202 Pv Jobs - Page 4

BBA / MBA / B.E. / B.Tech with min. 1 to 6 years of experience in sales profile in Solar Industry. Must have relevant sales experience in Solar Module Panel Sales & Solar Industry. Selling Solar Module Products (B2B Sales), Developing new business. Required Candidate profile Make client visits for marketing & promotion of Rooftop Solar Power system. Ready to Travel. Strong Understanding of Solar Industry trends and technologies. Growing the dealer & distributor network. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BBA / MBA / B.E. / B.Tech with min. 1 to 6 years of experience in sales profile in Solar Industry. Must have relevant sales experience in Solar Module Panel Sales & Solar Industry. Selling Solar Module Products (B2B Sales), Developing new business. Required Candidate profile Make client visits for marketing & promotion of Rooftop Solar Power system. Ready to Travel. Strong Understanding of Solar Industry trends and technologies. Growing the dealer & distributor network. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BBA / MBA / B.E. / B.Tech with min. 1 to 6 years of experience in sales profile in Solar Industry. Must have relevant sales experience in Solar Module Panel Sales & Solar Industry. Selling Solar Module Products (B2B Sales), Developing new business. Required Candidate profile Make client visits for marketing & promotion of Rooftop Solar Power system. Ready to Travel. Strong Understanding of Solar Industry trends and technologies. Growing the dealer & distributor network. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BBA / MBA / B.E. / B.Tech with min. 1 to 6 years of experience in sales profile in Solar Industry. Must have relevant sales experience in Solar Module Panel Sales & Solar Industry. Selling Solar Module Products (B2B Sales), Developing new business. Required Candidate profile Make client visits for marketing & promotion of Rooftop Solar Power system. Ready to Travel. Strong Understanding of Solar Industry trends and technologies. Growing the dealer & distributor network. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BBA / MBA / B.E. / B.Tech with min. 1 to 6 years of experience in sales profile in Solar Industry. Must have relevant sales experience in Solar Module Panel Sales & Solar Industry. Selling Solar Module Products (B2B Sales), Developing new business. Required Candidate profile Make client visits for marketing & promotion of Rooftop Solar Power system. Ready to Travel. Strong Understanding of Solar Industry trends and technologies. Growing the dealer & distributor network. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BBA / MBA / B.E. / B.Tech with min. 1 to 6 years of experience in sales profile in Solar Industry. Must have relevant sales experience in Solar Module Panel Sales & Solar Industry. Selling Solar Module Products (B2B Sales), Developing new business. Required Candidate profile Make client visits for marketing & promotion of Rooftop Solar Power system. Ready to Travel. Strong Understanding of Solar Industry trends and technologies. Growing the dealer & distributor network. Perks and benefits Negotiable - Depending Upon Candidate & Experience

1.Technical Head 2.Head Solar Design 3.Electrical Transmission Head. 4.Tendering Manager 5.Project Manager Technical 6.Execution Site Project Manager Required Candidate profile Travel to Africa: As and When Required IndustryManufacturing Production QualityQualificationB.E, M.TechKey Skills Solar Power Solar Business Project Manager Solar Panel Manager Technical Excellent Communication Solar Design Walk in

At Allstate, great things happen when our people work together to protect families and their belongings from lifes uncertainties. And for more than 90 years our innovative drive has kept us a step ahead of our customers evolving needs. From advocating for seat belts, air bags and graduated driving laws, to being an industry leader in pricing sophistication, telematics, and, more recently, device and identity protection. The Application Developer Lead Consultant provides code/design analysis and strategy, supports project planning, and develops code and designs for complex projects. They manage the review of code, design, and testing for lower band Application Developers and peers. They serve as a technical expert, coach and mentor for other application developer specialists and professionals. The Lead Consultant works closely with business partners to identify needs and design technology solutions toovercome process bottlenecks, reduce use of contingent claim resources, reduce compliance risks, or generally increase operational efficiency. They are often required to deliver tactical solutions that can be implemented within a few days. They are responsible for all phases of the application development cyclebeginning with requirements gathering, through release, and ultimately ongoing user support. Key Responsibilities Should have strong JAVA, spring boot, triage, TDD and test understanding. Assists with detailed project estimating and milestone planning. Reviews and validate accuracy of others estimates and works with project managers in continuous process improvement for estimating Develops code for complex to highly complex modules with high-level architecture, following documentation and development standards Ensures that design/code reviews are scheduled and executed; provide feedback and recommends solutions; ensures that design standards and documentation are followed and certifies that code meets quality standards; reviews and critiques code presented by team members. Critiques and evaluates detailed business, functional, and high-level technical requirements (including recovery, security and audit) Performs root cause analysis to prevent recurrence of problem and manages the resolution of complex problems Defines and manages process by which support and technical assistance is performed Leads and organizes testing reviews. Tracks and resolves complex defects and assists in planning efforts of complex functional tests in support of Quality Control (QC) Ensures project change management approach is followed and that enhancements are appropriately prioritized and developed, and delivered to Developers, Quality Control Analysts, and Environment Management personnel, and that all documentation is completed appropriately. Contributes to determining programming approach, tools, and techniques that best meet the business requirements. Promotes and defines development standards and high architectural standards. Education 4 year Bachelors Degree (Preferred) Experience 5 or more years of experience (Preferred) Supervisory Responsibilities This job does not have supervisory duties. Education & Experience (in lieu) In lieu of the above education requirements, an equivalent combination of education and experience may be considered. Primary Skills Application Development, Code Reviews, Process Improvements, Technical Consulting, Technical Shift Time Shift B (India) Recruiter Info Shriya Kumariskuow@allstate.com About Allstate Joining our team isnt just a job "” its an opportunity. One that takes your skills and pushes them to the next level. One that encourages you to challenge the status quo. And one where you can impact the future for the greater good. Youll do all this in a flexible environment that embraces connection and belonging. And with the recognition of several inclusivity and diversity awards, weve proven that Allstate empowers everyone to lead, drive change and give back where they work and live. Good Hands. Greater Together. The Allstate Corporation is one of the largest publicly held insurance providers in the United States. Ranked No. 84 in the 2023 Fortune 500 list of the largest United States corporations by total revenue, The Allstate Corporation owns and operates 18 companies in the United States, Canada, Northern Ireland, and India. Allstate India Private Limited, also known as Allstate India, is a subsidiary of The Allstate Corporation. The India talent center was set up in 2012 and operates under the corporations Good Hands promise. As it innovates operations and technology, Allstate India has evolved beyond its technology functions to be the critical strategic business services arm of the corporation. With offices in Bengaluru and Pune, the company offers expertise to the parent organizations business areas including technology and innovation, accounting and imaging services, policy administration, transformation solution design and support services, transformation of property liability service design, global operations and integration, and training and transition. Learn more about Allstate India here.

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy 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 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.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.Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. Basic knowledge in Medical TerminologyBasic knowledge about Pharmaceuticals & Clinical Research 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 Bachelor of Pharmacy

Roles and Responsibilities Manage a team of sales executives to achieve targets in auto loans, car finance, commercial vehicle loans, refinancing, and used car loans. Develop and maintain relationships with dealerships across India to increase business opportunities. Identify new business prospects through market research and networking within the industry. Collaborate with internal teams to resolve customer complaints and improve overall customer satisfaction. Analyze sales data to optimize sales strategies and improve performance metrics.

Job Summary The SME-Pharmacovigilance role is crucial for ensuring the safety and efficacy of pharmaceutical products. The candidate will leverage their expertise in PV Case Processing and customer service to enhance pharmacovigilance operations. This position requires a proactive approach to monitoring drug safety and contributing to research and development efforts. Responsibilities Triage & intake of ICSRs in ARGUS databases within agreed timelines Download and monitor valid ICSRs from Eudra Vigilance (EV)- or any other sources Process literature, spontaneous, clinical trial, and solicited cases Search for valid ICSRs in Literature search tools Generate reports and submit to health authorities and business partners Enter serious and non-serious ICSRs in ARGUS per client SOP and WI with high accuracy Code events, indications, patient history using MedDRA Code suspect products, amend narratives, and label events Obtain follow-up information for all cases per applicable guidelines Submit processed cases to regulatory authorities and distribute reports to Partners Communicate effectively with client stakeholders and internal teams Attend all internal and client trainings to ensure guideline compliance Ensure adherence to regulatory requirements and industry standards in all aspects of pharmacovigilance and safety operations. Assist in the development and maintenance of standard operating procedures to ensure consistency and quality in process execution. Support training and development initiatives to enhance team capabilities and knowledge in pharmacovigilance and safety operations. Utilize technical skills to troubleshoot and resolve process-related issues, minimizing disruptions and ensuring smooth operations. Engage in rotational shifts to provide consistent support and coverage across different time zones. Requirements Bachelor’s / Master’s degree in pharmacy. Minimum 3 years relevant work experience in case processing activities. Experience in Cardiovascular (CVS), Neuroscience (CNS), Oncology, Immunology therapeutic areas and Gene Therapy will be an added advantage. Experience with global pharma sponsor will be preferred. In-depth knowledge and understanding of applicable global, regional, and local regulatory requirements, including Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and International Conference of Harmonization (ICH) guidelines, SOPs. Excellent organizational and time management skills. Proficiency in Microsoft Office and web-based applications (e.g., Word, Excel, PowerPoint). Good knowledge of medical terminology.

JOB DESCRIPTION Job Title: Manager Sub-function: Pharmacovigilance- Quality Assurance (PV-QA) Function Corporate Quality Assurance Location - Vikhroli Job Details Job Purpose Pharmacovigilance (PV) Audits and risk assessment: Planning and conducting audits of PV processes, business partners, Cipla Offices, service providers and other departments related to PV function. Preparation and implementation of strategic and tactical level audit plan. To perform PV risk assessment. Facilitating external audits and regulatory inspections: Experience on handling of PV regulatory inspection eg. USFDA, MHRA, EMA, TGA etc. Quality Management System (QMS): Handling on deviation, CAPA, change management, documentation control on electronic software. Preparation, review and approval of QMS and PV SOPs. Record management process. End to end PV knowledge: Different source of safety information, PV mailbox case processing and literature screening, regulatory submission, knowledge of dictionaries (MedDRA, WHO DD, CPD), PV vendor management, Lavel update, PV/QMS training, Safety data exchange agreement, PSMF, Aggregate reports (RMP, PSUR/PBRER, PADER) and signal management. Key Accountabilities Accountability Cluster Major Activities / Tasks Pharmacovigilance Audits and Inspection Planning and conducting audits of PV processes, business partners, Cipla Offices, service providers and other departments related to PV function. Perform Vendor Qualification and its related activities. Conduct risk assessment of all PV processes, departments of Cipla other than DSD involved in PV System, Cipla Country offices, Cipla subsidiaries, business partner and service providers. Preparation and implementation of Audit schedule Facilitating external audits and regulatory inspections Deviation Handling and CAPA management Logging, approving, tracking and closing the deviations and CAPA raised in DSD. Initiation, Follow up and monitoring of open CAPAs. Closing and effectiveness review of CAPAs. Document Control Issuance, distribution, withdrawal, destruction of all the forms generated through approved written procedures for DSD. Preparation and review of written procedures related to Drug Safety Division (DSD) Quality Management System (QMS). Document retention and archival of all the DSD related documents. Training Training to DSD on QMS and related topics Identify need of training on QMS and related topics Change Request Coordinate change requests raised by DSD Review of PSMF, PvMF, or equivalent documents through change control system End to end Pharmacovigilance related activities Collection of safety information from Different source, PV mailbox case processing and literature screening, regulatory submission, knowledge of dictionaries (MedDRA, WHO DD, CPD), PV vendor management, Lavel update, PV/QMS training, Safety data exchange agreement, PSMF, Aggregate reports (RMP, PSUR/PBRER, PADER) and signal management. QMS software Trackwise, Vivo or any QMS software Major Challenges Communication with Cross function team to implement CAPA plan. Collection of data required to perform risk assessment Timely close of QMS activity Key Interactions InternalExternal Team Member, for discussion on concern to their activity / task and each and every assigned task on daily basis. DSD Team: Interaction with DSD team for closure of QMS document. CFT: Medical service depart, Corporate communication department, Corporate quality assurance, Clinical research department, CSV, IT, REMS. CFT: Cipla country offices and Subsidiaries External: Pharmacovigilance vendor, business partner for discussion of Audit requirement and implementation of CAPA plan. Dimensions Meet 100% compliance to Tactical level audit plan and risk assessment Ensure change request, Deviation and CAPA shall get raised within timeline. Meet 100% compliance timely closure of QMS documents i.e. Deviation, CAPA and change management. Ensure timely training imparted in QMS topics for key PV personnel. Ensure completeness, accuracy of QMS documents. Timely resolution of internal and external queries. Key Decisions: DecisionsRecommendations Inputs on resolution of queries from CFTs. Approve Process Deviations Make process improvements as needed. Mentoring CAPA owners on proper techniques Inspection Readiness Assistance to cross functional team To Share industry best practices To increase the awareness on regulatory intelligence. Process simplifications. Comments: The said Job description will involve adequate knowledge PV audit, QMS and End to end knowledge of PV system. Skills & Knowledge Educational qualifications: Qualified pharmacist (B. Pharma / M. Pharma). Relevant experience: He / She must have 10-14 years of Pharmacovigilance experience including audits and QMS. He / She must be technically sound on QMS function and exposure of regulatory audits like USFDA, MHRA, TGA, EMA, SHAPRA etc.

1. Sales and Marketing of Solar Projects (Power) 2. Build and Manage Sales team 3. Engage with corporate customers for setting up Solar Power Projects 4. Project Negotiation 5. Grow current customers Required Candidate profile 1.Proven experience in Solar Power Projects. 2.Should be currently managing a Sales Team 3.Strong knowledge of Solar Project Sales 4.High Level of initiative and a self starter. 5.Good Comm Skills Perks and benefits Excellet Renumeration,Perks and Incentives

Responsibilities: * Collaborate with cross-functional teams on solar projects from concept to commissioning. * Develop solar designs using Pvsyst, AutoCAD, Helioscope, Sketchup, Dialux & ETAP software.

Your Role: Own end-to-end the mechanical + electrical delivery of every rooftop solar project after design lock-in: from material QA at gate-in to net-meter synchronisation and client sign-off. You will manage a lean internal crew plus specialist subcontractors, and youll be the final gatekeeper for safety, quality and performance. Key responsibilities: Project mobilisation & sequencing convert Gantt to day-wise work-packs; secure crane, scaffold and HT-licensed electricians ahead of schedule if needed. Technical authority on-site verify structure pull-out tests, string configuration, torque logs and IV-curve results before energising. Regulatory interface : File CEIG Form-B / obtain DISCOM net-meter & synchronisation approvals; maintain as-built drawings for audit. People & vendor management coach two certified installers Quality-control sign-offs approve every checklist from roof-leak test to insulation resistance; issue Punch-List & Closure Memos. Must-have qualifications: Diploma / B.Tech in Electrical or EEE ; 2-5 yrs rooftop PV or industrial HT experience, incl. 500 kW cumulative installs. Diploma / B.Tech in Electrical or EEE ; 2-5 yrs rooftop PV or industrial HT experience, incl. 500 kW cumulative installs. Proven track-record with string/central inverters, HT/LT switchgear and BIS-QCO components. Good working knowledge of CEA Safety Regulations, IEEE-1547 anti-islanding and Telangana net-metering norms . Competence in PVsyst / HelioScope , MS-Project (or equivalent) & digital QC tooling (IV-curve logger, thermal cam). Hands-on with insulation-resistance, IV-curve, thermal imaging, drone shade scans Telugu & functional English communication; Hindi bonus Why GroSure? We build 25 kW 1 MW private power plants for leading factories, warehouses and campuses. Reliability is our product, so we staff only A-grade supervisors who can deliver a zero-rework site in 60 days. Performance bonus - Attractive incentives on successful project installations Chance to scale the department be the voice that shapes GroSure's SOPs and future Residential division.

Title Solar PV Design/Estimation & Purchase Engineer Reporting to Director Sales & Marketing / Managing Director Description The PV Design & Purchase Engineer will be responsible for all PV solution designs, costing/estimation and purchases. The profile is a high visibility role that directly reports to the senior management of the company and ensures that solar projects are designed as per specification and delivered as per budget. The role also involves site survey and remote project management to ensure projects in execution are managed/delivered as per schedule. Responsibilities Design and Costing for Retail/Commercial Solar PV Solutions Turnkey design of solar Photovoltaic (PV) Systems for domestic/residential, commercial and industrial applications Prior experience in design, installation and commissioning of the following solutions Rooftop Solar on-grid solutions upto 500 KW Rootfop Solar off-grid/hybrid solutions Solar street lights Solar pumps Solar lanterns and other solar PV based solutions Expertise in understanding engineering drawings to prepare and study technical data, specifications of electrical systems to ensure that installation and operations conform to standards and meet customer requirements. Ability to create accurate and fully detailed Bill of Materials (BOMs)/Bill of Quantities (BOQs) in response to customer requirements with accurate cost estimates based on prevalent market rates for components. Prepare specifications for purchase of materials and equipment estimate labor, material, construction and installation costs Ability to prepare details techno-commercial proposals that include detailed payback and ROI calculations for customers to make investment decisions. Working knowledge of industry standards in PV design, installation and installation codes Extensive knowledge of output, performance and reliability factors of various commercially available PV modules and inverters Experience working with HV system design BOS Design/Estimation Good knowledge of power cables/ electrification for residential, commercial, and industrial sectors Responsible for providing optimized module mounting structure design and solutions required to meet customer / project needs Assessment and evaluation of technologies for module support structure: fixed & tracking, rooftop & ground mount Drawing Preparation and Performance Analysis Experience preparing GA Layout drawings for placement of solar panels, Single Line Drawings (SLD) for electrical schematic/wiring and 3D drawings of wiring/routing on AutoCAD Experience preparing shadow analysis and analysing PV generation/performance on PVSyst or equivalent software. Experience with PV System Energy Modelling tools. Assessment and evaluation of technologies for module support structure: fixed & tracking, rooftop & ground mounted. Purchase/Procurement Negotiating purchase for all PV solution components and ensuring the rates are within budgeted cost Vendor relationship management and vendor development for PV solutions Adding new solutions to portfolio by bringing new solution vendors Software/Other Skills AutoCad, PVSyst (mandatory) Sketchup, other softwares (optional) Proficient in MS Excel, MS Word and proposal/report creation of solar projects Strong written/verbal skills and ability to communicate effectively with customers and participate in sales driven techno-commercial discussions Open for travel within India for site surveys and technical discussions. Languages - English, Hindi (preferred) , Marathi or other languages (optional) Position Requirements A graduate degree/diploma in Electrical Engineering or associated degree relevant to PV Design Atleast 5 Years of prior experience in PV Design & Purchase Working Hours & Culture Office Hours 9 am – 5:30 pm on weekdays, 6 days a week (Monday – Saturday) Presence on field will be mandatory, hence office presence will depend on necessity to travel We have an open and transparent culture freedom to express views and provide ideas.

Role & responsibilities Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level. Perform case follow up activities such as identification of information to be collected during follow-up. Creating and reviewing case narratives. Providing client notifications as required for case management. Case downloading from regulatory authority websites Submission to applicable regulatory authorities within stipulated timelines Supporting and contributing to the development of training materials and training delivery. Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs. Acquire and maintain an up-to-date knowledge of global safety regulations for medicines. Peer reviews of cases for quality, consistency, and accuracy as needed. Other duties as assigned Preferred candidate profile Strong verbal, written and interpersonal communication skills. High level of accuracy and attention to detail. Excellent organization and prioritization skills; able to multitask. Basic knowledge of Pharmacovigilance. Interested applicants can also apply directly with updated CV to hr@qpsbioserve.com

Help us bring cutting-edge medical treatments to life! Become a key player in clinical research and accelerate advancements in healthcare. Opportunities We offer two paths into the exciting world of clinical research: Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager to experience the field. Fresher-Level Position: Launch your career as a Clinical Research Coordinator! This position offers ongoing employment for those committed to this exciting field. Regardless of path, you'll get to: Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure the study progresses smoothly. Be a meticulous record-keeper: Collect and safeguard essential research data with the highest industry standards. Champion safety and ethics: Protect patient rights and ensure all research practices are ethical and compliant. Work within a team of like-minded professionals: Collaborate with investigators, healthcare providers, and fellow research enthusiasts. Qualifications Internship: Enrolled in or a recent graduate of a degree program in life sciences, health sciences, nursing, or a related field. Fresher-Level Position: Recent graduate with a degree in life sciences, health sciences, nursing, or a related field. For both: Passion for research, detail-orientation, strong organizational skills, clear communication, and willingness to learn. What We Offer Hands-on experience: Jumpstart your career or get real-world training. Training and mentorship: Get guidance from experienced researchers in the field. Professional development: Access resources or company-sponsored coursework to enhance your potential. Competitive compensation: Interns receive a stipend; fresher-level position offers salary and benefits. A role at the forefront of medical innovation: Shape the future of healthcare.

We are seeking a highly motivated and detail-oriented recent graduate to join our Drug Safety team as an Entry-Level Drug Safety Associate. This is an excellent opportunity to launch your career in the pharmaceutical industry and contribute to the safety surveillance of our products. You will gain practical experience in various aspects of drug safety, including adverse event processing, data entry, and safety reporting. This role is perfect for individuals with a strong interest in drug safety and a desire to learn and grow in a fast-paced environment. Responsibilities: Adverse Event Case Processing: Receive, triage, and accurately enter adverse event reports into the drug safety database. Ensure timely and accurate data entry in compliance with company Standard Operating Procedures (SOPs) and regulatory guidelines. Assist in the follow-up of adverse event reports to obtain complete and accurate information. Perform quality control checks on case data to ensure accuracy and consistency. Data Management and Safety Reporting: Assist in the preparation of safety reports and data summaries. Maintain accurate and organized drug safety records. Assist in the tracking and monitoring of adverse event trends. Learn to identify and escalate potential safety signals. Regulatory Compliance: Develop a basic understanding of global drug safety regulations and guidelines (e.g., ICH guidelines). Adhere to company SOPs and regulatory requirements. Assist in the preparation of regulatory submissions. General Support: Assist in the maintenance of drug safety databases and systems. Participate in team meetings and training sessions. Support senior drug safety staff as needed. Perform other duties as assigned. Qualifications: Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or a related healthcare field. Strong interest in drug safety and pharmacovigilance. Excellent attention to detail and accuracy. Strong organizational and time-management skills. Ability to work independently and collaboratively within a team. Good communication and interpersonal skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate. Preferred Qualifications (but not required): Basic understanding of medical terminology. Familiarity with drug safety databases or systems. Coursework related to pharmacology or drug safety.

(1) Experience in PV design engineering (2) preparing and sending document transmittal letters for designs and drawings (3) project mgt, strong communication and supervision skills Required Candidate profile Interested Candidate Share Your Updated CV in whatsapp no +91 9724346949

Job Description:. Weekly Hours:. 40. Time Type:. Regular. Location:. IND:AP:Hyderabad / Argus Bldg 4f & 5f, Sattva, Knowledge CityAdm: Argus Building, Sattva, Knowledge City. It is the policy of AT&T to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, AT&T will provide reasonable accommodations for qualified individuals with disabilities. AT&T is a fair chance employer and does not initiate a background check until an offer is made.. Show more Show less

Roles and Responsibilities Manage car loan sales from lead generation to disbursement, ensuring timely processing and customer satisfaction. Identify new business opportunities through networking, referrals, and market research to expand the customer base. Develop strong relationships with customers by providing exceptional service, resolving queries promptly, and addressing concerns effectively. Collaborate with internal teams (e.g., underwriting, operations) to ensure seamless execution of loan applications and documentation processes. Maintain accurate records of transactions, updates customers on application status, and adheres to compliance requirements.

PVSyst and Advanced Excel for solar plant performance analysis, including monthly simulations and energy modeling. Skilled in stakeholder communication, SOP preparation, record-keeping, and contractual deliverable monitoring operational efficiency. Role: Other Industry Type: Power (Solar) Department: Other Employment Type: Full Time, Permanent Role Category: Other Education UG: B.Tech/B.E. in Electronics/Telecommunication, Electrical

Description Safety & PV Specialist I-Japanese -Pune Office Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required, Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required, Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability, Enters data into safety database, Codes events, medical history, concomitant medications, and tests, Compiles complete narrative summaries, Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved, Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements, Maintains safety tracking for assigned activities, Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required, Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA, Manual recoding of un-recoded product and substance terms arises from ICSRs, Identification and management of duplicate ICSRs, Activities related to SPOR / IDMP, Quality review of ICSRs, Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate, Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process, Fosters constructive and professional working relationships with all project team members, internal and external, Participates in audits as required/appropriate, Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities, Qualifications Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job,

Misson: Within the Global Business Unit RenewablesWe 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 engineers?focused on Digital Twin & SCADA Integration and AI & Data Analytics?and 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: The scope of the role includes, but is not limited to, the following functional areas: 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 O&M 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, Business Unit: GBU Renewables Division: REN AMEA India Legal Entity: ENGIE Energy India Private Limited Professional Experience: Skilled ( >3 experience <15 years) Education Level: Technical Qualification