For more than 20 years, Trinity Consultants has assisted facilities in the aerospace industry with regulatory compliance and environmental management issues. Trinity has a long history of assisting facilities with their regulatory compliance and environmental management systems. Trinity helps chemical and pharmaceutical manufacturers to achieve regulatory and environmental compliance. Due to their nature, general manufacturing facilities are often faced with reviewing a wide range of regulations to determine applicability. Trinity provides a variety of services to government entities, including environmental permitting and compliance management. Trinity Consultants has long been committed to assisting lime and aggregates facilities with their regulatory compliance needs. Trinity takes pride in understanding the regulatory issues affecting our clients facilities and their industry. Oil and gas facilities must contend with a variety of regulatory compliance and environmental management demands. Trinity Consultants has long been committed to assisting cement facilities with their regulatory compliance and environmental management needs. Trinity has extensive experience assisting the pulp and paper industry with its regulatory compliance and environmental management requirements. Railroads are faced with rapidly evolving state, regional, and federal regulatory framework in the United States. Trinity prepares hundreds of air quality compliance reports for landfills and industrial facilities across the United States on an annual basis. For nearly 30 years, Trinity Consultants has assisted facilities such as those in the highly regulated wood products industry. The June 2016 Lautenberg amendments to the Toxic Substances Control Act (TSCA) required EPA to improve the TSCA Inventory by identifying which \"chemical substances\" are actively in commerce in the United States, allowing the agency to better The Regional Haze Rule (RHR) establishes a comprehensive visibility protection program for Class I areas and requires states to set reasonable progress goals (RPGs) towards achieving natural visibility conditions in all Class I areas by 2064. EPA In January 2019, Trinity Consultants (Trinity) acquired The Redstone Group (Redstone), a consulting services provider of international chemical control laws, and EHS auditing, compliance and permitting.Redstone has deep expertise and advises clients In 2016, the U.S. Customs and Border Protection (CBP) revised its importer compliance monitoring approach, although the change garnered little press. The agency's new priority involves re-focusing existing resources and using methods that more Leak Detection and Repair (LDAR) involves finding facility components that are leaking and fixing them. The U.S. Environmental Protection Agency (EPA) has a long history of regulating industries (such as petroleum refining and chemical View our monthly digests of environmental regulatory actions published in the U.S. Federal Register, with hyperlinks to the complete Federal Register notices. all summaries from 2011 These papers, presentations, and articles were authored by the staff of Trinity Consultants for presentation at various conferences. all papers & presentations View recorded webinars on important regulatory developments and their implications for the regulated community. all videos Since its founding in 1974, Trinity has expanded its geographic footprint and breadth of services. We attribute our continued growth to a focus on cornerstone values of top-notch technical performance and excellence in client service. ADVENT Engineering, a Trinity Consultants company, is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Headquartered near San Francisco, California, and with operations in the Eastern US and Canada, ADVENT is involved in almost every facet of global pharmaceutical and biotechnology facility design and process engineering and quality system projects. ADVENT's services include process engineering, automation engineering, project engineering, facility/system design, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies. The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set. This is an outstanding opportunity to join our growing team! Positions available in multiple U.S. locations - North Carolina, Boston, San Francisco Bay Area, Texas, etc. Responsibilities Provide technical leadership on design, commissioning, and start-up of control systems supporting manufacturing, testing, and storage of biotech and pharmaceutical processes, systems, and facilities. Undertake technical reviews for documents generated by others to ensure that technical and regulatory requirements are met. Working with full range of Biotech/pharma project phase execution including all design phases (conceptual design, basic design, detailed design), construction support and commissioning. You may support CQV (Commissioning, qualification and validation), shut-down, and project hand-over activities. Generating, revising, and troubleshooting automation code and associated specifications and drawings as required. Performing code review to ensure code meets its specifications and requirements and is fit for purpose Assisting process and validation teams in execution of process, cleaning, equipment, and utility C&Q efforts. Writing and executing commissioning and/or qualification protocols and associated reports to verify systems are qualified for use May require oversight, management, and partnerships with process and equipment engineers to provide guidance and leadership to colleagues in technical aspects, thoroughness and detail oriented in ensuring fulfillment of project deliverables of team. You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and ADVENT resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc. Associated topics: bioinformatic, biology, bioprocess, biosynthetic, genetic, medical, metabolic, pain, parenteral, pharmaceutical
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.