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Job Description Compli, LLC was founded in 2001 to provide Commissioning, Validation, and Regulatory Support Services to the Life Sciences industry. We serve pharmaceutical companies across the United States, offering a wide range of services that help companies exceed their goals and objectives. In today’s world, understanding regulations and quality assurance activities related to operations, vendors, engineering, construction, and contractors is more important than ever. In 2020, Compli, LLC became a wholly owned subsidiary of George Butler Associates, Inc. This acquisition integrated Compli into a network of services, providing clients with more options to engage an impressive suite of in-house services. Compli is a full-service firm specializing in Commissioning, Qualification, Regulatory Compliance, and On-Demand services. Essential Functions: Function as an owner’s representative and report to the client’s management lead. Coordinate internal and external resources for flawless project execution. Ensure all projects are delivered on time and within scope. Assist in defining project scope and objectives, involving all relevant stakeholders and ensuring technical feasibility. Develop detailed project plans to monitor and track progress. Manage changes to project scope, schedule, and costs using appropriate verification techniques. Measure project performance using suitable tools and techniques. Manage relationships with clients and stakeholders. Perform risk management assessments to minimize project risks. Establish and maintain relationships with third-party vendors. Meet with clients to clarify specific requirements of each capital project. Track project performance and analyze the successful completion of short- and long-term goals. Perform other related duties as assigned by the client’s representative. Education & Experience: Bachelor’s degree in engineering, preferably in mechanical engineering or construction management. At least seven (7) years of pharmaceutical engineering and capital project management experience. Familiarity with aseptic manufacturing processes and specifying aseptic processing equipment. PMP (Project Management Professional) certification preferred. Technical Skills & Abilities: Experience handling multiple projects with total values exceeding $5MM. Ability to discuss biologics and pharmaceutical manufacturing topics. Ability to work independently or collaboratively. Deep understanding of project management principles, concepts, and practices. Proficiency in current Good Manufacturing Practices and applicable FDA, USDA, and EU regulations. Excellent client relationship skills. Strong written and verbal communication skills. Excellent organizational skills with attention to detail and multitasking abilities. Proficient in MS Excel, Word, Project, PowerPoint, Access, and AutoCAD Lite. Willingness to travel regionally and/or nationally across the U.S. Travel: Based in Denver, CO, with willingness to travel regionally and nationally throughout the U.S. Salary Range: $90,000 to $115,000 per year. It’s more than just a job… At Compli, we value innovative and intelligent individuals who want to solve problems. We’re known for technical excellence and aim to create remarkable solutions for a higher quality of life. We are transforming the industry by integrating design and construction processes with new technology. At Compli, we are an Equal Employment Opportunity Employer, promoting diversity and inclusion regardless of race, gender, age, marital status, genetic information, expression, veteran status, or any other protected status by law. #J-18808-Ljbffr