Regulatory Compliance Specialist II
4 weeks ago
Overview:
This position entails conducting routine reviews of personnel training documentation and training records, review of applicable environmental regulations to assure thorough implementation, conducting periodic compliance assessments, and reporting regulatory compliance status under the direction of management. The WIPP facilitys mission is to emplace the nations defense-generated transuranic (TRU) mixed waste in an underground ground mine for permanent disposal. TRU mixed waste is TRU radioactive waste co-mingled with hazardous waste. Because the WIPP facility disposal facility of TRU mixed waste, it is subject to the permitting requirements of the Resource Conservation and Recovery Act (RCRA) at 40 CFR Part 264 for Treatment, Storage, and Disposal Facilities. This includes the requirements at 40 CFR 264.16, Personnel Training.
Responsibilities: Review RCRA job position assignments at the WIPP facility to ensure they are accurately identified on the human-resources required form; evaluate newly created job positions at the facility to determine the RCRA requirements for training; perform periodic reviews of personnel training lists to ensure that required updates have been made.
Review inspection records for compliance with the RCRA Permit.
Conduct periodic assessments of the RCRA training program to ensure compliance with the record-keeping requirements of 40 CFR 264.16.
Possess people and teaming skills necessary to provide guidance to facility organizations relative to RCRA training requirements for their personnel, developing positive working relationships in the process. The job will entail regulator interface with the technical training department as well as with individuals within various WIPP operational, engineering, and emergency management organizations, including managers and designated training coordinators, as appropriate.
Possess excellent writing and verbal communication skills.
Summarize assessments, develop corrective action plans, and cohesively describe areas where enhancements to the facility environmental compliance.
Support facility inspections by regulatory agencies.
Be proficient with appropriate computer skills to work within Word and Excel to develop files, draft letters, create spreadsheets and modify such documents as required to manage job tasks.
Be able to work both independently and with a team and demonstrate the flexibility to smoothly transition between multiple tasks.
Complete other permitting and compliance related tasks, as assigned.
Bachelor's of Science degree in a technical discipline with two years technical experience or equivalent experience.
Preferred environmental compliance/regulatory assurance experience.
Effective verbal and written communication skills are required.
The ability to work independently as well as collaboratively with other individuals and project groups is highly encouraged.
Attention to detail and initiative is required.
The ability to use Microsoft Office to prepare Excel spreadsheets, PowerPoint presentations, and reports is required.
The ability to develop knowledge of, respect for, and skills to engage with those of varying departments site-wide is required.
USD $56,388.00 - USD $101,460.00 /Yr.
-
Sr. Specialist, Regulatory Affairs
4 days ago
Carlsbad, United States Internetwork Expert Inc Full timeThe Regulatory Affairs Senior Specialist will be responsible for providing regulatory support of spinal implant and instrument product launches for domestic and international countries; as well as the support of daily activities related to product design teams, design control, and regulatory product submissions. Essential Duties and...
-
Regulatory Affairs Specialist
5 days ago
Carlsbad, United States Internetwork Expert Inc Full timeATEC Spine has an exciting opportunity for a Regulatory Affairs Specialist to work on-site at our location in San Diego, California. The Regulatory Affairs Specialist will support the development of submissions for domestic and international clearances for spine surgery products; as well as the support of daily activities related to product design teams,...
-
Sr. Specialist, Regulatory Affairs
4 days ago
Carlsbad, United States Atec Spine Full timeThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities * Collaborates as a core team member on new...
-
Sr. Specialist, Regulatory Affairs
3 days ago
Carlsbad, United States Atec Spine Full timeThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities * Collaborates as a core team member on new product...
-
Sr Regulatory Affairs Specialist
4 days ago
Carlsbad, United States Actalent Full timeDescription: The Sr. Regulatory Affairs Specialist - Europe participates and manages necessary regulatory and project management activities required for medical device registration and compliance, with a focus on European Medical Device registration. The candidate must have successfully demonstrated technical proficiency, creativity, initiative, independent...
-
Sr Regulatory Affairs Specialist
4 days ago
Carlsbad, United States Actalent Full timeDescription: The Sr. Regulatory Affairs Specialist - Europe participates and manages necessary regulatory and project management activities required for medical device registration and compliance, with a focus on European Medical Device registration. The candidate must have successfully demonstrated technical proficiency, creativity, initiative, independent...
-
QA & Regulatory Compliance Manager
6 days ago
Carlsbad, United States Galderma Full timeWith a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable...
-
QA & Regulatory Compliance Manager
1 week ago
Carlsbad, United States Galderma Full timeWith a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable...
-
Sr. Specialist, Regulatory Affairs
5 days ago
Carlsbad, United States Alphatec Spine Full timeThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities Collaborates as a core team member on new product...
-
Sr. Specialist, Regulatory Affairs
3 days ago
Carlsbad, United States Alphatec Spine Full timeJob DescriptionJob DescriptionThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties and Responsibilities Collaborates as a core...
-
Sr. Specialist, Regulatory Affairs
4 days ago
Carlsbad, United States Alphatec Spine Full timeThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product...
-
Sr. Specialist, Regulatory Affairs
5 days ago
Carlsbad, United States Alphatec Spine Full timeThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product...
-
Regulatory Affairs Specialist
3 days ago
Carlsbad, United States Alphatec Spine Full timePrimary responsibilities include the development of submissions for domestic and international clearances. Additionally, will assist to support daily activities such as new product development, change control, and post market surveillance. Essential Duties And Responsibilities Collaborates as a core team member on new product development teams. Determines...
-
Regulatory Affairs Specialist
4 days ago
Carlsbad, United States Alphatec Spine Full timePrimary responsibilities include the development of submissions for domestic and international clearances. Additionally, will assist to support daily activities such as new product development, change control, and post market surveillance.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product development teams. Determines and...
-
Regulatory Affairs Specialist
3 days ago
Carlsbad, United States Alphatec Spine Full timeJob DescriptionJob DescriptionPrimary responsibilities include the development of submissions for domestic and international clearances. Additionally, will assist to support daily activities such as new product development, change control, and post market surveillance.Essential Duties and Responsibilities Collaborates as a core team member on new product...
-
Regulatory Affairs Specialist
5 days ago
Carlsbad, United States Alphatec Spine Full timePrimary responsibilities include the development of submissions for domestic and international clearances. Additionally, will assist to support daily activities such as new product development, change control, and post market surveillance.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product development teams. Determines and...
-
Manager, Site Environmental Compliance
1 month ago
Carlsbad, United States Los Alamos Technical Associates Full timeOverview: LATA POSITION: Manager, Site Environmental ComplianceDepartment: Site Environmental Compliance (Carlsbad, NM)Job description: LATA is currently searching for a Manager of the Site Environmental Compliance section for the project in Carlsbad, New Mexico. This is a government contract to the U.S. Department of Energy (DOE) supporting the Waste...
-
Director, Compliance
2 weeks ago
Carlsbad, United States Arlo Inc Full timeWe are looking for a Compliance Director to join our team. Leading a small team, you will be responsible for managing the following aspects of compliance for Arlo: * Regulatory Compliance* ESG & CSR You are expected to be the subject matter expert of the above, and represent Arlo on these topics. Key Responsibilities of the position include:- Regulatory...
-
Director, Compliance
1 week ago
Carlsbad, United States Arlo Full timeWe are looking for a Compliance Director to join our team. Leading a small team, you will be responsible for managing the following aspects of compliance for Arlo: * Regulatory Compliance * ESG & CSR You are expected to be the subject matter expert of the above, and represent Arlo on these topics. Key Responsibilities of the position include:- Regulatory...
-
Benefits and Compliance Specialist
3 days ago
Carlsbad, United States Natural Alternatives International Full timeSince 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing...