16 Jobs für Product Reviewer
Stellenangebote Product Reviewer Jobs
Job vor 11 Tagen bei Jooble gefunden
Stryker
• Duisburg
[. .. ] for software components in compliance with regulatory requirements Generate and review the necessary documents with project teams. Perform Software verification and/or validation testing Perform code reviews as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an independent reviewer following best coding standards and practices. Who you are: Bachelor s degree in software engineering/ Computer Science or related discipline with 2+ years of relevant work experience OR Masters in relevant disciplines OR Ph D degree in relevant disciplines. At least 4+ years of Python and C++ development experience. 3+ years [. .. ] AI frameworks for orchestrating complex workflows. Experience with Kubernetes for orchestrating AI microservices. Familiarity with monitoring and logging (Prometheus, Grafana, Azure Monitor, etc. ) . Experience with medical devices and product development standards in a regulated environment (ISO 13485, IEC 62304, ISO 14971) . Role impact: As a valued member of Strykers AI innovation unit, you will work alongside trailblazers, industry visionaries, innovators, and inventors who are committed to bringing computer vision, machine learning and generative AI and digital innovation to [. .. ]
Job am 20.01.2026 bei Jooble gefunden
SGS
• Meinerzhagen
Führungs-/ Leitungspositionen
[. .. ] coordinating the operational delivery of all medical schemes including MDR and IVDR conformity assessment activities under SGS NB 1639. This role ensures the effective performance of clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] audits, technical, and product assessment functions, driving operational excellence, regulatory compliance, and strategic resource management. Oversees all technical teams, manages performance, and supports the development of processes, systems, and personnel to meet business and regulatory objectives. The role reports to the Head of Notified Body 1639. Key Accountabilities The role encompasses a wide range [. .. ] management capabilities. Strong commercial understanding and appreciation of the TIC industry. Experience in resource planning. Qualification as Lead Auditor or Product Assessor under EU MDR/ EU IVDR. Qualification as Final Reviewer and Decision Maker under MDR or IVDR. Experience in a Notified Body or equivalent regulatory organization. Experience Essential Minimum 10 years in the medical device or IVD industry, including experience in design, manufacturing, auditing, or technical documentation assessment. At least 5 years senior leadership in a Notified Body managing technical [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Moore TK
• Berlin
Why Moore TK? Together with our partner bunch capital we are building the next generation of fund services: technology-driven, automated and seamlessly integrated with
product engineering. For our VC PE [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clients, we deliver high-quality investor reporting and financials fast, standardized, audit-proof. We rely on modern tools, clean data models and automation instead of Excel overload. We develop an integrated end-to-end operating model (accounting, reporting, tax) standardized, quality-assured and knowledge-driven [. .. ] value chain, not just report assembly. Top Clients I First-class VC/ PE client portfolios and a cooperation based on partnership. Time for Quality I Realistic number of clients, templates, reviewer models, QA checklists. Risk-based sampling reviews and defined QA gates. Training Development I Develop into a subject matter expert based on your interest (valuation, IFRS, crypto, fund-of-funds etc. ) , support in obtaining certifications, tech-trainings. Moore Global Exciting and diverse field of activity with a broad [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Stryker
Senior AI Deployment Engineer
• Regierungsbezirk Freiburg
[. .. ] for software components in compliance with regulatory requirements Generate and review the necessary documents with project teams. Perform Software verification and/or validation testing Perform code reviews as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an independent reviewer following best coding standards and practices. Who you are: Bachelor s degree in software engineering/ Computer Science or related discipline with 2+ years of relevant work experience OR Masters in relevant disciplines OR Ph D degree in relevant disciplines. At least 4+ years of Python and C++ development experience. 3+ years [. .. ] AI frameworks for orchestrating complex workflows. Experience with Kubernetes for orchestrating AI microservices. Familiarity with monitoring and logging (Prometheus, Grafana, Azure Monitor, etc. ) . Experience with medical devices and product development standards in a regulated environment (ISO 13485, IEC 62304, ISO 14971) . Role impact: As a valued member of Strykers AI innovation unit, you will work alongside trailblazers, industry visionaries, innovators, and inventors who are committed to bringing computer vision, machine learning and generative AI and digital innovation to [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
• Böblingen, Baden- Württemberg
[. .. ] in algorithm design, development, and evaluation (requirements/ design/ architecture/ bugs/ tests) . Write efficient, reusable, scalable, testdriven and well documented code. Lead code reviews for projects/ systems [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as an independent reviewer applying design principles, coding standards and best practices. Youre the right fit if: Minimum Required Qualifications Education MSc. or Ph D Degree in Computer Science, Software Engineering, Electrical Engineering or equivalent. Work Experience Minimum 10 years of experience in areas such as Software Development, Software Design and Architecture, Testing and Quality Assurance or equivalent. Preferred Qualifications Track record in designing developing medical devices/ products as a product (requirements) owner holding a system thinking mindset. 10+ years of experience in software development, and at least 3 years of experience as an architect, technical product owner or staff engineer in an agile development environment with a passion for software and keeping up to date with software technology and related [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] data, infrastructure, and constraints into production systems. You will measure success through production adoption, measurable workflow impact, and eval-driven feedback loops, including evaluation benchmarks and acceptance criteria, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] that inform product and model roadmaps. Youll work closely with our Product, Research, Partnerships, GRC, Security, and GTM to deliver in regulated contexts, including inspection readiness with audit trails and traceable evidence. This role is based in Munich. We use a hybrid work model of 3 days in the office per week. We [. .. ] analysis, and iterative evidence generation that tightens acceptance criteria over time. Have delivered AI systems in trial design, regulatory writing, or scientific operations where validation strategy, auditability, compliance constraints, and reviewer expectations shaped system design and rollout. Communicate clearly across scientific, clinical, model research, technical, and executive audiences, translating technical tradeoffs into decision quality, risk posture, and measurable outcomes with credibility. Apply systems thinking with high execution standards, consistently turning failures, escalations, and audit findings into improved operating standards, validation artifacts, [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] balanced and compliant medical information. Key Responsibilities Support the Global Medical Information and local European markets operational strategies/ objectives and provide medical, scientific and technical support for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Madrigal Pharmaceuticals product portfolio and/or products under clinical development Support project plans that ensure pre-and post-product launch preparedness of the Medical Information department, including support of Medical Information Call Center, Medical Affairs, Medical Science Liaisons, Payer, and Commercial teams Provide quality review for inquiry handling by Medical Information Call Center, [. .. ] scientifically developed and maintained to ensure current/ relevant data is disseminated upon request Train Medical Information Call Center agents and Medical Affairs colleagues on Medical Information content Act as Medical Reviewer for promotional and medical content, including data check and reference requirements to ensure medical accuracy of both promotional and non-promotional materials as required Support the technology needs across the Medical Information function Contribute to submission (s) of compendia listings Contribute to the development of Medical Information processes and SOPs [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Heidelberg, Baden- Württemberg
[. .. ] evidence generation, clinical education, and regulatory compliance, while collaborating with cross-functional teams to deliver impactful solutions for healthcare professionals and patients. Main Responsibilities Medical Review Compliance: Act [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Medical Reviewer for Veeva Ad Prom MLR approval processes, ensuring scientific accuracy and regulatory compliance. Manage Veeva Vault Medical content and analyze feedback from Global Medical Information. Training Education: Build and implement training packages for UCC in collaboration with EMEA Marketing and Business Development teams. Support internal projects such as BDLA at [. .. ] regulatory standards for HCP interactions. Evidence Generation: Support clinical studies, publication strategies, and dissemination of real-world evidence. Monitor study progress and manage associated risks. Clinical Technical Support: Assist with product evaluations, clinical documentation, and user training activities. Project Management: Utilize tools such as Pub Med and regulatory databases for data analysis. Track budgets and oversee administrative processes for timely payments. About You Education: Advanced degree in medicine, nursing, pharmacy, or life sciences (MD, RN, Pharm D, Ph D, MSc preferred) . Experience: [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
• Krefeld, Nordrhein- Westfalen
[. .. ] invoicing. Independently determines project scope, develops a preliminary plan of investigation, and determines project specifications such as cost, time, and sample requirements by analyzing client input, available [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supplemental data, and product construction. Subcontractor inquiry, materials/ equipment/ personnel planning to meet job and project requirements. Perform sample testing and measurements at ULs laboratories. Projects may include frequent travel to conduct or witness tests at client sites. Initiates communication with clients to promote and explain the benefits of new and existing services. Communicates [. .. ] the obtained testing data. Prepare technical reports and present their results to customers. Maintain daily work records with accuracy and integrity. Serves as Project Handler of record and signs as Reviewer of record as assigned. Develops UL requirements for testing products beyond the scope of existing standards, or those involving unique features requiring frequent use of independent judgment. Develops special test methods and test equipment. Coordinates and/or performs File Reviews. May represent UL on technical committees and/or industry-related [. .. ]
Job am 23.01.2026 bei Jobleads gefunden
Global Head of Delivery and Operations
• Meinerzhagen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] coordinating the operational delivery of all medical schemes including MDR and IVDR conformity assessment activities under SGS NB 1639. This role ensures the effective performance of clinical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] audits, technical, and product assessment functions, driving operational excellence, regulatory compliance, and strategic resource management. Oversees all technical teams, manages performance, and supports the development of processes, systems, and personnel to meet business and regulatory objectives. The role reports to the Head of Notified Body 1639. Key Accountabilities The role encompasses a wide range [. .. ] management capabilities. Strong commercial understanding and appreciation of the TIC industry. Experience in resource planning. Qualification as Lead Auditor or Product Assessor under EU MDR/ EU IVDR. Qualification as Final Reviewer and Decision Maker under MDR or IVDR. Experience in a Notified Body or equivalent regulatory organization. Experience Essential Minimum 10 years in the medical device or IVD industry, including experience in design, manufacturing, auditing, or technical documentation assessment. At least 5 years senior leadership in a Notified Body managing technical [. .. ]
Job am 15.12.2025 bei Jobleads gefunden
Auditor-Technical File Reviewer
[. .. ] diagnostics products. Conduct conformity assessment to international/ regional standards (ISO13485 etc. ) and evaluate technical documents. Ensure technical files are compiled in accordance with standards and identify [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] any problems with product safety, documents, or files. Qualifications Familiarity with active medical device products. Have either a Bachelors, Master s or Doctoral degree (Biology, Chemistry, Pharmacy, Medicine, Agriculture, Veterinary Medicine, etc. ) . Experience in active medical device technical file reviews and testing/ inspection. Fluent in German language (written and spoken) . Communication [. .. ]
Job am 14.12.2025 bei Jobleads gefunden
(SENIOR) MANAGER FUND ACCOUNTING REPORTING (m/w/D)
• Berlin
Why Moore TK? Together with our partner bunch capital we are building the next generation of fund services: technology-driven, automated and seamlessly integrated with
product engineering. For our VC [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] PE clients, we deliver high-quality investor reporting and financials fast, standardized, audit-proof. We rely on modern tools, clean data models and automation instead of Excel overload. We develop an integrated end-to-end operating model (accounting, reporting, tax) standardized, quality-assured and knowledge-driven [. .. ] value chain, not just report assembly. Top Clients I First-class VC/ PE client portfolios and a cooperation based on partnership. Time for Quality I Realistic number of clients, templates, reviewer models, QA checklists. Risk-based sampling reviews and defined QA gates. Training Development I Develop into a subject matter expert based on your interest (valuation, IFRS, crypto, fund-of-funds etc. ) , support in obtaining certifications, tech-trainings. Moore Global Exciting and diverse field of activity with a broad [. .. ]
Job am 05.10.2025 bei Jobleads gefunden
Senior AI Deployment Engineer
• Duisburg, Nordrhein- Westfalen
[. .. ] for software components in compliance with regulatory requirements. Generate and review the necessary documents with project teams. Perform Software verification and/or validation testing Perform code reviews as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an independent reviewer following best coding standards and practices. Bachelors degree in software engineering/ Computer Science or related discipline with 2+ years of relevant work experience OR Masters in relevant disciplines OR Ph D degree in relevant disciplines. At least 4+ years of Python and C++ development experience. 3+ years of experience developing and [. .. ] AI frameworks for orchestrating complex workflows. Experience with Kubernetes for orchestrating AI microservices. Familiarity with monitoring and logging (Prometheus, Grafana, Azure Monitor, etc. ) . Experience with medical devices and product development standards in a regulated environment (ISO 13485, IEC 62304, ISO 14971) . As a valued member of Strykers AI innovation unit, you will work alongside trailblazers, industry visionaries, innovators, and inventors who are committed to bringing computer vision, machine learning and generative AI and digital innovation to the operating [. .. ]
Job am 01.10.2025 bei Jobleads gefunden
Regulatory Technical Reviewer (m/f/d) - Healthcare
• Plattling, Bayern
Overview BUILDING A WORLD CLASS TEAM STARTS WITH YOU CSA Group has an immediate opportunity for a Healthcare Regulatory Technical
Reviewer (f/m/d) to join our Healthcare Regulatory Services Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Germany and throughout Europe. CSA Group has a history of developing standards and providing certification services to help ensure safety, performance and environmental responsibility of a wide range of products. Headquartered in Canada, CSA Group operates globally with more [. .. ] looking for people like you to help make it happen. Responsibilities To ensure that assessments conducted have properly examined and addressed the regulatory responsibilities of the manufacturer with respect to product clinical performance including alignment with state-of-the-art expectations and defended risk/ benefit for the product. To formulate, maintain and improve assessment procedures and protocols in line with both CSA Group and external Authority expectations. Independently manages certification projects concurrently ensuring compliance with all applicable safety requirements achieving completion [. .. ]
Job am 18.01.2026 bei Neuvoo gefunden
OpenAI
Forward Deployed Engineer (FDE) , Life Sciences-Munich
• Munich, Bavaria
[. .. ] data, infrastructure, and constraints into production systems. You will measure success through production adoption, measurable workflow impact, and eval-driven feedback loops, including evaluation benchmarks and acceptance criteria, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] that inform product and model roadmaps. Youll work closely with our Product, Research, Partnerships, GRC, Security, and GTM to deliver in regulated contexts, including inspection readiness with audit trails and traceable evidence. This role is based in Munich. We use a hybrid work model of 3 days in the office per week. We [. .. ] analysis, and iterative evidence generation that tightens acceptance criteria over time. Have delivered AI systems in trial design, regulatory writing, or scientific operations where validation strategy, auditability, compliance constraints, and reviewer expectations shaped system design and rollout. Communicate clearly across scientific, clinical, model research, technical, and executive audiences, translating technical tradeoffs into decision quality, risk posture, and measurable outcomes with credibility. Apply systems thinking with high execution standards, consistently turning failures, escalations, and audit findings into improved operating standards, validation artifacts, [. .. ]
Job am 22.12.2025 bei Neuvoo gefunden
LEO Pharma
Medical Advisor-Critical Care-Germany
• Neu- Isenburg, Hessen
[. .. ] and support broader business plans Proactively contribute medical clinical expertise and insights to the development of the brand strategy for thrombosis therapeutic area Present the clinical data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] set for assigned product (s) at meetings e. g. Ad Boards, Investigator meetings, KEE meetings, CME medical society meetings as appropriate (and according to local regulations) Work closely with KEEs to develop and drive the medical strategy and provide medical direction to the brand plan Performance Delivery Lead development of local medical communication/ publications, [. .. ] strategy Create and deliver product training to the MSL team and other functions within the TA as appropriate (e. g. sales marketing) Governance Compliance Promotional review/compliance: Act as medical reviewer for activities and promotional materials in accordance with local compliance guidelines Ensure scientific and medical accuracy of outgoing materials, research papers and other reports, and may have sign off authority. Collaboration Partnership Collaborate closely with internal LEO stakeholders GMA, BU/ marketing, market access, regulatory, medical information, patient safety and clinical [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Product Reviewer pro Jahr?
Als Product Reviewer verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Product Reviewer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 16 offene Stellenanzeigen für Product Reviewer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Product Reviewer Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Product Reviewer Jobs.
Welche Unternehmen suchen nach Bewerbern für Product Reviewer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Product Reviewer Stellenangebote:
- Stryker (2 Jobs)
- SGS (1 Job)
- Moore TK (1 Job)
- OpenAI (1 Job)
- LEO Pharma (1 Job)
In welchen Bundesländern werden die meisten Product Reviewer Jobs angeboten?
Die meisten Stellenanzeigen für Product Reviewer Jobs werden derzeit in Nordrhein-Westfalen (3 Jobs), Bayern (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Product Reviewer Jobs?
Product Reviewer Jobs gehören zum Berufsfeld Produktmanagement.
