| Note: We are exclusively looking for candidates having Pharma/ Lifesciences /Bio pharma background.
The Process Architect – Architectural (CSA) is generally assigned to a project as a someone with specialist skills acquired on the job or through formal qualifications in the field of Pharmaceutical/Life Sciences facilities and site master planning. He/she is responsible for client interactions to understand their needs and requirements, creating concept layout options, site master planning, presentations and getting an “buy in” from clients on an option to proceed further. He/she is also responsible for ensuring that the Company and Group’s technical policies are followed, considering any special contractual requirements. · Prepares architectural layout options, site master plan options, Architectural narratives/philosophies, architectural flow diagrams, architectural schedules, room data sheets, implement cGMP requirements, support in permitting application drawings, support in tender, specification preparations. |
Ensure that all work is compliance with the Client’s Standards and Engineering Practices as described in the Project Co-ordination Procedure.
| · Provide support and technical assistance to the Project Lead Architect to translate and implement the client approved design during Basic and Detail Design Phases.
· Able to work as an individual contributor to develop layout options, concept 3D models, renderings, presentations to clients with little or no input from other disciplines at the Feasibility and concept phases. |
In addition, carry out such tasks from time to time as directed by the Project Lead Architect, Group Lead, People Leader, Department Manager with the work expected of this position.
| Technical and Development
· Degree in Architecture from a institute whose B. Arch is recognised by the Council of Architecture. · Have In-depth knowledge in Layout development and general process requirements of pharmaceutical / Life Science Pharmaceutical production facilities including but not limited to for API, Sterile Products, OSD, Bio-Pharma, Gene Therapy products, related R&D labs etc. · Ability and the initiative learn new types of facilities as required by clients requirements. |
Detailed knowledge in requirements of NBC and major statutory and regulatory bodies such as states, local bodies, and Industrial area bodies such as MIDC, KSIIC, HSIIDC etc.