Process Engineer (Pharma/Design/GMP Manufacturing)

Responsibilities:-

• 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.

Qualification and Experience:-

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

Location:-

• Mumbai, Maharashtra.

Company Overview:-

Arcadis is the leading global Design & Consultancy for natural and built assets. Applying our deep market sector insights and collective design, consultancy, engineering, project and management services we work in partnership with our clients to deliver exceptional and sustainable outcomes throughout the lifecycle of their natural and built assets. We are 28,000 people, active in over 70 countries that generate €3.5 billion in revenues. We support UN-Habitat with knowledge and expertise to improve the quality of life in rapidly growing cities around the world.