RevereIT LLC offers its employees opportunities to work on exciting and innovative projects that influence the lives of people worldwide. The company is committed to helping employees achieve financial security and improved quality of life.
In addition to receiving an equitable salary and having an equal opportunity for professional development and advancement, employees enjoy other benefits which enhances job satisfaction. Our package has been designed keeping in view about the short and long term requirements of the employees. Full time employees at RevereIT LLC are eligible for a wide range of benefits. Some of them are listed below.
- A competitive base salary, with periodic reviews and increments
- Relocation Assistance
- Health care package
- Employee Referral Program
- Life Insurance
- Fully Paid Training to keep your skills updated
Our referral program is easy, email us the resume. Contact your recruiter for further details, or firstname.lastname@example.org
What makes RevereIT LLC a preferred service provider?
- Our experts are available at competitive rates, considering their skills and experience.
- We specialize in Regulatory Affairs, QA/QC, Clinical Operations, Clinical Research, Project Management, Business Development.
- We choose experts with the relevant skills for each project. This keeps the clients' expenses down, as they don't have to worry about the employee administration costs.
- Frequently emerging new technologies make it hard for the client to constantly keep the employees trained in the latest techniques. Our team is constantly being trained in new technologies and so is always up-to-date. Hence, our team is ready to work on the projects at a very short notice.
- Our ability to fulfill the IT solutions in a short period of time makes the project cycle simpler, with resources not being an issue.
- We have a very friendly team who will train our clients on the developed project with their extensive knowledge about the project.
- Willingness of our consultants to relocate, travel and work during non-business hours.
RevereIT is always looking forward to hire professionals who can develop solutions that help customers achieve their business goals. Are you ready to make a difference in the lives of people?
We are currently hiring professionals for the below stated job profiles.
Senior Validation Engineer
Analyze validation test data to determine whether systems or processes have met validation criteria and to identify root causes of production problems. Prepare validation and performance qualification protocols for new or modified manufacturing processes, systems, or equipment for pharmaceutical, electronics, and other types of production. Coordinate the implementation or scheduling of validation testing with affected departments and personnel. Study product characteristics or customer requirements and confer with management to determine validation objectives and standards. Create, populate, or maintain databases for tracking validation activities, test results, or validated systems. Prepare, maintain, or review validation and compliance documentation such as engineering change notices, schematics, and protocols. Resolve testing problems by modifying testing methods or revising test objectives and standards. Prepare detailed reports and design statements based on results of validation and qualification tests or reviews of procedures and protocols. Identify deviations from established product or process standards and provide recommendations for resolving deviations. Master's in Biomedical Engineering, Bio-Engineering, Biotechnology & Chemical Engineering. Job location: our office at 45640 Willow Pond Plaza # 200, Sterling, VA 20164. Travel and/or relocation to client site any- where in U.S.A. is a must. Likely candidates will be tested on their general ability to perform the above tasks. Mail resumes to HR Manager, RevereIT LLC, 45640 Willow Pond Plaza # 200, Sterling, VA 20164. No PHONE CALLS PLEASE. RevereIT LLC is an EQUAL OPPORTUNITY EMPLOYER.
Senior Validation Analyst (Regulatory Affairs)
Senior Validation Analyst (Regulatory Affairs) RevereIT, LLC has job openings for Sr. Validation Analyst (Regulatory Affairs). Analyze requirements for various equipment or systems in compliance with Federal Rules and Regulations related to various pharmaceutical and/or medical device manufacturing facilities. Coordinate, prepare, or review documents related to regulatory submissions for various domestic and/or international projects. Write or update standard operating procedures, work instructions, or policies. Prepare and review protocols and identify gaps performing Root Cause Analysis. Track defects using Defect Management Tool and create deviation summary report. Provide technical review of data or reports that will be incorporated into FDA submissions to assure scientific rigor, accuracy, and clarity of presentation. Maintain or coordinate current knowledge base of existing and emerging regulations, regulatory standards, or guidance documents. Prepare and assist in development and review of Validation Protocols. Compile and maintain regulatory documentation databases or systems. Participate in internal or external audits. Travel/relocate to various unanticipated locations throughout the U.S. for long and short-term assignments at client sites. Master's degree or foreign equivalent in Regulatory Affairs, Pharmaceutical Sciences, Pharmacy, Chemistry, Biology, Molecular Biology and Microbiology or in a related life sciences discipline. Job location: our office at 45640 Willow Pond Plaza # 200, Sterling, VA 20164. Travel and/or relocation to client site any- where in U.S.A. is a must. Likely candidates will be tested on their general ability to perform the above tasks. Mail resumes to HR Manager, RevereIT LLC, 45640 Willow Pond Plaza # 200, Sterling, VA 20164. No PHONE CALLS PLEASE. RevereIT LLC is an EQUAL OPPORTUNITY EMPLOYER.
Senior Engineer (Medical Device)
Senior Engineer (Medical Device) Ensure the quality of the medical device system meets the design requirements, develop, implement and maintain test plans, protocols, test scripts and traceability matrix for design verification & validation, execute protocols/test scripts and document results. Ensure compliance with FDA device regulatory requirements (21 CFR Part 11), including Design History File and 510(k). Provide technical support in identifying continuous improvements to manufacturing operations and implementing new technologies. Perform assignments designed to continue the development of professional work knowledge and abilities requiring application of standard engineering techniques, procedures and criteria in carrying out a sequence of related engineering tasks, project management, statistical analysis and presentation of data and technical writing, assist in performing engineering projects, execute engineering studies process validation protocols and summary reports (IQ, PQ, OQ, Computer Software Validation and Test Method Validation). Master of Science Degree in Engineering discipline in Mechanical, Electrical, Electronics, Industrial and Engineering Management are acceptable. Job location: our office at 45640 Willow Pond Plaza # 200, Sterling, VA 20164. Travel and/or relocation to client site any- where in U.S.A. is a must. Likely candidates will be tested on their general ability to perform the above tasks. Mail resumes to HR Manager, RevereIT LLC, 45640 Willow Pond Plaza # 200, Sterling, VA 20164. No PHONE CALLS PLEASE. RevereIT LLC is an EQUAL OPPORTUNITY EMPLOYER.