4 Protocol Review Jobs nearby Mysore

As an Operations Manager at GRS UpDown Museum located within GRS Fantasy Park in Mysore, your role will involve overseeing the daily operations of the museum. You will be responsible for managing staff, ensuring customer satisfaction, maintaining safety standards, and enhancing the overall visitor experience. Your coordination with various departments and vendors, handling of budgets and inventory, and implementation of operational policies will be crucial to the success of the museum. **Key Responsibilities:** - Oversee end-to-end operations of the Up Down museum to ensure a seamless visitor experience and compliance with safety standards. - Manage all staff, including guest service, ticketing, housekeeping, and technical teams. - Develop and enforce SOPs for cleaning, maintenance, crowd control, and emergency procedures. - Maintain consistent housekeeping standards for hygiene and visitor comfort. - Plan staff schedules, training sessions, and performance reviews to uphold operational efficiency. - Monitor exhibits, lighting, and equipment for continuous functionality and safety. - Coordinate with marketing teams for events, promotions, and special programs. - Manage budgets, inventory, vendor contracts, and reporting to ensure smooth administrative operations. **Qualifications Required:** - Bachelor's degree in Business Administration, Management, or a related field. - Experience in the hospitality industry is a plus. - 5 to 7 years of experience in Operations Management. - Strong customer service, communication, and problem-solving skills. - Knowledge of safety standards and compliance. - Ability to work independently and manage multiple tasks simultaneously. As an ideal candidate for this position, you should possess 5+ years of experience in operations and administrative management, preferably in museums or hospitality. Your strong leadership and team management abilities will be essential for handling multi-department operations. Excellent communication and interpersonal skills are necessary for staff coordination and guest relations. You must have knowledge of safety regulations, compliance, and crowd management protocols, along with problem-solving and decision-making capabilities for high-pressure situations. Experience in budget planning, procurement, vendor management, and operational planning tools will be advantageous. A customer-centric mindset with a focus on service excellence will further contribute to your success in this role.,

You will be part of the Renewable Energy sector with a focus on utility-scale Solar PV EPC and site delivery across India. As an on-site engineer, your role will involve managing civil execution, quality control, and contractor delivery at remote project sites in the Civil & Construction discipline. **Key Responsibilities:** - Supervise and coordinate day-to-day civil construction activities for solar PV projects including earthworks, access roads, drainage, cable trenches, piling, and foundation works. - Execute site layout and surveying using Total Station/GPS to ensure accurate alignment of module tables, trackers, piling positions, and equipment platforms. - Validate construction quality through onsite testing and inspections such as concrete slump and compaction tests, enforce specification compliance, and manage third-party testing. - Prepare and maintain as-built drawings, mark-ups, and measurement sheets; review shop drawings and respond to RFIs with the design/PMC team. - Track quantities, progress, and productivity, maintain daily reports, material checklists, and support planning for manpower and equipment allocation. - Enforce HSE protocols onsite, manage subcontractor performance, conduct inspections, and implement corrective actions to meet schedule and cost targets. **Qualifications Required:** - AutoCAD for preparation and interpretation of civil drawings. - Total Station and GPS surveying for layout and alignment. - Quantity take-off and site layout skills for earthworks and foundation works. - Concrete testing and compaction testing familiarity for field QC. - Proven experience working on Solar PV EPC civil activities for ground-mounted/tracker projects. - Willingness to be based on site with frequent travel to remote locations. The company encourages applicants with additional qualifications such as a degree in Civil Engineering or equivalent, practical field experience in utility-scale solar or civil EPC projects, and familiarity with Indian codes and site regulatory compliance. If you join, you can expect competitive site allowances, travel reimbursement for on-site postings, hands-on growth path in utility-scale solar delivery, cross-functional exposure (design/PMC/planning), and a safety-first work culture with structured onboarding and field mentoring. Make sure to demonstrate your concrete field-delivery examples (site diaries, as-built samples, testing records) and readiness for sustained on-site engagement on utility-scale Solar PV projects.,

You will be working at a Fertility centre that is dedicated to providing compassionate and evidence-based fertility care to couples. As one of India's leading fertility networks, the centre aims to make parenthood possible for more families through advanced technology and a highly skilled team. **Key Responsibilities:** - Conduct detailed fertility evaluations and create personalized treatment plans for patients. - Perform and oversee ART procedures such as IVF and IUI. - Collaborate with multidisciplinary teams to ensure seamless patient care. - Maintain accurate patient records and uphold compliance with clinical protocols. - Offer empathetic counseling and support to patients throughout their fertility journey. - Participate in clinical audits, case reviews, and continuous improvement initiatives. **Qualifications & Experience:** - Education: MBBS with MD/MS/DNB in Obstetrics & Gynaecology - Specialization: Fellowship or MCH in Reproductive Medicine/ART (mandatory) - Experience: Minimum 1+ years of post-qualification experience in fertility or ART practices **Skills:** - Strong clinical and diagnostic acumen - Patient-centric approach with empathetic communication - Proven counseling skills for managing complex fertility cases - Commitment to ethical medical practice If you join this team, you will: - Work with a nationally recognized fertility care provider - Collaborate with experts in reproductive medicine - Have access to cutting-edge technology and world-class laboratories - Experience a supportive and growth-oriented work environment,

Role Overview: As an Embedded Firmware Developer, your main responsibility will be designing, developing, and testing firmware for 8-bit and 32-bit microcontrollers. You will focus on developing and debugging firmware in C/C++ to ensure reliability and performance, as well as working on real-time operating systems (RTOS) to integrate firmware with hardware seamlessly. Key Responsibilities: - Collaborate with cross-functional teams to define firmware requirements and specifications. - Implement and troubleshoot communication interfaces such as SPI, I2C, UART, ADC, DAC, and timers. - Develop and maintain secure boot mechanisms and secure firmware update processes. - Conduct code reviews, support hardware bring-up, and system integration. - Document development processes, code functionality, and testing procedures. - Participate actively in both development and testing phases of the firmware lifecycle. Qualifications Required: - Bachelor's degree in Computer Science, Electronics, Electrical, or a related engineering field. - Minimum of 5 years of professional experience in embedded software development. - Strong programming skills in C/C++ and experience in debugging embedded systems. - Deep knowledge of real-time operating systems, firmware architecture, and secure boot implementations. - Familiarity with hardware interfaces and communication protocols such as ADC, SPI, I2C, UART, DAC, and timers. - Solid understanding of hardware subsystems, peripheral integration, and strong analytical skills. - Excellent interpersonal and written communication skills. - Ability to thrive in a collaborative environment and strong problem-solving abilities. - Preferred qualifications include experience in developing firmware for safety-critical or secure systems, familiarity with version control systems like Git, and exposure to firmware testing methodologies and tools.,

Role Overview: As a Team Leader at Equiniti India - Operations, your main responsibility will be to lead a team efficiently to provide high-quality service to customers while ensuring adherence to agreed standards. You will be required to oversee and support the work of your colleagues, contribute to departmental planning, and coordinate resources effectively to ensure daily workloads are completed in a timely manner. Key Responsibilities: - Organise, plan, control, and monitor workflow to ensure daily workload completion in line with service standards. - Monitor team performance, recommend operational changes, and implement improvements to enhance service quality and process efficiency. - Facilitate the development of individual team members through cross-training and ensuring adequate knowledge and resources for coverage. - Collaborate with the US operational team to align communication and operations effectively. - Identify trends in problem occurrence and workflow, investigate root causes, implement necessary changes, and coordinate support from other parties to prevent re-occurrences. - Monitor team compliance with internal policies, procedures, external regulations, and data security protocols, reporting non-conformances as required. - Uphold quality and information security policies, along with all aspects of the Integrated Management System within the operational unit. - Support team deliverables by performing various roles and tasks as needed. - Continuously enhance personal skills and technical knowledge to adapt to evolving business environments. Qualifications Required: - Excellent English oral and written communication skills, capable of explaining information clearly and concisely to individuals or groups. - Proficient in self and work organization, utilizing time management techniques to plan, manage, and prioritize work effectively. - Skilled in performance review and development, objectively assessing capabilities and giving constructive feedback to identify development needs. - Experienced in change management, effectively communicating changes, planning implementations, and minimizing service disruptions. - Demonstrated organizational awareness, understanding the company's aims, policies, culture, and operational strategies. - Knowledgeable in environmental awareness, understanding the business environment, industry best practices, and potential impacts of economic, political, and social changes on the business. (Note: The additional details of the company were not provided in the job description.),

As a Senior Clinical Data Associate at [Company], you will be responsible for providing data management support and assistance throughout the clinical trial data management process. Your role will involve following Standard Operating Procedures (SOPs) and regulatory directives to ensure the successful completion of assigned projects. Some key responsibilities include: - Supporting the Lead DM as a back-up and/or team member to ensure tasks are performed in a timely manner - Performing data entry for paper-CRF studies and conducting quality control of data entry - Assisting in developing CRF specifications and coordinating the review/feedback from stakeholders - Building clinical databases and conducting database build UAT - Specifying requirements for edit checks and maintaining data management documentation - Training clinical research personnel on study-specific items - Reviewing and querying clinical trial data according to the Data Management Plan - Performing medical coding of medical terms for consistency - Coordinating SAE/AE reconciliation and liaising with third-party vendors - Identifying and troubleshooting operational problems for studies - Reviewing and providing feedback on protocols and reports - Participating in the development and maintenance of SOPs - Ensuring all data management project team members are sufficiently trained - Communicating with study sponsors, vendors, and project teams regarding project issues - Presenting software demonstrations/trainings and may require some travel Qualifications required for this role are: - 5+ years of experience - Bachelors and/or a combination of related experience - Proficiency in Microsoft Office - Ability to handle various clinical research tasks - Excellent organizational and communication skills - Basic knowledge of drug, device, and/or biologic development - Preferred experience in clinical, scientific, or healthcare discipline - Skills in dictionary medical coding, CDISC standards, and therapeutic experience in Oncology and/or Orphan Drug In terms of skills and competencies, you should demonstrate strong knowledge of ICH-GCP, precision oncology SOPs, and regulatory guidance. You should be able to motivate project team members, focus on continuous improvement, resolve project-related problems, work independently and in a team, and exhibit professionalism in interactions with customers and teammates. Please note that any data provided as part of the application process will be handled in accordance with our Privacy Policy. If you require a reasonable accommodation to complete the application process, please contact us at QuestionForHR@precisionmedicinegrp.com. Also, be aware of fraudulent job offers not associated with our company, as we do not extend job offers without prior communication and a formal interview process.,

Role Overview: As a Team Manager in the company, your main role will be to lead and supervise a team of assembly technicians. You will guide and mentor the team members, conduct performance reviews regularly, and ensure compliance with safety protocols and company policies. Key Responsibilities: - Plan, schedule, and oversee daily assembly operations to meet production targets - Monitor production processes, adjust schedules as necessary, and collaborate with other departments to resolve production issues - Implement and maintain quality control procedures, conduct inspections, and address quality issues promptly - Identify opportunities for process improvements, implement changes for enhanced efficiency, and stay updated with industry trends in injection molding technology - Manage inventory levels, coordinate with the procurement team, and maintain accurate records of production and inventory - Prepare and present regular reports on production performance, quality metrics, and process improvements - Maintain comprehensive documentation of assembly processes Qualifications Required: - Bachelor's degree in Engineering, Manufacturing, or a related field - Minimum of 5 years of experience in plastic injection molding and assembly operations - Proven experience in a managerial or supervisory role - Strong knowledge of injection molding processes, materials, and equipment - Excellent leadership, communication, and interpersonal skills - Proficiency in using manufacturing software and tools - Strong problem-solving abilities and attention to detail - Knowledge of lean manufacturing principles and continuous improvement methodologies Additional Company Details: The company offers benefits such as food, health insurance, leave encashment, and provident fund. The work schedule includes day shift, morning shift, night shift, and rotational shift, with additional perks like performance bonus, shift allowance, and yearly bonus. This is a full-time, permanent position that requires in-person work at the specified location.,

**Role Overview:** As a Hardware Penetration Tester on our Device Penetration Testing team at Cisco, you will proactively engage in technical and hands-on security assessments to strengthen the security of millions of Cisco devices. Your main responsibilities will include dissecting hardware, analyzing firmware, identifying critical vulnerabilities, and contributing to the security and trustworthiness of Cisco's product portfolio. **Key Responsibilities:** - Perform technical and hands-on security assessments by analyzing hardware components and interactions, including JTAG, UART, SPI, and I2C communication analysis. - Conduct in-depth analysis of firmware interactions with underlying hardware, extract content from SPI flash and other on-board memory, and audit the security of hardware protocols. - Engineer and implement exploit chains to bypass advanced hardware and firmware security mechanisms, demonstrating full compromise scenarios. - Research emerging hardware attack surfaces, develop innovative exploitation techniques, and enhance offensive security skillset. - Document identified vulnerabilities with detailed technical write-ups and collaborate with engineering teams for effective remediation. - Utilize automation, custom scripting, and AI/ML technologies for vulnerability discovery and streamline security analysis workflows. - Analyze recurring vulnerability patterns, translate findings into actionable security insights, and influence secure design to prevent future vulnerabilities. **Qualifications Required:** - Security-focused mindset with a genuine passion for penetration testing and vulnerability research. - Familiarity with firmware extraction techniques and methodologies. - Strong understanding of embedded hardware interfaces, protocols, and conducting JTAG, UART, and SPI-based testing. - Ability to identify and bypass hardware security mechanisms, familiarity with embedded operating systems, and architectures. - Proficiency in programming and scripting (e.g., Python, C, Bash), experience with hardware debug tools, and test equipment. - Solid understanding of network security, penetration testing methodologies, and industry frameworks such as OWASP. - Bachelor's degree in Computer Science, Information Security, or 5+ years of related work experience. - 4+ years of hands-on experience in web application security, firmware security, authentication, and security protocols. - Strong written and verbal communication skills to explain complex security issues clearly to technical and non-technical audiences. **Additional Details:** Cisco is revolutionizing how data and infrastructure connect and protect organizations in the AI era and beyond. With over 40 years of fearless innovation, Cisco provides solutions that power how humans and technology work together across the physical and digital worlds. The company encourages diversity and offers limitless opportunities for growth and collaboration on a global scale. Cisco empowers its employees to make a meaningful impact worldwide.,

As a Protocol Review Specialist, you will play a crucial role in the clinical trials process. Your responsibilities will include reviewing protocols, responding to queries and clarifications from EC/IRB, answering medical questions, attending drug safety meetings, reviewing AE/SAEs, and providing protocol training to site staff, CRAs, etc. during investigator meetings. Key Responsibilities: - Reviewing protocol and providing suggestions to enhance the process - Responding promptly to queries/clarifications from EC/IRB - Addressing medical questions from sites or project teams effectively - Attending important drug safety meetings and external meetings - Thoroughly reviewing and documenting AE/SAEs - Conducting comprehensive protocol training for site staff, CRAs, etc. during investigator meetings Qualifications Required: - Prior experience in clinical trials is essential - Proficiency in handling SAES will be advantageous - Ability and willingness to actively participate in external meetings Please note that the company operates within the ITES/BPO/KPO industry, with a strong focus on the pharmaceutical sector. This role is categorized under Life Sciences and Pharma. If you have any further questions or need clarification, please feel free to reach out. Job Code - GO/JC/20991/2025 Recruiter Name - HariharanA,

As an experienced Lead Data Engineer, your role will involve driving data engineering initiatives, architecting scalable data solutions, and leading a team of engineers. You specialize in Snowflake, Matillion, and Cloud platforms (Azure/AWS) and have expertise in BI tools like Power BI, Tableau. You are required to have strong SQL skills, analytical capabilities, excellent communication, and leadership abilities. Your responsibilities will include: - Designing and developing scalable, high-performance data solutions using Snowflake, Matillion, and cloud environments (Azure/AWS). - Building and optimizing ETL/ELT pipelines leveraging Matillion, Snowflake native capabilities, dbt, and other data integration tools. - Using Power BI, Tableau, and DOMO to develop insightful reports and dashboards, ensuring seamless data flow from the backend to visualization layers. - Writing and optimizing complex SQL queries for performance tuning, data transformation, and analytics. - Implementing data lakes, data warehouses, and data marts on Azure/AWS, ensuring security, scalability, and cost efficiency. - Designing and implementing dimensional models, star/snowflake schemas, and data warehouse best practices. - Collaborating with stakeholders to understand business requirements, define project scope, and deliver tailored data solutions. - Leading a team of data engineers, conducting code reviews, mentoring junior engineers, and establishing best practices. - Automating workflows, monitoring system performance, and optimizing data processes for efficiency. - Ensuring compliance with industry best practices, data privacy laws, and security protocols. - Implementing and managing orchestration tools like Apache Airflow, Prefect, or Dagster for automated data workflows. Required Skills & Qualifications: - 10+ years of experience in data engineering and cloud-based data solutions. - Expertise in Snowflake, including performance tuning, data sharing, and security management. - Strong experience with Matillion for ETL/ELT development. - Proficiency in Azure or AWS Cloud Services (e.g., AWS Redshift, S3, Glue, Azure Synapse, Data Factory). - Hands-on experience with BI tools such as Power BI, Tableau. - Exceptional SQL skills for query optimization and data modeling. - Strong analytical and problem-solving skills to translate business needs into technical solutions. - Proven ability to lead teams, mentor engineers, and manage projects effectively. - Excellent communication skills to collaborate with clients, stakeholders, and cross-functional teams. - Experience with Python or other scripting languages for data processing is a plus. - Experience with dbt for data transformation and modeling. - Knowledge of workflow orchestration tools like Apache Airflow, Prefect, or Dagster.,

Job Description: Huron helps its clients drive growth, enhance performance, and sustain leadership in the markets they serve. Collaborating with education organizations to develop strategies and implement solutions that enable transformative change. Empowering clients to drive innovation, create sustainable funding streams, and deliver better student outcomes. In your role as a Managed Services Associate at Huron, you will be joining a vibrant cross-shore team responsible for executing a portion of the overall Research Office portfolio. You will expand on your existing research foundation and collaborate with team members to propose unique solutions for a wide range of clients across the research industry. Your responsibilities will include developing coverage analysis reports, study budgets, study calendars, and other clinical trial documentation. You will gain experience with CRM tools, proprietary Huron Research Suite technology, clinical research protocols, and workflow facilitation in regulatory areas of the business. Responsibilities: - Managing your workload across multiple clients and ensuring target dates are met - Supporting Client Leads by preparing and managing client communications - Supporting Client Leads through Quarterly Report generation and updates - Protocol review and interpretation to support Coverage Analysis and Calendar Builds - Providing leadership for the Analyst team and supporting their development and growth - Analyzing workflows across various clients to identify escalation points - Engaging in continuous improvement efforts to solidify foundations for growth - Collaborating with internal team members during projects, including presenting key takeaways, communicating project updates, and organizing overall project logistics - Updating workplans to support overall project execution Core Qualifications: - Bachelor's degree required - 3-5 years relevant workflow execution or process improvement experience in a team-based environment within research operations - Experience within clinical research or sponsored awards is a plus - Proficient in Microsoft Office (Word, PowerPoint, Excel) - Eagerness to engage in ongoing professional development and apply skills in the workplace to foster a continuous improvement environment - Familiarity with clinical trials policy, research billing rules, and regulatory compliance - Experience with clinical trials management systems - Strong written and verbal English skills - Effective critical thinking, problem-solving, and analytical skills; attentive to detail - Capable of maintaining a 34-hour overlap with US Eastern Time - Located in or near Bangalore; role requires individual in the office,

Role Overview: As a Technical Lead in debugging, automation, and content development, you will be responsible for providing technical expertise to medium to large sized teams, mentoring team members, and inspiring them to excel in their roles. You will be expected to be proficient in bug monitoring, tracking bug lifecycle, coding modules, low-level debugging, and code analysis. Additionally, you will need to adhere to project timelines, mentor teams in automation/debug, and stay updated with the latest technologies in automation, debug, and content development. Key Responsibilities: - Expertise in bug monitoring, tracking bug lifecycle, and isolation - Proficiency in coding modules, libraries, low-level debugging, and code review - Perform component selection, isolation, and RCA in case of failure - Adherence to latest versions of feature documents, source code, and binaries - Mentor teams in Automation/Debug for enhanced effectiveness - Thorough analysis of requirements to provide measurable inputs - Train teams to analyze traces/core dump for defect resolution - Conduct regular sync meetings with stakeholders for issue resolution - Solicit feedback and implement changes for better customer satisfaction - Provide strategic and tactical solutions for technical issues - Motivate and encourage team members to stay updated with technical requirements - Act as a single point of contact for all technical solutions within the team Qualification Required: - Expertise in hardware engineering with knowledge of C, C++, C#, Python, and relevant languages - In-depth knowledge of automation programming or debugging techniques and methodologies - Familiarity with protocols, interfaces, and debugging tools - Experience with source code management tools like GIT - Proficiency in MS Office and Visio Additional Details: UST is a global digital transformation solutions provider with over 30,000 employees in 30 countries. UST partners with clients to embed innovation and agility into their organizations, impacting billions of lives in the process.,

As a Pega CSSA Certified Specialist joining our offshore delivery team for a Tier 1 Australian Bank, your role will involve designing, developing, and implementing Pega applications in alignment with banking business requirements. Collaborating with onshore and offshore teams, business analysts, and stakeholders to deliver high-quality solutions will be essential. You will provide technical leadership and guidance to junior developers, ensuring adherence to Pega best practices, guardrails, and coding standards. Additionally, you will support solution design sessions, architectural reviews, and code reviews, working closely with stakeholders within the Tier 1 Australian Bank to understand and translate requirements into Pega solutions. Your expertise will be crucial in assisting in performance tuning, troubleshooting, and production support. **Key Responsibilities:** - Design, develop, and implement Pega applications in alignment with banking business requirements. - Collaborate with onshore and offshore teams, business analysts, and stakeholders to deliver high-quality solutions. - Provide technical leadership and guidance to junior developers. - Ensure adherence to Pega best practices, guardrails, and coding standards. - Support solution design sessions, architectural reviews, and code reviews. - Work closely with stakeholders within the Tier 1 Australian Bank to understand and translate requirements into Pega solutions. - Assist in performance tuning, troubleshooting, and production support. **Qualifications Required:** - 5+ years of Pega development experience, with at least 2+ years as CSSA. - Pega CSSA Certification (Certified Senior System Architect). - Proven experience working on large-scale enterprise programs, ideally within a Tier 1 banking environment. - Strong understanding of banking operations and financial workflow automation. - 2+ years of experience as a Certified Senior System Architect, creating complex designs, reusable functions, user interfaces, reporting, and integration solutions for multi-process Pega applications. - Strong design skills with deep knowledge of Pega application design concepts, case design principles, and development best practices. - Track record of successful Pega application implementations that meet user needs. - Strong understanding of system architecture and administration concepts. - Proficient in REST/SOAP APIs, database integration, and authentication protocols (OAuth, SAML). - Experienced in Agile/Scrum methodologies with excellent analytical and critical thinking skills. - End-to-end lifecycle expertise with a focus on delivering agile, sustainable solutions. - Solid understanding of SDLC and DevOps practices. - Strong problem-solving and analytical skills. - Excellent communication and collaboration skills. This role offers the opportunity to work with a leading financial services organization globally and contribute to the delivery of beautiful experiences and exceptional capabilities to branch applications.,

As an experienced React Native developer with 2+ years of experience, you will be responsible for developing robust and scalable cross-platform mobile applications and delivering high-quality solutions with a team of designers and developers at Wokay. **Key Responsibilities:** - Creating mobile apps for different platforms using React Native. - Writing clean, efficient React Native code for mobile devices. - Working in a team of other developers and designers, sharing ideas and developing cross-platform mobile applications. - Improving React Native app performance on different devices. - Conducting code reviews and providing React Native code quality and standards compliance. - Connecting React Native apps with services and tools designed for mobile platforms. - Fixing bugs during React Native development. - Managing React Native app deployment to various stores and platforms. - Being involved in React Native-related processes of agile development. **Qualifications Required:** - 2+ years of experience with React Native. - Proficiency in JavaScript and the React Native framework. - Familiarity with mobile databases like SQLite or Firebase. - Knowledge and application of SOLID principles, algorithms, and design patterns in React Native development. - Understanding of web technologies and UI/UX standards for mobile platforms. - Experience integrating APIs and utilizing third-party libraries within React Native applications. - Understanding of mobile security protocols and experience with secure coding practices. - Familiarity with continuous integration and delivery methodologies in mobile app development. - Demonstrated commitment to staying updated on emerging React Native technologies and industry best practices. - Prior experience with TypeScript, Re.pack, Rspack and/or Expo would be a plus. - Excellent communication and collaboration abilities, with a proven track record of working effectively within a team environment. - Strong analytical and problem-solving skills, dedicated to delivering high-quality solutions. - Proficiency in English is required. *Note: Additional details of the company were not provided in the job description.*,

As a member of the project team at Fortrea, you will be responsible for conducting clinical data review, query generation/resolution, and reconciliation activities to ensure the delivery of clinical data meets client quality and integrity specifications, project timelines, and productivity targets. Your tasks will include assisting in developing the project Data Management Plan, executing data review guidelines/edit check, and eCRF specification, and contributing to the setup of data management systems based on project requirements. Your key responsibilities will involve: - Ensuring strict adherence to relevant protocols, global harmonized SOPs, and GCP standards for allocated projects. - Following study timelines for on-time deliverables and providing inputs on study design or timelines adjustments. - Reviewing clinical trial data, raising queries, and running additional programs to support data review. - Interacting with project team members for Data Management aspects setup, maintenance, and closure. - Generating and QC data listings, testing edit checks, database screen design, and functionality. - Supporting the training of new staff on project-specific Data Management processes. - Running study status reports, assisting in Database Lock and Unlock activities, and performing other assigned duties. Qualifications required: - University/college degree in life sciences, health sciences, information technology, or related fields, or certification in allied health professions. - Proficiency in English, both written and verbal. Experience required: - 3 to 5 years of relevant work experience in data management with knowledge of one or more therapeutic areas. - Demonstrated time management skills, knowledge of medical terminology, clinical data management practices, and effective communication skills. The job may involve working in an office or home-based environment, potential overtime, weekend work, and flexible shifts as per business requirements. Fortrea is dedicated to finding problem-solvers and creative thinkers who share a passion for overcoming clinical trial barriers. Join a collaborative workspace focused on revolutionizing the development process to deliver life-changing therapies swiftly to patients in need. Visit www.fortrea.com for more information. Fortrea is an Equal Opportunity Employer.,

As a Production Supervisor, your role involves overseeing various aspects of production operations to ensure smooth functioning and adherence to quality standards. Your key responsibilities include: - Indenting, approving, and receiving batch production records, cleaning records, and packing records based on production requirements. - Raising raw material indents and approving indented raw materials in alignment with production planning. - Maintaining good housekeeping in the plant environment. - Coordinating with cross-functional teams to execute plant operations efficiently. - Monitoring equipment utilization and manpower distribution for optimal productivity. - Initiating, reviewing, and approving indents for procuring production needs. - Ensuring the implementation of all schedules, including production planning, preventive maintenance, and calibration. - Ensuring compliance with production activities and meeting target timelines. - Monitoring and closing QMS documents, participating in internal audits, and supporting customer/regulatory audits. - Involving in qualification activities and providing training to the shop floor team. - Ensuring adherence to safety rules and regulations during work. - Attending training programs on GMP, job training, and safety as per the schedule. - Reviewing completed batch production records, equipment log books, and shift handover log books regularly. - Monitoring online BPR entries and providing new products training before batch execution. - Preparing, reviewing, and approving controlled documents related to the quality of APIs and intermediates. - Initiating, implementing, and closing QMS activities such as change control, deviation, OOS, investigation, and CAPA. - Reviewing validation protocols and reports, including campaign reports. - Acting responsibly for the activities of the immediate superior in their absence. - Performing any other assigned activity by the superior or Plant Head. This role offers a diverse range of responsibilities aimed at ensuring efficient production processes and maintaining quality standards throughout the operations.,

As a Junior Clinical Research Associate at Clinogenesis Research Organization, you will play a crucial role in supporting the clinical operations team and contributing to high-quality clinical trials. **Key Responsibilities:** - Assist in site initiation, monitoring & close-out activities - Support review of study documents & source data verification - Maintain trial documentation & ensure GCP compliance - Coordinate with site teams & internal stakeholders - Assist in reporting, study tracking & CAPA follow-ups - Ensure patient safety and protocol adherence **Qualifications:** - Bachelors/Masters in Life Sciences / Pharmacy / Nursing / Biotechnology - 01 year of experience - Understanding of ICH-GCP & clinical trial process - Strong communication & organizational skills Clinogenesis Research Organization is a growing, innovation-driven CRO committed to excellence in clinical research and data-driven healthcare. We provide aspiring professionals with a strong foundation to build rewarding careers in the clinical research field. If you are a fresher or an early-career professional passionate about clinical research and eager to grow in the industry, we welcome your application to join us in shaping the future of clinical research together.,

Role Overview: As a Feasibility Manager at Precision for Medicine, you will be a key member of the expert Feasibility Department team. Your role involves supporting the delivery of various projects including pre-award, post-award, rescue, and stand-alone feasibility projects. You will be responsible for conducting feasibility analysis to support business development, operational strategy teams, and site identification for both new and ongoing projects. Additionally, you may also have the opportunity to contribute to innovative projects that keep Precision for Medicine at the forefront of scientific innovation in the biotech and pharma industry. Key Responsibilities: - Support pre-award feasibility projects by providing analysis and input for pre-award RFPs, including competitive analysis, historical recruitment analysis, standards of care evaluation, and site/country analysis. - Review clinical protocols, study assumptions, client information, and study plans for US and global trials. - Present and explain feasibility analysis to BD/Clients, including recommendations and rationale. - Collaborate with colleagues, consultants, and partners to gather and share feasibility information. - Undertake feasibility site outreach for pre-award opportunities and participate in BDM and client calls. - Provide support to post-award feasibility projects by delivering feasibility analysis aligned with study requirements. - Engage with patient advocacy groups and site networks to support study feasibility and successful delivery. - Analyze collected site data to identify sites accurately, model enrollment, and develop study strategies. Qualifications Required: - Bachelor's degree in a life sciences discipline. - Minimum of 5 years of related experience. - Relevant experience in feasibility analysis and site identification activities. - Proficiency in English communication, both verbal and written. - Strong management, organizational, analytical, and presentation skills. - Advanced computer skills, including MS Word, Excel, PowerPoint, and data analysis platforms. - Knowledge of ICH-GCP guidelines. - Postgraduate degree preferred. Note: Any data shared as part of the application process will be handled in accordance with the company's Privacy Policy. If you require accommodations due to a disability or need an alternative method for applying, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. Please be cautious of fraudulent job offers and note that the company follows a formal interview process before extending any job offers.,

As a web application penetration tester at Redinent Innovations, you will play a crucial role in our research team by conducting penetration testing, reverse engineering, threat assessments, static and dynamic code analysis, and executing test attacks to discover vulnerabilities for some of the leading players in embedded devices globally. Key Responsibilities: - Conduct penetration testing, reverse engineering, threat assessments, static and dynamic code analysis - Execute test attacks to discover vulnerabilities in embedded devices - Develop next-generation cybersecurity technologies for embedded systems, operational technologies, and connected IoT devices - Contribute fresh ideas from diverse areas like data mining, system design, distributed computing, networking, and data storage - Possess strong hands-on penetration skills and in-depth knowledge of web technologies such as HTML5, Java, JavaScript, Tomcat, etc. - Understand application security mechanisms including authentication, authorization, data validation, output sanitization/encoding, and encryption practices - Utilize common penetration testing tools like Burp Suite, Nessus, sqlmap, Nmap, Wireshark - Have expertise in network protocols, protection techniques (firewalls, filtering), and methods to bypass them - Deep understanding of web service technologies like WebSockets, SOAP, REST, JSON, XML, and security schemes such as OAuth, SAML - Working knowledge of scripting languages/frameworks like Python, Ruby, NodeJS, PHP, basic cryptographic principles, fuzzing, and security code review - Experience with RDBMS systems like MySQL, PostgreSQL, ORACLE, proficiency in Linux and Windows OS Qualifications Required: - Strong hands-on penetration skills and knowledge of web technologies - Familiarity with web applications, web servers, web browsers, and frameworks - Proficiency in using common penetration testing tools - Expertise in network protocols and protection techniques - Deep understanding of web service technologies and security schemes - Working knowledge of scripting languages/frameworks, cryptographic principles, fuzzing, and security code review - Experience with multiple RDBMS systems, proficiency in Linux and Windows OS - At least 5 years of relevant work experience If you are ready to contribute to cutting-edge cybersecurity solutions and work alongside top engineers, apply now by clicking the button below.,

As the Quality Management Systems Specialist, your role will involve initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. Additionally, you will handle Return Goods and ensure the proper functioning of the quality system by performing risk assessments as needed. Conducting regular internal audits will also be part of your responsibilities. Key Responsibilities: - Initiate, review, and approve quality management systems including Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints - Handle Return Goods and perform risk assessments to ensure the proper functioning of the quality system - Conduct regular internal audits to maintain compliance - Review and approve all documents such as SOPs, Spec & STPs, Forms, protocols, and reports - Review annual product quality review reports and provide training on cGMP topics to site employees - Support customer audits/visits and regulatory audits - Provide necessary documentation for amendments, annual updates, regulatory filings, and CMC supporting documentation - Fill out questionnaires, declarations, and quality agreements - Execute any additional responsibilities assigned by the Head of Department Qualifications Required: - Bachelor's degree in a relevant field - Prior experience in quality management systems within the pharmaceutical industry - Strong knowledge of cGMP guidelines and regulatory requirements - Excellent attention to detail and organizational skills - Effective communication and interpersonal abilities Note: The company values continuous learning and development, providing opportunities for professional growth and advancement within the organization.,