Minimum Qualification Criteria: Bachelor’s degree in Pharmacy or Biotechnology (mandatory) Master’s degree in Pharmacy (preferred) A Project Associate plays a pivotal role in supporting end-to-end pharmaceutical project activities including planning, documentation, regulatory coordination, and client communication. This role is designed for individuals with a strong academic foundation and the eagerness to grow in project management, technical operations, and compliance within the pharmaceutical domain. Roles & Responsibilities Assist in planning and executing pharmaceutical facility design and validation projects. Coordinate between client teams, internal engineering experts, and regulatory bodies. Prepare and review technical documentation such as URS, SOPs, qualification protocols, and reports. Monitor project timelines, deliverables, and maintain accurate records of progress. Research and analyze regulatory guidelines to ensure project compliance. Support client interactions during audits, inspections, and key deliverable presentations. Contribute to continuous improvement initiatives and knowledge sharing sessions. Core Competencies: Technical Knowledge: Strong understanding of pharmaceutical manufacturing, GMP, and regulatory frameworks. Documentation Skills: Ability to prepare structured, compliant documents and reports. Communication Ability: Clear and professional communication with clients and internal teams. Analytical Thinking: Ability to analyze data, solve problems, and make informed decisions. Organizational Skills: Effective planning, task prioritization, and deadline management. Team Collaboration: Willingness to work collaboratively and learn from cross-functional teams. Job Type: Full-time Pay: ₹180,000.00 - ₹240,000.00 per year Work Location: In person Application Deadline: 05/08/2025 Expected Start Date: 05/08/2025
Minimum Qualification Criteria: ITI in Draftsmanship (Civil) Diploma in Civil Engineering Bachelor’s degree in Civil Engineering (preferred for advanced roles) A Draftsman/woman will be responsible for creating detailed technical drawings and documentation to support pharmaceutical facility design, equipment layout, process flow, and other engineering requirements. This role demands precision, compliance awareness, and coordination with multidisciplinary teams. Roles & Responsibilities: Produce 2D and 3D CAD drawings for architectural, mechanical, piping, electrical, and HVAC systems. Prepare layouts for cleanrooms, labs, production suites, and utility areas based on GMP standards. Revise drawings based on client feedback, engineer input, or regulatory changes. Ensure documentation accuracy in alignment with pharmaceutical industry codes and project specifications. Collaborate with project engineers and architects to interpret technical designs and specifications. Maintain drawing logs, version control, and documentation archives. Assist in site measurements, drafting as-built drawings, and coordinating with contractors. Core Competencies: Technical Proficiency: Strong command of AutoCAD, Revit, and other design software tools. Regulatory Awareness: Familiarity with GMP, USFDA, WHO, and other pharmaceutical regulatory norms. Team Collaboration: Ability to work closely with project managers, engineers, and QA teams. Attention to Detail: High precision in drawings to prevent costly errors in implementation. Time Management: Efficient handling of multiple drafts within tight deadlines. Communication Skills: Clear documentation and reporting skills for technical and non-technical stakeholders. Job Type: Full-time Pay: ₹180,000.00 - ₹220,000.00 per year Work Location: In person Application Deadline: 05/08/2025 Expected Start Date: 01/08/2025
Minimum Qualification Criteria: Bachelor’s degree in Pharmacy or Biotechnology (mandatory) Master’s degree in Pharmacy (preferred) A Project Associate plays a pivotal role in supporting end-to-end pharmaceutical project activities including planning, documentation, regulatory coordination, and client communication. This role is designed for individuals with a strong academic foundation and the eagerness to grow in project management, technical operations, and compliance within the pharmaceutical domain. Roles & Responsibilities Assist in planning and executing pharmaceutical facility design and validation projects. Coordinate between client teams, internal engineering experts, and regulatory bodies. Prepare and review technical documentation such as URS, SOPs, qualification protocols, and reports. Monitor project timelines, deliverables, and maintain accurate records of progress. Research and analyze regulatory guidelines to ensure project compliance. Support client interactions during audits, inspections, and key deliverable presentations. Contribute to continuous improvement initiatives and knowledge sharing sessions. Core Competencies: Technical Knowledge: Strong understanding of pharmaceutical manufacturing, GMP, and regulatory frameworks. Documentation Skills: Ability to prepare structured, compliant documents and reports. Communication Ability: Clear and professional communication with clients and internal teams. Analytical Thinking: Ability to analyze data, solve problems, and make informed decisions. Organizational Skills: Effective planning, task prioritization, and deadline management. Team Collaboration: Willingness to work collaboratively and learn from cross-functional teams. Job Type: Full-time Pay: ₹180,000.00 - ₹240,000.00 per year Work Location: In person Application Deadline: 05/08/2025 Expected Start Date: 05/08/2025
Minimum Qualification Criteria: ITI in Draftsmanship (Civil) Diploma in Civil Engineering Bachelor’s degree in Civil Engineering (preferred for advanced roles) A Draftsman/woman will be responsible for creating detailed technical drawings and documentation to support pharmaceutical facility design, equipment layout, process flow, and other engineering requirements. This role demands precision, compliance awareness, and coordination with multidisciplinary teams. Roles & Responsibilities: Produce 2D and 3D CAD drawings for architectural, mechanical, piping, electrical, and HVAC systems. Prepare layouts for cleanrooms, labs, production suites, and utility areas based on GMP standards. Revise drawings based on client feedback, engineer input, or regulatory changes. Ensure documentation accuracy in alignment with pharmaceutical industry codes and project specifications. Collaborate with project engineers and architects to interpret technical designs and specifications. Maintain drawing logs, version control, and documentation archives. Assist in site measurements, drafting as-built drawings, and coordinating with contractors. Core Competencies: Technical Proficiency: Strong command of AutoCAD, Revit, and other design software tools. Regulatory Awareness: Familiarity with GMP, USFDA, WHO, and other pharmaceutical regulatory norms. Team Collaboration: Ability to work closely with project managers, engineers, and QA teams. Attention to Detail: High precision in drawings to prevent costly errors in implementation. Time Management: Efficient handling of multiple drafts within tight deadlines. Communication Skills: Clear documentation and reporting skills for technical and non-technical stakeholders. Job Type: Full-time Pay: ₹180,000.00 - ₹220,000.00 per year Work Location: In person Application Deadline: 05/08/2025 Expected Start Date: 01/08/2025
As a Draftsman/woman in the pharmaceutical industry, you will play a crucial role in creating detailed technical drawings and documentation essential for various aspects of pharmaceutical facility design, including equipment layout, process flow, and other engineering requirements. Your responsibilities will encompass producing 2D and 3D CAD drawings for architectural, mechanical, piping, electrical, and HVAC systems. Your work will involve preparing layouts for cleanrooms, labs, production suites, and utility areas based on Good Manufacturing Practice (GMP) standards. Your role will also entail collaborating with project engineers and architects to interpret technical designs and specifications accurately. Furthermore, you will be expected to maintain drawing logs, version control, and documentation archives while ensuring documentation accuracy aligned with pharmaceutical industry codes and project specifications. To excel in this role, you must possess technical proficiency in tools like AutoCAD and Revit. Regulatory awareness, especially concerning GMP, USFDA, WHO, and other pharmaceutical regulatory norms, will be essential. Your ability to collaborate effectively with project managers, engineers, and quality assurance teams will be crucial for successful project outcomes. Attention to detail is paramount to prevent costly errors during implementation, and efficient time management will be required to handle multiple drafts within tight deadlines. Strong communication skills for clear documentation and reporting to both technical and non-technical stakeholders will also be necessary. This is a full-time position that requires in-person work at the designated location. The minimum qualification criteria for this role include an ITI in Draftsmanship (Civil), a Diploma in Civil Engineering, and a Bachelor's degree in Civil Engineering (preferred for advanced roles). If you meet these requirements and are enthusiastic about contributing to pharmaceutical facility design through precision, compliance awareness, and collaboration with multidisciplinary teams, we encourage you to apply before the application deadline on 05/08/2025. The expected start date for this position is 01/08/2025.,