Job Description
We are seeking a skilled Process Engineer to join our team on-site at a client facility specializing in Human Health Vaccine Manufacturing. The role involves meeting with customers to develop process solutions for CapEx expansion projects, conducting commissioning activities, leading HAZOP studies, and implementing risk management strategies. The Process Engineer will optimize manufacturing processes using simulation tools and provide technical support for upstream and downstream bulk sterilization processes.
ResponsibilitiesEnsure 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.Facilitate the identification and communication of the root causes of losses in the operation of production equipment and processes.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.Essential SkillsBachelor’s degree in chemical engineering, biochemical engineering, mechanical engineering, or a related field.At least five years of aseptic pharmaceutical manufacturing/engineering experience.In-depth understanding and application of cGMP principles, concepts, practices and standards.At least three years of upstream and downstream bulk sterile processing experience.Understanding of the operating principles of bioreactors, chrome skids, and filtration skids working in a pilot plant.Equipment commissioning and/or qualification experience.Process Safety Management understanding.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.Willingness to travel regionally and/or nationally throughout the U.S.A.Additional Skills & QualificationsMaintenance and Reliability Engineering experience is a plus.Work Environment
Fully on-site in Upper Merion/King of Prussia, PA area. Working with clients, other consultants, and vendors.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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