting into...

Join our comfortable, friendly, business casual work environment. Full time with half day Fridays. No weekends! Writing ability is a plus, but we will train. Do you have a mechanical background and a great interest in all things mechanics? Are you looking to change up your work environment and try something new? We are looking for a mechanic to hire...