Regulatory Affairs

Regulatory Affairs Project Manager / Regulatory Affairs Manager (m/f/d) Mannheim projects simultaneously Self-motivated and capable of working independently in a self-management environment Profound English and German skillsAffinity for IT and good MS Office skills 30 days leave per
Regulatory Affairs Project Manager / Regulatory Affairs Manager (m/f/d) Mannheim projects simultaneously Self-motivated and capable of working independently in a self-management environment Profound English and German skillsAffinity for IT and good MS Office skills 30 days leave per
Manager Regulatory Affairs (m/f/d)* Mainz in regulatory affairs or medical devices, with a focus on interfaces with quality management.Proven skills in project management and ability to think interdisciplinary.Profound knowledge of the regulatory
Global UDI Data Business Manager – Regulatory Affairs Hamburg (STS) within regulatory affairs. This is a broad, global role with many interesting and exciting projects to be part of. You will be joining a highly motivated team, who share a passion for regulatory and
Regulatory Affairs Manager - (Swiss Submissions, home-based) (m/w/d) Frankfurt, Hesse, Germany register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• Provide Regulatory Consulting for ODS Applications, New
Delivery & Operations Lead, IQVIA Regulatory Intelligence London, United Kingdom projects by:o Prioritize, scope and drive content improvement/enhancement projects to identify the relevant regulatory contento Contribute to the content identification and requirements and the
Regulatory Affairs Manager (f/m/d) Mannheim manage multiple projects simultaneously Self-motivated and capable of working independently in a self-management environment
Regulatory Affairs Manager (f/m/d) Ludwigshafen market products internationally Coordinate and complete documents required by federal agencies, maintaining complex files and electronic document management systems and work with project teams to obtain
Regulatory Affairs Manager (m/f) EMEA - Specialist who is able to make hands-on decisions and set-up a long term strategy (abgeschlossen) International projects, e.g. reducing complexity for product approvals, label management, ingredient acceptance and specification managementProviding practical solutions for the business, in a quick and efficient
with business partner screening to ensure and comply with legal requirements, such as supply chain due diligence. Participate in the implementation of compliance software / legal tech projects (AEB
/ reports Enable/direct internal department digital improvement initiatives encompassing: interactive training material, global portals, project reporting tools and dashboards, process flow data
/ reports Enable/direct internal department digital improvement initiatives encompassing: interactive training material, global portals, project reporting tools and dashboards, process flow data
Regulatory Manager, Clinical Trials Regulatory Management- Home-based, Europe Reading, Berkshire, United Kingdom Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIESActs as a
Senior Director, Regulatory Strategy Lead (home-based) Reading, Berkshire, United Kingdom for the development of regulatory business, in accordance with RADDS and Corporate business plans. Participates in project-related work, as necessary. Provide scientific, regulatory, and product
Associate Manager, Clinical Trials Regulatory Management- Home-based, Europe Reading, Berkshire, United Kingdom Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIESActs as a Clinical Trial
Regulatory and Start Up Specialist 2 (FSP) (m/w/d) Home Based Frankfurt, Hesse, Germany (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions and CTIS experience. German and English fluent
Finance Project Director (m/f/d) Hannover Head of New Product Development (abgeschlossen) Relevant project management experience, preferably in manufacturing Understanding of EU food regulatory environment Able to deal with and manage complexity, building strong relationships, striving for
& Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to
Senior Statistical Programmer - Global BIOS Frankfurt, Hesse, Germany & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to
& Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to
Safety Manager - San Antonio San Antonio,Texas Knowledge & experience to provide effective training on all appropriate safety related topics Ability to travel Excellent Computer skills Power point, Excel, Word, Visio and ProjectPreferred Requirements
assure alignment around strategic projects and day-to-day activities and to assure mutually successful working relationships Completed Master's degree in natural sciences e.g. chemistry, biotechnology or
Senior Compliance Manager / Legal Professional (m/w/d) - EMEA Region Pliezhausen legal and regulatory developments potentially impacting Renishaw's businesses. Conduct and manage internal investigations, including as related to whistleblowing reports. Complete other legal projects as
assure alignment around strategic projects and day-to-day activities and to assure mutually successful working relationships Completed Master's degree in natural sciences e.g. chemistry, biotechnology or
Technical Developer Quality Lead (f/m/d) Holzkirchen, Oberbayern key stakeholders to ensure clinical Quality-by-Design for the projects under responsibility Establish and lead core Quality Issue Management governance for critical or major quality issues pertinent to
MARISK Compliance Manager (m/f/d) Hamburg SCAYLE Payments You are responsible for (technical) compliance projectsRequirementsYou have minimum of 3-4 years' experience in the field of compliance in the Financial Service Industry or FinTech
Quality Assurance Manager GMP/GDP (m/f/d) Allschwil drug product, and finished products manufactured by contract manufacturersMonitor performance metrics, provide regular updates to management on assigned project progress, and escalate challenges as
Quality Assurance Manager GMP/GDP (m/f/d) Allschwil drug product, and finished products manufactured by contract manufacturersMonitor performance metrics, provide regular updates to management on assigned project progress, and escalate challenges as
Verbal Communication skills Excellent computer Skills Power Point, Excel, Word, Visio, and ProjectPreferred Qualifications:Bachelor Degree in a safety related Field 3 years in Safety Management Formal
Operational Excellence projects in the area of QualityLead the communications channel between Quality at regional level and the Global and Cluster key stakeholders
Local Trial Manager or Senior LTM (m/w/d) Frankfurt, Hesse, Germany The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials. Joining the team provides
cabin projects, achieving best in class cabin interior within budget and meeting program timelines Responsible for assigned cabin interior from concept through to delivery. Ensuring timelines, budget and
Parenteral formulation and Process Development Scientist (m/f/d) Basel Stadt , biologics (e.g. oligonucleotides) and long acting injectable within a multifunctional project team coordinated by a Project LeaderLead and manage all project activities, support team members, participate
Parenteral formulation and Process Development Scientist (m/f/d) Basel Stadt , biologics (e.g. oligonucleotides) and long acting injectable within a multifunctional project team coordinated by a Project LeaderLead and manage all project activities, support team members, participate
Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to
Project Engineer Urban Water Management (m/f/d)Your assignments Producing designs, both initial outlines and full plans, of sewerage, water treatment and flood defence structures such as pump
all industries and so can provide specialists with exciting projects and attractive job opportunities. Whether it's working within an international group or with a regional market leader: we look at
all industries and so can provide specialists with exciting projects and attractive job opportunities. Whether it's working within an international group or with a regional market leader: we look at
related business Experience in working in an international environment, as well as team leading and project management experiences Ideally good knowledge and understanding of the regulatory and GMP/GCP
several projects simultaneously and within a dynamic, fast-paced, and growing organization Experience of working in a bank and/or a commodity trading environment Experiences with Product Organization and
StellenbeschreibungTake off with us! We offer exciting projects at our renowned customer Airbus Operations and we are looking for a motivated employee for the position "Commercial Planning
across all industries and therefore can provide engineering specialists with exciting projects and attractive job opportunities, drawing on your personal interests and experience. As your professional
authoritiesEnsure that Validation Master plans are up to date and established for all ongoing projectsAssess and produce the CSV package(s) on an assigned project. Taking accountability for the work to be
development (f.e. in Project Management, Quality Assurance and Testing, Requirements Engineering, Customer and Stakeholder Engagement, Continuous Improvement Culture ). Contribute on a strategic vision for the
Specialist Private Label Development (m/w/d) and effective product development (f.e. in Project Management, Quality Assurance and Testing, Requirements Engineering, Customer and Stakeholder Engagement, Continuous Improvement Culture ). Strategic
environment, leadership experience, ability to build relationships with customers,- Capability to define strategic plan for the site, negotiation, project management and presentation skills
packaging. You execute complex innovation and customer specific projects from idea all the way to market launch. You are responsible to plan technical work packages and deliver them according to quality
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