Company Description SyMetric is a provider of web-based, end-to-end solutions for clinical research. Our Product suite is built as an ERP on a single database, providing a seamless flow of data across modules. Role Description This is a full-time on-site role for a Quality Assurance Manager located in Bengaluru North. The Quality Assurance Manager will be responsible for ensuring that SyMetric's products and Processes meet or exceed customer expectations, regulatory requirements, and quality standards. The Quality Assurance Manager will also be responsible for managing the QA team and developing, implementing, and maintaining the Quality Management System, Infrastructure and Security Management Systems. Qualifications Quality Assurance processes and procedures, drafting an Maintenance of SOP,s Understanding of CSV and SDLC software development life cycle. Experience in managing QMS( Quality Management System) and Infrastructure and Security Management Systems as per ISO standards Experience in leading and managing a QA team Internal and External Audits, MRM, risk Management Excellent communication and interpersonal skills Strong analytical and problem-solving skills Bachelor's degree in Pharmacy or Science Experience in the Life Sciences industry, Pharma Industry is preferable. Certifications in Quality Assurance like ISO is a plus. The ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners. Candidates with 6-8 years of experience, with an understanding of Clinical Trial Domain and Computer System Validation are welcome to apply. Show more Show less
Microsoft Office Suite, especially Excel and PowerPoint skills. Operating system and server. Cloud Computing ,Azure Troubleshooting skills.· Knowledge of ISMS /ISO27001 is an advantage. Responsibilities Thorough Knowledge of IT infrastructure in the following areas (Change management, Incident management, Problem management, Capacity Management and Infrastructure Security) Maintain all local software and hardware licensing to ensure conformance. Support implementation and planning of deletions, additions and major changes to IT infrastructure. Recommend software and hardware solutions comprising of upgrades and new acquisitions. Maintain and update documentation of procedures and configurations. Manage cloud services. Qualifications Should possess a Postgraduate or bachelor’s degree in engineering. Specialization in IT Support skills are desirable Operating system and Server both Windows and Linux.
Microsoft Office Suite, especially Excel and PowerPoint skills.Operating system and server. Cloud Computing ,Azure Troubleshooting skills. Knowledge of ISMS /ISO27001 is an advantage. Responsibilities Thorough Knowledge of IT infrastructure in the following areas (Change management, Incident management, Problem management, Capacity Management and Infrastructure Security) Maintain all local software and hardware licensing to ensure conformance. Support implementation and planning of deletions, additions and major changes to IT infrastructure. Recommend software and hardware solutions comprising of upgrades and new acquisitions. Maintain and update documentation of procedures and configurations. Manage cloud services. Qualifications Should possess a Postgraduate or bachelors degree in engineering. Specialization in IT Support skills are desirable Operating system and Server both Windows and Linux. Show more Show less
Company Description SyMetric provides web-based, end-to-end solutions for clinical research from manufacturing to submission. Our product suite is built as an ERP on a single database, providing seamless flow of data across modules. We offer Project Management and Clinical Data Management Services for Clinical Studies globally. Role Description This is a full-time on-site role in Bengaluru for Clinical Data Management Specialist. The Specialist, Clinical Data Management will be responsible for day-to-day tasks associated with Clinical Data Management such as Study setup, UAT, Query Management, Study start-up and Conduct and close-out phase. Qualifications Clinical Data Management and Electronic Data Capture (EDC) skills Experience in Project Management, Preferred. Excellent data management skills Familiarity with clinical data and GCP/ICH Guidelines Strong analytical and communication skills Bachelor’s or Master’s degree in Science, Biotechnology, or related fields Experience with clinical operations or clinical data management is preferred
Role Overview: You will be working as a Clinical Data Management Specialist at SyMetric in Bengaluru. Your main responsibilities will include tasks related to Clinical Data Management such as Study setup, UAT, Query Management, Study start-up, Conduct, and close-out phase. Key Responsibilities: - Perform Study setup activities - Conduct User Acceptance Testing (UAT) - Manage queries related to clinical data - Coordinate Study start-up and close-out phase Qualification Required: - Possess Clinical Data Management and Electronic Data Capture (EDC) skills - Previous experience in Project Management is preferred - Demonstrate excellent data management skills - Have familiarity with clinical data and GCP/ICH Guidelines - Showcase strong analytical and communication skills - Hold a Bachelors or Masters degree in Science, Biotechnology, or related fields - Experience in clinical operations or clinical data management is advantageous,
As a Quality Assurance Manager at SyMetric, located in Bengaluru North, your role will involve ensuring that the company's products and processes meet or exceed customer expectations, regulatory requirements, and quality standards. You will be responsible for managing the QA team, as well as developing, implementing, and maintaining the Quality Management System, Infrastructure, and Security Management Systems. Your responsibilities will include: - Implementing Quality Assurance processes and procedures, including drafting and maintenance of SOPs - Understanding CSV and SDLC software development life cycle - Managing QMS and Infrastructure and Security Management Systems as per ISO standards - Leading and managing a QA team - Conducting Internal and External Audits, MRM, and risk management To excel in this role, you should possess: - Excellent communication and interpersonal skills - Strong analytical and problem-solving abilities - A Bachelor's degree in Pharmacy or Science - Experience in the Life Sciences industry, with a preference for the Pharma Industry - Certifications in Quality Assurance such as ISO would be a plus The ideal candidate for this position is a critical thinker who will actively contribute to improving the company's quality systems through internal audits, participation in process improvement programs, and collaboration with key partners. Candidates with 6-8 years of experience, including knowledge of the Clinical Trial Domain and Computer System Validation, are encouraged to apply.,
Roles And Responsibilities Research, outline, write and edit new and existing content, working closely with various departments to understand project requirements Independently gather information from subject matter experts to develop, organize, and write procedure manuals, technical specifications, and process documentation Work with development and support leads to identifying all documentation repositories, revising and editing, and determining the best solution for data compilation and centralized storage Research, create, and maintain information architecture templates that uphold organizational and legal standards, and allow for easy data migration Develop content in alternative media forms for maximum usability, with a consistent and cohesive voice across all documentation Objectives of This Role Develop comprehensive documentation that meets organizational standards Obtain a deep understanding of products and services to translate complex product information into simple, polished, and engaging content Write user-friendly content that meets the needs of the target audience, turning insights into language that sets our users up for success Develop and maintain detailed databases of appropriate reference materials, including research, usability tests, and design specifications Evaluate current content and develop innovative approaches for improvement Technical Skills Bachelors degree in a relevant technical field (Ex: Computer Science, Healthcare,.) 3 years of industry experience as an effective technical writer Proven ability to quickly learn and understand complex topics Previous experience writing documentation and procedural materials for multiple audiences Superior written and verbal communication skills, with a keen eye for detail Experience working with engineering to improve the user experience: design, UI, and help refine content and create visuals and diagrams for technical support content Competencies Proven ability to handle multiple projects simultaneously, with an eye for prioritization Firm understanding of the systems development life cycle (SDLC) Previous software development experience Certification through the Society for Technical Communicators Experience using XML tools to create documentation