4 Pharmaceutical Engineering Jobs

Participate in finalizing Basic and Detailed Engineering concepts (Mechanical/ HVAC/ Modular Panel/ Utility/ Firefighting & other disciplines, as applicable). Review/Approve MEP services drawings & documents supplied by the consulting firm. Ensure Installation/ Execution of MEP package services inline to GMP, GEP, ISPE & other applicable standards as applicable. Perform in - depth review of the project to schedule deliverables and estimate costs. Oversee all onsite and offsite MEP services to monitor compliance with building and safety regulations. Perform due diligence for identifying latest Installation trends, material, quality, reliability, cost etc. Prepare drawing and documents required for statutory approvals, as applicable Conduct, minute weekly project coordination meetings with all the consultants, contractors. Mediate any conflicts that are arise with various contractors and consultants Participate in resolving any technical hurdles during project executions with the help of consultants Ensure that Installation activities move according to predetermined schedule. Communicate effectively with the contractors responsible for completing various phases of the project. Co-ordinate the efforts of all parties involved in the project, which include the consultants, contractors, sub-contractors and labourers . Monitor the progress of the construction activities on a regular basis and hold regular status meetings with all the sub-teams. Maintain strict adherence to the budgetary guidelines, quality and safety standards. Following & documenting the Project Change control management as per the agreed procedures Ensure project documents are complete. Essential Requirements: Degree in Mechanical Engineering with 8 - 10 years of experience in Pharmaceutical/ Chemical/ FMCG Industry. Deep understanding of Project MEP services like Mechanical/Piping/HVAC/Clean room / Black & Clean Utility services within pharmaceutical Formulation facility. Good Knowledge of Project management like - Project planning, Cost Management, Time Management, Construction management, Quality Management, Contract Administration, Safety Management & required Statutory approvals management. Desirable Requirements: Bachelor s degree in mechanical engineering. Good English both spoken and written.

As a Project Planner at NNE, your role will involve being a part of a dynamic team of experienced professionals in the Project Management department. You will receive the necessary training and support to excel in planning large multi-disciplinary projects in the biotech and pharmaceutical field. Your responsibilities will include ensuring project planning activities are executed efficiently, adhering to project schedules, and implementing GMP requirements seamlessly. Additionally, you will contribute to the development and implementation of procedures and tools to enhance project execution within the department. Your daily tasks will revolve around creating project time schedules, identifying solutions to time constraints, advising project managers, evaluating progress reports, and providing schedule data for project reporting requirements. You will work collaboratively with a multi-disciplinary team, utilizing your expertise in project planning procedures and communication skills to drive successful project outcomes. To qualify for this role, you should have a minimum of 8-10 years of planning experience in an engineering or manufacturing company, proficiency in Primavera P6 and Microsoft Project, and a background in Quantity Surveying, Engineering, or Construction Management. Experience in the pharmaceutical, biotech, food, or chemical industries and the ability to handle multiple projects simultaneously are essential. Strong communication skills, both written and oral in English, and a structured approach to work are key attributes we are looking for in the ideal candidate. At NNE, we value individuals who are result-oriented, team players, and possess a flexible approach to work. If you are passionate about contributing to the design and construction of critical pharmaceutical facilities that impact millions of patients worldwide, we welcome you to apply for this position. Join our team of experts at NNE and be part of a work environment that fosters collaboration, innovation, and excellence in pharma engineering. If you believe you meet the qualifications and are ready to unleash your potential in a challenging yet rewarding role, we encourage you to apply before the deadline of 20th March 2025. For any inquiries or clarifications, please feel free to contact pvyn@nne.com or RHM@nne.com. We will be conducting interviews on an ongoing basis, and we look forward to the possibility of having you on our team at NNE India, Bangalore.,

As a Process Head at Kavs Spectronova Technologies Pvt Ltd, you will be responsible for leading the process engineering aspects of pharmaceutical plant projects. Your role will involve overseeing optimal process design, ensuring regulatory compliance, and facilitating seamless coordination among internal and external stakeholders for both greenfield and brownfield facility projects within the pharmaceutical industry. Your key responsibilities will include leading the end-to-end process design for various types of pharmaceutical facilities such as OSD, Injectable, Vaccine, or Biotech. You will be required to develop and review essential documents including P&ID, Process Flow Diagrams, Mass Balances, Equipment Sizing, and Critical Design Parameters. Additionally, you will prepare and evaluate User Requirement Specifications (URS) and oversee various tests and validation protocols such as FAT, SAT, DQ, IQ, OQ, and PQ to ensure compliance with regulatory standards like GMP, WHO, USFDA, and EU. Collaboration with cross-functional teams such as R&D, Quality Assurance, HVAC, Utility, Electrical, Instrumentation, and Automation will be a crucial part of your role. Your technical expertise and leadership will be essential during project execution, commissioning, and regulatory audits. Client meetings, technical presentations, and troubleshooting activities will also be a part of your regular responsibilities, along with international travel for projects, site visits, audits, and technical review meetings. To qualify for this position, you should hold a Bachelor's or Master's degree in Chemical Engineering or Pharmaceutical Engineering with 8 to 12 years of experience in process design and execution of pharmaceutical plant projects. A deep understanding of regulatory requirements including GMP, WHO, USFDA, and EU is essential. Demonstrated leadership skills in managing diverse teams and external consultants/vendors, excellent communication, documentation, and presentation abilities, as well as the capability to handle multiple projects under strict timelines are required. A valid passport is mandatory for this role, and prior international exposure is highly desirable. In return, we offer you a challenging leadership role in global pharmaceutical projects, opportunities for international exposure and career advancement, a collaborative work environment that emphasizes innovation and compliance, as well as competitive compensation and benefits in line with industry standards. To apply for this position, please send your updated resume to suchita@spectronova.com with the subject line: Application for Process Head Pharma Projects.,

Role & responsibilities Inspect, maintain, and troubleshoot tablet compression tooling systems as part of both Breakdown Maintenance (BM) and Preventive Maintenance (PM) routines. This includes tools of EURO and TSM standards . Ensure the efficient performance, durability , and long life of all tablet tooling components. Follow Good Manufacturing Practices (GMP) and carry out regular maintenance to avoid machine breakdowns and ensure smooth production. Operate and maintain tablet press machines , identify tool wear patterns , and address machine/tool-related issues on time. Use precision measuring tools such as profile projectors, micrometers, dial gauges, hardness testers , and die bore gauges to check and calibrate tools accurately. Read and understand engineering drawings and tablet designs , including B&D tooling standards , multi-tip tooling , and special shapes . Know and apply correct tolerance limits , materials of construction (MOC) , and tool coatings for better tool performance and longer life. Coordinate with other departments to bring improvements in tooling care and machine efficiency .