Product Reviewer Stellenangebote


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19 Stellenangebote


Stellenangebote Product Reviewer Jobs bei StepStone


Stellenangebot Product Reviewer Job bei Otsuka Pharma GmbH Job vom 30.11.2024 Otsuka Pharma GmbH

Director, Global CMC Regulatory Affairs (EU) (m/f/d)

• Frankfurt am Main Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten
MEHR[...] C Act, EMA FDA quality guidelines, ICH and regional compendial requirements as well as EMA and FDA policies and practices for drugs, devices and drug- device combinations Comprehensive knowledge and experience in preparing CMC (Quality) sections for investigational and marketed product submissions (IND, NDA, DMF) for FDA and equivalent submissions for Europe (CTA, IMPD, MAA) Comprehensive understanding of the global regulatory [...] Pacific, Latin America and middle- east countries will be a plus 3 to 5 years of hands- on pharmaceutical product development, including scale- up and technology transfer to manufacturing and/ or manufacturing experience is highly desirable As a CMC Quality reviewer (assessor) with FDA or EMA is highly desirable Bachelors degree in Pharmaceutical Sciences or Chemistry or Pharm. D. Masters degree [...]
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Stellenangebote Product Reviewer Jobs gefunden bei Jobbörse Jobleads

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Job vor 10 Tagen gefunden Director, Global CMC Regulatory Affairs (EU) (m/f/d) • Osterwieck, Sachsen- Anhalt Führungs-/ Leitungspositionen
MEHR[...] C Act, EMA FDA quality guidelines, ICH and regional compendial requirements as well as EMA and FDA policies and practices for drugs, devices and drug- device combinations. Comprehensive knowledge and experience in preparing CMC (Quality) sections for investigational and marketed product submissions (IND, NDA, DMF) for FDA and equivalent submissions for Europe (CTA, IMPD, MAA) . Comprehensive understanding of the global [...] Pacific, Latin America and middle- east countries will be a plus. 3 to 5 years of hands- on pharmaceutical product development, including scale- up and technology transfer to manufacturing and/ or manufacturing experience is highly desirable. As a CMC Quality reviewer (assessor) with FDA or EMA is highly desirable. Bachelors degree in Pharmaceutical Sciences or Chemistry or Pharm. D. Masters degree [...]
Job vom 02.12.2024 Director, Global CMC Regulatory Affairs (EU) (m/f/d) • Frankfurt, Hesse Führungs-/ Leitungspositionen
MEHR[...] C Act, EMA FDA quality guidelines, ICH and regional compendial requirements as well as EMA and FDA policies and practices for drugs, devices and drug- device combinations. Comprehensive knowledge and experience in preparing CMC (Quality) sections for investigational and marketed product submissions (IND, NDA, DMF) for FDA and equivalent submissions for Europe (CTA, IMPD, MAA) . Comprehensive understanding of the global [...] Pacific, Latin America and middle- east countries will be a plus. 3 to 5 years of hands- on pharmaceutical product development, including scale- up and technology transfer to manufacturing and/ or manufacturing experience is highly desirable. As a CMC Quality reviewer (assessor) with FDA or EMA is highly desirable. Bachelors degree in Pharmaceutical Sciences or Chemistry or Pharm. D. Masters degree [...]
Job vom 22.11.2024

Sector Expert (Agriculture LCA)

• Berlin, Stuttgart, Baden- Württemberg
MEHR[...] Develop, maintain and pro- actively share with the global consulting and business development organization an appropriate sector knowledge. Pro- actively support the Food, Agriculture and Renewable Materials (FARM) team members in reaching team goals. Support projects from other teams across Product and Corporate Sustainability, particularly by providing FARM expert LCA know- how and guidance. Support standardization, workflow improvement and documentation to [...] QA guidelines, e. g. , according to the latest methodology standards. Pro- actively research for relevant QA topics and where relevant provide internal guidance and external thought leadership. Pro- actively engage with relevant external stakeholders and bodies (such as critical reviewer, EPD Program Operators) with regards to QA. Support organizing meetings/ trainings for QA experts and organize at least one yearly [...]
Job vom 12.11.2024

Senior Director, Oncology Genomics

• Heidelberg, Baden- Württemberg Führungs-/ Leitungspositionen
MEHR[...] Genetics and Genomics organization. Contribute scientific expertise to identify and deliver drug discovery or development efforts within and outside own discipline. Lead and influence the outcome of multidisciplinary projects and meetings. Contribute to projects and programs as an Expert Peer Reviewer. Represent GSK on cross- industry teams on initiatives, maintaining an extensive network of specialists within and outside GSK. Effectively communicate [...] and senior leaders across GSK. Utilize your track record of effecting substantial change to impact discovery/ development policy, processes or guidelines in the pharmaceutical industry. Define and execute a coordinated and highly influential scientific strategy. Accountable for decisions affecting major product development activities or business directives and their implementation and for recommending allocation of resources with key matrix partners. Basic Qualifications [...]
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Job vom 11.11.2024

Sr. Program Manager, Artificial General Intelligence

• München, Bayern
MEHR[...] help us build the future. As a Program Manager, you will be responsible for identifying and executing on opportunities to bring information to our teams customers and beyond. Key job responsibilities In this role you will: Lead the AGI Information product, and its application for customers in Germany, setting and tracking country- specific goals and business metrics. Ensure the product meets high standards of engagement and quality. Act as the final reviewer for all customer experiences, ensuring they are culturally relevant and linguistically appropriate for German users. Define and enforce customer experience [...]
Job vom 09.11.2024 Sr. Program Manager, Artificial General Intelligence • München, Bayern
MEHRMinimum Qualifications: Bachelor s degree in a field such as Science, Business Administration, Computer Science, Engineering, or a related technical field. Proven experience in program or product management. Proven track record of delivering complex projects, from concept to execution, in a fast- paced environment. Experience in managing [...] and beyond. Key job responsibilities: Lead the AGI Information product, and its application for customers in Germany, setting and tracking country- specific goals and business metrics. Ensure the product meets high standards of engagement and quality. Act as the final reviewer for all customer experiences, ensuring they are culturally relevant and linguistically appropriate for German users. Define and enforce customer experience [...]
Job vom 07.11.2024

Software Engineer- Architect (m w d)

MEHR[...] Hannover, Munich, Regensburg, Rosenheim, Leipzig, Vienna. PERFECT MATCH You actively support your agile team in the daily development work. You keep an eye on the software architecture as well as the functional and non- functional requirements. You are interested in product development during all project phases, from discovery to delivery, and advise customers on the latest technical trends. We offer you [...] desired activities with you individually and openly and would like to make these possible for you. You are a technical lead, moderator and mentor in our teams. You enjoy solving tricky code problems and are a popular contact person and reviewer. Partnering with our customers to take a product from concept to implementation. Evaluating trade- offs and making decisions on common [...]
Job vom 07.11.2024

Productmanager Food (m/w/d) / Lead Auditor Food

• Frankfurt, Hesse Führungs-/ Leitungspositionen
MEHR[...] die Durchführung von fachlichen Prüfungen sowie und Unterstützung externer FP s. Sie nehmen bei Audits durch Akkreditierungsstellen/ Standard Owner teil Sie informieren Änderungen der Akkreditierungsanforderungen und Ergebnisse von Office Audits Ihr Profil Zugelassener IFS- Auditor für Food Alternativ zugelassener IFS- Reviewer mit folgenden Anforderungen Ein lebensmittelbezogener oder ein im Bereich der Biowissenschaften abgeschlossener Studiengang (mindestens ein Bachelor bzw. ein gleichwertiger Abschluss) [...]
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Stellenangebote Product Reviewer Jobs gefunden bei Jobbörse Neuvoo

Stellenangebote Product Reviewer Jobs bei Neuvoo


Stellenangebot Product Reviewer Job bei Medtronic Job vor 9 Tagen gefunden Medtronic

Senior Software Engineer Surgical (m/f/d) .

• Weßling, Bavaria
MEHR[...] the rest of the robotic platform Contribute to the continuous improvement of verification methods Partner with the greater software organization, systems engineering, and validation groups Define and review software requirements Conduct hardware- in- loop testing of prototype as well as product software Act as an independent reviewer of Simulink models to ensure that all software meets quality standards Prepare and participate in design reviews Document or participate [...]
Stellenangebot Product Reviewer Job bei DQS Group DE Job vor 10 Tagen gefunden DQS Group DE Productmanager Food (m/w/d) / Lead Auditor Food • Frankfurt am Main, Hesse Führungs-/ Leitungspositionen
MEHR[...] die Durchführung von fachlichen Prüfungen sowie und Unterstützung externer FP s. Sie nehmen bei Audits durch Akkreditierungsstellen/ Standard Owner teil Sie informieren Änderungen der Akkreditierungsanforderungen und Ergebnisse von Office Audits Ihr Profil Zugelassener IFS- Auditor für Food Alternativ zugelassener IFS- Reviewer mit folgenden Anforderungen Ein lebensmittelbezogener oder ein im Bereich der Biowissenschaften abgeschlossener Studiengang (mindestens ein Bachelor bzw. ein gleichwertiger Abschluss) [...]
Stellenangebot Product Reviewer Job bei BSI Job vor 13 Tagen gefunden BSI EU IVD Regulatory Lead Führungs-/ Leitungspositionen
MEHR[...] and authorisations of employees to conduct specified conformity assessment, certification and supporting activities linked to the assigned competence codes; Establish qualification criteria for competence codes; Verify the competence for roles Scheme Manager, Technical Specialist, Certificate Decision Maker, Unannounced Auditor, Clinical Reviewer, Competence Verifier, Document Approver. Process Requirements:Build relationships with authorities, i. e. , the European Commission, the Designating Authorities (NL- VWS; [...] Conformity Assessment Body (i. e. NB2797 and AB0086) for the Medical Devices Regulations (EU UK, respectively) . Notified Body listing the designations and scope of designation on the EC Website NANDO; Conformity Assessment Body (i. e. , NB AB) , product and quality systems standards and requirements; An understanding of product and QMS conformity assessment routes and certification concepts and principles; [...]
Stellenangebot Product Reviewer Job bei CSA Group Job vom 02.12.2024 CSA Group Clinical Reviewer MDR/ IVDR (f/m/d) • Plattling, Bavaria
MEHR[...] environmental impact. Our employees take pride in making a difference in peoples lives through the work that we do. Were looking for people like you to help make it happen. Job Summary:CSA Group Europe has an opportunity for a Clinical Reviewer MDR/ IVDR (f/m/d) to join our Healthcare Regulatory Services Team in Germany and throughout Europe. The Clinical Reviewer will support [...] team in the delivery of clinical assessments of products under the European Regulations towards Medical and In Vitro Diagnostic Devices Regulation. 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. In this responsibility [...]
Stellenangebot Product Reviewer Job bei Vestas Job vom 21.11.2024 Vestas Specialist Blades • Hamburg
MEHR[...] and engineering teams with global functions, ensuring knowledge sharing in virtual and physical forums Identify key performance drivers within relevant functional areas and ensure there is an agreed action plan to deal with the issue Act as technical and operational reviewer of solutions and deliverables during RCA, development and implementation when addressing quality issues with service impact Ensure service requirements are captured during new product development and key deliverables are ready for introduction to service operations Identify areas for operational improvement of WTG servicing and [...]
Stellenangebot Product Reviewer Job bei Medtronic Job vom 20.11.2024 Medtronic Principal Software Engineer- Surgical Robotics. • Weßling, Bavaria
MEHR[...] mechanical, electrical and software engineers responsible for further development and enhancement of the globally launched Robotic Assisted Surgery platform within the Surgical Operating unit: Medtronic s Surgical Operating Unit is one new, powerful operating unit bringing together the people and product portfolio of Surgical Robotics and Surgical Innovations. With the Medtronic Mission as our North Star, we will build on our [...] methods and update/ tune existing software implementation to support released products. Contribute to the continuous improvement of verification methods. Partner with the greater software organization, systems engineering, and validation groups to define and review software requirements. Act as an independent reviewer of MATLAB/ Simulink models to ensure that all software meets quality standards and follow proper architecture. Prepare and participate in [...]
Job vom 25.07.2024 Cloud Factory Agronomist (Data Reviewer)
MEHR[...] particular crop and weed species. Through this collaboration with the delivery team, you will support in fostering high- quality datasets for AI model development. Bridge the Gap Between Ag and AI: Participate in client calls to understand how business and product objectives translate into annotation requirements. Continuous Learning: Stay up- to- date on the latest advancements in agronomy and relevant AI [...]
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Stellenangebote Product Reviewer Jobs gefunden bei Jobbörse NewScientist Jobs

Stellenangebote Product Reviewer Jobs bei NewScientist Jobs


Job vom 28.11.2024 Hogarth Worldwide AI Solutions Architect • London, Greater London, United Kingdom, London (Greater)
MEHR[...] de r s This role reports to the MD, Strategic Consulting AI. You will work closely with our Production Studio, Strategic Consulting, Martech, VFX and pipeline development teams Responsibilities Lead and develop our NVIDIA/ Hogarth partnership Define go- to market product and service offerings built on NVIDIA solutions Develop new business opportunities and leads across NVIDIA and WPP Lead and co- [...] automated anonymisation system. This aims to ensure that all candidates are considered for interview based solely on their experience and what they can bring to the role. The solution, provided by Me Vitae, scans and redacts CVs to reduce potential reviewer bias. Please contact careers hogarth. com if you need the job advert or form in another format. Data We rely [...]
Job vom 28.11.2024 Siemens Energy Reliability Engineer • Lincoln, United Kingdom, Lincolnshire
MEHRJob Title: Reliability Engineer Department: Product Lifecyle Reports To: Product Lifecyle Director Location: Lincoln, Lincolnshire or Houston, Texas Job Summary: Siemens Energy Industrial Turbomachinery Ltd. Is [...] for turbine failures and performance issues, and collaborate with maintenance and operations teams to identify corrective actions and prevent recurrence. Innovative Design Integration: Partner with design and manufacturing teams to incorporate reliability considerations into new turbine designs, acting as a reviewer in design reviews, and develop optimised maintenance strategies to enhance turbine reliability and reduce downtime. Continuous Improvement and Training: Promote [...]
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Job vom 13.10.2024 Bio Marin Pharmaceutical Inc. Associate Director, Clinical Medical Writing • London, Greater London, United Kingdom, London (Greater) Führungs-/ Leitungspositionen
MEHR[...] for Medical Writing staff, including authoring/ editing documents. The Associate Director may participate in review and approval of regulatory submission documents and publications, and will work with the Head of CMW in departmental resource planning, submission planning for program and product development, and other resource or budgetary medical writing requirements for that/ those program (s) RESPONSIBILITIES Oversight responsibilities for Medical Writing [...] Writing to ensure appropriate CMW deliverables planning for specified clinical development program (s) , including resource forecasting and allocation, timelines, and budget Works with CMW line management to establish and maintain timelines for program planning. Acts as management- level author/ reviewer for CMW and other Development Sciences deliverables, where such review/ authoring is required by SOPs or other controlled process documentation [...]
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