205 Pv Jobs - Page 8

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations. Key Responsibilities: Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements. Site Management: Assist in site selection, initiation, monitoring, and close-out activities. Documentation: Maintain accurate and complete study records, including case report forms, source documents, and regulatory binders. Communication: Facilitate effective communication between study sites, sponsors, investigators, and internal team members. Data Management: Ensure timely and accurate data collection, entry, and query resolution. Regulatory Compliance: Ensure compliance with all applicable regulations, guidelines, and standard operating procedures. Patient Recruitment: Support patient recruitment and retention efforts. Training: Provide training and support to study staff on study protocols and procedures. Quality Assurance: Participate in quality control activities and internal audits. Qualifications and Skills: Education: Bachelor's degree in life sciences, nursing, or a related field. Experience: Fresher or recent graduate with a strong interest in clinical research. Knowledge: Basic understanding of clinical research principles and Good Clinical Practice (GCP). Skills: Excellent organizational, communication, and interpersonal skills.

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.

WSP has a long history in the delivery of high-quality technical advisory and management consultancy services focused on renewable energy. We have worked on ground mount, floating and rooftop solar developments, including some of the world’s largest solar PV projects. We have established client relationships with some of the largest and most well-known developers, investors and lenders in the industry and we support their projects across the globe. Delivering high quality, proactive, prompt and up to date technical services to our clients is paramount. We offer services at all stages of the project lifecycle, with a particular focus on the following core services: Energy yield and resource assessments, Site layouts and optimisation, concept design and feasibility studies, Technical due diligence for Merger and Acquisition (M&A) transactions, Lender’s Technical Advisor (LTA) scopes of work, Project development and Owner’s Engineer (OE) scopes of work, including tendering and contracting support, construction monitoring and management, and technical advisory services. WSP has ambitions to significantly expand our renewable energy team. We have a range of roles available to suit people at all points of their career and development. We are seeking talented engineers or renewable energy professionals with experience in the delivery of any of WSP’s core scopes for solar PV development. Applications are encouraged from those who have experience as a contractor, developer, financier/lender, or manufacturer, in addition to those with consultancy experience. WSP’s aim is to build a team with broad range of experience to allow us to allow the best value and advice to our clients. This role will report to the Solar PV Technical Lead and will require working closely with the other renewable energy sector teams, technical discipline leads, and WSP’s international offices. In addition to providing technical expertise, a key element of this role is to contribute to the development of a close-knit high-performing specialist team. We'd love to hear from you if you have: A degree in a relevant engineering, technical or scientific discipline, ideally with a graduate qualification related to electrical engineering and/or renewable energy with experience of 10 to 15 years. Experience in the delivery of solar PV projects, ideally within the UK and internationally on utility scale projects, and at least one of WSP’s core services. Knowledge of solar PV technology (incl. different types of Modules, Tracker, MMS etc.) and the project development process. Cost optimization and capitalization for engineering for both AC & DC BOS Preparation Technical specification of DC system. Sound in design knowledge in areas of solar plant layouts, tray Layout, cable routing layouts, ICR Blocks layouts and Switchyard layouts of large-scale solar power plants Review & approval of design calculation, drawings, etc. Expert on areas like transformers, Inverters, Transmission, and other major electrical components. Engineering monitoring and control, in relation to Project Setup. Detailed Engineering Drawings and Design Study. AC/DC Design and Component Knowledge. Equipment Sizing and Selection. Pre bid Engineering, Tendering, basic and design Engineering. OPTIONAL- Experience in managing projects, developing client relationships, and working in a consultancy environment. OPTIONAL- Some experience in business development and/or winning work.

Urgent requirement our Clint Job Profile : QA , QC , CRA , RA , R&D , Pharmacist , Medical Billing , Medical Record summarization , Medical Reviewer , Clinical Research EXP : 0 to 4 Years Salary : 18 to 5 L Job Locations - Pune , Mumbai, Goa. Required Candidate profile BSc , MSc , D.Pharm , B.Pharm, M.Pharm , all pharmaceutical , health care , life science ,heath care IT , CRO Background candidates required fresher & experienced

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt Ltd. We are hiring General Manager - Plant Operations (Solar PV) for our client a leading pharmaceutical manufacturing company dedicated to API/Intermediate. Company: Solar photovoltaic (PV) panels Production Company and Products. Location: 1) Hyderabad, 2) Visakhapatnam About the Company: Our client is a leading manufacturer of high-quality solar photovoltaic (PV) panels in India, covering the entire solar value chain from polysilicon (in some cases) to finished panel assembly. We are committed to driving innovation and sustainability in the renewable energy sector. Our operations encompass the production of solar cells, wafers, glass, backsheets, encapsulants, junction boxes, frames, connectors, and the final assembly of PV modules. We are experiencing rapid growth and seek a dynamic and experienced General Manager. About the Role: We are seeking a dynamic and experienced General Manager - Plant Operations to oversee the day-to-day operations of our solar photovoltaic (PV) unit. The ideal candidate will be a strategic thinker with a proven track record in managing large-scale manufacturing operations. You will be responsible for driving operational excellence, ensuring safety, and maximizing plant efficiency. Key Responsibilities: Operational Leadership: Oversee all aspects of plant operations, including production, quality control, maintenance, and safety. Develop and implement operational strategies to achieve production targets and optimize resource utilization. Monitor key performance indicators (KPIs) and take corrective action to improve performance. Team Management: Lead and motivate a team of skilled professionals to deliver exceptional results. Recruit, hire, and develop talent to build a high-performing team. Foster a positive and collaborative work environment. Quality Assurance: Ensure adherence to stringent quality standards and regulatory compliance. Implement robust quality control procedures to minimize defects and maximize product quality. Continuously improve product quality and reduce costs. Maintenance and Reliability: Develop and execute a comprehensive preventive maintenance program to minimize downtime and optimize equipment reliability. Manage the maintenance budget and ensure efficient utilization of resources. Safety and Environmental Compliance: Prioritize safety and environmental sustainability. Implement rigorous safety protocols and ensure compliance with all relevant regulations. Promote a culture of safety and environmental responsibility. Cost Management: Identify and implement cost-saving initiatives to improve profitability. Monitor and control operational expenses to optimize resource utilization. Strategic Planning: Contribute to the development and execution of the company's strategic plan. Identify opportunities for growth and expansion. Stay updated on industry trends and technological advancements. Qualifications and Experience: Bachelor's degree in Engineering (Electrical, Mechanical, or Electronics) or a related field. Minimum of 10 years of experience in a plant operations role, preferably in the solar PV industry. Proven track record in managing large-scale manufacturing operations. Strong leadership and interpersonal skills. Excellent problem-solving and decision-making abilities. Proficiency in lean manufacturing principles and Six Sigma methodologies. Knowledge of relevant safety and environmental regulations. Strong financial acumen and cost management skills. If you are a highly motivated and results-oriented individual with a passion for renewable energy, we encourage you to apply. (Interested candidates can share their CV to aradhana@hungrybird.in or call on 9959417171) Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Relevant Experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Aradhana +91 9959417171

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt Ltd. We are hiring General Manager - Projects for our client a leading pharmaceutical manufacturing company dedicated to API/Intermediate. Company: Solar photovoltaic (PV) panels Production Company and Products. Location: 1) Hyderabad, 2) Visakhapatnam About the Company: Our client is a leading manufacturer of high-quality solar photovoltaic (PV) panels in India, covering the entire solar value chain from polysilicon (in some cases) to finished panel assembly. We are committed to driving innovation and sustainability in the renewable energy sector. Our operations encompass the production of solar cells, wafers, glass, backsheets, encapsulants, junction boxes, frames, connectors, and the final assembly of PV modules. We are experiencing rapid growth and seek a dynamic and experienced General Manager. Job Summary: As the General Manager - Operations, you will play a pivotal role in shaping the operational foundation of our newly established solar company. This is a unique opportunity to build and lead the operations function from the ground up. You will be responsible for developing and implementing operational strategies, establishing processes, and building a high-performing team. This role requires a hands-on leader with a strong entrepreneurial spirit, a deep understanding of the solar industry, and the ability to thrive in a fast-paced, dynamic environment. Job Description: Operational Strategy & Setup: Develop and implement the overall operational strategy for the company, aligning it with the business plan. Establish key operational processes, procedures, and systems. Facility Setup (if applicable): Oversee the setup of manufacturing facilities, project sites, or other operational infrastructure, ensuring compliance with regulations and timelines. Team Building: Recruit, train, and manage a high-performing operations team. Foster a culture of collaboration, innovation, and continuous improvement. Supply Chain Management: Establish and manage a robust supply chain, including sourcing of materials, vendor selection, and inventory management. Manufacturing/Project Execution Oversight (depending on focus): Manufacturing: Oversee the manufacturing process, ensuring quality, efficiency, and cost-effectiveness. Develop and implement production plans, monitor performance, and drive continuous improvement. Project Execution: Manage the complete project lifecycle, from design and engineering to installation, commissioning, and maintenance. Ensure timely completion of projects within budget and quality parameters. This includes managing design engineering, supply chain, quality, installation, commissioning & maintenance teams for On-Grid, Off-Grid, Solar Water pumping and Solar PV systems. Quality Control: Implement and maintain a comprehensive quality management system to ensure the highest standards of product and service quality. Regulatory Compliance: Ensure compliance with all relevant regulations and industry standards, including safety, environmental, and quality requirements. Budget Management: Develop and manage the operational budget, monitor performance against targets, and implement cost optimization strategies. Performance Reporting: Develop and provide regular reports on operational performance, key metrics, and progress against goals. Relationship Building: Build and maintain strong relationships with key stakeholders, including suppliers, contractors, government agencies, and customers. Continuous Improvement: Identify opportunities for process improvement, implement best practices, and drive operational efficiency. Qualifications: Bachelors degree in Engineering (Electrical, Mechanical, or related field) or equivalent. A Master's degree is preferred. Minimum of [Number] years of experience in a senior operational leadership role within the solar industry. Experience in a startup environment is a plus. Strong technical expertise in solar technologies, including [mention specific technologies relevant to the company's focus, e.g., module manufacturing, battery storage, power electronics]. Deep understanding of the Indian solar market, including regulations, policies, and industry trends. Excellent leadership, communication, and interpersonal skills. Strong analytical and problem-solving abilities. Entrepreneurial mindset with a hands-on approach. Ability to thrive in a fast-paced, dynamic environment. (Interested candidates can share their CV to aradhana@hungrybird.in or call on 9959417171.) Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Relevant Experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Aradhana +91 9959417171

Hiring: Solar Sales Manager and Sales Executives Job Details: Position: Solar Sales Manager / Executive Industry: Solar / Renewable Energy / Finance Salary: Up to 9 LPA for Sales Executives For Mehsana: Sales Manager position available Up to 16 LPA Eligibility Criteria: CIBIL Score: 700+ Education: Graduation is mandatory Experience: Candidates must have experience in Solar Sales or Finance Knowledge: Must be familiar with Government Subsidy Schemes for Solar Age Requirement: Must be above 35 years Locations: Tamil Nadu: Virudhunagar, Viluppuram, Tirupattur, Tenkasi, Pudukkottai, Mettupalayam, Mayiladuthurai, Kanchipuram Andhra Pradesh: Guntakal, Rayachoti, Jaggayyapeta, Rajam Maharashtra: Baramati, Pandharpur, Khopoli, Ratnagiri Gujarat: Halol, Dahod, Mehsana (Sales Manager also needed here) Job Responsibilities: Promote and assist with finance options for solar products Educate customers on solar benefits & government subsidy schemes Maintain strong relationships with distributors and financial partners Follow up with customers and help them avail finance options Develop and manage relationships with clients, distributors & government agencies Achieve sales targets and expand the business in the assigned region Conduct site visits and provide customized solar solutions How to Apply? Interested candidates can send their resume to Pooja@vsharptalent.in or WhatsApp CV at 9998683788

India's No. 1 IT Company is Hiring for Medical Reviewer MBBS/MD Graduates with 1 yr to 5 yr Experience in Clinical Trials, PV, ICSR, SUSAR, Clinical Trial Operations Salary up-to 18LPA Call-Prachi-8287816038/ Rukhsar- 9899875055

Job Description Solar Resource and Performance analysis Role Proposal Stage Yield Assessment a. Solar Resource Assessment covering comparison with nearby plants, aerosol/pollution study and climate study b. Energy yield assessment for solar projects and solar part in hybrid projects c. TL line loss assessment, Tilt-Pitch analysis, Tracker Vs Fixed Tilt analysis d. Maintaining the Solar resource database of the company and conversant with SGIS data e. Should be fully conversant with latest version of PVsyst. As-Built Solar Yield Assessment based a. Actual plant configuration, b. Number of land parcels, c. Actual Transmission Line Losses d. Exact location irradiation and weather data Support in O and M generation budget preparation Preparation of Detailed Project Reports for solar and hybrid projects for funding Site Audits: a) Evaluate sites independently for generation improvement

Greetings from You & I Consulting! You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. Hirings for MNC : - Great Opportunity in Giant MNC .Grab the Opportunity to grow and explore We are hiring for: Medical Writer CTC : upto 17 LPA Mode : Work From Office Location- Mumbai, Pune, Bengaluru Preferred experience for the role: • Overall ~5 years of authoring/editing experience in medical writing domain across different therapeutic areas in clinical documents including clinical study protocol, pediatric investigation plan, informed consent document, clinical study report, investigators brochure, clinical summary of pharmacology, clinical overview (efficacy and safety), briefing package/pre-meeting package preferred • Good knowledge of clinical research domain, ICH GCP principles, Common Technical Document (CTD) structure and regulatory requirements • Experience in preparation of clinical documents necessary for national and international regulatory submissions to the US, European and other regulatory agencies • Computer Literate: Knowledge of MS Word, PowerPoint, Adobe Acrobat, MS Excel, etc Responsibilities: • Setting, discussing and meeting expectations of the document during kick off and subsequent meetings Lead the authoring/editing of clinical documents, as mentioned above. Ensure adherence to established processes, timelines, regulatory guidelines and applicable standards, styles, guidelines Perform quality review of the clinical documents within established timelines with adherence to applicable guidelines, templates, and processes Ability to effectively and proactively communicate with internal and external stakeholders, including authors and key opinion leaders as appropriate (including problem-solving and resolution of issues) • As required, take on functional role and responsibilities of the role of Documentation Lead o Lead PDRD deliverables for project and act as first point of contact for any information that is required for content/document preparation Ensure alignment and content re-use across documents for a product Onboard lead document writers on document content alignment and timelines. Provide required source documents incl. information pertaining to study documentation, relevant project contacts (authors, reviewers), developmental strategy Actively participate in Regulatory Affairs Functional or other cross functional team meetings Review content of document prior to finalization to ensure high quality prior to initiation of author review or Expert Team Review Perks and benefits: ONLY 5 Days Work CAB Fecility Medical Benefits To Apply Call on 8250242229 (Puja) / Whats app on the same Number ***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: - 8250242229 (Puja) Name- Mobile number - Mail - Highest Qualification Highest qualification University Name Total work experience - Date of birth- Current Organization- Preferred Location Last CTC- Expected CTC: *Interested candidates can even refer their friends or relatives provided the criteria *FOR interview Call Now our HR Specialist: -----@ ** 8250242229 (Puja) (call or WhatsApp)

Role & responsibilities Solar AC/DC Systems: Supervise the installation and commissioning of solar AC/DC systems for the ground-mounted solar power plant. Ensure all electrical systems are correctly configured and operational, following safety standards and project specifications. 2. Module Mounting Systems (MMS) Erection: Oversee the erection of Module Mounting Systems (MMS) , ensuring proper alignment and stability. Coordinate with the installation team to ensure MMS is installed according to design specifications and manufacturer guidelines. 3. Solar Table Erection: Manage the erection of solar tables where solar panels will be mounted. Ensure the correct installation of tables, focusing on structural integrity and alignment to support the modules effectively. 4. Module Installation: Supervise the installation of solar modules onto the MMS and solar tables. Ensure proper alignment, secure mounting, and connection of modules to optimize system performance. 5. Module Alignment: Conduct precise alignment of solar modules to ensure optimal tilt and orientation for maximum energy capture. Use appropriate tools and techniques to achieve accurate module positioning and alignment. 6. Erection and Commissioning: Lead the overall erection and commissioning activities, ensuring all components and systems are installed, tested, and operational. Perform initial system checks, troubleshooting, and adjustments to confirm proper functionality before project handover. 7. Safety and Compliance: Adhere to all safety protocols and standards during installation and commissioning activities. Ensure compliance with project specifications, industry standards, and local regulations. 8. Documentation and Reporting: Maintain detailed records of all installation and commissioning activities. Prepare and submit reports on progress, issues encountered, and completed tasks to the Project Manager. 9. Coordination and Communication: Coordinate with project teams, contractors, and suppliers to ensure timely and efficient completion of tasks. Communicate effectively with stakeholders regarding project status, schedules, and any issues that arise. 10. Quality Assurance: Implement quality control measures to ensure all installations meet required standards and specifications. Conduct inspections and tests to verify the integrity and functionality of the installed systems. Preferred candidate profile Minimum 3-7 years of experience in solar power plant erection and commissioning, with hands-on experience in solar AC/DC systems, MMS, and module installation. Proficiency in solar module alignment, MMS erection, and commissioning procedures. Strong knowledge of safety standards and project specifications.

Roles and Responsibilities Manage auto loan sales from lead generation to disbursement, ensuring timely processing and customer satisfaction. Develop strong relationships with customers through effective communication, negotiation, and problem-solving skills. Identify new business opportunities by prospecting for leads, networking with dealerships, and leveraging market knowledge. Collaborate with internal teams to resolve issues related to loan applications, documentation, and collections. Maintain accurate records of transactions, updates customers on loan status, and provides regular feedback. Desired Candidate Profile 1-6 years of experience in auto finance or banking industry (preferably). Strong understanding of various types of loans such as Car Loan, Commercial Vehicle Loans, Used Car Loan etc. . Excellent communication skills with ability to work independently as well as part of a team. Proficiency in MS Office Suite (Excel) is essential; familiarity with CRM software an added advantage. For more details or to apply for this opportunity email your updated Resume or CV on hr819.o3hire@gmail.com

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Sr Analyst Qualifications: Bachelor of Pharmacy Years of Experience: 5 to 8 years 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 world's 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.In this role, you will be expected to 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? Ability to establish strong client relationship Ability to work well in a team Collaboration and interpersonal skills Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Bachelor of Pharmacy

Dear Candidates, Greetings from Brunel!!! www.brunel.net Brunel India Private Limited, a subsidiary of Brunel Holding Group Company (Brunel Intl. N.V.) a company registered in the Netherlands with over 10,000 employees in 104 offices across 35 countries. The Energy Division of Brunel Group comprehensively provides manpower services for Upstream Oil & Gas, Downstream Oil & Gas, Renewables, Power Generation, Mining & Resources, Civil Engineering, Automotive, Rail, Life Sciences, Finance, Legal and ICT. Our core services are Pay Rolling, Contract Hire and Direct Hire services for major Operating companies and EPC contractors. Basic terms of employment are mentioned below: - Positions: Civil Engineer Experience : 8 -10 years Qualification: B.E in Civil or Structural Engineering Job Location : Remote, Office located at Bangalore Work Mode: Remote working. In a month candidate have to work from Bangalore office for Three to Four days. Role & responsibilities 1. Good Communication, Presentation and Leadership skill 2. MNC Experience 3. Candidates who can join early 4. Experience in Civil Design of energy or heavy industrial facilities. A concentration in renewable energy industry is a plus including PV, Wind and/or BESS.6. Excellent communications skills, with the ability to provide training on complex operations 7. Demonstrate continuous commitment to safe operations. Be an active role model and constant resource to the organization. 8. Experience in renewable energy construction and design. Experience in heavy bid or similar software. 9. Must be able to use Microsoft Word, Excel, PowerPoint, Project and AutoCAD. 10. Ability to communicate detailed information accurately to internal / external customers 11. Ability to professionally represent the company when dealing with external organizations 12. Able to work in an indoor or outdoor environment. 13. Have a valid drivers license and satisfactory driving record. Interested candidates can share CVS on o.komal@brunel.net/ Contact No 8655929878

Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years Language - Ability: Japanese - Elementary 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 world's 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.In this role, you will be expected to 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? Agility for quick learning Collaboration and interpersonal skills Commitment to quality Ability to perform under pressure Prioritization of workload Roles and Responsibilities: In 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 The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Any Graduation

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy Years of Experience: 0 to 1 years Language - Ability: English - Advanced 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 world's 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.In this role, you will be expected to 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? 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 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 Qualifications Bachelor of Pharmacy

Hi We are hiring for ITES Company Role -Medical Reviewer Qualification : MBBS/MD only (MCI Certification is not mandate**) Experience Range : 1 to 7 Years Preferred Experience: Minimum of 1 years of experience in PV/ Clinical Research (drug safety) Job Description: Author a company clinical comment (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. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. • Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. 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 To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Medical Reviewer Mumbai (Job Code # 47) b) For Position in Pune Search : Medical Reviewer Pune (Job Code # 48) c) For Position in Bangalore Search : Medical Reviewer Bangalore (Job Code # 51)

Hi Hiring for the leading ITES Company for Regulatory Medical Writer Profile. Job Description: Experience : 4 - 11 years of experience in Medical Writing domain. Location: Mumbai, Pune, Bangalore Salary: 8 LPA to 12 LPA To Connect WhatsApp 'Hi' @9151555419 and search for Job in Mumbai / Pune / Bangalore Roles and Responsibilities: Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas. Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required. To work in coordination with all the members in the study team- internal and external for the development of clinical documents. Share project timelines amongst the study team for the development of document. Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document. Review statistical analysis plans and table/figure/listing, when required. Ensure uniformity and consistency in the scientific content of the regulatory documents To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Medical Writing Mumbai (Job Code # 56) b) For Position in Pune Search : Medical Writing Pune (Job Code # 57)

Hi, We are hiring for Leading ITES Company for Medical Writer Profile. Role & Responsibilities: Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas. Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required. To work in coordination with all the members in the study team- internal and external for the development of clinical documents. Share project timelines amongst the study team for the development of document. Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document. Review statistical analysis plans and table/figure/listing, when required. Ensure uniformity and consistency in the scientific content of the regulatory documents Preparation of documents in the scope and other Medical Writing documents that may be required for domestic and international regulatory submissions to the US, European, and other regulatory agencies. Prepare Medical Writing documents within established timelines that are of high quality for scientific content, organization, clarity, accuracy, format, and consistency, with adherence to regulatory guidelines and applicable standards, styles, guidelines, and processes. Perform peer review and quality control review of the documents within established timelines with adherence to applicable guidelines, and processes, using appropriate checklists. Take an active role on assigned projects with respect to planning of content, format, and timing of documents, report scheduling/tracking, etc. Provide support to the assigned clinical development or project team to ensure that project needs, and department standards are met, while completing reports within established schedules/timelines. Plan and organize project and non-project meetings, as and when required To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Medical Writing Mumbai (Job Code # 56) b) For Position in Pune Search : Medical Writing Pune (Job Code # 57)

We are hiring for the below role: Job Title: Lead Engineer - Battery Integration & Energy Storage Systems CTC- 5LPA About Us: KSL Cleantech Limited is one of the largest and most experienced solar companies in India. We design, manufacture, build, and operate photovoltaic power plants from kilowatt to multi-megawatt. At KSL Cleantech, we are dedicated to creating a sustainable future by implementing innovative technologies and eco-friendly practices. Our unwavering commitment aims to reduce our carbon footprint and promote environmental responsibility, ensuring a greener planet for future generations. Join our dynamic, inclusive team and contribute to projects that matter. Role & responsibilities Designing & testing Battery Energy Storages Systems Working in Solar + Storages + grid integration solutions Study global energy storages trends Comprehensive Competitor Analysis for BESS/ESS product & services Making business models Continuous research on energy storage systems breakthrough in Battery Chemistry & Storage Solutions Preferred candidate profile : -Degree in Electrical Engineering or Renewable Energy or related field -Comprehensive knowledge working in Solar+ Storage+ Grid integration solutions -Should be fluent in Communications -Data-driven -Good Market Research skills -Proactive -Tech Savvy -Proficient in MS Office Suite Perks and benefits : Monthly CTC- 40K If your profile suits the above criteria, please do share your cv at hr@kslcleantech.com or drop your cv on WhatsApp at +919230913827 (No Calls Please).

We are seeking a highly motivated and detail-oriented recent graduate to join our Pharmacovigilance team as an Entry-Level Pharmacovigilance Associate. This is a fantastic opportunity to begin your career in the pharmaceutical industry and contribute to the safety monitoring of our products. You will gain hands-on experience in various aspects of pharmacovigilance, including adverse event reporting, data entry, and case processing. This role is ideal for individuals with a strong interest in drug safety and a desire to learn and grow in a dynamic environment. Responsibilities: Adverse Event Case Processing: Receive, triage, and accurately enter adverse event reports into the pharmacovigilance database. Ensure timely and accurate data entry according to company Standard Operating Procedures (SOPs) and regulatory guidelines. Assist in the follow-up of adverse event reports to obtain complete information. Perform quality checks on case data to ensure accuracy and consistency. Data Management and Reporting: Assist in the preparation of safety reports and data summaries. Maintain accurate and organized pharmacovigilance records. Assist in the tracking and monitoring of adverse event trends. Regulatory Compliance: Gain a basic understanding of global pharmacovigilance regulations and guidelines. Adhere to company SOPs and regulatory requirements. Assist in the preparation of regulatory submissions. General Support: Assist in the maintenance of pharmacovigilance databases and systems. Participate in team meetings and training sessions. Support senior pharmacovigilance staff as needed. Any 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 as part of a team. Good communication and interpersonal skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate.

Industry :- BFSI Designation :- State Head - Car Loan Manage the Auto Loans vertical for Karnataka region with P&L Accountability for auto loans products. Building distribution channels/ channel partners in Karnataka with an objective to penetrate deep into the market. Acquire a network of influencers and ensure activation of these channels by virtue of various initiatives and activities. Ensuring compliance with regulations and procedures as laid down, by keeping up to date with all changes in the regulatory framework Understand the market dynamics and technological advancements in the Banking & Finance/Fintech industry and build strategies around the same. Create a road map for the business, based upon the vision of the organization, encompassing value creation for stakeholders, customers, channel partners and employees Responsible for overall Business/Distribution Strategy function, driving key business objectives centrally. Sound understanding of the distribution business. Responsible for channel profitability & strategic initiatives to grow the business Topline/Initiatives to grow the business, Topline/Bottomline target achievement. Developing and maintaining good working relationships with business associates. Effective relationship management with the Banks/Financial Institutions. Monitoring and reporting on performance against agreed sales targets, including monitoring the performance of other staff. For more details or to apply for this opportunity email your updated Resume or CV on nitish.o3hire@gmail.com

Role & responsibilities : Achievement of business plan targets in terms of volume growth, product mix and market share. Responsibility for Dealer network management & expansion. Promotion of business & Institutional sales. Planning& executive sales promotion plans & activities. Effective cost management. Conducting detailed market study to analyze the latest market trends and tracking competitor activities and providing valuable inputs for fine tuning the selling strategies Preferred candidate profile Graduate 3-5 yrs. experience in Auto Loans business is a must. Good communication and pleasing personality. High level of Self Drive/Enthusiasm Team handling experience Key Responsibilities : Strong commercial and business acumen Strong customer focus Excellent communication and presentation skills. Strong analytical and problem solving skills. Knowledge of service and warranty system.

Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Senior Analyst Qualifications: BCom Years of Experience: 5 to 8 years 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? Team lead experience Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications BCom

Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: BCom/Any Graduation Years of Experience: 1 to 3 years 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? ** Roles and Responsibilities: In 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 The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications BCom,Any Graduation