Engineering Administrator - Product Manufacturing

Job DescriptionEngineering AdministratorTHIS IS AN ON-SITE POSITION**SummarySupporting of the development of new products and continuous improvement of existing products by creating, editing and writing various types of technical documentation, including how-to guides, operating, user and maintenance manuals, instructions and other technical publications related to the equipment.Primary responsibilities:Work closely with the members of the engineering teams to understand client’s/new product requirements (content, format and schedule). Contribute to development and management of project documents, Project Tasks, Milestones, and outline content, requirements, budget, and deliverables. Support the PDM administration with clerical data updates. Support the development and maintenance of technical specifications. Update user documentation for a variety of materials, including how-to guides and instruction manuals. Maintain and update departmental procedures and tools. Research, collect and organize information on the subjects in libraries and on the web. Support product testing and data collection. Prepare charts, graphs, or forms to be incorporated into the final documentation package. Edit and update current publications. Follow a document development life cycle. Release the documents following final approval, if necessary. Support detailed web searches for commercial or technical material. Requirements:Proven history of working in small teams and independently. Motivated self-starter with ability to function independently or in a team. Mechanical, electrical and fluid mechanics aptitude is a strong benefit. Proficient in MS Office Suite (MSOffice, MS Project, Visio, MS Access). Strong grammatical skills. Experience:5 Years Experience in a Product Manufacturing environment. Experience with the assembly, installation, start-up of industrial equipment (highly preferred). Familiarity of the use of standard hand tools necessary to communicate with team members. The ability to read and understand mechanical and electrical drawings in both European and North American formats is required. Familiarity with PLC’s and HMI's/SCADA will be an advantage and experience in the medical / clean room industry as well as in Validation is a plus. BenefitsMonthly Benefit Allowance awarded to all employees. Comprehensive Benefits Package401(k) Match – up to 6.6% match / fully vested immediately. PTO and Holiday PayOpportunities for growthMonday - FridayRad Source Technologies, Inc. is an equal opportunity employer where employment is based upon personal capabilities and qualifications without discrimination because of race, color, religion, gender, age, national origin, disability, veteran status, or any other protected characteristic as established by law.Disclaimer: This job description may not be inclusive of all assigned duties, responsibilities, or aspects of the job described, and may be amended at any time at the sole discretion of the Employer.Company DescriptionRad Source was founded in 1997 for the purpose of creating non-gamma irradiation alternatives. Even prior to the more recent security issues associated with radioactive gamma sources, the company’s vision was to solve environmental disposal and related practical issues associated with “hot” source equipment.Based on that, we introduced our first products in 1999 incorporating x-ray technology including the first FDA cleared x-ray blood irradiator as well as our laboratory research x-ray irradiator, the RS 2000.Since then, we’ve continued expanding our capabilities and adding to our proprietary x-ray based irradiation technology, developing proprietary x-ray sources and new equipment. We are a global enterprise and our equipment resides in major pharmaceutical labs, healthcare institutions and renowned universities around the world. We are based in Buford, Georgia, USA where our highly qualified and dedicated staff continues to develop our technology, design and produce our equipment.Rad Source was founded in 1997 for the purpose of creating non-gamma irradiation alternatives. Even prior to the more recent security issues associated with radioactive gamma sources, the company’s vision was to solve environmental disposal and related practical issues associated with “hot” source equipment. Based on that, we introduced our first products in 1999 incorporating x-ray technology including the first FDA cleared x-ray blood irradiator as well as our laboratory research x-ray irradiator, the RS 2000. Since then, we’ve continued expanding our capabilities and adding to our proprietary x-ray based irradiation technology, developing proprietary x-ray sources and new equipment. We are a global enterprise and our equipment resides in major pharmaceutical labs, healthcare institutions and renowned universities around the world. We are based in Buford, Georgia, USA where our highly qualified and dedicated staff continues to develop our technology, design and produce our equipment.