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
