464 Jobs in Anupgarh - Page 11

32766BR Hyderabad Job Description Java Backend Developer Spring Boot Experience Micro Services Experience Telecom Experience is preferable Qualifications B.Tech Range of Year Experience-Min Year 5 Range of Year Experience-Max Year 8

34145BR Bangalore - Campus Job Description Enthusiastic Rails developer needed for an expanding set of business-critical applications, both in-house and customer-facing. Work with a friendly and helpful team, always looking to share and learn from the most recent best practices in Ruby and Rails. We need a Rails guru, with an ability to write quality code for very large systems. Knowledge of Javascript/front-end frameworks, RSpec and Linux is helpful. We work in small, self-directed, project-based groups, using an Agile methodology and two-week iterations. Every developer does some requirements gathering, design and coding. New projects and groups form throughout the year. We encourage exploration of new tools and techniques. We're looking for someone who enjoys solving problems and taming complexity. Technologies You Get To Work With Ruby on Rails, relational databases, Cloud Technologies and CI Tools Responsibilities Create high-level application analysis based on business requirements Create program designs based on high-level analysis Modify and write application software and unit tests to meet business requirements Work with other developers, providing coaching and training and checking deliverables Estimate and prioritize items in development iterations and releases Participate in code reviews Document program and API operation Required Skills Bachelor’s degree in a technical field or equivalent work experience 8+ years professional programming experience Experience creating web services and web applications Ruby on Rails and JavaScript Experience with API development Experience with cloud-based services Experience with distributed source code systems SQL querying skills Excellent troubleshooting and root cause analysis skills Excellent time management and prioritization skills Excellent written and verbal communication skills High attention to detail Qualifications Any Bachelor's Degree Range of Year Experience-Min Year 5 Range of Year Experience-Max Year 8

34240BR Georgia Job Description Senior Technical Consultant Qualifications Graduate Range of Year Experience-Min Year 8 Range of Year Experience-Max Year 10

33940BR Hyderabad Job Description JD for SOA Senior developer. 8 to 10 experience in Oracle integration cloud (OIC ) , Oracle Fusion Middleware (12c) and Skillful in BPEL Development, Oracle Service Bus Development (OSB) 12c, and Service Composite Architecture with minimum two live project experience. Strong knowledge on OIC with integration development (Scheduled and App driven integrations) Able to create integration in OIC by understanding SOA code Good knowledge integrating HCM Strong knowledge and experience with SOA frameworks and web service integration model Strong knowledge and experience with SOAP UI and REST WS-service client / postman. Strong knowledge and experience with XML, XSD, XSLT, XPath, XQuery, REST and WSDL technologies Knowledge and experience with Oracle’s (BEA) WebLogic , Application Server. Experience in working with various Oracle adapter technologies such as: Database, REST, File/ FTP , Oracle MQ, and JMS adapter Ability to write SQL queries Experience working with Relational databases Experience working with messaging infrastructure Qualifications B.Tech Range of Year Experience-Min Year 8 Range of Year Experience-Max Year 12

34241BR Georgia Job Description Tivoli Workload Scheduler SME Qualifications Graduate Range of Year Experience-Min Year 8 Range of Year Experience-Max Year 10

33456BR Chennai Job Description 8-10 Years of REST API Testing Experience using Postman. US Healthcare Experience is required. Basic SQL Experience is required. Agile Scrum experience is required. have knowledge of FHIR Specifications. Strong communication and ability to interact with US customers without assistance Essential experience with building Test Automation frameworks (Cucumber, Selenium) and Automated Testing. Strong delivery ownership. Collaborate with stakeholders to understand application needs and objectives. Participate in Agile ceremonies required for the project (daily stand-ups, sprint planning, backlog grooming, retrospectives, etc.) Demo the feature/story on sprint/release demos.Work Timing - 1:30 PM to 10.30 PM IST Location: Chennai/Bangalore. Qualifications BE Range of Year Experience-Min Year 8 Range of Year Experience-Max Year 10

34151BR Bangalore Job Description Job Title: L2 Network & Security Engineer Location: [Noida, Bangalore] Job Type Full-time | [Hybrid] Job Summary We are seeking a motivated and technically skilled L2 Network & Security Engineer to join our IT infrastructure team. The ideal candidate will be responsible for supporting and maintaining the organization’s network and security infrastructure, providing advanced troubleshooting, and implementing the best practices for secure and reliable operations. Key Responsibilities Monitor, maintain, and troubleshoot network infrastructure (routers, switches, firewalls). Investigate and resolve L2-level tickets escalated from the Service Desk or L1 engineers. Proficiency in VLAN, STP, RSTP, PVST, HSRP, NAT, PAT, and IPSLA. Ability to configure and troubleshoot EtherChannel issues. Conduct vulnerability scans, analyze security alerts, recommend mitigation strategies, network and security audits and compliance checks. Maintain network diagrams, documentation, SOPs and RCAs. Assist in deploying and configuring new network and security devices. Collaborate with L3 engineers to implement infrastructure changes and upgrades. Respond to and support incident management and problem resolution processes. Required Skills & Qualifications 5+ years of experience in networking and IT security support. Strong understanding of TCP/IP, DNS, DHCP, VLANs, subnetting, and routing protocols (e.g., OSPF, EIGRP, BGP). Hands-on experience with firewall Palo Alto, VPN, and security appliances. Working knowledge of tools (e.g., SolarWinds, Wireshark, NetFlow). Familiarity with access control, identity management, and patch management. Ability to analyze packet captures and troubleshoot network/security incidents. Preferred Certifications Cisco CCNA (Routing & Switching or Security) Palo Alto PCNSA / similar vendor certs Soft Skills Strong analytical and problem-solving abilities. Excellent communication and documentation skills. Ability to work independently and as part of a team. Willingness to participate in on-call rotation or after-hours support, as needed. Nice To Have Exposure to cloud networking/security (GCP, AWS, Azure,). Knowledge of scripting (PowerShell, Python) for automation tasks. Familiarity with ITIL processes and ticketing systems (e.g., ServiceNow, Jira). Qualifications Bachelor's Degree Range of Year Experience-Min Year 5 Range of Year Experience-Max Year 8

33647BR Chennai Job Description 5-7 Years of SF Service Cloud/Health Cloud Testing Experience. US Healthcare Experience is required. Agile Scrum experience is required. Strong communication and ability to interact with US customers without assistanceEssential experience with building Test Automation frameworks (Cucumber, Selenium, Jenkins, BDD) and Automated Testing. Strong delivery ownership. Collaborate with stakeholders to understand application needs and objectives. Participate in Agile ceremonies required for the project (daily stand-ups, sprint planning, backlog grooming, retrospectives, etc.) Demo the feature/story on sprint/release demos. Qualifications BE Range of Year Experience-Min Year 5 Range of Year Experience-Max Year 7

Organization- Hyatt Regency Shanghai, Wujiaochang Resumo Qualificações

Organization- Hyatt Regency Shanghai, Global Harbor Resumo Qualificações

Description Regulatory Associate Beijing/Shanghai Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Assists with preparation of product development documents including gap analyses and clinical development plans, Assists with preparation of regulatory submission documents including components of investigational new drug applications (INDs), new drug applications or new marketing applications (NDAs/MAAs), drug master files (DMFs), variations, renewals, marketing authorisation transfers (MATs) and other lifecycle maintenance activities, according to current government regulations and guidelines, Conducts regulatory research to identify regulatory precedents and to support the preparation of orphan drug designation requests, Performs quality checks on related documents, Assists with submissions of other regulatory documents and other regulatory research as needed, Assists clients, customers, or others with general information Gathers, compiles, analyzes, and reports information, Gathers information, searches files and records, and makes personal contacts to obtain specific information in order to prepare detailed reports and compose routine correspondence, Qualifications BS in science/healthcare field, or equivalent combination of education and experience, Excellent interpersonal / communication skills, Advanced skills in Microsoft Office Applications, Good time and project management skills, preferred, Strong analytical skills and attention to detail, Ability to work both as a team member and independently and to understand and carry out detailed instructions, Ability to interact with staff from multiple departments, Ability to work concurrently on projects, each with specific instructions that may differ from project to project preferred, Fluent in speaking, writing, and reading English, Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job,

Description Medical Scientist Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan) Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans, Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews, Authors medical data queries and reviews query responses, approves query closure in association with Medical Director, May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed, Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed, Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review, Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner, Attends at Trusted Process meetings and may participate in internal and external audits, Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology, Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans Adheres to customer policies and standard operating procedures, as required in project plans, Qualifications Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline, Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential, A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work, Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership, Understanding of scientific principles to assure effective and high-quality medical data analysis, Excellent written and oral communication skills, Excellent computer skills: MS Office programs, spread sheets, presentations, Prefer knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines, Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment, Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job,

Description CRA II (Single Sponsor dedicated) Croatia Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes, Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate Demonstrates diligence in protecting the confidentiality of each subject/patient Assesses factors that might affect subject/patients safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues, Per the Clinical Monitoring/Site Management Plan (CMP/SMP): o Assesses site processes o Conducts Source Document Review of appropriate site source documents and medical records o Verifies required clinical data entered in the case report form (CRF) is accurate and complete o Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines o Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture o Verifies site compliance with electronic data capture requirements May perform investigational product (IP) inventory, reconciliation and reviews storage and security Verifies the IP has been dispensed and administered to subjects/patients according to the protocol Verifies issues or risks associated with blinded or randomized information related to IP Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned, Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness Reconciles contents of the ISF with the Trial MasterFile (TMF) Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations, Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan Supports subject/patient recruitment, retention and awareness strategies Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution, For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met Must be able to quickly adapt to changing priorities to achieve goals / targets, May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements, Prepares for and attends Investigator Meetings and/or sponsor face to face meetings Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements, Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions, Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes; completes assigned training as required, For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II Additional responsibilities include: o Site support throughout the study lifecycle from site identification through close-out o Knowledge of local requirements for real world late phase study designs o Chart abstraction activities and data collection o Collaboration with Sponsor affiliates, medical science liaisons and local country staff o The SMA II may be requested to train junior staff o Identify and communicate out of scope activities to Lead CRA/Project Manager o Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associations Qualifications Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, presentation and interpersonal skills Ability to manage required travel of up to 75% on a regular basis Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job, Show more Show less

Description CRA II (Sponsor dedicated) Athens Homebase Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes, Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate Demonstrates diligence in protecting the confidentiality of each subject/patient Assesses factors that might affect subject/patients safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues, Per the Clinical Monitoring/Site Management Plan (CMP/SMP): o Assesses site processes o Conducts Source Document Review of appropriate site source documents and medical records o Verifies required clinical data entered in the case report form (CRF) is accurate and complete o Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines o Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture o Verifies site compliance with electronic data capture requirements May perform investigational product (IP) inventory, reconciliation and reviews storage and security Verifies the IP has been dispensed and administered to subjects/patients according to the protocol Verifies issues or risks associated with blinded or randomized information related to IP Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned, Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness Reconciles contents of the ISF with the Trial MasterFile (TMF) Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations, Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan Supports subject/patient recruitment, retention and awareness strategies Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution, For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met Must be able to quickly adapt to changing priorities to achieve goals / targets, May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements, Prepares for and attends Investigator Meetings and/or sponsor face to face meetings Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements, Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions, Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes; completes assigned training as required, For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II Additional responsibilities include: o Site support throughout the study lifecycle from site identification through close-out o Knowledge of local requirements for real world late phase study designs o Chart abstraction activities and data collection o Collaboration with Sponsor affiliates, medical science liaisons and local country staff o The SMA II may be requested to train junior staff o Identify and communicate out of scope activities to Lead CRA/Project Manager o Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associations Qualifications Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, presentation and interpersonal skills Ability to manage required travel of up to 75% on a regular basis Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job, Show more Show less

Description Quality and Compliance Assessor Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Performs Routine and Non-Routine Monitoring Evaluation Visits (MEVs) and/or Sign Off Visits (SOVs) as assigned, Assists in the analysis of qualitative oversight data to identify quality improvement signals, Conducts root cause analysis of the quality signals and develops a plan and/or recommended action(s) that may include assisting with implementation of process and efficiency improvements, Identifies training needs for CRAs through the analysis of aggregated oversight data to meet expected standards in quality and efficiency across Global Clinical Operation (GCO), May conduct training on areas of improvement as identified through the quality oversight data analysis and/or audit and inspection findings in collaboration with Learning Center of Excellence, Corporate Quality and Clinical Operations Management, Supports Clinical Operations in addressing ad hoc or escalated quality concerns within region, Acts as consultant to local/regional operations related to quality oversight best practices and tools, May assist in the review of Clinical Monitoring SOPs, tools or templates related to monitoring oversight, Performs other work-related duties as assigned, Requirements Bachelor's degree in biological science or healthcare-related field required Minimum of 5 years of experience in monitoring or auditing clinical research programs at a CRO, biotech or large pharmaceutical company Additional industry experience as a CRA Line Manager, Project Manager, Clinical Team Manager or Quality Control role preferred In-depth knowledge of ICH/GCP, local regulations, drug development process and clinical operations required Knowledge of multiple therapeutic areas Must be able to work independently within a matrixed environment across multiple projects, geographical locations and organizational levels to accomplish business goals Strong attention to detail with excellent organizational, documentation and presentation skills Strong interpersonal and communication skills with the ability to identify and solve problems and communicate issues tactfully Ability to perform root cause analysis Ability to manage required travel of up to 75% on a regular basis; including internationally Proficiency in written and spoken English with additional languages preferred in regional locations where the assessor will support multiple countries Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job, Summary The Quality and Compliance Assessor will collaborate with Clinical Research Associate ?CRA? line management to conduct quality oversight activities of CRAs to achieve consistent, high-quality performance and output for our clients Coordinates analysis of aggregated quality oversight data and communicates findings to CRA line management and Clinical Operations leadership with critical attention to addressing issues with solution-oriented proposals,

Description Site Activation Specialist II Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Responsible for the quality deliverables at the country level; follows project requirements and applicable country rules, with moderate oversight from the SSU Country Manager, Works within the forecasted submission/approval timelines and ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time; if forecasted timelines are not reached: investigates and provides clear rationale for delays, provides support on contingency plan to mitigate impact, and escalates the issue as soon as identified, Monitors basic financial aspects of the project and the number of hours/tasks available per contract; escalates discrepancies in a timely fashion, Reviews and complies with Standard Operating Procedures (SOPs) and Work Instructions (WI) in a timely manner, keeps training records updated accordingly and ensures timesheet compliance, Supports continuous improvement of quality in all Site Start-Up (SSU) components at the country level where assigned (submissions, essential document collection, communication to Competent Authorities and ECs, etc ), Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements, Responsible for one or more of the following functions at the country level: Local Submissions Specialist Follows the project direction provided by the designated country start-up advisor (CSA) and SAL May serve as a point of contact for the PM/SAL (or designee) during start-up on allocated projects Complies and/or reviews essential document packages for site activation and may also be involved in essential document collection from site Prepares and submits Central EC Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required, Prepares ongoing submissions, amendments, and periodic notifications required by central and local EC and RA and other local regulatory authorities as needed within the country; includes safety notifications as required by local rules, with moderate oversight from the SSU Country Manager, May act as liaison and facilitator between investigational sites and functional leads for related tasks and/or issues Oversee site activation end toend process at country/ site level, Country Start-Up Advisor Acts as Subject Matter Advisor for in-country performance within the Site Start-Up Supports country-level intelligence on start-up (SU) and clinical trial regulatory (CTR) Ensures that local country regulatory intelligence, as it pertains to the activities of the local SU and CTR team, is maintained on the central repository, e-g , Competent Authority submissions, EC submissions, notifications to data protection authorities, notifications/applications to any other local/federal/national body, and import/export license applications where these are obtained with RA applications In absence of legal advisor or dedicated subject matter may provide support for data protection at the country and provide guidance at a country level on data protection statements that need to be included on those documents which the Sponsor has contracted to the Company start-up group to adapt to local requirements This may include the Principal Investigator/Informed Consent and the Confidential Disclosure Agreement/contract template Provides input in local SOPs and WI Supports the creation of internal training materials on local legislation requirements Provides input to the team to assist with EC or CA issue resolution at the country level, Local Site ID and Feasibility Support Provides support with site selection lead and PM/SAL to ensure that the appropriate sites are selected for individual studies based on the requirements of the clinical trial, Local Investigator Contract and Budget Negotiator Provides support to SAL to agree on country template contract and budget Produces site-specific contracts from country template Provide support in submissions for proposed contract and budget for site Provides support in negotiating budget and contract with site via Site Contracts Service Centre and SAL with Sponsor until resolution of issues and contract execution Performs quality control and arranges execution of CTAs as well as archival of documents into repositories and capture of metadata, Qualifications Bachelors Degree Detailed understanding of clinical trial process across Phases II-IV and ICH GCP, Ability to understand clinical protocols and associated study specifications, Detailed understanding of clinical trial start-up processes, Ability to manage external vendors to contract effectively, Strong organizational skills with ability to handle multiple tasks effectively, Strong written and verbal communication and interpersonal skills, Ability to manage multiple project budgets with increased complexity and value, Quality-driven in all managed activities, Good negotiating skills, Good problem-solving skills, Demonstrated ability to work independently as well as part of a team, Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job, Summary Roles within the Site Start-Up/Site ID job family at the P21 level are responsible for managing and executing the site identification process in accordance with regulations, SOPs, and project requirements These roles involve completing and negotiating site confidentiality agreements (CDAs) and site information forms (SIFs) with sites, maintaining, reviewing, and reporting on site performance metrics, serving as the primary point of contact for investigative sites, and tracking the completion of site identification for sites Impact and Contribution Individuals in these roles are established and productive contributors who may manage defined components of projects or processes within their area of responsibility They utilize their practical knowledge of the professional area, typically obtained through education combined with experience, to contribute to the design, implementation, or delivery of processes, programs, and policies Their work ensures that site identification processes are completed efficiently and effectively, supporting the overall success of clinical trials and research projects Core Focus Managing and executing the site identification process in accordance with regulations, SOPs, and project requirements Completing and negotiating site confidentiality agreements (CDAs) and site information forms (SIFs) with sites Maintaining, reviewing, and reporting on site performance metrics Serving as the primary point of contact for investigative sites Tracking the completion of site identification for sites Show more Show less

Financial Planning And Budgeting Develop and manage project budgets. Forecast financial needs and ensure sufficient funding. Analyze project costs and variances. Project Monitoring And Reporting Track project financial performance against budget. Prepare and present financial reports and dashboards. Conduct regular project financial reviews with project managers. Cost Control Identify and mitigate financial risks and issues. Implement cost-saving measures and efficiency improvements. Ensure compliance with financial policies and procedures. Stakeholder Management Collaborate with project managers to ensure financial objectives are met. Communicate project financial status to stakeholders. Provide financial insights and recommendations to support decision-making. Audit And Compliance Ensure adherence to regulatory requirements and internal controls. Assist with internal and external audits. Maintain accurate financial records and documentation.

### Job Title: Project Head / Deputy General Manager (DGM) - Solar Projects #### Job Overview: The Project Head / Deputy General Manager (DGM) for Solar Projects will oversee the planning, execution, and completion of large-scale solar power projects. This leadership role requires extensive experience in project management, deep knowledge of solar technologies, and the ability to lead a multidisciplinary team to deliver projects on time, within scope, and budget. The DGM will be responsible for ensuring compliance with industry standards, regulations, and company policies while achieving project objectives. #### Key Responsibilities: **Project Planning and Development:** Lead the development of solar power projects from inception to completion. Develop comprehensive project plans, including scope, timelines, budget, and resource allocation. Conduct feasibility studies, site assessments, and due diligence to evaluate project viability. Secure necessary permits, licenses, and approvals from regulatory bodies. **Execution and Management:** Oversee all aspects of project execution, including engineering, procurement, construction, and commissioning. Coordinate with cross-functional teams, including engineering, procurement, construction, legal, finance, and environmental specialists. Ensure that all project activities align with the strategic goals and objectives of the company. Implement and monitor project controls to track progress, manage risks, and ensure quality and safety standards. **Team Leadership and Development:** Lead, mentor, and develop a high-performing project team. Foster a collaborative and inclusive team environment. Provide guidance and support to team members, promoting professional growth and development. **Stakeholder Management:** Act as the primary point of contact for all project-related matters. Develop and maintain strong relationships with stakeholders, including clients, contractors, suppliers, government agencies, and community representatives. Communicate project status, challenges, and successes to senior management and stakeholders. **Financial Management:** Develop and manage project budgets, ensuring cost-effectiveness and adherence to financial targets. Monitor and control project expenditures, identifying and mitigating financial risks. Prepare financial reports and forecasts for senior management review. **Quality and Compliance:** Ensure all project activities comply with industry standards, regulations, and company policies. Implement quality assurance and quality control processes to maintain high standards of workmanship. Conduct regular project reviews and audits to identify and address any issues. #### Qualifications and Experience: Bachelor's degree in Engineering (Electrical, Mechanical, Civil) or a related field; a Master’s degree or MBA is preferred. Minimum of 10 years of experience in project management, with at least 5 years in the solar power industry. Proven track record of successfully managing large-scale solar projects. Strong understanding of solar technologies, renewable energy systems, and construction methodologies. Excellent leadership, communication, and interpersonal skills. Proficiency in project management software and tools. Strong analytical and problem-solving abilities. Ability to travel to project sites and work in a dynamic and fast-paced environment. #### Skills and Competencies: **Leadership and Management:** Demonstrated ability to lead large teams and manage complex projects. **Technical Expertise:** In-depth knowledge of solar power systems and related technologies. **Financial Acumen:** Strong budgeting, financial management, and reporting skills. **Regulatory Knowledge:** Familiarity with relevant industry standards, regulations, and compliance requirements. **Problem-Solving:** Ability to identify issues, analyze data, and develop effective solutions. **Communication:** Excellent verbal and written communication skills for effective stakeholder engagement.

Financial Planning And Budgeting Develop and manage project budgets. Forecast financial needs and ensure sufficient funding. Analyze project costs and variances. Project Monitoring And Reporting Track project financial performance against budget. Prepare and present financial reports and dashboards. Conduct regular project financial reviews with project managers. Cost Control Identify and mitigate financial risks and issues. Implement cost-saving measures and efficiency improvements. Ensure compliance with financial policies and procedures. Stakeholder Management Collaborate with project managers to ensure financial objectives are met. Communicate project financial status to stakeholders. Provide financial insights and recommendations to support decision-making. Audit And Compliance Ensure adherence to regulatory requirements and internal controls. Assist with internal and external audits. Maintain accurate financial records and documentation.

Een goede financiële administratie is van groot belang om sturing te geven aan inhoudelijke opgaven van onze gemeente. De vraagstukken worden steeds complexer en onze opgave is om te bouwen aan een toekomstbestendige Bedrijfsadministratie en (financiële) Informatievoorziening die klaar is voor de ontwikkelingen van morgen. We zoeken twee managers die sturing gaan geven aan het bureau. Samen geven jullie richting aan de verdere ontwikkeling vorm Onze medewerkers kenmerken zich door vakmanschap, samenwerking, oplossingsgerichtheid en nauwkeurigheid. In onze organisatie staat de Nijmegenaar centraal, een gemeente is er tenslotte niet voor zichzelf. We zoeken verbinding, nemen initiatief en kijken vooruit. Ook jouw werk als manager Bedrijfsadministratie raakt de samenleving. Jouw werk doet ertoe! Wat ga je doen? Als manager geef je sturing aan een deel van het bureau Bedrijfsadministratie en Informatievoorziening. Samen met je collega-manager zorg je voor de koers en de bedrijfsvoering van het bureau op inhoud, mensen en middelen. Jij bent de HR-leidinggevende van je eigen deel van de medewerkers (plusminus 20 medewerker) binnen het bureau. We verwachten dat de ene manager zich richt op de de in- en verkoopadministratie en de andere op (financiële) informatievoorziening, aangevuld met enkele specifieke processen (zoals bijvoorbeeld verzekeringen en aansprakelijkheid). De precieze taakverdeling en teamindeling stemmen we samen af, op basis van ervaring, affiniteit en teamdynamiek. Je faciliteert een lerende, professionele werkomgeving waarin mensen met plezier werken aan resultaten. Je bent verantwoordelijk voor de kwaliteit van het werk van jouw teams en stimuleert medewerkers om zich te ontwikkelen en mee te bewegen met veranderingen. Je stuurt, samen met je collega MT-leden, integraal op de gehele afdeling Financiën. De komende jaren staan in het teken van verdere professionalisering en digitalisering van de administratie. Dit vraagt om stevig en zichtbaar leiderschap, met oog voor mensen en ontwikkeling. Als coachende leidinggevende geef je richting, maak je duidelijke keuzes en stimuleer je eigenaarschap in het team. In jou zien de medewerkers een leidinggevende die helder is, ruimte geeft, koers bepaalt en zich uitspreekt als iets goed gaat of beter kan. De medewerkers in het team zijn divers, jij bent flexibel in je stijl om zo goed in verbinding te zijn. Je motiveert, enthousiasmeert en ondersteunt medewerkers om mee te gaan in ontwikkelingen. Wie zijn wij? Als manager bedrijfsadministratie ben je onderdeel van het MT Financiën. De afdeling Financiën heeft in totaal 140 medewerkers verdeeld over drie bureaus. Je werkt nauw samen met de collega-manager binnen het bureau bedrijfsadministratie en benut elkaars kwaliteiten om het bureau toekomstbestendig te maken. Daarbij onderhoud je waar nodig de verbinding met andere afdelingen. Je geeft duidelijke signalen af richting de concernmanager en het management van de organisatie. Wat bieden wij jou? Werken bij de gemeente Nijmegen doe je vanuit je hart en daar belonen wij je graag voor. Benieuwd wat je ervoor terug krijgt? Lees dan verder! Een salaris in schaal 12. Afhankelijk van jouw ervaring ontvang je een salaris tussen de € 5.070,- en € 6.862,- bruto per maand bij een volledige werkweek van 36 uur. (dit is exclusief de aanstaande cao verhoging) Een individueel keuzebudget van 17,05% per maand. Extra verlof dagen bijkopen behoort dus tot de mogelijkheden. Een contract voor 32 tot 36 uur per week. Een hybride manier van werken. Jij past jouw werkplek en tijden aan zodat het past bij jouw functie en persoonlijke situatie. Een mooi opleidingsaanbod. We bieden je de ruimte om je te kunnen blijven ontwikkelen en het beste uit jezelf te halen. Zowel fysiek als digitaal. De keuze is aan jou! Lees hier meer over op onze pagina arbeidsvoorwaarden. Wie zoeken wij? Wij zoeken daadkrachtige managers die op inspirerende wijze leidinggeven en open staan voor vernieuwing en creativiteit. Jij bent een echte netwerker zowel binnen als buiten de organisatie. Je bent goed in verbinding met je collega-managers, zowel op de inhoud als in de bedrijfsvoering. Verder ben je een manager met oog voor een gezonde en veilige werkomgeving. Je neemt de zorgplicht voor de werkomstandigheden van je mensen serieus. Daarnaast zien we graag terug op jouw cv: Wo werk- en denkniveau Leidinggevende ervaring in een gemeentelijke- of andere publieke organisatie Ervaring als financial, bedrijfs-, of bestuurskundige en/of hebt kennis van en affiniteit met (werk)processen in het financiële vakgebied Waar kom je te werken? Werken bij de gemeente Nijmegen doe je vanuit je hart. Omdat je graag meedeint met het ritme van de stad. Als onderdeel van een bruisend geheel. Verbonden met- en verantwoordelijk voor een oude stad die niet stil kan blijven staan. Een stad met een prachtige historie en een nog mooiere toekomst. Want hier blijven mensen zichzelf keer op keer uitvinden. Hier is ruimte om te experimenteren en van elkaar te leren. Je krijgt het vertrouwen om je werk op jouw manier te doen. Zodat de oudste stad van Nederland voorop blijft lopen. Zonder daarbij iemand achter te laten. Want Nijmegen is van ons. Voor iedereen met hart voor de stad. En oog voor de toekomst. Meer weten en solliciteren? Maakt jouw hart een sprongetje bij het lezen van deze vacature? Solliciteer dan direct! Je kunt reageren tot en met 30 juni 2025. Gesprekken vinden plaats op woensdag 9 en donderdag 10 juli 2025. We zijn benieuwd waar jouw zwaartepunt ligt: voel jij je meer thuis in de administratieve processen, of spreekt juist de informatievoorziening met bijbehorende specifieke thema’s jou aan? Deel dit in je motivatie. Heb je toch nog vragen? Tom Merkx, concernmanager Financiën vertelt je graag meer! Je kunt hem bereiken via: t.merkx@nijmegen.nl of 06 11 95 62 73. Bij ons willen we dat jij jezelf kan zijn. We vinden het belangrijk om verschillende leeftijden, kwaliteiten en achtergronden in onze teams te hebben. Met verschillende perspectieven kunnen we ons werk beter doen. Herken jij eigenschappen en vaardigheden die genoemd zijn in de vacature? Voel je dan welkom om te solliciteren. Show more Show less

İdxalat üzrə satınalma mütəxəssisi vakansiyasına müraciət et Ad * Soyad * Ata adı * Son iş yeri Xananı doldurun Departament/Şöbə/Vəzifə Xananı doldurun Email Şifrə Şifrə Şifrəni təsdiqləyin Şifrəni təsdiqləyin Telefon nömrəsi * Faktiki yaşayış ünvan * CV yüklə DOC, PDF, JPEG 5 MB-dən çox olmayan Cv yükləyin Xananı doldurun Şəhər Bakı Məşğulluq növü Tam iş günü Maaş Son müraciət tarixi 30 Jun Ünvan 8 noyabr Müraciət et Ümumi məlumat Araz Supermarketlər Şəbəkəsi "İdxalat üzrə satınalma mütəxəssisi" vakansiyası üzrə işə qəbul elan edir! Vakansiya ilə bağlı müraciət etmək istəyənlər “İdxalat mütəxəssisi” adını mövzu hissəsində qeyd etməklə CV formalarını Career@retail.az elektron poçt ünvanına göndərə bilərlər. Öhdəliklər İxracat və idxalat əməliyyatlarında təcrübə; Beynəlxalq ticarət qaydaları və gömrük prosedurlarını bilmək; Müqavilələrin hazırlanması və danışıqlar aparılması bacarığı; Lojistik və tədarük zənciri ilə bağlı təcrübə; Bütün sənədləşmə və əməliyyatları düzgün şəkildə həyata keçirmək: Tələblər Ali təhsil; Sahə üzrə 1-2 il iş təcrübəsi arzu olunandır; Rus dili və ingilis dili yüksək səviyyədə; Güclü Kommunikasiya Bacarığı Bənzər vakansiyalar Show more Show less

Position Summary, 职位概述 Summer intern need to do some supports for Treasury team on a day-to-day basis and for the following projects, Bank Note H2H Internal Audit Statutory Cash Flow Mapping UAT Job Responsibilities, 工作职责 Check the completeness of data flow from accounting/purchase/reimbursement system to tax system, Check the calculation logic of separate tax filing module, Attend the meetings with vendor to summarize issues and follow-up actions, Compare the tax filing results coming from off-line approach and on-line tax automatic filing approach, Support the accounting treatment discussion with accounting team for those tax relevant matters. Requirements, 要求 Check the completeness of data flow from accounting/purchase/reimbursement system to tax system, Check the calculation logic of separate tax filing module, Attend the meetings with vendor to summarize issues and follow-up actions, Compare the tax filing results coming from off-line approach and on-line tax automatic filing approach, Support the accounting treatment discussion with accounting team for those tax relevant matters. Show more Show less

글로벌 오디오 라이브 콘텐츠 플랫폼, Spoon 과 함께 하실 Global CX Manager 를 지금 찾고 있어요 | 오디오(Spoon)와 비디오(Vigloo)를 아우르는 콘텐츠 플랫폼으로의 더 큰 도약을 위해, 스푼라디오에서 스푼랩스로 사명을 변경하였습니다 | 계약 기간은 최소 1년이며, 종료 시점에 내부 논의를 거쳐 계약 연장 여부가 검토될 수 있습니다. 🧑‍🤝‍🧑 [Spoon User Support 팀을 소개합니다] User Support 팀은 이런 일을 해요! 스푼랩스 User Support 팀은 한국 및 일본 스푼 서비스 운영을 담당해요. DJ가 팬 및 타 DJ와 더 깊고 넓은 관계를 맺도록 돕기 위해 VIP 및 유저 커뮤니티 관리, VoC 개선, 활동 정책 수립 등을 담당하며 유저 경험의 질적 개선을 도모해요. 이용자가 즐거운 경험만을 얻어갈 수 있도록, 이용자와 가장 가까운 위치에서 이용자의 경험을 공감하고 이해해요. 적극적인 소통을 통해 문제를 해결하여 스푼 서비스의 성장을 이끄는 중요한 역할을 수행해요. User Support 팀은 이런 문화로 일해요! 우리 팀은 이용자와 가장 가까이에 있어요. 때문에 팀원 모두가 이용자들이 쉽고 편하게 스푼을 이용할 수 있도록 뜨겁게 논의하고 빠르게 실행해요. 소소한 상황들도 같이 공유하고 해결하며 어려움은 나누고 기쁜 일은 2배로 기뻐하며 끈끈한 팀워크를 유지해요. Spoon 서비스는요, 누구나 목소리 하나로 방송하고, 팬과 실시간으로 소통할 수 있는 오디오 라이브 플랫폼이에요. No.1 오디오 라이브 콘텐츠 플랫폼을 향해, 한국·일본·대만 등지에서 글로벌 MAU 100만 명 이상으로 성장 중이에요. 2022년 첫 흑자 전환 이후, 지금까지도 꾸준한 성장세를 이어가고 있어요. Spoon 즐기러 가기: https://www.spooncast.net/kr 모두가 즐거운 스푼을 향한 여정에 동참하실 분을 기다릴게요! 💼 [주요 업무 - 주로 이런 업무를 수행해요] Global VoC 데이터 가공 및 분석 Global VoC 분석 기반 유저 경험 개선점 도출 및 반영 Global CS 오퍼레이션 기획 및 운영 (품질 관리 포함) Global 리스크 개선을 위한 기획 및 운영 Global 대외기관 분쟁 대응 📌 [자격 요건 - 이런 분과 함께하고 싶어요] 3년 이상의 Global CS 운영 혹은 Global CX 혹은 Global Customer Success 경험을 보유하신 분 Global CS 대응 경험이 있는 분 IT 스타트업 / 콘텐츠 관련 업계 재직 경험이 있는 분 데이터, 이용자 반응 등을 기반으로 문제점과 니즈를 파악하고, 상담, 운영, 정책 등을 개선한 경험이 있는 분 ➕ [우대 사항 - 이런 분은 더욱 반가워요] 이용자 불편사항과 문제점에 대한 원인을 파악하고, CS 운영 측면에서의 개선을 통해 해결한 경험이 있는 분 국가별 유저 문화, 커뮤니케이션 스타일, 민감 이슈에 대해 공감하고 이해할 수 있는 분 민감한 이슈(콘텐츠 삭제, 차단, 과금 오류 등)에 대한 신속하고 신뢰감 있는 응대가 가능한 분 명확한 상황 파악이 가능하고 정보를 논리적으로 정리, 전달하며 관계부서와 원활한 커뮤니케이션이 가능한 분 한국 소비자원, 콘텐츠 분쟁 조정 위원회, 수사기관 등에서 접수된 분쟁을 대응한 경험이 있는 분 일본어 네이티브 혹은 비즈니스 대화가 가능한 정도 혹은 한국어 비즈니스 레벨 이상 대화 가능한 분 📑 [제출 서류 - 지원자님을 알기 위해서는 다음 서류가 필요해요] 이력서 (필수 제출) 이력서 외 추가로 공유하고 싶은 자료가 있다면 함께 제출하셔도 무방합니다. 🎯 [채용 전형 - 다음 과정을 거쳐 스푼랩스에 합류하게 돼요] 서류 전형 > 1차 직무 인터뷰 전형 > 2차 컬처핏 & 3차 경영진 인터뷰 전형 > 레퍼런스 체크 전형 > 처우 협의 > 최종 합격 및 입사 1차 직무 인터뷰 전형 Spoon User Support 팀과의 직무 인터뷰를 진행합니다. 대면으로 진행되며, 예상 소요시간은 약 1시간입니다. 2차 컬처핏 인터뷰 전형 스푼랩스 EX팀(인사팀)과 컬처핏 인터뷰를 진행합니다. 대면으로 진행되며, 예상 소요시간은 약 1시간입니다. 2차 인터뷰가 끝나고 잠깐 휴식을 하신 이후, 3차 인터뷰가 바로 진행됩니다. (2, 3차 인터뷰는 하루에 연이어 진행됩니다.) 3차 인터뷰 전형 스푼 사업부 리드와의 경영진 인터뷰를 진행합니다. 대면으로 진행되며, 예상 소요시간은 약 1시간입니다. 레퍼런스 체크 전형 > 처우 협의 > 최종 합격 및 입사 상황에 따라 채용 절차가 생략 혹은 추가될 수 있습니다. (과제 전형/코딩 테스트/커피챗/추가 인터뷰 등) 이력서 및 제출 서류에 허위 사실이 발견되거나 근무 이력 중 징계사항이 확인될 경우, 채용이 취소될 수 있습니다. 스푼랩스 취업규칙 제10조(채용결격)에 따라 결격사유에 해당하는 자는 채용이 취소될 수 있습니다. 지원서에 기재된 개인정보를 제외한 경력·프로젝트 정보는 채용 진행 과정에서 AI 분석 도구로 검토될 수 있습니다. 👀 [스푼랩스는 어떻게 일하나요? 여기에 답이 있어요] 우리는 더 빠르게, 더 치열하게, 더 단단하게. 완벽보다 속도, 완성보다 실행. 스푼랩스는 빠르게 시도하고, 실패는 안고 다시 달립니다. 결국 답에 닿을 때까지, 우리는 계속 몰입합니다. 반짝이는 아이디어, 밤을 새워 몰입했던 순간, 깨달음에서 전율을 느끼던 날들. 속도는 빠르고, 기준은 높고, 불확실성은 큽니다. 누군가에게 이곳은 버거울 수 있지만, 우리는 그 안에서 치열하게 성장하며 매일 조금씩 더 나아갑니다. 더 멀리, 더 빠르게 나아가기 위해 어깨를 맞대되 각자의 빛을 잃지 않고, 앞서가되 독주하지 않습니다. 함께할 때 더 단단하기에, 우리는 서로를 믿고 배우며, 겸손하게 성장합니다. 원하는 게 ‘편한 일’인지, ‘치열한 성장’인지 스스로에게 물어보세요. 우리는 이미 ‘치열한 성장’을 선택했습니다. 단순한 일이 아닌, 내 인생과 세상을 바꾸는 전력질주를 위한 무대. 몰입과 끈기로 성장할 준비가 된 사람을 환영합니다. 스푼랩스 문화 블로그 스푼랩스 테크 블로그 스푼랩스 링크드인 스푼랩스 채용 사이트 🌱 [몰입하고, 성장할 수 있도록 이런 제도가 준비되어 있어요] [성장을 위한 제도] 끊임없이 도전하고 더 나은 결과를 만들어내는 구성원을 위해 월 10만원 한도의 자기계발비 지원 월 20만원 한도의 일본어, 영어, 한국어 외국어 학습비 지원 AWS re:Invent, Digital Marketing Summit, MAU Conference 등 업무 관련 국내외 교육 및 세미나 참석 지원 우리 같이 공부해요! 사내 스터디 모임 지원 사내 도서관 운영 및 신청 도서 구매 입사자와 추천자 모두 후한 보상을! 사내 직원 추천 제도 우리는 빠르게 배우고, 더 나은 방향으로 스스로 성장하는 사람들이 함께 모인 팀입니다. [일하는 방식] 몰입과 실행의 밀도를 높이기 위해 창의적 몰입을 위한 워케이션 프로그램 오전 8시~10시 30분 사이 자유롭게 출근하는 자율출근제 열심히 일하고 안전하게 퇴근해야죠. 야근 식비 및 택시비 지원 월요일은 4시간의 몰입을! 더욱 집중해서 몰입하는 주 4.5일제 우리는 더 깊이, 함께 몰입할 수 있는 환경을 선택합니다. [함께하는 팀을 위한 환경] 치열하게 일한 만큼, 서로를 챙기기 위해 함께해 주셔서 감사해요! 근속 기간별 리프레시 휴가 및 휴가비 지원 생일을 진심으로 축하합니다. 생일자를 위한 반반차 휴가 개개인의 일상에도 진심을 담아, 경조 휴가 및 경조비 지원 개인 근무 일정에 맞게 알아서 사용하는 휴가/반반차 제도 든든히 드세요. 아침 식사 제공 및 점심 식비 지원 무엇보다 건강이 우선이죠. 연 1회 종합건강검진 제공 강남역 역세권의 깔끔하고 세련된 사무실 에너지는 항상 충전되어야 하니까. 무제한 카페테리아 운영 힘들 땐 잠시 쉬어요. 고급 안마의자, 게임기, 다트, 탁구대 구비 치열하게 일한 만큼, 재충전도 중요하니까. 우리는 일하는 순간뿐 아니라, 그 사이사이도 함께 고민합니다. 채용에 대해 궁금한 점이 있다면? 아래 메일로 문의 주세요! 스푼랩스 채용: recruit@spoonlabs.com 주식회사 스푼랩스는 채용 ATS 그리팅의 개인정보 처리방침에 따라 개인정보를 수집 및 이용하고 있습니다. Show more Show less

Pavago is an innovative offshore recruitment company dedicated to connecting global companies with exceptional remote talent from multiple regions, including Latin America, Pakistan, the Philippines, and South Africa. This role is embedded within Pavago’s mission to build remote teams that combine cultural fit and professional excellence. Exclusive to Get on Board. Responsibilities Inbox & Slack Management: Oversee daily email and Slack communications, ensuring timely responses, organization, and prioritization across internal and external stakeholders. Schedule Management: Manage calendars, book meetings, and coordinate time zones to optimize productivity and eliminate friction. Task Coordination: Track, prioritize, and follow up on open items and deadlines, keeping things moving at a fast pace. Information Management: Capture notes, create to-do lists, and organize documentation to keep the founder fully aligned and on track. Proactive Support: Anticipate needs, offer solutions before being asked, and remove bottlenecks to allow the founder to focus on high-impact work. High-Level Communication: Act as a liaison with internal teams and external contacts—communicating with clarity, professionalism, and speed. What Makes You a Perfect Fit Admin & EA Experience: You’ve supported high-level executives or fast-paced teams before and know how to keep everything running smoothly. Exceptional Organization: You’re detail-obsessed, structured, and always thinking three steps ahead. Fast-Paced & Hungry: You thrive in intensity, enjoy being challenged, and are eager to take on responsibility in a high-performance environment. Excellent Communicator: You write and speak clearly, know how to adapt your tone, and can be assertive when needed. Problem Solver: You don’t just execute tasks—you find better ways to do them and stay ahead of potential issues. Discreet & Trustworthy: You’ll be handling sensitive information and must maintain confidentiality and discretion at all times. Required Experience & Skills Admin / EA Background: 2–4 years supporting fast-moving executives or founders, ideally in a startup or high-growth environment. Communication Tools Mastery: Experience using Slack, Google Workspace (Gmail, Calendar, Docs), Zoom, and Notion or similar tools. Calendar & Inbox Management: Proven ability to manage busy inboxes and complicated calendars with minimal oversight. Top-of-Market Talent: You’re sharp, switched-on, and operate at a high level of performance and accountability. Thrives in High Expectations: You don’t get overwhelmed by intensity—you rise to the challenge and deliver reliably. What Does a Typical Day Look Like? You’ll start your day reviewing and organizing emails, messages, and calendars—clearing blockers, prioritizing tasks, and prepping for upcoming meetings. Throughout the day, you’ll manage communications, book appointments, track to-dos, and follow up on outstanding items. You’ll work closely with CEO, making sure nothing slips through the cracks and helping him stay laser-focused. Everything moves quickly, so being proactive and responsive is key. GETONBRD Job ID: 54327 Remote work policy Locally remote only Position is 100% remote, but candidates must reside in South America, Costa Rica, Guatemala, Honduras, Nicaragua, El Salvador, Panama, Mexico, Jamaica or Belize. Show more Show less

Date 04/11/2024 Raison sociale Pi acoustique Poste TECHNICIEN(NE) EN ACOUSTIQUE - (Gironde) Descriptif société BET Pi acoustique - Bureau d'études en acoustique. Descriptif poste Vous serez chargé(e) de mesures et d'études acoustiques dans les domaines du Bâtiment, Environnement et Industrie. Tâches diverses et variées telles que : mesures acoustiques sur site, études acoustiques, analyses de mesures, rédactions de rapports, dimensionnements de dispositifs acoustiques, visites de chantiers, visas, etc. Poste basé en Gironde (33) à l'agence de La Lande de Fronsac, proche Bordeaux. Rémunération selon expérience. Profil recherché Technicien(ne) en acoustique de formation BAC+2 ou BAC+3 (DUT ou BUT Mesures Physiques ou autre, BTS, Licence …), ayant le sens du concret et un minimum de connaissances en chauffage ventilation climatisation et techniques de construction du bâtiment. Profil débutant ou expérimenté. Maîtrise des outils informatiques et logiciels de traitements de textes et tableurs (word, Excel, Publisher, etc). Connaissance des logiciels d'acoustique (dans l'idéal Cadnaa, Acoubat, dbtrait et dBbati). Connaissance des logiciels de plans (Sketchup, Autocad, etc). Idéalement connaissances et savoir-faire en traitements phoniques de bruits d'équipements (CVC, groupes froids, groupes électrogènes, etc) Qualité rédactionnelle et bon niveau en orthographe, indispensables. Permis B indispensable. Contact Transmettre SVP, CV et lettre de motivation à " contact@pi-acoustique.fr ", en mentionnant la référence suivante en objet "CANDIDATURE_AC_TECH_B_2411". Courriel contact@pi-acoustique.fr Site internet https://pi-acoustique.fr/ Show more Show less