2 Maas Jobs nearby Vellore

Job Description: You will be responsible for overseeing daily operations, coordinating administrative functions, and ensuring efficient office management. Your tasks will include budget planning and management, customer service excellence, strategic planning, and handling new projects while maintaining the existing infrastructure. Key Responsibilities: - Overseeing daily operations - Coordinating administrative functions - Ensuring efficient office management - Budget planning and management - Customer service excellence - Strategic planning - Handling new projects - Maintaining existing infrastructure Qualifications Required: - Strong communication skills - Proficient in analytical skills and planning - Excellent customer service abilities - Experience in budgeting and financial management - Strong leadership and organizational skills - Bachelor's degree in Business Administration, Management, or related field - Previous administrative experience in an educational institution is an advantage,

As an Applied Scientist at the Digital Acceleration (DA) team in India, your role will involve prototyping, optimizing, and deploying ML algorithms to solve Digital business problems. You will work on advancing the state of the art in AI & ML by researching, experimenting, and building Proof Of Concepts. Additionally, your responsibilities will include collaborating with engineering, product, and business teams to understand customer needs, drive science solutions from conception to delivery, and adapt quickly to evolving technical requirements. Effective technical communication, documentation of algorithms, methodologies, and findings, as well as supporting on-call activities for critical issues, are also key aspects of your role. Key Responsibilities: - Research, experiment, and build Proof Of Concepts advancing AI & ML - Collaborate across teams to understand customer needs and drive science solutions - Adapt quickly to evolving technical requirements - Engage in effective technical communication with coordination across teams - Conduct thorough documentation of algorithms, methodologies, and findings - Publish research papers in internal and external venues - Support on-call activities for critical issues Qualifications Required: - 3+ years of building models for business application experience - PhD, or Master's degree with 4+ years of experience in CS, CE, ML, or related field - Experience in patents or publications at top-tier conferences or journals - Programming experience in Java, C++, Python, or related language - Knowledge in areas such as algorithms, data structures, parsing, numerical optimization, data mining, parallel and distributed computing, and high-performance computing,

As an ideal candidate for this role, you should possess the following qualifications: - Proficiency in bookkeeping, account reconciliation, and financial reporting - Strong knowledge of budgeting, forecasting, and financial analysis - Experience in using accounting software and advanced Excel skills - Understanding of tax laws, compliance regulations, and audit processes - Attention to detail, analytical skills, and the ability to manage deadlines effectively - Bachelor's degree in Accounting, Finance, or a related field - Professional certification such as CPA or equivalent is a plus As an ideal candidate for this role, you should possess the following qualifications: - Proficiency in bookkeeping, account reconciliation, and financial reporting - Strong knowledge of budgeting, forecasting, and financial analysis - Experience in using accounting software and advanced Excel skills - Understanding of tax laws, compliance regulations, and audit processes - Attention to detail, analytical skills, and the ability to manage deadlines effectively - Bachelor's degree in Accounting, Finance, or a related field - Professional certification such as CPA or equivalent is a plus

As a Sr Regulatory Consultant specializing in Biologics/Biosimilars at Syneos Health, you will play a crucial role in authoring and reviewing CMC sections of regulatory submissions for various applications. Your responsibilities will include: - Authoring and reviewing CMC sections of regulatory submissions such as INDs, IMPDs, CTAs, BLAs, and MAAs, as well as briefing packages and health authority responses. - Ensuring completeness and compliance of CMC sections within IND and IMPD applications based on regulatory guidance (FDA, EMA, ICH). - Providing peer review and mentorship to junior writers or team members to maintain consistency and scientific accuracy across deliverables. - Staying updated with evolving regulatory expectations and industry best practices related to CMC submissions for biologics and biosimilars. - Demonstrating a good understanding of analytical method development, validation, comparability, upstream and downstream process development. In addition to the primary skills, the following secondary skills are also required for this role: - Deep understanding of CMC regulatory requirements for biologics/biosimilars, including ICH and region-specific guidance. - Experience with biosimilars, monoclonal antibodies, recombinant proteins, or other biologics. Qualifications for this position include: - Minimum of 8 years of experience in CMC-Biologics with a Masters degree in pharmaceutical sciences (preferred) or Masters degree in other life sciences. - Ability to work independently, manage multiple priorities in a fast-paced consulting environment, and strong organizational skills. - Experience with RIMS/Veeva Vault for submission management, document lifecycle tracking, and regulatory compliance. At Syneos Health, we are committed to developing our employees, fostering a Total Self culture, and creating a diverse and inclusive workplace where everyone feels valued and respected. Join us in our mission to accelerate customer success and change lives through innovative solutions in the biopharmaceutical industry.,

As a global leader in cybersecurity, CrowdStrike protects the people, processes, and technologies that drive modern organizations. Since 2011, CrowdStrike's mission is to stop breaches and redefine modern security with the world's most advanced AI-native platform. With a focus on large-scale distributed systems processing almost 3 trillion events per day, CrowdStrike's customers from various industries rely on the company to keep their businesses running smoothly and communities safe. **Role Overview:** As a Senior Systems Engineer at CrowdStrike, you will join the Production Infrastructure Engineering team and play a crucial role in the architecture and management of production systems environments. **Key Responsibilities:** - Oversee and coordinate technical resources to drive internal and external team projects to completion - Analyze requirements and develop solutions for technical problems based on complex business needs - Hold regular project meetings, address challenges, and drive milestones - Report project status regularly to leadership - Understand complex technical systems architecture and recommend improvements - Represent the systems team as a technical leader, providing direction and insight for projects and problem management - Familiarity with large-scale production deployments of servers and applications in internal data centers - Ability to write moderate to complex scripts and programs for automation and tools development **Qualifications Required:** - Experience leading projects and delivering solutions - Expertise with Bare Metal Orchestration services like OpenStack, Canonical MaaS - Proficiency in Linux engineering and administration for bare metal and virtual machines - Experience with container orchestration services such as Kubernetes - Knowledge of virtualization technologies like OpenStack Nova, VMWare ESXi - Familiarity with CI/CD systems like GitLab CI/CD, Jenkins - Experience with configuration management tools like Chef, Ansible, Salt - 7+ years of engineering experience, preferably in a production role - Ability to travel 2-3 times per year for business-related group meetings **Additional Company Details:** CrowdStrike offers a remote-friendly and flexible work culture, market-leading compensation, and equity awards. The company provides comprehensive physical and mental wellness programs, competitive vacation and holidays, paid parental and adoption leaves, and professional development opportunities for all employees. Employee Networks, geographic neighborhood groups, and volunteer opportunities are available to build connections. CrowdStrike is committed to fostering a culture of belonging and supporting veterans and individuals with disabilities through affirmative action programs.,

As a Vice President Operations at MAA INFRATECH PRIVATE LIMITED, your role will involve overseeing day-to-day operations in Patna, focusing on strategic planning, project management, and ensuring successful delivery of infrastructure projects. Your responsibilities will include managing financial performance with P&L responsibilities, establishing operational benchmarks, and driving customer-centric strategies to enhance service delivery and client satisfaction. Collaborating with various teams to align on business goals and maintaining organizational efficiency will be crucial to your success in this role. Key Responsibilities: - Oversee day-to-day operations, strategic planning, and project management - Ensure successful delivery of infrastructure projects - Manage financial performance, including P&L responsibilities - Establish operational benchmarks and drive customer-centric strategies - Collaborate with various teams to align on business goals - Maintain organizational efficiency Qualifications: - Proven expertise in Operations Management and strong P&L Management skills - Experience in Customer Service and designing customer-focused strategies - Proficiency in Strategic Planning and executing long-term business growth initiatives - Project Management skills with a track record of successfully delivering large-scale infrastructure projects - Strong leadership, decision-making, and team collaboration abilities - Experience in the construction or infrastructure sector is highly advantageous - Bachelor's or Master's degree in Business Administration, Engineering, or a related field preferred,

As a Diamond Assorter, your role involves assorting polished diamonds according to company-defined quality standards. You will be responsible for grading diamonds based on cut, color, clarity, and carat weight to ensure consistency and accuracy in diamond assortment. Collaborating closely with the quality control team is essential to maintain high standards. Your duties also include identifying and reporting any discrepancies or irregularities in diamond grading and maintaining records and documentation related to assortment. Qualifications Required: - Previous experience in diamond assorting and grading - Knowledge of cut, color, clarity, and carat weight standards - Attention to detail and accuracy in diamond assessment Please feel free to reach out to HR Kanika at 9251554005 for further information on this full-time position. As a Diamond Assorter, your role involves assorting polished diamonds according to company-defined quality standards. You will be responsible for grading diamonds based on cut, color, clarity, and carat weight to ensure consistency and accuracy in diamond assortment. Collaborating closely with the quality control team is essential to maintain high standards. Your duties also include identifying and reporting any discrepancies or irregularities in diamond grading and maintaining records and documentation related to assortment. Qualifications Required: - Previous experience in diamond assorting and grading - Knowledge of cut, color, clarity, and carat weight standards - Attention to detail and accuracy in diamond assessment Please feel free to reach out to HR Kanika at 9251554005 for further information on this full-time position.

Job Description As a Personal Assistant to the Director at Maa Bhawani Construction, you will play a crucial role in providing comprehensive support to the director. Your responsibilities will include managing the director's diary, handling administrative and clerical tasks, organizing meetings, and coordinating travel arrangements. Your effective communication, organization, and time-management skills will be essential in ensuring the efficient operations within the director's office. Key Responsibilities - Manage the director's diary effectively - Handle administrative and clerical tasks efficiently - Organize meetings and ensure smooth coordination - Coordinate travel arrangements for the director Qualifications Required - Proficiency in Personal Assistance and Executive Administrative Assistance skills - Strong Diary Management skills - Demonstrated Administrative Assistance and Clerical skills - Excellent organizational and time-management abilities - Effective written and verbal communication skills - Ability to maintain confidentiality and handle sensitive information - Proficiency in office software such as Microsoft Office - Bachelor's degree in Business Administration, Management, or related field is a plus,

As a Business Promotion Executive in Distt Mohali, your role will involve promoting the company's products or services. You will be required to be computer proficient, hold a valid driving license, and have a minimum qualification of 10+2 pass. Key Responsibilities: - Promote the company's products or services effectively - Utilize computer skills to enhance promotional activities - Drive to different locations as required for promotional activities Qualifications Required: - Must be computer proficient - Should hold a valid driving license - Minimum qualification of 10+2 pass Work Location: You will be required to work in person at various locations in Distt Mohali. Job Types: This is a full-time position suitable for freshers.,

As a Technical Support Analyst (Data-Focused) at our growing Analytics/tech-support team, your role involves investigating and resolving data inconsistencies or anomalies raised by business or engineering teams. You will write and debug Python scripts to automate checks, extract insights, or fix data issues. Running and adapting SQL queries (Athena and standard RDBMS) for data investigations will also be a key responsibility. Additionally, you will analyze logs and data flows to troubleshoot technical problems and build or support internal tools for monitoring, analysis, or reporting. Collaboration with product, data, and engineering teams to ensure data quality and integrity will be crucial, along with maintaining clean documentation of findings, tools, and processes. **Key Responsibilities:** - Investigate and resolve data inconsistencies or anomalies raised by business or engineering teams - Write and debug Python scripts for automation, data extraction, and issue resolution - Run and adapt SQL queries (Athena and standard RDBMS) for data investigations - Analyze logs and data flows to troubleshoot technical problems - Build or support internal tools for monitoring, analysis, or reporting - Collaborate with product, data, and engineering teams to ensure data quality and integrity - Maintain clean documentation of findings, tools, and processes **Qualifications Required:** - Strong Python skills for scripting, automation, and basic data processing - Proficiency in SQL, including joins, filtering, and analytical queries - Hands-on experience using AWS Athena or other distributed query engines - General coding/debugging experience and strong technical curiosity - Comfortable in CLI/terminal environments and working with structured/unstructured data - Proven attention to detail, able to detect subtle anomalies or logic issues - Strong analytical and problem-solving mindset In addition to the technical skills, the ideal candidate would have experience with AWS tools (S3, Glue, Lambda, CloudWatch), familiarity with Git and basic version control workflows, understanding of ETL pipelines, data validation, or schema management, exposure to dashboards (e.g., Metabase, Looker, Tableau), and ability to understand and use REST APIs for debugging or automation. Experience working in cross-functional, collaborative teams is also preferred. --- **About Affle:** Affle is a global technology company with a proprietary consumer intelligence platform that delivers consumer recommendations and conversions through relevant Mobile Advertising. The platform aims to enhance returns on marketing investment through contextual mobile ads and also by reducing digital ad fraud. Affle powers unique and integrated consumer journeys for marketers to drive high ROI, measurable outcome-led advertising through its Affle2.0 Consumer Platforms Stack which includes Appnext, Jampp, MAAS, mediasmart, RevX, Vizury, and YouAppi. Affle 3i Limited successfully completed its IPO in India and now trades on the stock exchanges (BSE: 542752 & NSE: AFFLE). Affle Holdings is the Singapore-based promoter for Affle 3i Limited, and its investors include Microsoft and Bennett Coleman & Company (BCCL) amongst others. For more information please visit: [www.affle.com](https://www.affle.com) **About BU (YouAppi):** YouAppi is a programmatic mobile app retargeting products that put your app where you want it - top of mind. A holistic marketing funnel approach activates valuable users, keeping them engaged, and growing your app revenue. For every app that helps in retargeting DSP offers a tailored approach with flexible integrations, optimizations, and transparent reporting going beyond downloads. For more information please visit [YouAppi Website](https://youappi.com/),

As an experienced doctor at Maa G Emergency Clinic Centre, your role will involve managing the OPD on a daily basis for 2 hours. Key Responsibilities: - Manage the OPD efficiently - Attend to patients" medical needs - Collaborate with the medical team for patient care - Maintain accurate medical records - Adhere to medical protocols and guidelines Qualifications Required: - MBBS degree for the female doctor role (1 position available for 24x7) - MD/MS in OBS/Gynecology (1 position available) - MD/MS in Internal Medicine (1 position available) - MD/MS in Orthopedics (1 position available) - MD/MS in Radiology (1 position available) If you meet the qualifications and are interested in working in a dynamic medical environment, please consider applying for the available positions at Maa G Emergency Clinic Centre.,

As a Program Lead at Elektrofi, you will play a crucial role in leading cross-functional program teams from early development through launch. Your main responsibilities will include: - Driving the development and implementation of integrated scientific, technical, and regulatory strategies for programs in the portfolio, ensuring alignment with overall program objectives and regulatory requirements. - Partnering with program managers, functional heads, and technical Subject Matter Experts (SMEs) to integrate nonclinical, formulation, process and analytical development, manufacturing, and regulatory plans. - Identifying risks and implementing mitigation strategies for each program in collaboration with the program manager, functional heads, and technical SMEs. - Supporting regulatory strategy development and health authority interactions as the lead contributor. - Acting as the primary technical interface between Elektrofi and Alliance Partners, ensuring transparent communication and alignment. - Facilitating effective decision-making by preparing clear program updates, risk assessments, and recommendations for governance and senior leadership. - Leading technical governance meetings, decision-making forums, and stage-gate readiness reviews. - Serving as the primary interface between the Program team and Company leadership to ensure alignment with Elektrofi's short- and long-term goals. - Fostering a collaborative and high-performing team environment that encourages accountability and solution-oriented thinking. Qualifications required for this role include: - Advanced degree (BS considered with strong experience) in a scientific or engineering discipline. - 12+ years of biotech/pharma industry experience, including 5+ years of CMC program leadership in biologics development. - Proven ability to lead complex, cross-functional teams in a matrix environment. - Ability to operate strategically while managing tactical execution details. - Strong team player with the ability to rapidly build positive relationships, proactively partner across teams, motivate and influence others, and negotiate diplomatically. - Deep understanding of end-to-end drug product development, manufacturing, and regulatory expectations for biologics, with a preference for experience in high-concentration and subcutaneous formulations. - Strong understanding of biologics CMC development, from preclinical through clinical stages, with regulatory submission experience (IND/CTA, BLA/MAA). - Excellent oral and written communication skills, and attention to detail to ensure high-quality presentations and regulatory submissions. Elektrofi is dedicated to transforming pioneering ideas into life-transforming solutions. While remote work is acknowledged for its merits, Elektrofi values an in-office work ethos. If you are looking to be part of a team that is revolutionizing the delivery of biologic therapies, please apply at elektrofi.com/careers. As a Program Lead at Elektrofi, you will play a crucial role in leading cross-functional program teams from early development through launch. Your main responsibilities will include: - Driving the development and implementation of integrated scientific, technical, and regulatory strategies for programs in the portfolio, ensuring alignment with overall program objectives and regulatory requirements. - Partnering with program managers, functional heads, and technical Subject Matter Experts (SMEs) to integrate nonclinical, formulation, process and analytical development, manufacturing, and regulatory plans. - Identifying risks and implementing mitigation strategies for each program in collaboration with the program manager, functional heads, and technical SMEs. - Supporting regulatory strategy development and health authority interactions as the lead contributor. - Acting as the primary technical interface between Elektrofi and Alliance Partners, ensuring transparent communication and alignment. - Facilitating effective decision-making by preparing clear program updates, risk assessments, and recommendations for governance and senior leadership. - Leading technical governance meetings, decision-making forums, and stage-gate readiness reviews. - Serving as the primary interface between the Program team and Company leadership to ensure alignment with Elektrofi's short- and long-term goals. - Fostering a collaborative and high-performing team environment that encourages accountability and solution-oriented thinking. Qualifications required for this role include: - Advanced degree (BS considered with strong experience) in a scientific or engineering discipline. - 12+ years of biotech/pharma industry experience, including 5+ years of CMC program leadership in biologics development. - Proven ability to lead complex, cross-functional teams in a matrix environment. - Ability to operate strategically while managing tactical execution details. - Strong team player with the ability to rapidly build positive relati

As a member of the Enterprise Monitoring team at ADP, you will play a crucial role in designing and implementing intelligent monitoring solutions using the power of Artificial Intelligence and Machine Learning. You will be responsible for the following key tasks: - Designing and enhancing Monitoring-as-a-Service (MaaS) frameworks by leveraging Dynatrace APIs and automation capabilities. - Creating reusable templates, self-help solutions, and dashboards for application, infrastructure, and cloud monitoring. - Automating setup and configuration of Dynatrace entities using Python or CI/CD pipelines. - Building and maintaining React-based front-end portals for monitoring self-service and visualization. - Developing automation scripts and backend services to integrate Dynatrace with other tools. - Utilizing Dynatrace Davis AI for anomaly detection, root cause analysis, and proactive alerting. - Collaborating with SRE, DevOps, and Cloud teams to define monitoring standards and SLAs. - Documenting processes, APIs, and monitoring playbooks to support self-service adoption. Qualifications required for this role include: - Degree in Computer Science or a related technical field. - Experience in software development projects including front-end and backend development. - Hands-on coding experience in Java and other languages such as JavaScript, Python, and Typescript. - Familiarity with frameworks like React, Spring boot, Spring MVC, and Java Spring. - Experience with software development tools like Jira, Confluence, Git, SVN, and Jenkins. - Interest in designing and building solutions using cloud platforms like AWS and Azure. - Strong problem-solving skills and a collaborative mindset. - Good presentation and communication skills in English. Additionally, previous experience or interest in the following areas would be valued: - Container technologies such as Docker, Kubernetes, and OpenShift. - Knowledge of UNIX or Linux environments. - J2EE, Restful Webservices, Node.js. - Proficiency in Build Management, Configuration & Release Management, Design & Build Enablement.,

You will be part of a rapidly growing digital news and infotainment platform, Maa Bhavani Infotainment, with an audience base of over 250,000+ active viewers and readers. The platform focuses on news, documentaries, and public opinions, and aims to bring fresh voices and perspectives to the forefront. **Key Responsibilities:** - Research, report, and produce stories on current affairs, public issues, and trending topics. - Conduct field interviews, gather public opinions, and create engaging on-camera reports. - Collaborate with the editorial and production team for script development and story framing. - Participate in live reporting and contribute to digital content creation for various platforms. - Uphold journalistic ethics, accuracy, and credibility in all reporting activities. **Who Can Apply:** - Students or recent graduates in Journalism, Mass Communication, Political Science, or related fields. - Enthusiastic individuals with a strong interest in news, current events, and storytelling. - Candidates comfortable with speaking on camera and interacting with the public. - Ability to work independently, meet deadlines, and handle fast-paced assignments. You will have the opportunity to receive an Official Internship Certificate upon completion, gain practical exposure to live news and media production, benefit from mentorship from experienced media professionals, and have the chance for Full-Time Employment (FTE) based on performance. Additionally, you may receive featured content credits on official social media and video platforms. This certification-based internship has a duration of 6 months, with no salary during the initial period. Outstanding performers will be considered for Full-Time Employment (FTE) upon successful completion. Please note that the work location can be remote or on-field based on assignments. The internship is based in Bailey Road, Patna, Bihar, and candidates who are able to commute/relocate to this location are preferred. *Education:* - Higher Secondary(12th Pass) (Preferred) *Language:* - Hindi (Preferred),

As a Global Strategy Leader for a pharmaceutical portfolio, you will play a crucial role in leading the strategic direction and execution of regulatory strategies. Your responsibilities will include: - Developing global regulatory strategies for the company's pharmaceutical portfolio, such as IND/CTAs, NDAs, NDSs, MAAs, and other key regulatory submissions. - Collaborating with senior leadership in various functional areas to align regulatory strategy with overall product development and business objectives. - Providing expert guidance on regulatory requirements, market access strategies, and potential risks to inform decision-making across the organization. - Overseeing the planning, preparation, and execution of global regulatory submissions to ensure timely approval and market access across key regions (e.g., FDA, EMA, Health Canada, etc.). - Serving as a regulatory contact for cross-functional teams to ensure alignment on regulatory strategy and execution across global markets. - Identifying and managing regulatory risks associated with the global development and commercialization of pharmaceutical products. - Leading, mentoring, and developing a high-performing team of regulatory professionals. - Assessing and anticipating the competitive landscape and market trends to inform regulatory strategy and market access plans. Qualifications and Required Skills: - Education: Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field (Advanced degree preferred). Regulatory Affairs Certification (e.g., RAC) is a plus. - Experience: 12+ years of regulatory affairs experience in the pharmaceutical industry, with expertise in regulatory strategy, submissions, and global market access. - Skills & Competencies: Strategic thinker with deep understanding of global regulatory environment, exceptional leadership and team-building skills, strong project management abilities, excellent communication and negotiation skills, analytical mindset, and proven ability to navigate complex regulatory landscapes. The job requires 10-15% domestic and international travel. The position also offers a comprehensive benefits package including medical, dental, and vision insurance, a 401(k) with company match, paid time off, parental leave, and potential for performance-based bonuses. Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.,

You will be responsible for performing comprehensive Quality Control (QC) review of clinical sections of regulatory documents to ensure the highest quality from technical, regulatory, and compliance perspectives. This includes verifying all references and source data, ensuring internal consistency within documents, and documenting QC findings appropriately. Additionally, you will be involved in content QC of clinical data/reports across different therapeutic areas, development phases, modalities, and geographic regions. - Conduct comprehensive QC review of clinical sections in regulatory documents such as IBs, INDs, NDAs, BLAs, CTAs, MAAs, and briefing packages for regulatory agency meetings. - Verify data presented in text, tables, and figures against source documents for consistency and accuracy. - Ensure 100% verification of data/content as per the source documents. - Review documents for grammar, punctuation, spelling, and compliance with specified styles/standards. - Maintain QC records and checklists. - Hands-on experience in regulatory toxicology and writing of Non-clinical Regulatory/Non-Regulatory documents. - Proficiency in drafting and reviewing Modules 2.4 and 2.6 (pharmacology, pharmacokinetics, and toxicology) for regulatory submissions. - Good knowledge of pharmaceutical impurities, degradation products, and excipients in the context of nonclinical writing. - Experience in content QC, including checking and verifying data presented in text, tables, and figures against source documents. - Project management skills and ability to work closely with cross-functional teams. - Familiarity with attending cross-functional project calls and managing due diligence activities. - Technical review experience of submission output and operational support activities in a non-clinical setting.,

As a Senior Linux Systems Administrator at Neysa, you will play a crucial role in the engineering backbone of the company's infrastructure. This hands-on position is perfect for individuals who excel in high-performance environments, enjoy mentoring others, automating tasks, and ensuring system reliability and security. - Administer and troubleshoot Linux servers including RHEL, CentOS, and Ubuntu - Configure and maintain automation scripts using Bash or Python - Implement and manage tools such as Ansible, Puppet, Foreman, Terraform, or MAAS - Set up and monitor system health utilizing tools like Zabbix, Grafana, Prometheus, or Nagios - Harden systems, manage firewalls, and ensure compliance - Work with containers (Docker, Kubernetes), virtualization (VMware, KVM), and cloud providers (AWS, Azure, GCP) - Collaborate with DevOps and software teams to ensure seamless integration - Mentor junior administrators and create detailed documentation and reports - Expert-level knowledge in Linux systems (RHEL/CentOS/Ubuntu) - Proficiency in scripting with Bash, Python (knowledge of Perl is a plus) - Deep understanding of TCP/IP, DNS, DHCP, and Firewalls - Hands-on experience with Infrastructure as Code (IaC) tools like Ansible, Puppet, and Terraform - Familiarity with CI/CD tools such as Jenkins, GitLab CI/CD - Proficiency in monitoring tools like Grafana, Prometheus, Zabbix, and Nagios Bonus Experience: - Experience with Docker & Kubernetes deployments and orchestration - Proficiency in MySQL/PostgreSQL administration - Familiarity with Agile and DevOps best practices - Previous experience in leadership/mentoring roles Soft Skills: - Patience and clarity in dealing with end-users - Strategic thinking and risk assessment for configuration/system changes - Team-first mindset with excellent communication skills,

Job Description: As a candidate for this role, you are expected to exhibit high standards, excellent communication skills, and possess the ability to take initiative and prioritize daily tasks. Your strong ability to take charge and meet tight deadlines will be crucial for success in this multi-faceted position. Key Responsibilities: - Handle and coordinate active calendars - Schedule and confirm meetings - Ensure file organization based on office protocol - Provide ad hoc support around the office as needed Qualifications: - Bachelor's degree or equivalent experience - Strong interpersonal, customer service, and communication skills - Ability to multitask - Proficient in Microsoft Office suite,

Role Overview: As a member of the Enterprise Monitoring team at ADP, you will play a crucial role in designing and implementing monitoring solutions, developing applications for monitoring self-service and visualization, leveraging AI and analytics for anomaly detection, and collaborating with various teams to define monitoring standards and SLAs. Your work will contribute to the transformation of IT operations and product reliability through the power of Artificial Intelligence and Machine Learning. Key Responsibilities: - Design and enhance Monitoring-as-a-Service (MaaS) frameworks using Dynatrace APIs and automation capabilities. - Create reusable templates, self-help solutions, and dashboards for application, infrastructure, and cloud monitoring. - Automate setup and configuration of Dynatrace entities using Python or CI/CD pipelines. - Build and maintain React-based front-end portals for monitoring self-service and visualization. - Develop automation scripts to integrate Dynatrace with other tools such as ServiceNow, Jenkins, AWS, and Kubernetes. - Utilize Dynatrace Davis AI for anomaly detection, root cause analysis, and proactive alerting. - Collaborate with SRE, DevOps, and Cloud teams to define monitoring standards and SLAs. - Document processes, APIs, and monitoring playbooks to support self-service adoption. Qualification Required: - Degree in Computer Science or Technical Science or similar. - Experience in software development projects including front-end and backend development. - Strong hands-on coding experience in Java and other languages such as JavaScript, Python, and Typescript. - Experience in frameworks like React, Spring boot, Spring MVC, Java Spring, and software development tools like Jira, Confluence, Git, SVN, and Jenkins. - Experience and interest in designing and building solutions using cloud platforms such as AWS & Azure. - Strong interest in growing technical skills and ability to be an innovative, resourceful, and collaborative problem solver. - Good presentation and communication skills in written and spoken English. (Note: Additional details about the company were not provided in the job description.),

As a Regulatory Affairs Manager for biologic products, your responsibilities will include: - Developing global regulatory strategies for biologic products throughout all development phases in the US, EU, and rest of the world, ensuring alignment with business objectives and regulatory requirements in different regions (FDA, EMA, emerging markets). - Preparing, reviewing, and managing high-quality regulatory submissions such as INDs/IMPDs, BLA/MAA, CTA, DSUR, Annual Reports, and post-approval changes (variations, amendments). - Engaging with global regulatory agencies to support product approvals and address inquiries, collaborating with R&D, Quality, Clinical, and national regulatory teams to ensure regulatory compliance during the product lifecycle. - Providing regulatory advice during product development, technology transfer, and clinical trial execution, monitoring and interpreting evolving global regulations, guidelines, and industry trends related to the product category, and offering interpretive analyses of regulatory guidance impacting product(s) or CMC operations. To qualify for this role, you should have: - A Master's degree (M.Sc./M.Pharm/M.Tech) in Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field. - At least 5-7 years of regulatory affairs experience with a focus on biologics like mAbs, biosimilars, vaccines, or novel biologics in emerging markets. - A strong understanding of ICH guidelines, FDA, EMA, and other regulatory frameworks in emerging markets, along with experience in IND/BLA submissions and lifecycle management of biological products.,