• Edit and format technical/security deliverables • Maintain document consistency and quality standards • Support Section 508/accessibility compliance checks • Review cross-references, tables, and compliance artifacts • Assist with final package assembly and submission readiness

Role Description Join a UK-based website design agency that delivers high-conversion, bespoke websites with a concierge-style client experience. In this role, you will act as the central link between clients, designers, and developers, ensuring that each project moves seamlessly from concept to launch with precision, consistency, and care. - Manage 10–20 active projects at any time. - Oversee timelines and coordinate communication. - Populate and format content. - Perform detailed quality checks across all devices and browsers. - Test, identify errors, log issues, and re-test fixes to ensure every website meets the agency’s high standards. This is a hands-on, detail-driven coordination role suited to professionals who enjoy structure, autonomy, and building strong client relationships. Accuracy, organisation, and calm persistence are essential, as you will juggle multiple projects simultaneously while maintaining impeccable attention to detail. This is not a coding role but rather a coordination and quality-assurance position focused on content population, detailed testing, and managing project workflows. Qualifications - Experience managing high-volume project portfolios (10–20 projects simultaneously preferred). - Strong content formatting skills in WordPress. - Basic understanding of HTML, CSS, and web concepts. - Comfort working with tools such as Figma and browser inspector tools. Requirements - Extreme attention to detail, with the ability to pick up micro-errors. - Process-oriented, following strict SOPs, workflows, and QA checklists. - Highly organised, able to manage large volumes of tasks with structured systems. - Clear and proactive communicator, both written and verbal. - Patient and persistent, able to handle repetitive testing cycles without losing accuracy. - Able to learn new software tools, digital systems, and web processes quickly. Responsibilities - Project Coordination & Workflow Management - Oversee concurrent projects, each at different stages of development. - Prioritise tasks effectively across multiple clients and internal stakeholders. - Track progress using project management tools, checklists, and structured workflows. - Ensure all deadlines are met and escalate risks or delays proactively. - Content Population & Formatting - Upload and format content, media, and images on websites, primarily in CMS environments such as WordPress. - Ensure consistency in styling, layout, and brand alignment across all pages. - Manually adjust and optimise content for clarity, readability, and visual appeal. - Quality Assurance (Primary Focus) - Perform detailed QA on all website pages and features using structured checklists. - Test functionality, including buttons, forms, links, menus, and user interactions. - Conduct content accuracy reviews, ensuring all text, imagery, and media are correct and error-free. - Validate styling and layout across all major browsers (Chrome, Firefox, Safari) and devices (desktop, tablet, mobile). - Check for broken links and 404 errors. - Log, track, and communicate bugs or issues with development, coding, and design teams. - Re-test after fixes are applied to ensure issues have been fully resolved. - Communication & Coordination - Act as a key point of contact for both internal teams and multiple clients. - Communicate bugs, delays, priorities, or required changes clearly and proactively. - Manage client expectations with transparency and professionalism. - Collaborate with developers, designers, and content teams to move tasks to completion. Benefits - Salary: R30 - 35 000 per month. - Employment Type: 12-Month Renewable Contract.

Role Description We are seeking experienced Automation QA Engineers to support our clients in North Carolina. These roles will support automation quality assurance activities within a GMP-regulated pharmaceutical manufacturing environment, with a strong focus on commissioning, qualification, validation, and lifecycle documentation for automation systems. This is an excellent opportunity for candidates with pharmaceutical or biotech automation QA experience who are comfortable working cross-functionally with Validation, Engineering, Manufacturing, and Quality teams in support of large-scale capital and operational projects. Key Responsibilities - Provide QA oversight and support for automation-related qualification and validation activities - Review and approve validation lifecycle documentation including: - IQ/OQ/PQ protocols and reports - Risk assessments - Traceability matrices - Change controls - Deviations and CAPAs - Support automation systems operating within GMP manufacturing environments - Ensure compliance with FDA, cGMP, GAMP 5, and 21 CFR Part 11 requirements - Partner with Automation, CQV, CSV, Manufacturing, and Quality teams to ensure compliant execution of project deliverables - Participate in document reviews, project meetings, and quality assessments - Support audit readiness and inspection preparedness activities - Assist with implementation and continuous improvement of validation and QA processes Preferred Systems / Technologies - Experience with one or more of the following is highly preferred: - DeltaV - Rockwell / PLC systems - SCADA or HMI platforms - MES systems (Syncade experience is a plus) - Historian systems - Automated manufacturing equipment within pharma/biotech environments Qualifications - Bachelor’s degree in Engineering, Life Sciences, Computer Science, or related field preferred - 3+ years of experience in Automation QA, CSV, CQV, or Validation within the pharmaceutical, biotech, or regulated manufacturing industry - Strong understanding of GMP compliance and validation lifecycle principles - Experience reviewing and approving GMP documentation - Familiarity with data integrity and 21 CFR Part 11 requirements - Excellent communication and cross-functional collaboration skills - Ability to work independently in a remote environment Benefits - Flexible career options - Paid time off - Paid holidays - Medical - 401K match - Other unique incentives Company Description Valpro is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.

• As a Senior QA Engineer at Scribe, you will take ownership of quality across our desktop and browser extension platforms. • Partner closely with engineering, product, and design to define and execute testing strategies that scale with our growth. • Shape processes, introduce automation, and bring structure to how we validate across multiple platforms and release channels. • Collaborate with a distributed team based in Serbia.