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About No deviation
At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.
We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development - empowering our team members to grow personally and professionally.
Position Overview
The Process Engineer is responsible for supporting the introduction, qualification, and commercialization of new products and processes within the manufacturing facility. This role ensures production readiness through process assessment, material planning, system setup, and manufacturing execution support, while maintaining compliance with quality and operational requirements.
Key Responsibilities
Process Assessment & Manufacturing Readiness
Process Qualification (PQ) Support
Manufacturing Documentation Development
MES & System Implementation
Cross-Functional Collaboration
Required Qualifications
Why join us
How to apply
Are you ready to play a key role in shaping the future of pharmaceutical solutions If you're passionate about making an impact, we want you on our team!
Please submit your resume, outlining your qualifications and experience relevant to the role, here.
Job ID: 152028313
Skills:
process flow , Solidworks, Wi, Bom, Welding symbols, Autocad, Geometric tolerances, CAM programming, Manufacturing documentation, Sop, Process Validation, Manufacturing process optimization, Pfmea, Nesting software, Surface finishes
Skills:
Commissioning, Filtration, Root Cause Analysis, Lean Management, Validation, Data Analysis, Good Manufacturing Practice, Digital tools for documentation, Control Systems, Process troubleshooting, Capa, Chromatography, Fluid handling, Six Sigma
Skills:
Technical Documentation, Technology Transfer, GMP compliance, Aseptic manufacturing, Process development, Troubleshooting, Material assessment
Skills:
automation, process calculations, industrial communication protocols, Siemens PCS7, process control strategies, Emerson DeltaV, validation and technical documentation, sterile manufacturing, Process Engineering, Rockwell Automation PlantPAx, optimisation studies, Industry 4.0 concepts, GMP-compliant production facilities, controllogix, advanced pharmaceutical manufacturing, upstream downstream bioprocessing, risk assessments, digitalization
Skills:
regulatory standards , Troubleshooting, Gmp, biologics manufacturing, Purification, Fermentation, Filtration, drug substance processes, Process Validation