203 Pv Jobs - Page 2

Role & responsibilities Leads and optimizes QA function that supports organizations QMS in compliance with respective international regulatory requirements. • Hosting and support in external/client audits and regulatory inspections hosted by Auriga. • Audits and inspection handling. • Conduct internal system and process audits within Auriga systems. • Conduct external audits including the audit of vendors, clients and/or clients business partners and service providers. • Lead and manage a team of clinical audit professionals, providing guidance, training, and mentorship. • Support the operations team for adequate root cause identification, conducting gap analysis and implementation of corrective action plan. • Participate in risk assessments and preparation of risk-based audit plan for auditing internal processes, vendors and customers. • Supporting the CAPA management in audit and Inspection related CAPAs. • Support the document life cycle management, deviation handling process and change control process. • Prepare audit reports to communicate outcomes of quality review activities. • Preparation and or/review of company standard operating procedures (SOPs) and such other quality documents. • Interpret and implement quality assurance standards within the organization. • Liaise with quality representatives, internal customers and external customers across Auriga global access offices as required to achieve quality objectives. • Ensure development and maintenance of a PV Quality System for Standard Operating Procedures, auditing, review CAPAs, Change control and deviations. • Evaluate client audit and regulatory inspection findings and prepare and distributes reports to observation staff, management and customers.

Roles and Responsibilities: Perform coding of Adverse Events , Medical History, Indications, and Concomitant Medications using MedDRA and WHO Drug Dictionary. Ensure accurate and consistent data entry within global safety databases. Review case narratives and source documents to assign appropriate codes. Maintain compliance with ICH, GVP, and company SOPs. Coordinate with case processors, medical reviewers, and QA teams to resolve coding discrepancies. Stay updated with MedDRA and WHO-DD version updates and apply changes. Participate in coding audits, quality control, and data consistency checks. Support safety signal detection and regulatory queries with coded data. Qualifications: Bachelors degree in Pharmacy, Life Sciences, Nursing, or related field 2-5+ years of experience in pharmacovigilance or medical coding Hands-on experience. Familiarity with PV software. Basic understanding of ICSR and pharmacovigilance workflow. Certification in pharmacovigilance or medical coding is preferred. Interested to apply can share CV or call/WhatsApp to 9342735755

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview The Test Technician will support the execution of DV, PV and Development testing for Sensor Products across automotive, medical and industrial applications. This role requires a details-oriented, hands-on individual with a strong foundation in test methods, test setups, test execution, data analysis and compliance with international standards. DESIRED S: Strong Analytical and problem-solving skills Hands-on, detail oriented and eager to learn Excellent communicator with the ability to work in cross-functional and global teams Self-motivated, proactive, and capable of working under tight schedules, pressure with minimal supervision Passionate about technology, testing and continuous improvement. KEY RESPONSBILITIES: Experience2 to 4years of hands-on experience in product validation, reliability testing, preferably in sensors or automotive, medical domai Prepare and setup test fixtures, instruments, and chambers for executing DV, PV and qualification tests. Execute Functional Tests, Environmental tests (thermal cycling, vibration, humidity, pressure and electrical tests), etc Record and manage test data accurately and Test report generation. Interpret and apply standards such as IATF 16949, ISO 17025, ISO 13485, AEC-Q100/102/103. Support in developing test plans and procedures aligned with product requirements and regulatory needs. Maintain test methods, fixtures and documentation in compliance with ISO 17025 requirements. Operate and maintain test equipment for electrical, mechanical, and environmental testing for maintenance, calibration and test efficiency. Analyze test data using statistical tools (e.g., Minitab), identify trends, Coordinate with the design and development teams for test schedules and support root cause analysis and corrective action implementation for any test failures. Collaborate with global design and validation teams to align test scope, timeline and acceptance criteria. Contribute to lab standardization and continuous improvement initiatives in test methods, automation, and lab efficiency. Ensure Test activities are executed safely in compliance with EHS safety, quality, and documentation standards in the lab environment Must be willing to work in shifts and need to be in office weekly 5 days. Hands on experience with environmental chambers, DAQs, sensors, and measurement systems. Understanding basic electrical and mechanical testing principles. Experience in DV/PV test execution, data analysis and preparing test reports. Familiarity with test automation tools, ISO 17025, IATF, AEC-Q qualification Test methodologies. Experience with tools like LabVIEW, CANalyzer, Minitab, MS Excel, etc Skilled in use of DAQ, Oscilloscopes, Lab Instruments, Pressure / Vibration / Humidity, Climatic chambers, etc Proficiency in interpreting and applying international and customer-specific standards. Hands-on experience with test equipment and instrumentation. Competencies

Responsible for handling end to end Case management (ICSRs) activities and to ensure the compliance. Manage assigned team and ensure that all tasks are performed according to guidelines and standard operating procedures. Consulting and guiding the pharmacovigilance team for completion of aggregate reports (PSURs, PADERs, RMPs and applicable regulatory submission PV documents) as required for regulatory submission To develop and review pharmacovigilance SOPs. Coordination with MICC for ICSR activities and regulatory compliance. Coordinating the safety data exchange agreements between Hetero and business partners. Responsible for providing guidance and training to team as and when required. Responsible for identifying, implementation and continuous improvement activities. Responsible to handle audits and inspections

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integral to addressing climate change. With a total capacity of more than 13.4 GW (including projects in pipeline), ReNew’s solar and wind energy projects are spread across 150+ sites, with a presence spanning 18 states in India, contributing to 1.9 % of India’s power capacity. Consequently, this has helped to avoid 0.5% of India’s total carbon emissions and 1.1% India’s total power sector emissions. In the over 10 years of its operation, ReNew has generated almost 1.3 lakh jobs, directly and indirectly. ReNew has achieved market leadership in the Indian renewable energy industry against the backdrop of the Government of India’s policies to promote growth of this sector. ReNew’s current group of stockholders contains several marquee investors including CPP Investments, Abu Dhabi Investment Authority, Goldman Sachs, GEF SACEF and JERA. Its mission is to play a pivotal role in meeting India’s growing energy needs in an efficient, sustainable, and socially responsible manner. ReNew stands committed to providing clean, safe, affordable, and sustainable energy for all and has been at the forefront of leading climate action in India. Job Description Job Description POSITION TITLE AM – Module Quality (PV Module) BUSINESS/DEPARTMENT Quality-Solar JOB PURPOSE Assuring quality of PV Modules LINKAGES & REPORTING RELATIONSHIPS Reporting To: Head Solar Quality PRINICIPAL ACCOUNTABILITIES (a) Assuring Quality of PV Modules. (b) Planning and carrying out Module inspections at Module factories in India and outside India. (c) Planning third party lab testing as per IEC. (d) Preparation of Module QAP. (e) Review of QAPs and daily inspection reports. QUALIFICATIONS REQUIRED (a) B.Tech/Diploma in Electrical/ Electronics. WORK EXPERIENCE REQUIRED 5 to 10 years SPECIFIC SKILLS REQUIRED (a) Thorough knowledge about PV Module quality & Cell parameters. Good knowledge about PV module manufacturing. (b) Hands on experience of PV Module acceptance criteria and Reliability testing. In depth knowledge about BOM used in Modules and its selection critical parameters. (c) Knowledge about statistical sampling plans. (d) Experience of Calibration of Sun simulators and preparation of calibration Masters. (e) Experience in Third party lab testing of Modules. (f) Knowledge and understanding of IEC standards and MNRE requirements. (g) Skill of doing assessment and factory audits of Module Plants. SPECIFIC CHARACTERISTICS REQUIRED (a) Good at Auditing. (b) Good in managing 3rd party inspection agencies. (c) Good written and verbal communication. LOCATION Gurgaon TRAVELLING 70%

Urgent Clin Infotech Hiring B.Pharm Freshers With Certification in Clinical Research and Clinical Data Management Candidate With Hands On Experience In Clinical Data Management Is Preferrable Required Candidate profile Candidate With Knowledge in Clinical Research Roles and Responsibilities is Prefferable Candidate Should have Good Communication Skills is Mandatory

Responsibilities: * Collaborate with cross-functional teams on product development & marketing strategies * Lead sales team, drive revenue growth through solar solutions Annual bonus

Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory New Associate Qualifications: BBA/BCom/Master of Business Administration Years of Experience: 0 to 1 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whilst safeguarding the bank from risks associated with this business.Identify and assess, prevent and mitigate and account to provide reasonable measures to adapt before executing an agreement in relation to the real estate and immovable property. Valuation of commercial real estate using software like Argus, extracting key information from lease agreements (including amendments) and rent rolls. What are we looking for Ability to meet deadlinesAbility to perform under pressureAbility to work well in a teamAdaptable and flexibleAgility for quick learning Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined, narrow scope of work Please note that this role may require you to work in rotational shifts Qualification BBA,BCom,Master of Business Administration

Hiring Solar Trainer (Electrical) | WB | 5+ yrs exp | ITI/Diploma/B.Tech | Solar PV training, fieldwork, travel required | Salary: 2-3 LPA + perks | I Communication & Mobilization I I Apply: link - https://forms.gle/NmTGoJeumhFeSKkj8

Hiring an OpenShift L3 Support Engineer with 6+ years of experience for 24x7 onsite support in Noida. Role involves full lifecycle OpenShift cluster management, CI/CD, monitoring, patching, and RCA delivery. Required Candidate profile Experienced OpenShift L3 Engineer with 6+ years in container management, CI/CD, monitoring (Zabbix/Grafana), patching, and RCA reporting. OCP certified and available for 24x7 onsite support in Noida.

Looking for an OpenShift L2 Support Engineer with 4–6 years of experience for onsite support in Noida/Delhi. Must manage OpenShift clusters, container lifecycle, CI/CD, monitoring, patching, and incident resolution in a 24x7 setup. Required Candidate profile Experienced L2 Support Engineer with 4–6 years in OpenShift container platform, CI/CD pipelines, monitoring, OS patching, IAM, and troubleshooting. Available for 24x7 onsite support in Noida/Delhi.

Clinztech is looking for Pharmacovigilance Associate I to join our dynamic team and embark on a rewarding career journey. Monitor and assess the safety of pharmaceutical products through the collection and analysis of adverse event reports. Ensure compliance with regulatory requirements related to pharmacovigilance. Prepare and submit reports to regulatory authorities regarding product safety. Collaborate with internal teams to develop risk management strategies for pharmaceutical products. Provide training and guidance to staff on pharmacovigilance practices and policies. Maintain up - to - date knowledge of industry trends and regulatory changes.

Responsibilities Monitoring of Installation, Testing and Commissioning of Ground Mounted/Roof Mounted Solar Plants and Substations. Ensure that all projects are delivered on-time, within scope and within budget

Assist in the installation, testing, and commissioning of electrical systems for Solar PV projects. Support engineers in preparing electrical designs, drawings, and documentation Conduct routine inspections and maintenance of electrical equipment.

*Greetings From You & I Consulting ! You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. *Hurry Do Not Miss This Opportunity To Work For Global Giant MNC. We are hiring for the below locations under Medical Reviewer Role!! *Open Locations :- * Gandhinagar / Mumbai *Mode Of Interview - Virtual *Mode Of Work :- Work From Office * CTC Upto - 10 To 24Lpa *Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) or email your CV to puja@careersuni.com PFB Job Insights for Medical Reviewer Role!! Author a CCC for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. Detail any requests for changes to the case, including the narrative. Skills required:- Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills * * *Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) email your CV to puja@careersuni.com ***Note we also have open positions for the below skills :- *Aggregate Reporting / Clinical Data Management / Clinical SAS / SQL Programmer / EDC Programmer / Medical Monitor / HEOR Health Economist Role / SAS + R / Statistical Programmer / Study Data Manager *Though We Try and Answer The Calls Immediately, but Due to Heavy Call Flow The Below Numbers Might Be Busy At Times. In case you find the number busy, please whatsapp your details to us in the below format: - Name- Mobile number - Mail - Qualification - Total work experience - Current Organization- Location - Last CTC Expected CTC:- *Interested candidates can even refer their friends or relatives provided the criteria *FOR interview Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) email your CV to puja@careersuni.com

Job Title: Senior Medical Safety Advisor Education Qualification: MBBS/MD. Work Location: Anywhere in India. Work Mode: Home Based. Years of exp: 3yrs Clinical and 2+ yrs of PV (Exp in Oncology is a must) Pls note MCI reg is mandatory for all the foreign medical graduates. Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and standalone safety projects with appropriate oversight from management or more senior medical safety directors. Essential Functions Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a products safety profile Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data Represent safety and clinical data review findings during client meetings Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies Provide medical oversight for label development, review and change Provide medical support and attendance at Data Safety Monitoring Board Meetings • Attends and contributes medical safety evaluation on Safety Monitoring Committees Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture. Act as Global Safety Physician or Assistant or Back-up on projects as assigned Attend project meetings, medical safety team meetings, and client meetings as requested Ensure coverages for all medical safety deliverables within regulatory or contracted timelines Provide medical escalation support for medical information projects Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects • 24-hour medical support as required on assigned projects Maintain awareness of medical-safety-regulatory industry developments Qualifications Required MBBS/MD graduates from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Three (3) years of clinical practice experience with 2+ additional years in the pharmaceutical or associated industry in any role is required. Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice. Knowledge of clinical trials and pharmaceutical research process. Ability to establish and meet priorities, deadlines, and objectives. Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility. Ability to establish and maintain effective working relationships with coworkers, managers and clients. A valid medical license, or equivalent, from the country or region in which he/she resides and works Preferred.

Solar Energy Technician Job Title : Solar Energy Technician Location : Chennai, Hyderabad, Bangalore Experience : 0-3 Role Summary: Installs, maintains, and repairs solar photovoltaic (PV) systems for residential, commercial, and industrial applications. Key Responsibilities: Install solar panels, inverters, and related electrical components. Perform routine inspections and maintenance of solar systems. Troubleshoot and repair system faults. Ensure compliance with safety and electrical codes. Skills Required: Knowledge of PV systems and electrical wiring. Familiarity with tools and safety protocols. Ability to read blueprints and technical diagrams. Basic understanding of energy efficiency principles. Qualifications: Diploma or certification in Electrical Engineering or Renewable Energy. 13 years of experience in solar installation or maintenance.

As an experienced professional with 7-9 years of experience, you will be responsible for executing customer projects independently with minimal supervision in the field of VLSI Frontend Backend or Analog design. Your role will involve guiding team members technically and taking ownership of specific tasks/modules related to RTL Design, Module Verification, PD, DFT, Circuit Design, Analog Layout, STA, Synthesis, Design Checks, and Signoff. You will lead the team to achieve results, complete assigned tasks successfully and on-time, and anticipate, diagnose, and resolve problems as necessary. Your responsibilities will also include ensuring on-time quality delivery approved by the project manager and client, automating design tasks flows, writing scripts to generate reports, and coming up with innovative ideas to reduce design cycle time and cost. Additionally, you will be expected to write papers, file patents, and devise new design approaches. To measure the outcomes of your work, quality will be verified using relevant metrics by UST Manager/Client Manager, timely delivery will be assessed based on relevant metrics, and the reduction in cycle time and cost using innovative approaches will be monitored. The number of papers published, patents filed, and trainings presented to the team will also be considered. Your outputs are expected to demonstrate high quality deliverables with zero bugs in the design/circuit design, clean delivery of the design/module, meeting functional specs/design guidelines without deviation, and thorough documentation of tasks and work performed. Timely delivery, teamwork, innovation, and creativity will be key aspects of your role, along with participation in technical discussions and training forums. Your skills should include proficiency in languages and programming skills such as System Verilog, Verilog, VHDL, UVM, C, C++, Assembly, Perl, TCL/TK, and Makefile. You should have experience with EDA tools like Cadence, Synopsys, and Mentor tool sets, as well as technical knowledge in IP spec architecture design, bus protocols, physical design, circuit design, analog layout, synthesis, DFT, floorplan, clocks, P&R, STA, extraction, physical verification, and more. Strong communication skills, analytical reasoning, problem-solving abilities, attention to detail, and the ability to interact with team members and clients effectively are essential. You should also be well-versed in using available EDA tools, delivering tasks on time per quality guidelines, understanding standard specs and functional documents, and continuously learning new skills as needed. If you have led and executed projects in RTL Design, Verification, DFT, Physical Design, STA, PV, Circuit Design, Analog Layout, and possess a good understanding of design flow and methodologies, this role could be a great fit for you. Additionally, experience in analog circuit design and verifications, knowledge of TSMC FinFet technologies, and familiarity with Cadence Virtuoso circuit design suite would be beneficial. In this role, you will be responsible for circuit design and verification of analog modules like Voltage regulator, LDOs, developing circuit architecture, optimizing designs, guiding layout engineers, problem-solving, and effective communication skills. Desired skills include solid CMOS Analog design fundamentals, hands-on experience with Cadence Virtuoso, technical knowledge of power-performance trade-offs, understanding device parameter variation, and being a good team player in a multi-site work environment. Join us at UST, a global digital transformation solutions provider, where you will work alongside the world's best companies to make a real impact through transformation. With deep domain expertise, innovation, and agility, UST partners with clients to embed innovation and create boundless impact, touching billions of lives in the process.,

Designing & Costing the Solar PV system layout, including selection of system components, their integration and sizing. Designing of OFF Grid & ON Grid Solar system for Rooftop & Ground Mounted Solar Power plants. Ability to make accurate BOM Required Candidate profile Gender : Any Good knowledge of Auto Cad, Pv systs, STAAD.pro , Sketchup Updated with latest trends & Advancements in Solar Structure design. Knowledge of Project designing (Structural, 3D, Civil)

PaisaBuddy is looking for Operations Executive - [Operations -Solar Finance] to join our dynamic team and embark on a rewarding career journey Oversee the day-to-day operations of the company or organization. Monitor and evaluate the performance of operational processes and systems. Identify and resolve operational problems and inefficiencies. Stay up-to-date with industry trends and advancements in operations management. Continuously assess and improve operational processes and systems to ensure they meet business requirements

Responsibilities: * Collaborate with cross-functional teams on product development & marketing strategies * Lead sales team, drive revenue growth through solar solutions

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy Years of Experience: 1 to 2 year About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. database as per client guidelines and applicable global regulatory requirements. What are we looking for Looking for the candidate with Good Communication and written skills, Bachelor of Pharmacy,Bachelor of Physiotheraphy,BSc. Nursing Roles and Responsibilities: n this role you are required to solve routine problems, largely through precedent and referral to general guidelines, Your expected interactions are within your own team and direct supervisor.You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments Qualification Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy Years of Experience: 1 to 2 year About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases. What are we looking for Looking for the candidate with Good Communication and written skills, Bachelor of Pharmacy,Bachelor of Physiotheraphy,BSc. Nursing Roles and Responsibilities: n this role you are required to solve routine problems, largely through precedent and referral to general guidelines,Your expected interactions are within your own team and direct supervisor. You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments Qualification Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy

We are seeking an experienced Senior Project Manager to lead a specialized team dedicated to the automation of SCADA data integration and digital twin creation for our renewable energy projects. This role will manage a core team of two expert engineersfocused on Digital Twin SCADA Integration and AI Data Analyticsand will coordinate external resources during peak project phases. The ideal candidate is a proactive leader with a strong background in Wind, PV and/or BESS technology, demonstrates excellent communication skills, and a proven ability to drive projects to successful completion within the renewable energy sector. This position is crucial for our ambition to enhance operational efficiency and improve data accuracy across our renewable energy portfolio. Responsibilities: Team Leadership Coordination: Direct and mentor a core team of two engineers specializing in digital twin integration and AI-driven data analytics. Establish clear roles, responsibilities, and performance metrics for the team. Facilitate effective communication and collaboration within the team and with other departments. Project Planning Execution: Develop comprehensive project plans, including timelines, budgets, risk assessments, and resource allocation strategies. Monitor project progress against milestones, ensuring deliverables are met on time and within budget. Implement Agile or similar project management methodologies to adapt to evolving requirements. External Resource Management: Identify, onboard, and coordinate with external contractors and consultants during peak seasons or specialized project phases. Manage contracts, scope, and performance of external resources to ensure alignment with project goals. Maintain quality control and seamless integration of external contributions into the overall project. Stakeholder Vendor Management: Act as the primary liaison between the project team, senior management, and external vendors. Prepare and deliver regular status reports, project updates, and presentations to key stakeholders. Ensure effective communication of project risks, issues, and dependencies to drive timely decision-making. Quality Assurance Continuous Improvement: Oversee the integration of quality assurance processes to maintain ensure high First time right rate. Leverage your engineering expertise to conduct cross-check validations using critical documentation such as SLD AC/DC, Points List, DBR-Electrical, Tracker Configuration (including NCU and Tracker Motor Mapping), Block Layout, and SCADA IFC Combined Set. Interfaces: R-GBU HQ Countries IT/OT teams Countries Construction and OM teams OEM representatives Internal development and IT teams Education: Bachelors or Masters degree in Computer Science, Electrical Engineering, Industrial Automation, or a related field. Experience: 8+ years of hands-on experience Wind, PV or BESS construction projects, specialized in engineering Proven track record in managing multidisciplinary teams and coordinating external resources for complex projects.

We are looking for a Wind Turbine Engineer with a strong knowledge and understanding of wind turbine technology including the aerodynamics of turbine blades and the mechanics of gearboxes, generators, power converter and USS transformer. The position is based in Pune, with potential business travel within India and internationally. Candidate will report to the Head of Engineering(Wind). Job Responsibilities: Manage and coordinate engineering work packages with respect to choice of wind turbine technologies, technical configurations and for setting relevant performance, statutory, safety and quality requirements for multiple projects. Knowledge of various IS, IEC and IEEE etc standards related to the Turbine Design. Work closely with the procurement and construction team in line with the procurement strategies and construction strategies. Prepare RFP, BOQ and comparison for the Project (Pre-Bid/Post-Bid) coordinating with BD, OM other departments input. Factory Visit for evaluating different OEMs for major equipments Conduct feasibility studies and site assessments to identify suitable locations for wind energy projects. Review technical analyses to determine the optimal size, type, and placement of wind turbines within the wind farm with the help of WRA team. Collaborate with electrical engineers to design and integrate wind turbines into the power grid. Monitor and evaluate the performance of wind turbines, troubleshoot issues, and propose solutions for optimization. Stay updated with industry trends, technological advancements, and regulatory requirements related to wind energy. Conduct regular inspections and maintenance activities to ensure the reliability and longevity of wind energy systems. Collaborate with project teams to develop project plans, manage budgets, and adhere to project timelines. Utilize proven RCA methodologies and tools to identify basic or causal factors in failure events or variances in performance to eliminate repeated occurrences optimize performance and prepare reports and/or presentations to summarize findings for internal and external stakeholders. Provide technical guidance to support site operations and provide training to operational teams Prepare SOPs, technical documentation, including reports and manuals. Collaborate with cross-functional teams to ensure project success. Stay updated on advancements in turbine technology and industry trends. Review and Monitor balance of plant (BOP) construction, generator installation, testing, commissioning, or supervisory control and data acquisition (SCADA) to ensure compliance with specifications. Knowledge of various IS, IEC, IEEE and grid codes etc standards related to Wind Turbine. Experience: 10 to 15 years of relevant experience.