Role Description Octopus by RTG is hiring a Salesforce QA Engineer for one of our partners. We are looking for an experienced Software Tester to execute comprehensive testing strategies that ensure the quality, functionality, and performance of software applications. This role involves both manual and automated testing, including integration and regression testing, as well as defect identification and resolution. The ideal candidate will have a strong background in QA practices, test tool setup, and collaboration with cross-functional teams. Role Responsibilities: - Execute comprehensive test strategies and plans to ensure software meets functional and non-functional requirements. - Collaborate with developers and other stakeholders to identify and resolve defects. - Create and conduct automated testing of software applications, including integration and regression testing. - Identify, report, and track software defects to resolution, ensuring that all critical issues are prioritized and resolved promptly. - Participate in the review of requirements and design documents to ensure testability. - Document testing results and create test reports for various stakeholders, including senior management. - Continuously improve testing processes and methodologies, driving the adoption of best practices and standards. - Act as a subject matter expert in software testing, staying up to date on industry trends and advancements. Qualifications - 5+ years of demonstrated experience as a Software Tester or in a QA-related role with emphasis on Salesforce development and testing. - Demonstrated experience in setting up test tools. - Experience with automation testing tools. - Proven experience in solution testing. - QA experience with manual testing and writing automated tests. - Has worked on multiple clouds with at least Sales Cloud, Service Cloud, and Community Cloud. - Other Salesforce clouds experience: Marketing, Commerce, CPQ, Education, and Analytics is an added advantage. Requirements - Required Certifications: - Certified Salesforce Administrator - Certified Salesforce Advance Administrator Other Skills - Proactiveness - Ownership and accountability of the project tasks - Open communication and transparency about day-to-day work, issues, risks, and progress - Experience in Agile project methodology - Collaboration and being a team player - Estimation of timelines and solution approaches

Bridge quality-system expertise with software development, document functional requirements, lead data migration processes, and design training programs to ensure compliance and enhance quality engineering initiatives.

Role Description We are sharing a specialised part-time consulting opportunity for professionals experienced in medical devices, regulatory affairs, quality engineering, design controls, manufacturing validation, supplier quality, clinical affairs, and structured regulated-device documentation. This role supports current and upcoming remote consulting opportunities focused on structured medical device workflow review, regulatory documentation, quality system assessment, design history file review, validation documentation, CAPA analysis, and high-quality project execution. Selected professionals will apply their medical device expertise to review realistic regulated-device scenarios, evaluate technical and compliance requirements, prepare structured written outputs, and support accurate, evidence-based medical device workflow tasks. Key Responsibilities - Regulatory Affairs & Submission Documentation - Review medical device scenarios involving 510(k), PMA, De Novo, EU MDR, technical files, regulatory submissions, and supporting documentation. - Evaluate regulatory materials against source records, device requirements, submission expectations, and documented review criteria. - Support structured review of regulatory correspondence, submission packages, technical documentation, and device classification materials. - Identify missing information, documentation gaps, regulatory inconsistencies, and expected submission review outcomes. - Quality Systems, Risk & CAPA Review - Review quality scenarios involving DHF, DMR, risk-analysis matrices, CAPA records, eQMS workflows, validation protocols, and quality documentation. - Evaluate materials against 21 CFR 820, ISO 13485, ISO 14971, design control requirements, risk management expectations, and quality system procedures. - Support structured review of CAPA documentation, risk files, quality records, post-market surveillance materials, and MDR/vigilance reporting workflows. - Prepare clear written explanations for quality and regulatory decisions based on source materials and verifiable criteria. - Design Controls, Manufacturing & Validation Support - Review device R&D and manufacturing scenarios involving design controls, software-related device workflows, process validation, supplier quality, and manufacturing engineering documentation. - Evaluate validation protocols, supplier records, manufacturing workflows, and device development materials against defined technical requirements. - Support structured review of materials connected to ANSYS Fluent, STAR-CCM+, Siemens Opcenter, Rockwell FactoryTalk, DocuSign, eQMS systems, or similar regulated-device tools. - Maintain accuracy, consistency, and professional judgment across submitted work. Qualifications - 3+ years of experience in medical devices, regulatory affairs, quality engineering, design controls, R&D, manufacturing engineering, process validation, supplier quality, clinical affairs, post-market surveillance, or related regulated-device roles. - Experience in one or more areas such as 510(k), PMA, De Novo, EU MDR, technical files, 21 CFR 820, ISO 13485, ISO 14971, CAPA, DHF, DMR, SaMD, process validation, supplier quality, or vigilance reporting. - Familiarity with tools and systems such as ANSYS Fluent, STAR-CCM+, Siemens Opcenter, Rockwell FactoryTalk, DocuSign, eQMS platforms, PLM systems, MES platforms, or similar medical device workflow tools. - Comfort reading and preparing medical device artifacts such as design history files, regulatory submissions, DHF/DMR documents, risk-analysis matrices, validation protocols, CAPA records, supplier files, and technical summaries. - Strong analytical thinking and written communication skills. - Ability to translate regulated medical device workflows into clear, structured task documentation. Educational Background - A degree or professional background in biomedical engineering, mechanical engineering, electrical engineering, regulatory affairs, quality engineering, life sciences, clinical research, manufacturing engineering, or a related field is helpful. - Equivalent practical experience in medical device regulatory, quality, R&D, manufacturing, clinical affairs, or validation workflows is also highly relevant. Nice to Have - Experience at a medical device manufacturer, contract developer, contract manufacturer, healthcare technology company, or regulated life sciences organization. - Familiarity with design controls, risk management, FDA submissions, EU MDR, SaMD, eQMS, supplier quality, process validation, CAPA, clinical affairs, or post-market surveillance. - Experience preparing or reviewing regulatory submissions, technical files, validation protocols, DHF/DMR materials, CAPA records, risk files, or quality documentation. - RAC, ASQ CQE, CRE, CBA, regulatory affairs, quality, validation, or medical device certifications are helpful. - Strong attention to detail in regulated, documentation-heavy, and cross-functional medical device environments. Why This Opportunity - Apply medical device regulatory, quality, and engineering expertise to structured remote project work. - Contribute to high-quality device documentation review, regulatory workflow assessment, quality system analysis, and validation scenario development. - Work on flexible, project-based assignments aligned with your medical device background. - Use your regulated-device judgment in a focused, detail-oriented review environment. - Remote structure with competitive hourly compensation. Contract Details - Independent contractor role. - Fully remote with flexible scheduling. - Part-time commitment depending on project availability. - Competitive rates between $60–$85 per hour depending on expertise. - Weekly payments via Stripe or Wise. - Projects may be extended, shortened, or adjusted depending on scope and performance. - Work will not involve access to confidential or proprietary information from any employer, client, or institution. About the Platform This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams. By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy .

• Ensure the integrity, accuracy, and reliability of the Athena Master Reference Data Platform • Design, document, and execute comprehensive automated testing plans covering unit, integration, and end-to-end regression testing • Develop and maintain automated test scripts specifically for data validation • Integrate automated test suites into the CI/CD pipeline • Collaborate with developers to define 'Definition of Done' criteria • Perform deep-dive data validation using SQL • Collaborate with Data Engineers and Architects to identify, document, and track defects • Build and maintain automated regression test suites to support continuous integration and delivery (CI/CD) cycles • Validate API endpoints and downstream data consumption points • Ensure data consistency, accuracy, and completeness