Role Description We currently have an exciting opportunity at SGS for a Final Reviewer & Certification decision maker to join our highly successful Global Medical Device team. In this role, you will be reporting to the Final Reviewer & Certification Decision Maker Medical Device Team leader and you will have a Global role. Main Purpose of Role: - The role of the Final Reviewer & Certification decision maker is to review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745. - Take decision on reviewed audit packs to determine if the certificate shall be issued and if there are any applicable restrictions. - Verify that audit documentation for QMS on-site as well as technical documentation assessment is in compliance with medical device regulations and internal procedures. - Ensure a good understanding of the audit trail and support the relevant evidence of compliance of the audited company. - Verify that all major non-conformity and any unsolved issues have been addressed and closed out before transferring the audit pack for certification decision. - Review whether the final review has been carried out by an approved Final Reviewer. - Ensure that the final review documentation has been completed satisfactorily. - Confirm whether all/any actions raised by the Final Reviewer have been satisfactorily addressed and closed out. - Make the final decision as to whether a certificate should be issued. - Check audit packs for QMS on-site audit for MDD / MDR / ISO13485, for technical documentation assessment and any changes. - Involve in concessions and certificate suspension when relevant. - Be in close contact with auditors, product assessors, Certificate Decision makers, and Global Medical Device Certification Manager. - Contribute in meeting operations objectives and Key Performance Indicators to deliver certificates to customers and maintain regulatory compliance. Key Accountabilities: - Establish whether the audit report pack demonstrates compliance with specific standards/normative documents. - Ensure the audit has been carried out and associated documentation completed in accordance with relevant procedures. - Verify that the auditor/audit team were confirmed as competent. - Ensure principles and practices associated with undertaking audits are applied, especially in reporting audit findings and decision-making processes. - Establish whether Final Technical Review addresses all Scope of Certification or accreditation issues relevant to specific standards/normative documents. - Ensure completion of technical review documentation and no outstanding issues remain unresolved. - Appreciate the business/industry environment in which the audit took place. - Understand and make judgment on the auditors’ interpretation and reporting of the audit findings and decision-making rationale. - Offer support and help to Certificate Decision Makers. - Ensure full compliance with the Company’s Code of Integrity & Professional Conduct. - Maintain and develop personal professional capabilities to ensure knowledge and understanding of sector expectations is up to date. - Ensure SGS operates in accordance with professional, ethical, legal and accreditation requirements to maintain all approvals. - Report data on your daily workload and any technical issues. It is remote based, and we are open to candidates located everywhere across Europe. But they must hold a valid work permit for their country of residency. Please send your CV in English! Qualifications - Experience in a similar position in a European notified body (must have). - Significant work experience in the medical device field as Lead Auditor or as Product Assessor in a Notified Body (must have). - Detailed understanding of global medical device Regulations and good analysis capacity to detect discrepancies or issues. - Good communication skills. - Strong team building skills. - Fluent in English. Other languages are a benefit. Benefits - Global and very stable company, world leader in the TIC (Testing, Inspection and Certification) industry. - Flexible schedule and hybrid model. - SGS university and Campus for continuous learning options. - Multinational environment where you will work with colleagues from multiple continents. - Benefits platform. Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. At SGS, we have an open corporate and international culture. We offer a dynamic work environment in a leading global company. Our high professional standards and our sustainability approach guarantee you a future-oriented work environment. We invest in our employees for the long term and are committed to supporting your development within the company. Our business principles include: Integrity, Health, Safety & Environment, Quality & Professionalism, Respect, Sustainability, and Leadership.

Role Description We are sharing a specialised part-time consulting opportunity for experienced visual quality professionals with expertise in: - Film - VFX - Rendering - Lighting - Color grading - Cinematography - Professional photography - Artifact detection - Pixel-level review - Super-resolution video evaluation This role supports current and upcoming remote consulting opportunities focused on: - Video sharpening - Upscaling - Super-resolution review - Frame-by-frame visual quality assessment - Artifact detection - Evaluation template development - High-quality project execution Selected professionals will apply a rigorously trained visual eye to assess whether enhanced video outputs hold up at a professional level across: - Detail - Sharpness - Texture - Color - Temporal consistency Qualifications - Fluent English - 7–10 years of experience in high-end visual evaluation across film, visual effects, professional photography, cinematography, rendering, or related fields - Training from a university or program with a highly respected film, visual effects, digital media, or imaging curriculum - Reliable access to a 4K-resolution monitor for precise pixel-level review - Familiarity with AI tools and workflows, including the ability to generate visual samples for testing and comparison - Ability to translate complex visual details into clear, precise language for captions, review notes, and evaluation templates - Ability to work independently in a remote, project-based environment Requirements - VFX supervisor with strong final image quality review experience - Rendering supervisor with experience reviewing dailies and pixel-level output quality - Lighting supervisor, lighting lead, or lighting artist with strong digital video and cinematic motion judgment - Colorist with deep experience in grading, artifact detection, and visual consistency - Director of photography or cinematographer with expertise in framing, sharpness, and high-resolution image detail - Effects artist, surfacing artist, high-end photographer, director, or digital projectionist with a trained eye for final-output quality Nice to Have - Experience reviewing final image quality for film, VFX, animation, games, commercial photography, or high-end video content - Experience with dailies review, color grading, projection review, visual QC, rendering review, or image finishing - Strong understanding of compression artifacts, grain structure, aliasing, noise, softness, texture fidelity, and high-resolution visual detail - Comfort with frame-by-frame review and structured visual evaluation - Experience creating or reviewing visual benchmarks, comparison samples, or expert evaluation templates Benefits - Apply professional visual quality expertise to structured remote evaluation work - Contribute to high-quality review of video sharpening, upscaling, and super-resolution outputs - Work on assignments aligned with your VFX, rendering, lighting, color, cinematography, photography, or projection background - Use your trained eye to identify subtle image-quality issues that matter at a professional level - Remote structure with competitive hourly compensation Contract Details - Independent contractor role - Fully remote with scheduling aligned to PST through EST working hours - Eligible professionals should be based in the United States depending on project needs - Part-time commitment depending on project availability - Competitive rates between $50–$80 per hour depending on expertise and project scope - 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

Role Description The Site Visit Report Reviewer (SVRR) is responsible for reviewing site qualification, site initiation, monitoring, and termination visit reports, ensuring they meet quality standards, regulatory requirements, Parexel Standard Operating Procedure (SOP), International Conference on Harmonization/ Good Clinical Practice (ICH/ GCP) guidelines, and protocol requirements. - Working in close collaboration with Clinical Research Associates (CRAs), Clinical Operations Leaders (COLs), and project teams. - Diligently monitors the progress of Open Issues, Protocol Deviations (PDs), and ongoing Serious Adverse Events (SAEs) as documented in Monitoring Visit Reports (MVRs), following up until closure. - May participate in project meetings as needed. - Conducts and communicates periodic analyses of monitoring visits and issues to project teams. - Assists the COL with additional tasks as required, contingent upon successful completion of appropriate training. Qualifications - Excellent interpersonal, verbal and written communication skills. - Flexible and positive attitude towards work assignments and new learning. - Ability to manage multiple tasks, prioritize workload, and maintain attention to detail while committing to high-quality work. - Willingness to work in a complex environment and value teamwork. - Client-focused approach to work. - Initiative to work independently and seek guidance when necessary. - Strong analytical and decision-making skills. - Proficient in computer skills, including Microsoft Office products. - Manage time effectively and demonstrate a sense of urgency in completing tasks. - Ability to work across cultures. - Successful work in a ('virtual') team environment and maintaining consistent performance. - Proactive issue identification and effective problem-solving skills. - Knowledge of and compliance with ICH-GCP Guidelines, regulations, and Parexel/Client procedures. Requirements - Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Education - Educated to degree level (biological science, pharmacy or other health-related discipline preferred), nursing or other relevant qualification/experience.

Role Description iMPROve Health is seeking an addiction medicine physician to serve as an independent contractor (1099) performing independent external medical reviews remotely on an ad hoc basis. As a peer reviewer, you will apply your clinical expertise to evaluate cases, specific to your specialty, medical necessity and/or standard of care, supporting efforts to enhance the overall quality and integrity of health care and your profession. Please note, this is not an employed position and our contracted fee is based on credential and specialty type. Qualifications - Medical License: Must hold an unrestricted medical license in any U.S. state. - Board Certification: Required (if applicable), through a board recognized by: - The American Board of Medical Specialties (ABMS) - The American Osteopathic Association (AOA) - Another nationally recognized board granting certification. - Clinical Experience: - Have at least five (5) years full-time equivalent experience providing direct clinical care to patients. - Have experience providing direct clinical care to patients within the past three (3) years. - Knowledgeable of the issue under review, or of the current, evidence-based clinical guidelines and novel treatments for the medical or behavioral health condition, disease, treatment, or procedure under review. - Have the clinical expertise to manage the medical or behavioral health condition or disease under review. - Must be actively engaged in direct or virtual patient care for at least 20 hours per week. Administrative work does not qualify. Requirements - Reliable Wi-Fi access. - Proficiency with Microsoft Word. - Access to a computer compatible with iMPROve Health’s IT systems. - Must complete the electronic credentialing application and receive organizational approval prior to performing a case review. - Must complete a conflict of interest attestation upon credentialing and prior to performing a case review. - Active hospital medical staff privileges may be required, as applicable. - Notify the organization in a timely manner of an adverse change in licensure or certification status, including board certification status. - Cannot have current employment or affiliation with any Veterans Affairs (VA) hospital, health care system, or medical center if applying to perform VA-related peer reviews. Benefits - Make a Difference: Use your clinical knowledge to improve the quality of care patients receive. - Professional Recognition: Join a network of highly respected experts in your specialty. - Competitive Compensation: Receive fair pay for your time and expertise. - Protect Standards of Care: Help uphold the integrity of your profession. - Work Remotely: Review cases from the convenience of your home or office.