Senior Process Engineer at Arcadis

Navi Mumbai, maharashtra, India -

Full Time

Start Date

Immediate

Expiry Date

09 Sep, 26

Salary

0.0

Posted On

11 Jun, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Engineering, Plant Equipment Layout, P&ID Preparation, OSD Facility Design, Parenteral Facility Design, Process Modelling, Process Safety, Risk Assessment, Project Management, cGMP Guidelines, DQ/IQ/OQ/PQ, FAT/SAT Protocols, Process Automation, CAD Tools, Hazardous Area Classification, Sterile Processing

Industry

Professional Services

Description

Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can solve the world’s most complex challenges and deliver more impact together. Role Description: This role will form a core part of our Global Excellence Centre (GEC) – Arcadis’ centralized and fully integrated project delivery group. Our GEC is made up of more than 3,000 talented individuals working in offices across India, Romania and Philippines, providing Capability, Capacity and a Competitive Advantage across a wide array of unique projects and services, in collaboration with our global businesses. Advanced Process Manufacturing within the GECs is comprised of cross-functional teams, that contribute to the design & development of innovative process engineering solutions in Pharmaceutical, Semi-Conductor & Process industries. Our ability to effectively manage projects, assess client needs, and provide technical guidance is crucial in delivering successful outcomes, using the most innovative way of doing computational design. Your Role will include, but not limited to: * Preparation of plant equipment layouts, process flow diagrams, equipment sizing & P & IDs. * Preparation of Specifications & data sheets, for Process Equipment, Utility Equipment Warehouse Equipment etc. * Experience with OSD projects, (Tablet, Capsule manufacturing), facility design, equipment involved in OSD facilities, like Granulator, FBD/FBP, compression, Coaters etc * Knowledge of equipment such as, Blister packing, Bottles packing lines, secondary packing lines, track & trace. Palletisers etc. * Experience with Small (Ampoule, Vial, PFS etc) & large Volume Parenteral Facility design. * Knowledge of equipment such as, Ampoule/Vail washers, dehydrogenation tunnels, filling machines, isolators, Autoclaves, inspection machine, secondary packing machines * Knowledge of instrumentation Control requirement & Preparation of plant process control Philosophies. * Provide required process input to Instrumentation team for instrument process data sheets. * Develop documentation, diagrams, and specifications to meet project requirements and compliances with regulatory standards and guidelines. * 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 Qualification Mandatory: * Bachelor’s degree in engineering [Chemical (Preferred)/Mechanical] * An experience as process engineer in design engineering consultancy environment. * 8-14 years of experience as a process engineer in a design consultancy. * 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. Why Arcadis? We can only achieve our goals when everyone is empowered to be their best. We believe everyone's contribution matters. It’s why we are pioneering a skills-based approach, where you can harness your unique experience and expertise to carve your career path and maximize the impact we can make together. You’ll do meaningful work, and no matter what role, you’ll be helping to deliver sustainable solutions for a more prosperous planet. Make your mark, on your career, your colleagues, your clients, your life and the world around you. Together, we can create a lasting legacy. Join Arcadis. Create a Legacy. Our Commitment to Equality, Diversity, Inclusion & Belonging We want you to be able to bring your best self to work every day which is why equality and inclusion is at the forefront of all our activities. Our ambition is to be an employer of choice and provide a great place to work for all our people. We are an equal opportunity employer; women, minorities, and people with disabilities are strongly encouraged to apply. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity. #GECPlacesProcessEngineering #LI-IP1

Responsibilities

Responsible for designing process engineering solutions, including equipment layouts, P&IDs, and specifications for pharmaceutical and process industries. The role involves preparing validation protocols (DQ, IQ, OQ, PQ) and ensuring compliance with cGMP and regulatory standards.