Process Engineer

Key Responsibilities

• Develop, Review, Approve technical content of P&IDs, and complete back-check process ensuring drawing accuracy based on defined scope and deliverables.
• Develop block flow and process flow diagrams based on client direction.
• Leverage appropriate Client standards, generate project specific Process Specifications.
• Generate vendor bid packages from equipment specifications and complete technical bid analysis based on vendor quotations.
• Evaluate and Define process equipment utility requirements from vendor data and complete utility system capacity studies based on this and site data.
• Review and perform basic process calculations including pump sizing, hydraulic/pipe flow, and heat transfer.
• Complete engineering field surveys and P&ID walkdowns, document findings and ensure resolution where issues are found.
• Attend relevant design and client-based meetings to drive Project scope and deliverables.
• Lead process related deviations and provide technical support to manufacturing.
• Investigate, identify root cause for critical deviations and determine CAPA for manufacturing.
• Write product impact assessments to support deviations.
• Write and review technical documentation (batch records, SOPs, protocols & reports).
• Participate and report to a cross-functional development team to advance production activities.
• Ensure successful manufacturing production runs by assessing risk, setting preventative measures in place, investigating, and troubleshooting equipment and process issues.
• Design and execute process development studies to develop a thorough understanding of operating and process performance parameters.
• Perform hands-on activities that support process engineering from drafting procedures to execution of commissioning start up studies.

Skills & Qualifications

• Degree in Biochemical Engineering, Chemical Engineering, Biotechnology or related discipline with at least 2 plus years of GMP Lifesciences, pharmaceutical manufacturing, technology transfer & process development experience required.
• Practical expertise with cGMP manufacturing and regulatory regulations and requirements for pharmaceuticals and devices.
• Mastery of scientific and engineering Principles.
• Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell therapy products and process development.
• Ability to think critically, and demonstrated troubleshooting and problem-solving skills.
• Excellent interpersonal, verbal, and written communication skills.
• Ability to function efficiently and independently in a changing environment.
• Self-motivated and willing to accept temporary responsibilities outside of initial job description.
• Well-developed computer skills.

The Company

DPS Group is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a 'client-first' mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.

DPS Engineering Inc. is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. DPS does not discriminate in employment opportunities or practices on the basis of: race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status or any other characteristic protected by country, regional or local law.