Senior Process Engineer (Pharma/Design/GMP Manufacturing)

Your role will include, but is not limited to:

• Preparation of plant equipment layouts, process flow diagrams, equipment sizing P IDs.
• Preparation of Specifications, for Process Equipment, Utility Equipment Warehouse Equipment etc.
• Mass Energy balances to calculate Utility Load requirement.
• Knowledge of instrumentation Control requirement Preparation of plant process control Philosophies.
• Provide required process input to Instrumentation team for instrument process data sheets.
• Input to project schedules and monitoring tasks to meet milestones during each phase.
• Develop documentation, diagrams, and specifications to meet project requirements and regulatory standards.
• Prepare scope of work documentation for use in project planning.
• Participate in project reviews to enable ongoing status tracking and reporting.
• Prepare review project documents i.e. DQ, IQ, OQ PQ Qualifications, FAT/SAT protocol reports etc.
• Ensure adherence to industry standards and best practices in Process designing.
• Adhering to cGMP guidelines and work as per Arcadis SOP/Work instructions.
• Compliance to SHE Sustainability
• Performs the tasks within the agreed-upon budget and schedule.

Qualifications

Mandatory:

• Bachelor s degree in engineering (chemical, mechanical, industrial or similar).
• 5-8 years of experience as a process engineer in a design consultancy or GMP manufacturing environment.
• Knowledge of process analysis 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