TCB CB Administrator

Job description

Core Responsibilities: To perform this role successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required: Collecting and performing cursory reviews on documents needed for certification and storing them in an organized job folder. Preparing applications for TCB technical review (via completed admin checklists). Updating the TCB Tracking Sheet to keep track of the number of applications processed Providing applicants/customers/engineers details of technical review results (RTs) Saving the RTs and Responses in the applicable job folder Uploading information when approved (FCC/Canada/MIC) and receiving/creating grants to be issued to the applicant/customer. Work directly with clients to create Technical Construction Files (TCFs) related to the Radio Equipment Directive (RED). Providing applicants/customers/engineers details of technical review results (RTs) for RED applications Issuing Notified Body Opinions (NBOs) Work with Program Manager for Surveillance functions throughout the year. Update documents within the TCB folder as necessary (training, procedures, checklists, work instructions, etc.) Prepare for and participate in audits conducted by regulatory bodies and accreditation organizations. Coordinate all TCB projects and provide Billing Forecast to TCB Director, ensure all projects are billed in METrak Ability to maintain confidentiality. Other duties as deemed appropriate by management and for which management believes adequate experience exists, or for which knowledge can be easily obtained to perform such duties. As-needed Responsibilities: Contribute to team efforts of customer arrivals, scheduling, and conflict resolution Other duties as deemed appropriate by management and for which management believes adequate experience exists, or for which knowledge can be easily obtained to perform such duties Travel as needed according to company guidelines Two-year college degree or relevant experience. Experience in regulatory compliance and certification processes. Strong written and verbal communications skills including the ability to communicate effectively in a group setting with colleagues and clients. Ability to perform multiple tasks. Ability to work independently. Ability to organize and prioritize workload to meet or exceed deadlines. Authorization to work in the United States indefinitely without restriction or sponsorship. Demonstrated excellent verbal and written communication skills Demonstrated attention to details and good documentation skills Must have computer (Word, Excel, Teams, Outlook) and office related skills Physical Demands: Office/Desk working environment Ability to sit for long periods of time. Compensation: $36.06-$48.08 per hour Schedule: The position is full-time, Monday - Friday, 8:00am - 5:00pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.