15 Jobs für Product Reviewer
Stellenangebote Product Reviewer Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• Basel, Basel- Stadt
[. .. ] to come. Join Roche, where every voice matters. The Position Senior/ Principal Agentic AI Engineer (Clinical Data Systems) This role resides in the Data Management team, a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] key function within Product Development Data Sciences (PDD) . At Roche, we lead the industry in speed and efficiency across all data management responsibilities. Through innovative tools, automation, and cutting-edge technologies, we streamline clinical trial data collection and delivery. As trusted partners in drug development, our team leverages deep expertise across therapeutic area [. .. ] Graph, Crew AI, or Auto Gen to automate complex clinical data management tasks Multi-Agent Systems: Develop production-grade multi-agent systems where specialized agents (e. g. , Planner, Validator, Protocol Reviewer) collaborate through tool-calling and retrieval-augmented workflows, with human-in-the-loop validation to ensure traceable, compliant outcomes. Maintain high-quality, testable code and service documentation Advanced Prompt Engineering: Utilize systematic prompt engineering techniques (Chain-of-Thought, Re Act, Reflection) for high-fidelity outcomes in clinical contexts Integration Scalability: [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Winzenberg, 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 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 employees. [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Global Head of 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 Head of Notified Body 1639. Key Accountabilities The role encompasses a wide range of [. .. ] 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 11.03.2026 bei Jobleads gefunden
• Nürnberg, Bayern
Führungs-/ Leitungspositionen
[. .. ] location in Nuremberg you will strengthen our Transceiver Development team. Cisco Optical is developing subsystems for high-speed optical networking applications in Ciscos optical transmission and routing products. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The current product portfolio includes advanced 100Gbps, 400Gbps and 800Gbps optical transceiver modules for mass-scale Datacenter and Campus applications. We focus on high speed, high performance optical system interfaces for cost-effective high-density system applications in Cisco differentiated by fulfilling specific Cisco requirements. Our core competencies are in digital signal processing [. .. ] This includes definition of calibration algorithms enabling highly efficient manufacturing. Perform and assist in manufacturing testing activities and ensure product delivered aligns with product requirements and customer expectations. Serve as reviewer of technical documentation in support of product development and release. Assist and lead in some early product demonstrations to customers. Plan and direct advanced, innovative technical projects. Pursue new technology for product suitability. Minimum Qualifications Experienced in optical transmission systems and a strong background in communication theory. Masters degree in [. .. ]
Job am 07.02.2026 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 am 04.02.2026 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 am 15.12.2025 bei Jobleads gefunden
[. .. ] 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
• 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 vor 2 Tagen bei Neuvoo gefunden
Elanco
• Cuxhaven, Lower Saxony
Führungs-/ Leitungspositionen
30+ Urlaubstage Tarifvertrag
[. .. ] Korrektur- und Vorbeugungsmaßnahmen (CAPAs) Qualitätsdokumentation: + Sicherstellung der Vollständigkeit und Integrität aller qualitätsbezogenen Aufzeichnungen, die während der Herstellung und Prüfung erstellt werden. + Überwachung der zeitnahen Erstellung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] und Überprüfung von Product Quality Reviews (PQRs) . Führung Teamentwicklung: + Führung, Mentoring und Entwicklung eines leistungsstarken Teams von Quality Operations-Experten. + Förderung einer proaktiven Qualitätsmentalität und einer Kultur der kontinuierlichen Verbesserung innerhalb des Quality Operations-Teams und in allen operativen Abteilungen. Kontinuierliche Verbesserung Lean: + Vorantreiben kontinuierlicher Verbesserungsinitiativen innerhalb von Quality Operations [. .. ] as reviewing applications against jobrelated criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice. 85463515 [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
SGS Australia
Global Head of Operations
• Meinerzhagen, North Rhine- Westphalia
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 vor 14 Tagen bei Neuvoo gefunden
SGS
Global Head of Operations
• Meinerzhagen, North Rhine- Westphalia
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 10.03.2026 bei Neuvoo.com gefunden
Lilly
Qualified Person (QP) - (m/w/d)
[. .. ] in Alzey, Germany. This is an outstanding opportunity to deliver on new manufacturing investments and new pioneering technologies. The QP is responsible for certifying that each batch [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of a medicinal product meets all required provisions when released from a manufacturing facility. These provisions include ensuring that the batch has been produced according to appropriate standards and has successfully passed all required tests. Certification and Release of Finished Batches Confirms, certifies, and releases batches of products manufactured, ensuring all manufacturing steps have [. .. ] products and active substances. Quality Assurance Performs analysis of corporate standards and participates in their implementation on site. Participates in the implementation of new regulations. Acts as approver and/or reviewer of procedural documents related to their activity. Approves regulatory specifications of manufactured products in the LIMS system. Approves in SAP the list of countries registered for finished product codes. Acts as reviewer for the Annual Product Review (APR) of the Alzey site, ensuring the quality of the analysis and conclusions. [. .. ]
Job am 12.02.2026 bei Neuvoo.com gefunden
Lilly
Qualified Person (QP) - (m/w/d)
• Alzey
[. .. ] in Alzey, Germany. This is an outstanding opportunity to deliver on new manufacturing investments and new pioneering technologies. The QP is responsible for certifying that each batch [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of a medicinal product meets all required provisions when released from a manufacturing facility. These provisions include ensuring that the batch has been produced according to appropriate standards and has successfully passed all required tests. Certification and Release of Finished Batches Confirms, certifies, and releases batches of products manufactured, ensuring all manufacturing steps have [. .. ] products and active substances. Quality Assurance Performs analysis of corporate standards and participates in their implementation on site. Participates in the implementation of new regulations. Acts as approver and/or reviewer of procedural documents related to their activity. Approves regulatory specifications of manufactured products in the LIMS system. Approves in SAP the list of countries registered for finished product codes. Acts as reviewer for the Annual Product Review (APR) of the Alzey site, ensuring the quality of the analysis and conclusions. [. .. ]
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 23.11.2025 bei Neuvoo gefunden
Moore TK
(SENIOR) MANAGER FUND ACCOUNTING REPORTING (m/w/D)
• Berlin
Abgeschlossenes Studium
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 [. .. ]
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 15 offene Stellenanzeigen für Product Reviewer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Product Reviewer Jobs?
Aktuell suchen 7 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:
- Lilly (2 Jobs)
- Elanco (1 Job)
- SGS Australia (1 Job)
- SGS (1 Job)
- OpenAI (1 Job)
- Moore TK (1 Job)
In welchen Bundesländern werden die meisten Product Reviewer Jobs angeboten?
Die meisten Stellenanzeigen für Product Reviewer Jobs werden derzeit in Nordrhein-Westfalen (4 Jobs), Bayern (3 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Product Reviewer Jobs?
Product Reviewer Jobs gehören zum Berufsfeld Produktmanagement.
