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129 Jobs für Regulatory Affairs Executive


Stellenangebote Regulatory Affairs Executive Jobs


Job gestern bei Jobleads gefunden

Regulatory Affairs Executive

Salary: Competitive Job Timings: 8 AM to 5 PM Requirements: Graduation in pharmacy background or any relevant degree. About the role: To contribute to the regulatory documents and reports to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] be included in regulatory submission. Documents and track regulatory submission and regulatory authority license approval for EU market and most probably Germany. Provide regulatory support to the teams and associates of the company. Responsibilities: Application for new registration to receive license from EMA. Cooperation with authorities [. .. ] and receipt of approval from MAH. Maintenance of existing approvals and maintaining formats and content review of packaging texts, Sm PC, PIL and labelling. Review task for, support and mentor Regulatory Affairs associates. Provide on-going regulatory support to the regulatory affairs team lead and to project teams to ensure regulatory concerns are planned and accounted for the relevant data are generated to meet project objectives. Provide format and contents review of packaging texts, Summary of Product Characteristics, Patient Information Leaflet and [. .. ]

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Job gestern bei Mindmatch.ai gefunden 8036 Takeda Pharmaceuticals International AG Associate Director, Medical Grants and Sponsorship • AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] operating model. Operates in a highly regulated, matrixed, multicountry environment with variation in local laws, industry codes, transparency/ disclosure requirements, HCP/ HCO rules, tax/ finance requirements, sponsorship [...]
MEHR INFOS ZUM STELLENANGEBOT[...] practices and Medical Affairs maturity. Acts as a strategic governance and quality partner, helping teams apply consistent standards in a practical, riskbased and auditready way. Balances scientific and educational impact, patient benefit, independence, transparency, compliance, budget discipline, operational agility and process simplicity. Establishes enterprise standards and oversight expectations that enable consistent, defensible and auditable [. .. ] Experience with grantmanagement systems, data quality, repository management, documentation standards, budget tracking, reconciliation, metrics and closeout processes preferred. Experience working across multiple countries, regions or markets with varied maturity levels, regulatory environments and industrycode expectations preferred. Competencies Skills Ability to translate enterprise governance expectations into simple, usable tools and guidance that support consistent execution without adding unnecessary complexity. Strong governance, riskbased thinking and systemsthinking capability, with the ability to convert complex funding and compliance requirements into practical enterprise standards and decision [. .. ] patterns, tradeoffs, budget implications and systemic execution risks across multiple Therapeutic Areas, geographies and funding categories. Excellent crossfunctional leadership, communication, influence and stakeholdermanagement skills across cultures, functions and seniority levels. Executive communication skills, with the ability to frame status, implications, options, risks and recommendations in a concise, leadershipready manner. Ability to balance compliance rigor with operational practicality, avoiding unnecessary bureaucracy while maintaining strong patient, scientific, quality and company safeguards. High attention to detail, clarity and documentation quality, with sound judgment in [. .. ]

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Job gestern bei Mindmatch.ai gefunden MSD

Director Procurement, Animal Health Technology Solutions (Global)

• AT- 3 Krems an der Donau Führungs-/ Leitungspositionen [. .. ] services and capital investment, covering categories such as plastics, printed circuit board assemblies, microchips, electronic components, metals, external manufacturing and other technology solutions supporting animal health operations. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Reporting to the Executive Director responsible for Indirect Services and Animal Health Technology Solutions Procurement, you will lead a global team of approximately six procurement professionals. You will partner with senior leaders across manufacturing, supply chain, research and development, commercial operations, finance, quality, regulatory affairs, engineering and technology to deliver value, strengthen supply resilience and support business growth and transformation. Primary location: United States (Rahway) or EURAM (Netherlands, Austria, Germany or Spain) . What You Will Do Develop and deliver global procurement and category strategies across direct materials, indirect services and capital investment. Lead strategic [. .. ]

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Job gestern bei Mindmatch.ai gefunden Johnson Johnson Director, Ext Mfg Reg Compliance • AT- 2 Lavamünd Führungs-/ Leitungspositionen Job Function: Legal Compliance Job Sub Function: Enterprise Compliance Job Category: People Leader All Job Posting Locations: Schaffhausen, Switzerland Job Description: Director, External Manufacturing Regulatory Compliance Oversight Location: EU Johnson [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Johnson Sites Reports To: Senior Director, External Manufacturing Regulatory Compliance Oversight Travel-Up to 25-40 (Global) Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by [. .. ] compliance oversight, risk visibility, inspection-readiness support, governance, and organizational learning across the Innovative Medicine External Manufacturing network. The role partners with External Manufacturing Operations, Quality, Supply Chain, Procurement, Regulatory Affairs, Technical Operations, and other stakeholders to identify emerging compliance risks, strengthen compliance performance, and support proactive risk management across contract manufacturers, contract laboratories, strategic partners, and other external suppliers. This role operates within the External Manufacturing Regulatory Compliance Oversight organization and supports implementation of the compliance oversight strategy established for [. .. ] and communicate complex compliance risks in a clear and actionable manner. Strong analytical, problem-solving, and decision-support capabilities. Ability to influence without direct authority across a global network. Strong executive communication and stakeholder engagement skills. Ability to balance independent oversight with productive cross-functional partnerships. #LI-Hybrid J-18808-Ljbffr 03497811 [. .. ]

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Job gestern bei Mindmatch.ai gefunden Revolution Medicines

Senior Director, Corporate Affairs, Communication and Policy Advocacy, CNE

• AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigorall in service of patients. The Opportunity: The [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Senior Director, Corporate Affairs will lead the development and execution of oncology-focused Corporate Affairs strategies in the CNE that support the companys mission of revolutionizing treatment for patients with RAS-addicted cancers. These Corporate Affairs strategies bring together media relations, corporate public affairs, product communications, corporate reputation management and internal communications. This is [. .. ] regional and global Corporate Affairs strategies. Key Responsibilities: Media Relations Acts as CNE spokesperson, directing enquiries to internal experts as needed. Drives proactive media content and strategy around trial results, regulatory milestones, and major oncology congresses (ASCO, ESMO) . Builds and maintains trusted relationships with top-tier CNE and trade media, ensuring accurate representation of company positions and achievements. Monitors media coverage and sentiment, flagging emerging narratives before they require a crisis response. Ensures consistent messaging across earned, owned, and shared [. .. ] reputation indicators and stakeholder sentiment, giving leadership early warning of emerging risks and opportunities. Leads local crisis and issues management, protecting and enhancing the companys reputation during sensitive events. Builds executive visibility and thought leadership within the local business, healthcare, and policy community, positioning leaders as trusted voices on oncology innovation. In partnership with the local Value, Market Access and Pricing team, pursues corporate Public Affairs activities, including engagement with government and stakeholder institutions in CNE on broader company issues. Maps [. .. ]

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Job gestern bei Mindmatch.ai gefunden Richemont Government Affairs Senior Manager, CH, US • AT- 2 Lavamünd [. .. ] the same time, we are committed to innovating and designing new products in line with the values of our Houses, through a process of permanent creativity. ROLE [...]
MEHR INFOS ZUM STELLENANGEBOT[...] PURPOSE The Government Affairs Sr Manager, CH, US will support the execution of the Groups global government affairs strategy, with responsibility for driving impact and building influence in priority international markets. The role is accountable for government affairs engagement in Switzerland and the United States, aligned with business priorities and in coordination with the [. .. ] luxury sector. Develop and execute annual stakeholder engagement plans with clear objectives, milestones and measurable outcomes aligned with Group priorities. Policy Monitoring Advocacy Monitor and assess relevant policy, legislative and regulatory developments across assigned markets. Develop and implement advocacy strategies in priority international markets. Monitor and assess geopolitical, trade and economic policy developments impacting the Groups international operations and support advocacy strategies to protect market access and business continuity Ensure alignment with Group positions before external engagement. Coordinate with trade associations [. .. ] ability to manage by influence. High energy and a positive attitude, with a pleasant and open personality. Sound judgment and strong intellect. Ability to be a trusted advisor for senior executive members. Proactiveness and flexibility, displaying a can-do attitude. Strong understanding of policy-making processes in key markets, particularly United States and Switzerland, with exposure to international environments. Must have a strong network in Switzerland and a well-established one in the United States. Demonstrated ability to build and manage [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Novartis

Manager, Senior Manager, Public Affairs

• AT- 2 Schweiz [. .. ] (PPE) activities to maximize the value of assigned products/ therapeutic areas in Japan, contribute to shaping the external policy environment, and support the effective operation and execution [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of broader Public Affairs priorities and initiatives Job Description Job Responsibilities: Maximize the value of products and platforms through public policy engagement with S G, TA, medical, V A and C PTA etc. Create Public Affairs (PA) strategy for product based on OGSM framework and One Brand Plan, and executive PPE activities. Gather policy trends and insights from policy makers related to diseases and products, and reflect them in business plans. Execute public policy engagement to optimize health policies Develop and maintain the relationship with policy stakeholders Promote PPE activities in Japan in collaboration with GPA counterparts and external stakeholders, [. .. ] guidelines related to public policy engagement Collaborative and team-oriented ways of working required (Preferable) At least 5 years experience in pharmaceutical industry (Preferable) Governmant/ Public Affaris, Marketing, Medical, Development, Regulatory, Patient Advocacy, Consulting Government Official background (Preferable) Experience in advocacy and lobbying for policy stakeholders Key performance indicators: Influence on priority policy agendas Strategic alignment with Novartis objectives Quality of deliverables and insights J-18808-Ljbffr 03444326 [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Fresenius Medical Care Global Category Lead (Contract Manufacturing) • AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] multiple regions. The Director leads a team of Category Managers and procurement professionals, providing strategic direction, talent development, and performance management while partnering with senior business leaders [...]
MEHR INFOS ZUM STELLENANGEBOT[...] across Manufacturing, Quality, Regulatory, Supply Chain, Operations, R D, Legal, and Finance. The incumbent acts as a trusted advisor to executive leadership and contributes to procurement transformation initiatives across the enterprise. Your Role: Strategic Leadership Define and own the global Contract Manufacturing category strategy and roadmap. Develop and implement multi-year category plans supporting business growth and manufacturing network optimization. Establish long-term supplier portfolio strategies aligned with business objectives. Drive [. .. ] strategic make-versus-buy decisions. Present category strategies, supplier performance, risks, and opportunities to senior leadership. Lead cross-functional initiatives involving Procurement, Manufacturing, Quality, Supply Chain, Finance, Legal, and Regulatory Affairs. Your Profile: Minimum 12 years of progressive procurement and strategic sourcing experience. Minimum 7 years leading Contract Manufacturing categories in a global environment. Minimum 5 years people management experience. Demonstrated success managing international supplier networks. Experience leading complex international negotiations and sourcing programs. Experience operating within regulated industries such as [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Phia LLC

Senior Program Leader (IVd/CDx) (Relocation to Switzerland)

• AT- 2 Lavamünd Führungs-/ Leitungspositionen Do you bring deep experience in IVD or companion diagnostic product development and a track record of leading complex programs through regulatory approval or pivotal clinical trials? Can you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] align cross-functional teams and biopharma partners around the scientific, regulatory, operational, and commercial milestones needed to deliver diagnostic solutions? If this sounds like you and you are driven by purpose, join the SOPHi A GENETICS Diagnostics Solutions team as a Program Leader and [. .. ] portfolio reviews, business stage gates, design reviews, Joint Steering Committees, and Joint Development Teamsto drive aligned, timely decision-making. Integrate Bioinformatics and Assay Development, Verification and Validation, Clinical Operations, Regulatory Affairs, Quality Assurance, Manufacturing, Product Management, and Biopharma teams around a coherent program strategy, milestones, resources, and shared accountability. Deliver diagnostic programs from requirements definition through product development, verification and validation, regulatory submission, and commercial launch while managing timelines, budgets, risks, resources, and contingency plans. We know that every background is [. .. ] social committee whose purpose is to make SOPHi A GENETICs both enjoyable as well as rewarding As our global HQ, youll have direct interaction and exposure to senior leadership and our executive team locally Our DNA Like the strands of DNA itself, SOPHi A GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient Nimble and Fearlessly Adventurous Our Virtues At [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Novartis Head of Public Affairs, Brazil • AT- 2 Schweiz Führungs-/ Leitungspositionen [. .. ] #LI-Hybrid 3 days/ week in office Were a team of dedicated and smart people united by a drive to achieve a higher purpose together. As Head of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Public Affairs, Brazil, you will have the unique opportunity to help shape the future of healthcare in one of the worlds most dynamic markets. Working at the intersection of policy, business, healthcare systems, and society, you will lead Novartis Public Affairs strategy in Brazil, driving the policy and stakeholder environment needed to [. .. ] helping shape country and regional priorities while ensuring Brazils perspectives and opportunities are reflected in broader business and policy discussions. This is a highly visible leadership role for an experienced executive who is passionate about healthcare transformation, leading and developing highperforming teams, and creating true impact for the business and society at large. Job Description Key Responsibilities: Develop and execute an integrated Public Affairs, policy, and stakeholder engagement strategy aligned with Novartis business priorities and patient needs in Brazil. Monitor, analyze, and communicate political, legislative, regulatory, and healthcare policy developments that may impact Novartis, patients, and the broader healthcare system. Shape healthcare policy discussions and advocacy initiatives that support sustainable access to innovation, strengthen healthcare systems, and improve patient outcomes. Build and maintain trusted relationships with senior government officials, policymakers, industry associations, think tanks, academic institutions, [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden NEVEON Executive Committee

Head of Project Management (all genders)

• AT- 4 Kremsmünster Führungs-/ Leitungspositionen Homeoffice möglich [. .. ] Zusammenarbeit mit Innovation Management sowie internationalen Schnittstellenfunktionen Vertretung des Fachbereichs gegenüber Behörden, benannten Stellen, Kunden sowie internen Stakeholdern Enge Zusammenarbeit mit Fachexperten aus, Innovation Development, Produktmanagement, Klinischen [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Fachbereichen, Qualitätssicherung, Produktion, Regulatory Affairs/ Registrierung Damit überzeugen Sie uns: Abgeschlossene relevante akademische Ausbildung, z B (Biomedical) Engineering, (Clinical) Chemistry, oder Material Science Mehrjährige Erfahrung in der Produktentwicklung von Medizinprodukten und in vitro Diagnostika in den Vorgaben der ISO13485, 820 CFR, EU MDR und IVDR Regularien Erfahrung in relevanten aspekten des Lifecycle Management Prozess unter ISO13485 [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden NEVEON Executive Committee Head of Project and Change Management (all genders) • AT- 4 Kremsmünster Führungs-/ Leitungspositionen Homeoffice möglich [. .. ] Zusammenarbeit mit Innovation Management sowie internationalen Schnittstellenfunktionen Vertretung des Fachbereichs gegenüber Behörden, benannten Stellen, Kunden sowie internen Stakeholdern Enge Zusammenarbeit mit Fachexperten aus, Innovation Development, Produktmanagement, Klinischen [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Fachbereichen, Qualitätssicherung, Produktion, Regulatory Affairs/ Registrierung Damit überzeugen Sie uns: Abgeschlossene relevante akademische Ausbildung, z B (Biomedical) Engineering, (Clinical) Chemistry, oder Material Science Mehrjährige Erfahrung in der Produktentwicklung von Medizinprodukten und in vitro Diagnostika in den Vorgaben der ISO13485, 820 CFR, EU MDR und IVDR Regularien Erfahrung in relevanten aspekten des Lifecycle Management Prozess unter ISO13485 [. .. ]

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Job vor 9 Tagen bei Mindmatch.ai gefunden MADx Macro Array Diagnostics GmbH

Head of Marketing Product Management (f/m/x)

• AT- 9 Wien Führungs-/ Leitungspositionen [. .. ] to shape the scientific product development pipeline, translating market and customer needs into clear product requirements and owning the product concept through to market launch. Partner closely [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with Sales, Medical, Regulatory Affairs, Quality and Executive Leadership to align scientific innovation, market needs, and commercial priorities. Act as the executive owner for market intelligence, customer segmentation, and competitive analysis as the basis for portfolio and commercial decisions. Build and maintain strong relationships with key customers, distributors, industry experts, and Key Opinion Leaders in the scientific and [. .. ]

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Job vor 9 Tagen bei Mindmatch.ai gefunden World Institute for Nuclear Security (WINS) Executive Director • AT- 9 Wien Führungs-/ Leitungspositionen Careers at WINS Executive Director LOCATION: Vienna, Austria TERM: Initial 3 years START: January 2027 The World Institute for Nuclear Security (WINS) is seeking an exceptional leader to serve [...]
MEHR INFOS ZUM STELLENANGEBOT[...] as its next Executive Director (ED) and lead the organisation into its next phase of development and global impact. The next ED will join WINS [. .. ] and can demonstrate the combination of organisational leadership, not-for-profit fundraising success, relationship development, and substantive credibility required for the role. Specific knowledge of the nuclear industry, including its regulatory standards, especially regarding the safe and secure management of nuclear materials and technologies across the broad range of civilian purposes (power generation, medical isotopes, research and development, advanced reactors) is essential. Of particular importance is demonstrating the ability to manage complex donor relationships, navigate complex geopolitical environments, and ensure strong [. .. ] independent organisation. Nuclear security technical leadership Candidates should demonstrate technical depth in nuclear security and show strong leadership, relationship development, and the ability to empower other experts. Public policy, international affairs, or diplomacy Candidates should demonstrate diplomatic judgement, influence, coalition building, exceptional communication, and the ability to translate technical issues for non-specialist audiences. EXPERIENCE QUALIFICATIONS Significant senior executive, organisational leadership or equivalent experience in the nuclear arena Strong record of organisational building, development or transformation Successful fundraising and resource development [. .. ]

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Job vor 10 Tagen bei Mindmatch.ai gefunden MADx Macro Array Diagnostics GmbH

Head of Product Strategy Marketing Life Sciences (f/m/x)

• AT- 9 Wien Führungs-/ Leitungspositionen [. .. ] to shape the scientific product development pipeline, translating market and customer needs into clear product requirements and owning the product concept through to market launch. Partner closely [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with Sales, Medical, Regulatory Affairs, Quality and Executive Leadership to align scientific innovation, market needs, and commercial priorities. Act as the executive owner for market intelligence, customer segmentation, and competitive analysis as the basis for portfolio and commercial decisions. Build and maintain strong relationships with key customers, distributors, industry experts, and Key Opinion Leaders in the scientific and [. .. ]

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Job vor 10 Tagen bei Mindmatch.ai gefunden Jobgether Senior Director, Quality Compliance • AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] in Switzerland. This senior leadership role is responsible for shaping and executing a global quality and compliance strategy across clinical research services. You will provide strategic direction [...]
MEHR INFOS ZUM STELLENANGEBOT[...] on quality management, regulatory compliance, inspection readiness, and enterprise risk. The position combines executive leadership with client-facing responsibilities, supporting sponsors, strategic partners, and internal operational teams. You will lead quality transformation initiatives designed to strengthen operational effectiveness, quality maturity, and client confidence. The role requires close collaboration with senior executives and cross-functional leaders across a global clinical research environment. You will also [. .. ] support effective mitigation strategies. Advise senior leadership on quality, compliance, inspection readiness, regulatory risk, and broader enterprise quality initiatives. Requirements: A bachelors degree in Life Sciences, Nursing, Pharmacy, Quality, Regulatory Affairs, or a related scientific discipline is required. An advanced degree such as an MSc, Pharm D, Ph D, or MBA is preferred. A minimum of 1015 years of progressive experience in Quality Assurance, Quality Management, Regulatory Compliance, Clinical Research, or a related field is required. At least seven years of leadership experience [. .. ]

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Job vor 12 Tagen bei Mindmatch.ai gefunden Phia LLC

Senior Program Leader (IVd/CDx)

• AT- 2 Lavamünd Führungs-/ Leitungspositionen Do you bring deep experience in IVD or companion diagnostic product development and a track record of leading complex programs through regulatory approval or pivotal clinical trials? Can you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] align cross-functional teams and biopharma partners around the scientific, regulatory, operational, and commercial milestones needed to deliver diagnostic solutions? If this sounds like you and you are driven by purpose, join the SOPHi A GENETICS Diagnostics Solutions team as a Program Leader and [. .. ] portfolio reviews, business stage gates, design reviews, Joint Steering Committees, and Joint Development Teamsto drive aligned, timely decision-making. Integrate Bioinformatics and Assay Development, Verification and Validation, Clinical Operations, Regulatory Affairs, Quality Assurance, Manufacturing, Product Management, and Biopharma teams around a coherent program strategy, milestones, resources, and shared accountability. Deliver diagnostic programs from requirements definition through product development, verification and validation, regulatory submission, and commercial launch while managing timelines, budgets, risks, resources, and contingency plans. We know that every background is [. .. ] social committee whose purpose is to make SOPHi A GENETICs both enjoyable as well as rewarding As our global HQ, youll have direct interaction and exposure to senior leadership and our executive team locally Our DNA Like the strands of DNA itself, SOPHi A GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient Nimble and Fearlessly Adventurous Our Virtues At [. .. ]

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Job vor 12 Tagen bei Mindmatch.ai gefunden Abbott Laboratories Global Associate Director, Patient Strategy Partnerships • AT- 2 Schweiz Führungs-/ Leitungspositionen [. .. ] patients and patient organizations around the world. This is a unique opportunity to build and evolve a global patient engagement capability, connecting patient insights with strategic decision [...]
MEHR INFOS ZUM STELLENANGEBOT[...] making across Medical Affairs, Market Access, Regulatory Affairs, Public Affairs, and Commercial teams. You will work with colleagues across regions and functions to ensure patient perspectives help inform healthcare solutions, policy discussions, evidence generation, and access initiatives. Most importantly, you will help create lasting partnerships that improve outcomes for patients and communities. What Youll Do Shape Abbotts [. .. ] complex global organizations and external healthcare ecosystems. Proven track record in external stakeholder management and partnership building. Experience in complex matrixed global health care organizations. Excellent communication, storytelling, facilitation, and executive presentation skills, with the ability to translate complex contexts into simple messages Fluency in English required; additional languages are a plus. Additional experience in oncology, biosimilars, health policy, HTA, or healthcare advocacy is valued but not essential. Why Abbott? At Abbott, youll have the opportunity to: Help shape a growing [. .. ]

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Job vor 12 Tagen bei Mindmatch.ai gefunden SOPHiA GENETICS Senior Program Leader (IVd/CDx) (Relocation to Switzerland) • AT- 2 Lavamünd Führungs-/ Leitungspositionen Do you bring deep experience in IVD or companion diagnostic product development and a track record of leading complex programs through regulatory approval or pivotal clinical trials? Can you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] align cross-functional teams and biopharma partners around the scientific, regulatory, operational, and commercial milestones needed to deliver diagnostic solutions? If this sounds like you and you are driven by purpose, join the SOPHi A GENETICS Diagnostics Solutions team as a Program Leader and [. .. ] portfolio reviews, business stage gates, design reviews, Joint Steering Committees, and Joint Development Teamsto drive aligned, timely decision-making. Integrate Bioinformatics and Assay Development, Verification and Validation, Clinical Operations, Regulatory Affairs, Quality Assurance, Manufacturing, Product Management, and Biopharma teams around a coherent program strategy, milestones, resources, and shared accountability. Deliver diagnostic programs from requirements definition through product development, verification and validation, regulatory submission, and commercial launch while managing timelines, budgets, risks, resources, and contingency plans. Requirements We know that every background [. .. ] social committee whose purpose is to make SOPHi A GENETICs both enjoyable as well as rewarding As our global HQ, youll have direct interaction and exposure to senior leadership and our executive team locally Our DNA Like the strands of DNA itself, SOPHi A GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient Nimble and Fearlessly Adventurous Our Virtues At [. .. ]

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Job vor 12 Tagen bei Mindmatch.ai gefunden Bridge Bio Pharma Head of International Communications • AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] 20 drug development programs, ranging from early discovery to late-stage clinical trials, across multiple therapeutic areas including precision oncology, cardiology, endocrinology, neurology, and renal disease. We have [...]
MEHR INFOS ZUM STELLENANGEBOT[...] already achieved regulatory approval for three therapies and continue to advance promising science from academia into meaningful treatments for patients worldwide. Who We Are Bridge Bio is a global biotechnology company with our Global Headquarters located in San Francisco, USA, and our International HQ located in Zug, Switzerland. Since establishing our European presence [. .. ] for patients. Our people are trusted and empowered, united by urgency, purpose, and the drive to advance science for patients around the world. What Youll Do You will report to Executive Vice President, Communications and work closely with SVP Head of International to drive strategic initiatives that support Bridge Bios mission of delivering transformative medicines to patients with genetic diseases and genetically driven cancers. We are entering our first multi-market ex-US launch cycle across a footprint that includes wholly [. .. ] voice, message pull-through, milestone coverage and report against it quarterly Protect reputation and manage issues Own corporate reputation and issues management outside the US, partnering with Legal, Regulatory, Medical Affairs, Compliance, Market Access and International Leadership team. Serve as regional lead for issues escalation: define the threshold at which an in-market issue becomes a global one, and who speaks at each stage. Govern the boundary where US-compliant content becomes non-compliant in-market: corporate website territory gating, social [. .. ]

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Job vor 12 Tagen bei Mindmatch.ai gefunden Bridge Bio Pharma Director, Patient Advocacy, International • AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] 20 drug development programs, ranging from early discovery to late-stage clinical trials, across multiple therapeutic areas including precision oncology, cardiology, endocrinology, neurology, and renal disease. We have [...]
MEHR INFOS ZUM STELLENANGEBOT[...] already achieved regulatory approval for three therapies and continue to advance promising science from academia into meaningful treatments for patients worldwide. Who We Are Bridge Bio is a global biotechnology company with our Global Headquarters located in San Francisco, USA, and our International HQ located in Zug, Switzerland. Since establishing our European presence [. .. ] decision-making. The Director oversees external international partnerships and educational initiatives, strengthening meaningful outreach across the region. As a strategic cross-functional partner, this leader collaborates with clinical development, medical affairs, commercial, and market access teams to integrate authentic patient perspectives into planning and execution. The role also champions a patient-focused culture within the international organization by elevating international community insights and ensuring regional perspectives inform strategy. Resposanbilities Develop and execute a comprehensive international patient advocacy and engagement strategy aligned [. .. ] into internal communications, programming, and regional initiatives. Maintain expertise in relevant healthcare policy and industry regulations governing patient advocacy engagement and ensure compliant execution of all external activities. Demonstrate strong executive presence and leadership, serving as a trusted advisor internally and externally while representing Calcilytix within the hypoparathyroidism community. The above job description documents the general nature and level of work but is not intended to be an exhaustive list of activities, duties, and responsibilities required of job incumbents. Therefore, job [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden SOPHiA GENETICS Senior Program Leader (IVd/CDx) • AT- 2 Lavamünd Führungs-/ Leitungspositionen Do you bring deep experience in IVD or companion diagnostic product development and a track record of leading complex programs through regulatory approval or pivotal clinical trials? Can you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] align cross-functional teams and biopharma partners around the scientific, regulatory, operational, and commercial milestones needed to deliver diagnostic solutions? If this sounds like you and you are driven by purpose, join the SOPHi A GENETICS Diagnostics Solutions team as a Program Leader and [. .. ] portfolio reviews, business stage gates, design reviews, Joint Steering Committees, and Joint Development Teamsto drive aligned, timely decision-making. Integrate Bioinformatics and Assay Development, Verification and Validation, Clinical Operations, Regulatory Affairs, Quality Assurance, Manufacturing, Product Management, and Biopharma teams around a coherent program strategy, milestones, resources, and shared accountability. Deliver diagnostic programs from requirements definition through product development, verification and validation, regulatory submission, and commercial launch while managing timelines, budgets, risks, resources, and contingency plans. Requirements We know that every background [. .. ] social committee whose purpose is to make SOPHi A GENETICs both enjoyable as well as rewarding As our global HQ, youll have direct interaction and exposure to senior leadership and our executive team locally Our DNA Like the strands of DNA itself, SOPHi A GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient Nimble and Fearlessly Adventurous Our Virtues At [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden Vice President, Regulatory Affairs Führungs-/ Leitungspositionen Develop and execute global regulatory strategies for the companys oncology portfolio Advise executive leadership and the Board of Directors on regulatory risks, opportunities, timelines, and competitive landscape considerations [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Establish regulatory strategies supporting global market expansion and lifecycle management Lead interactions with FDA, EMA, MHRA, PMDA, Health Canada, and other global regulatory agencies Serve as the principal regulatory representative in key agency meetings Direct [. .. ] regulatory expertise to corporate strategy, investor communications, and strategic planning Requirements Advanced degree in a scientific discipline required Ph D, Pharm D, MD, or equivalent strongly preferred 15+ years of progressive Regulatory Affairs experience or related experience within biotechnology and/or pharmaceutical organizations Significant experience leading regulatory strategy for late-stage clinical development Oncology and combination product development preferred Demonstrated success leading NDA, BLA, MAA, or equivalent global registration submissions and approvals Deep knowledge of U. S. and international regulatory frameworks governing drug [. .. ]

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Job vor 7 Tagen bei Jobleads gefunden Group General Counsel (f/m/d) • Starnberg, Bayern [. .. ] 15 sites. Our site in Starnberg is the headquarters of the Aenova Group. Your key responsibilities The Company seeks a Group General Counsel with overall responsibility for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the companys legal affairs, corporate governance and compliance. The General Counsel serves as a trusted advisor to the senior management and board and with a team of 10 colleagues supports the business group-wide in contract discussions with customers and suppliers, litigations, corporate affairs and other legal matters; he/ she also oversees compliance. The GC reports to the Chief Financial Officer and is based at the companys head office in Starnberg near Munich. More specifically, responsibilities include: Act as business partner and advisor to Executive Leadership Team on corporate, commercial, contractual, regulatory, and strategic matters incl. growth projects and corporate initiatives Manage external legal counsel, and support M A, strategic partnerships, licensing transactions, and dispute resolution Oversee the negotiation, drafting, and management of complex international agreements, including manufacturing, development, technology transfer, supply, procurement, real estate, IP, licensing, quality agreements Lead corporate governance [. .. ]

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Job am 30.08.2026 bei Jobleads gefunden Group General Counsel (f/m/d) • Percha, Bayern [. .. ] 15 sites. Our site in Starnberg is the headquarters of the Aenova Group. Your key responsibilities The Company seeks a Group General Counsel with overall responsibility for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the companys legal affairs, corporate governance and compliance. The General Counsel serves as a trusted advisor to the senior management and board and with a team of 10 colleagues supports the business group-wide in contract discussions with customers and suppliers, litigations, corporate affairs and other legal matters; he/ she also oversees compliance. The GC reports to the Chief Financial Officer and is based at the companys head office in Starnberg near Munich. Act as business partner and advisor to Executive Leadership Team on corporate, commercial, contractual, regulatory, and strategic matters incl. growth projects and corporate initiatives Manage external legal counsel, and support M A, strategic partnerships, licensing transactions, and dispute resolution Oversee the negotiation, drafting, and management of complex international agreements, including manufacturing, development, technology transfer, supply, procurement, real estate, IP, licensing, quality agreements Lead corporate governance [. .. ]

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Wieviel verdient man als Regulatory affairs executive pro Jahr?

Als Regulatory affairs executive verdient man zwischen EUR 60.000,- bis EUR 100.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Regulatory Affairs Executive Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 129 offene Stellenanzeigen für Regulatory Affairs Executive Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Regulatory Affairs Executive Jobs?

Aktuell suchen 16 Unternehmen nach Bewerbern für Regulatory Affairs Executive Jobs.


Welche Unternehmen suchen nach Bewerbern für Regulatory Affairs Executive Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Regulatory Affairs Executive Stellenangebote:


  • Novartis (2 Jobs)
  • Phia LLC (2 Jobs)
  • NEVEON Executive Committee (2 Jobs)
  • MADx Macro Array Diagnostics GmbH (2 Jobs)
  • SOPHiA GENETICS (2 Jobs)
  • Bridge Bio Pharma (2 Jobs)


In welchen Bundesländern werden die meisten Regulatory Affairs Executive Jobs angeboten?

Die meisten Stellenanzeigen für Regulatory Affairs Executive Jobs werden derzeit in Bayern (21 Jobs), Berlin (12 Jobs) und Nordrhein-Westfalen (7 Jobs) angeboten.


Zu welchem Berufsfeld gehören Regulatory Affairs Executive Jobs?

Regulatory Affairs Executive Jobs gehören zum Berufsfeld Regulatory Affairs & Management.


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Dauer: 0.0418 s., Vers. V.2025-d-2009-Ind-141