Process Engineer

Overview

Process Engineer role within Arcadis' Global Excellence Centre (GEC), delivering process engineering solutions for Pharmaceutical, Semi-Conductor and Process industries.

What you'll do

• Prepare plant equipment layouts, process flow diagrams, equipment sizing and P&IDs.
• Prepare specifications and data sheets for process equipment, utility equipment, warehouse equipment and similar.
• Provide required process input to the instrumentation team for instrument process data sheets.
• Knowledge of instrumentation control requirements and preparation of plant process control philosophies.
• Develop documentation, diagrams and specifications to meet project requirements and regulatory standards and guidelines.
• Participate in project reviews to enable ongoing status tracking and reporting.
• Prepare and review project documents, including DQ, IQ, OQ and PQ qualifications, and FAT/SAT protocols and reports.
• Ensure adherence to industry standards and best practices in process design.
• Adhere to cGMP guidelines and work as per Arcadis SOPs and work instructions.
• Comply with SHE and sustainability requirements.

What you'll need

• Bachelor's degree in engineering (Chemical preferred, Mechanical also accepted).
• Experience as a process engineer in a design engineering consultancy environment.
• 4-8 years of experience as a process engineer in a design consultancy.
• Knowledge of process analysis and process modelling.
• Working knowledge of process safety, risk assessment and compliance with regulatory standards.
• Good project management skills with the ability to prioritize tasks and meet deadlines.
• Effective communication and interpersonal skills to collaborate with cross-functional teams and stakeholders.
• Ability to manage multiple projects simultaneously and meet deadlines in a fast-paced environment.

Nice to have

• Master's degree in process engineering or a related field.
• Professional certification in process engineering or related areas.
• Experience with process automation and control systems.
• Knowledge of process simulation software and computer-aided design (CAD) tools.
• Solid understanding of quality management systems, such as ISO standards.
• Experience of sterile processing.
• Knowledge of hazardous area classification.
• Experience of high potency pharmaceuticals.
• Experience of both small molecule and large molecule process design.

Details

• Location: Navi Mumbai, Maharashtra, India.