CSV Lead​/Computer System Validation Lead

Compli, LLC was founded in 2001 to provide Commissioning, Validation and Regulatory Support Services to the Life Sciences industry.

• Supporting Validation of Computer systems in support of a newly constructed drug manufacturing facility.
• Position will serve a key role in delivery to accommodate the exit of the existing facility.
• Lead the development and execution of CSV documents
• Provide project / process engineering support for capital project delivery projects.
• Ensure planned progress with respect to the engineering deliverables for projects, process engineering planning & scheduling, preparation of progress reports, manpower & resource forecasts, and utilize resources effectively & efficiently.
• Provide process design & detailed engineering including performing process simulations, design calculations, process optimization, sizing & selection of equipment for projects.
• Prepare various engineering deliverables (drawings & documents) such as process flow diagrams, P & I diagram, process datasheets, equipment specifications, cause & effect diagrams, control philosophies, shutdown philosophies, and HAZOP studies & reports.
• Facilitates and executes engineering change control documentation.
• Provide the necessary process engineering inputs for capex projects to the other disciplines and other departments.
• Prepare and issue RFIs, evaluate vendor’s quotations, clarifications, and perform technical bid analysis. Review vendor’s documents, drawings, datasheets, specifications and calculations.
• Supports construction and trade groups with site safety programs and assist in safety documentation.
• Other duties as assigned.

• BS in related engineering field (Chemical / Mechanical / Architectural / Electrical) (required).
• 10 to 15 years of experience in support of project or production, processes and process optimization (required) // process engineering including process design (if possible).
• Prepare process engineering deliverables for investment projects (e.g., PFDs, Equipment Specifications), experience is preferred but not required.
• Act in assigned roles within capital investment projects (e.g., Project /Process Engineer), experience is preferred but not required
• Knate experience preferred.
• Prior experience in a pharmaceutical / biotech manufacturing environment
• Prior experience with Current Good Manufacturing Practices and other applicable regulations
• Excellent client-facing relationship building skills.
• Excellent written and verbal communication skills.
• Excellent math and problem-solving skills.
• Ability to work independently or in collaboration with others.
• Solid organizational skills including attention to detail and multitasking skills.
• Proficient in MS Excel, MS Word, MS Project, MS PowerPoint, MS Access

Travel
:
Local to the Marietta, PA Metropolitan area. No per diem or travel assistance currently offered.

* This role is not open to C2C staffing.

At Compli, we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender identity, gender expression, disability, veteran status, pregnancy status, or any other status protected by law.