249 Jobs für Pharmaceutical Regulatory Manager
Stellenangebote Pharmaceutical Regulatory Manager Jobs
Neu Job vor 3 Std. bei StepStone gefunden
CHEPLAPHARM Arzneimittel GmbH
• Berlin, Greifswald
Führungs-/ Leitungspositionen Homeoffice möglich
We are a global and growing specialty
pharmaceutical company with an exceptional, sustainable business model. Our mission: to be THE platform for established and trusted branded products in various therapeutic [...]
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[...] areas and indications and to ensure their availability in the highest quality as an important partner of the innovation-driven pharmaceutical industry for the global market We have [. .. ] due diligence and alignment of teams on common goals, plans and timelines. Lead Cross-Functional Execution and Accountability Leading a diverse team from M A, IMO, Commercial, Finance, Supply Chain, Regulatory Affairs, Quality, Medical and Legal (different departmends) . Coordinating all workstreams for regulatory approvals, CMO onboarding, tech transfers as well as production and delivery within deadlines. Identification and implementation of timeline optimizations and escalation of important topics to leadership. Manage Key External Stakeholders The Integration Project Manager is ultimately accountable for ensuring external stakeholders Divestment Partner, Contarct Manufacturing Organizations, Sales and Distribution Partners are effectively managed and aligned with integration objectives. Own Issue Resolution and Decision-Making Take active ownership of issue identification, resolution, and escalation. Navigate complex interdependencies, competing priorities, and market-specific challenges (e. g. [. .. ]
Neu Job vor 3 Std. bei StepStone gefunden
CHEPLAPHARM Arzneimittel GmbH
(Senior) Sales Alliance Manager Asia Pacific (m/f/d)
• Berlin, Greifswald
Homeoffice möglich
Work-Life-Balance
We are an owner-managed, globally active company in the specialty pharmaceuticals sector with a clear mission: to be THE sustainable platform for long-established and trusted
pharmaceutical brand products in various [...]
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[...] therapeutic areas. As a reliable partner to the research-based pharmaceutical industry, CHEPLAPHARM ensures the availability and supply of these medicines for the global market. This benefits not only our partners, but also patients around the world. We are proud that our specialised business model has [. .. ] commercial plans and recommendations. Enable Strategic Integration of Acquisitions Drive the strategic and sustainable integration of newly acquired products into the regional distribution network. Collaborate closely with internal stakeholders including Regulatory Affairs, Supply Chain, Marketing and other relevant functions to ensure seamless market entry and continuity. Ensure Compliance and Governance Excellence Ensure full compliance with American pharmaceutical regulations as well as distributor agreements. Monitor distributor performance and adherence to contractual and industry standards, proactively addressing risks and deviations. Manage Key Stakeholders [. .. ] to personal goals, as well as company and team events to strengthen cohesion and celebrate successes together. . CHEPLAPHARM Arzneimittel Gmb H sucht in Berlin, Greifswald eine/n (Senior) Sales Alliance Manager Asia Pacific (m/f/d) (ID-Nummer: 13994230) 91239501 [. .. ]
Neu Job vor 3 Std. bei StepStone gefunden
CHEPLAPHARM Arzneimittel GmbH
• Berlin, Greifswald
Homeoffice möglich
Work-Life-Balance
We are an owner-managed, globally active company in the specialty pharmaceuticals sector with a clear mission: to be THE sustainable platform for long-established and trusted
pharmaceutical brand products in various [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapeutic areas. As a reliable partner to the research-based pharmaceutical industry, CHEPLAPHARM ensures the availability and supply of these medicines for the global market. This benefits not only our partners, but also patients around the world. We are proud that our specialised business model has [. .. ] commercial plans and recommendations. Enable Strategic Integration of Acquisitions Drive the strategic and sustainable integration of newly acquired products into the regional distribution network. Collaborate closely with internal stakeholders including Regulatory Affairs, Supply Chain, Marketing and other relevant functions to ensure seamless market entry and continuity. Ensure Compliance and Governance Excellence Ensure full compliance with American pharmaceutical regulations as well as distributor agreements. Monitor distributor performance and adherence to contractual and industry standards, proactively addressing risks and deviations. Manage Key Stakeholders [. .. ] tailored to personal goals, as well as company and team events to strengthen cohesion and celebrate successes together. . CHEPLAPHARM Arzneimittel Gmb H sucht in Berlin, Greifswald eine/n Sales Alliance Manager Eastern Europe (m/f/d) (ID-Nummer: 13994234) 91264285 [. .. ]
Job vor 3 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
Supply Chain Specialist (f/m/d)
• Monheim
Angebote von Zeitarbeitsunternehmen Homeoffice möglich
Time for change time for a new job You are a supply chain
manager and looking for a new professional challenge? Then stop searching We offer the job you are [...]
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[...] looking for: Our subsidiary Randstad professional solutions offers a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Monheim. Apply online now We welcome applications from all suitably qualified persons regardless of any disabilities. Prepare sales forecasts and lead monthly demand meetings with stakeholders Plan and execute special promotions with Marketing/ Product Managers Ensure effective material flow in the supply network Process customer returns, credit, and [. .. ] continuously monitor stock coverage and expiration dates Analyze product portfolio for optimization potential Maintain, improve, and develop KPIs and KPI dashboards Support and coordinate packaging changes with Master Planning and Regulatory Drive/ assist the development of new processes whilst ensuring compliance with local and global requirements Strong knowledge of supply chain processes, including demand planning, inventory management, and logistics Good understanding of Gx P regulations and compliance requirements Proficiency in using supply chain management software and tools Effective communication skills, both written [. .. ]
Job vor 4 Tagen bei StepStone gefunden
K. D. Pharma Bexbach GmbH
• Bexbach
[. .. ] 3 fatty acids. This enables KD Pharma Group to provide tailored solutions, allowing each customer to differentiate themselves from competitors in the global marketplace. In this key [...]
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[...] role as IT Manager, you will be responsible for the sites entire IT and OT (Operational Technology) landscape and will drive the digital transformation forward. You lead and motivate an IT team and promote their ongoing development in an agile work environment. You are responsible for the local infrastructure, Active Directory, and our cloud [. .. ] in production. You develop the IT strategy for the site and ensure that local requirements align with the global standards and objectives of the corporate group. You ensure compliance with regulatory requirements (e. g. , CSV/ Computer System Validation: GAMP 5, FDA 21 CFR Part 11, EU-GMP Guideline Annex 11) and protect both office and production IT against cyber risks. You serve as the link to production and are responsible for IT support of the manufacturing environment. In this role, [. .. ] an IT specialist in system integration, or several years of professional experience with solid IT expertise. Several years of management experience in IT, ideally in a manufacturing company in the pharmaceutical or life sciences sector. In-depth knowledge of modern infrastructure technologies (virtualization, SD-WAN, hybrid cloud architectures) . Experience with ERP systems is a plus. Confident handling of validation processes and regulatory standards. Ability to translate complex global requirements into pragmatic local solutions. A thinker with a hands-on mentality. [. .. ]
Job vor 8 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
Clinical Trial Manager (f/m/d)
• Biberach an der Riß
Angebote von Zeitarbeitsunternehmen
Our mission: We bring people together Our subsidiary Randstad professional solutions is currently offering an attractive position as CTSU trial
manager with one of our customers-a
pharmaceutical company [...]
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[...] in Biberach. A fair compensation and personal support are of course included. You have a masters degree in natural science? Then you are a perfect match for us we look forward to hearing from you Apply online now We welcome applications from all suitably qualified persons regardless of any [. .. ] the responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs Provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies Support investigations as Subject Matter Expert for assigned trials Masters degree in natural sciences or similar disciplines or completed vocational training with experience [. .. ]
Job vor 8 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
• Ludwigshafen am Rhein
Beratungs-/ Consultingtätigkeiten Angebote von Zeitarbeitsunternehmen
Time for change time for a new job You are a
regulatory affairs specialist and looking for a new professional challenge? Then stop searching We offer the job you [...]
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[...] are looking for: Our subsidiary Randstad professional solutions offers a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Ludwigshafen. Apply online now We welcome applications from all suitably qualified persons regardless of any disabilities. Provide support to complete product dossiers, technical files and responses to information requests Coordinate and complete documents required by federal agencies, incl. maintaining complex files and electronic document management systems Work with [. .. ] scheme contribution after the end of the probationary period A wide range of employee benefits/ perks. Randstad Deutschland Gmb H Co. KG sucht in Ludwigshafen am Rhein eine/n Regulatory Affairs Manager (f/m/d) (ID-Nummer: 13982464) . Appcast 90265014 [. .. ]
Job vor 9 Tagen bei StepStone gefunden
Du Pont de Nemours (Luxembourg) S. . r. l.
Global Application Development Manager Tyvek Roll Goods f/m
• Luxemburg
[. .. ] from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the worlds most talented people are choosing to work at Du Pont. [...]
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[...] Global Application Development Manager Tyvek Roll Goods f/m Senior Leadership Position Global Scope Location: Luxembourg About Du Pont Healthcare Water Du Pont Healthcare Water is globally recognized for advanced materials and solutions in the medical, pharmaceutical, and water industries. The company specializes among others in healthcare packaging, personal protective equipment and consumer and industrial solutions notably with its Tyvek brand, aiming to improve safety health, innovation, and sustainability. 1. Strategic Technical Business Leadership Define the global Application Development vision and strategy for Tyvek Roll Goods. Partner [. .. ] Global Application Development Technical Service Oversee worldwide execution of technical service, application development, and technical customer engagement. Ensure rigor, consistency, and technical excellence across all regions. Direct compliance with QMS, regulatory expectations, and industry standards. Represent Du Pont in key global technical bodies, influencing industry norms and future regulatory frameworks. 3. Drive the Short Term Innovation Portfolio Identify, prioritize, and execute renewal and growth initiatives in established applications and markets. Oversee global VOC processes and competitive assessments to fuel the innovation [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Amplity
• AT- 9 Wien
[. .. ] Site Engagement (GPSE) Reports to Program Director, Amplity Health Location Home based anywhere in Germany or Austria Territory DACH, Israel, Turkey, 60 travel Therapeutic Areas Oncology and [...]
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[...] Neurology Individual or Manager Individual We are seeking an experienced Clinical Trial Liaison (CTL) to lead site engagement strategies and patient-focused initiatives. Join a dynamic team dedicated to improving operational excellence and inclusivity in clinical trials, while building strong relationships with healthcare providers and key opinion leaders (KOLs) . Key Responsibilities Develop peer-[. .. ] airport. Fluent in English and German. Preferred Solid tumor/ targeted therapy experience and a proven track record of success. Knowledge of healthcare environments and external experts in academia. Familiarity with regulatory requirements for field-based personnel. About Us Amplity powers biopharma innovation through expert-led teams that deliver. Whether you knew us in the 80s as Physician Detailing Inc. , or in the 00s as part of Publicis Health, the companies that came together in 2019 to form Amplity have delivered contract medical, commercial + communications excellence for 40+ years. Our people-driven, tech-enabled DNA fuels everything we do. Our professionals understand the pharmaceutical industry from the inside out. With a deep grasp on product lifecycles, marketing hurdles, operational nuances + the complex needs of providers and patients, we help our clients launch products + operate smoothly with precision across all business shapes, sizes + specialties. We are on a mission to improve patient [. .. ]
Job gestern bei Mindmatch.ai gefunden
Chiesi Farmaceutici S. p. A.
Pharmaceutical Affairs Manager All genders Full-time
• AT- 9 Wien
Pharmaceutical Affairs
Manager All genders Full-time Date: 5 May 2026 Department: Pharmaceutical Affairs Business Area: R D, Pharmacovigilance
Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary [...]
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[...] Location: Vienna, AT fixed-term employment contract (approx. 1 to 1.5 years) You will be responsible for Managing the Change Control process, including evaluation, coordination, and documentation of changes Updating, maintaining, and harmonising SOPs, including the implementation of global procedures into [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
• AT- 9 Wien
[. .. ] you will be responsible for onsite and remote monitoring activities, ensuring protocol adherence, data integrity, and subject safety. You will work closely with investigational sites and internal [...]
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[...] teams to oversee regulatory documentation, ethics committee and hospital submissions at site level, and trial conduct in accordance with SOPs, ICHGCP, and applicable regulatory requirements. All activities are performed with a strong focus on quality, inspection readiness, and timely delivery. If you enjoy working in a dynamic clinical research environment and want to contribute [. .. ] required by project needs What you bring to the table: 3+ years of Clinical Research Associate (CRA) experience in clinical monitoring and an advanced degree in Life Sciences, Medical, or Pharmaceutical studies, or an equivalent combination of education and experience Proven experience with regulatory authority, ethics committee, and hospital submissions Willingness and motivation to expand into clinical project manager responsibilities Excellent command of English (written and spoken) and working proficiency in German (B2 level or higher) Good teamwork skills Problemsolving skills Results and detailoriented approach to work delivery and output Ability to prioritize own workloads to meet deadlines Strong software and computer skills, including MS Office applications Ability to [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Mundipharma International
Associate Quality Manager (f/m/d)
• AT- 9 Wien
Associate Quality
Manager-FTC Location: Vienna, Austria (Hybrid) Department: Quality Assurance Job type: 12-month Fixed-Term Contract Join us and make a difference when it matters most At Mundipharma, we are [...]
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[...] proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, [. .. ] our employees. The Team We are looking for an Associate Quality Manager to join Mundipharma on a 12month fixedterm contract. In this role, you will support and maintain a robust pharmaceutical Quality Management System in line with the Austrian Medicines Act (AMBO) and EU GDP/ Gx P guidelines, covering Austria and selected CEE markets. You will work closely with crossfunctional and regional stakeholders and play a handson role in daytoday quality operations. This is an excellent opportunity to deepen your experience in [. .. ] Resolution and support the management of regional quality issues, including complaints, product recalls, and returns. Audit Management-Lead the preparation and support for internal and external GDP/ GMP audits and regulatory inspections. QMS Development-Maintain and evolve the Quality Management System in accordance with EU GDP/ GMP guidelines and national legislation. Quality Controls-Manage deviations, CAPAs, change controls, and conduct thorough quality risk assessments. Oversee technical documentation Quality/ Technical Agreements, pharmaceutical licenses, and ensure rigorous document control. Develop and maintain core [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Mundipharma
• AT- 9 Wien
Associate Quality
Manager-FTC Location: Vienna, Austria (Hybrid) Department: Quality Assurance Job type: 12-month Fixed-Term Contract Join us and make a difference when it matters most At Mundipharma, we are [...]
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[...] proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare [. .. ] our employees. The Team We are looking for an Associate Quality Manager to join Mundipharma on a 12month fixedterm contract. In this role, you will support and maintain a robust pharmaceutical Quality Management System in line with the Austrian Medicines Act (AMBO) and EU GDP/ Gx P guidelines, covering Austria and selected CEE markets. You will work closely with crossfunctional and regional stakeholders and play a handson role in daytoday quality operations. This is an excellent opportunity to deepen your experience in [. .. ] Resolution and support the management of regional quality issues, including complaints, product recalls, and returns. Audit Management-Lead the preparation and support for internal and external GDP/ GMP audits and regulatory inspections. QMS Development-Maintain and evolve the Quality Management System in accordance with EU GDP/ GMP guidelines and national legislation. Quality Controls-Manage deviations, CAPAs, change controls, and conduct thorough quality risk assessments. Oversee technical documentation Quality/ Technical Agreements, pharmaceutical licenses, and ensure rigorous document control. Develop and maintain core [. .. ]
Job am 22.04.2026 bei Mindmatch.ai gefunden
Novartis
Supply Chain Manager-Global Clinical Supply
• AT- 7 Langkampfen
Role Purpose The Supply Chain
Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished Good (CFG) to Drug Substance (DS) and Booklet labels, ensuring demand fulfillment [...]
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[...] for assigned projects. The SCM acts as a key contributor to the Clinical Supply Operations Planning (CS OP) process in TRd/GCS and provides transparency on supply [. .. ] supply strategy of CHAd/PHAd/Biologics. Participates in the GPMM along with the CSPL and CTSM ensuring alignment between demand and supply. Ensures demand fulfillment and coverage of supply and regulatory aspects by contributing to GCS agenda at TRD Sub team CMC meeting. Represents GCS at TRD Subteam on supply chain aspects. Actively contributes to the portfolio manufacturing schedule alignment (from DS to CFG) and defines most costefficient ordering levels from CFG to DS, minimizing waste and allowing flexibility to accommodate [. .. ] Integrates Comparator supply strategy into the TRD procurement, blinding release planning. Minimum Requirements Degree in science, engineering or equivalent. Fluent English. More than 5 years of practical experience in chemical/ pharmaceutical industry or more than 3 years of experience in field of expertise. Good expertise in related field. Good knowledge about the Drug Development process. Basic project management, good organization and planning skills. Knowledge of relevant regulations (e. g. , GMP, HSE, etc. ) and Novartis specific standards. Demonstrates problemsolving and [. .. ]
Job am 22.04.2026 bei Mindmatch.ai gefunden
Merck Gesellschaft mbH
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] sectors in Austria. In this role you will also work closely with the EU Regional Market Access Pricing function and Regional Government Affairs team. You will support [...]
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[...] the Country General Manager across the following functional domains and serve as a strong business partner to the Business Unit Heads, Country Medical Director, Regulatory Affairs, and other internal stakeholders. Market Access Pricing (MAP) Develop and implement an integrated market access strategy outlining the key priorities, plans and actions incl. external engagement Develop pricing access strategies for launch and in-line brands in collaboration with the business units and the EMEA region Provide MAP input [. .. ] of a communication strategy for the affiliate, aimed at driving internal engagement, but also raising the profile of Merck externally Who You Are: 10+ years of relevant experience in the pharmaceutical industry with a minimum 5 years in market access pricing and governmental affairs roles Graduate degree in healthcare, law or life science, ideally complemented with a graduate degree in management Fluency in written and spoken German and English language Experience in business partnering with members of a Country Leadership Team [. .. ]
Job am 20.04.2026 bei Mindmatch.ai gefunden
Biogen, Inc.
Manager, Standards Governance (f/m/d)
• AT- 9 Wien
Manager, Standards Governance (f/m/d) page is loaded # # Manager, Standards Governance (f/m/d) remote type: On Campuslocations: Vienna, Austriatime type: Full timeposted on: Posted Todayjob requisition id: REQ22811For our [...]
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[...] office in Vienna (hybrid working model) , we are recruiting for a Manager, Standards and Governance (f/m/[. .. ] both branded and non-branded local materials adhere to applicable laws, regulations, codices and aligning with marketing authorizations. This role is crucial in maintaining Biogens commitment to ethical standards and regulatory compliance, fitting seamlessly into the broader business structure and contributing to its overall success. What Youll Do : Own and drive improvements in Standards Governance processes to ensure compliant business operations in Austria. Serve as the primary point of contact for compliance-related questions and execution in line with Biogen [. .. ] in Pharmacy or equivalent (scientific studies) . Minimum 5 years of experience, consisting of at least 3 years of relevant experience in Medical Affairs, Regulatory Affairs or Compliance in the Pharmaceutical Industry. Knowledge of the Austrian AMG (Medicinal Products Act) and Co C. Strong understanding of compliance and governance frameworks. Preferred Skills : Prior experience in the field of Compliance. Familiarity with transparency reporting processes. Effective communication and collaboration skills. Minimum annual gross salary of 76.000, 00, depending on qualification and [. .. ]
Job am 14.04.2026 bei Mindmatch.ai gefunden
Novartis
• AT- 7 Langkampfen
A leading
pharmaceutical company located in Langkampfen, Austria, is seeking a Quality Assurance
Manager to ensure compliance with
regulatory requirements and internal quality standards. The ideal candidate [...]
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[...] will provide support to operational activities, manage quality initiatives, and assist with health authority inspections. A strong background in quality management systems and Gx P is required, along with fluency in German and English. The minimum salary is 65, 605.54/ year, with [. .. ]
Job am 13.04.2026 bei Mindmatch.ai gefunden
AOP Health
Senior Associate Serialization
• AT- 9 Wien
Homeoffice möglich
[. .. ] looking for a: We are looking for a Senior Associate Serialization who ensures the compliant and efficient execution of serialization processes in accordance with EU FMD, DSCSA, [...]
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[...] and other applicable regulatory requirements. What Your Day To Day Will Look Like Execute and monitor serialization processes in compliance with EU FMD, DSCSA, and countryspecific regulations Act as a user for serialization IT systems (e. g. , Avarto, Tracekey, Melior, LS Pedia) , ensuring secure, stable, and compliant system functionality Support managing and [. .. ] Your Qualifications And Experience Degree in Business Administration, Information Technology, Supply Chain Management, Life Sciences, or comparable qualification Experience with serialization systems or complex database systems preferred Basic understanding of pharmaceutical serialization regulations (EU FMD, DSCSA) preferred Good knowledge of Gx P requirements and validation principles Analytical mindset and strong data accuracy Structured, independent, and solutionoriented working style Strong communication skills and ability to work crossfunctionally Fluent in English (German advantageous) Our offer An open corporate culture with the opportunity to contribute [. .. ] Flexible working hours Laptop Initial and continuing education Canteen Good transport connection Employee events Meal allowance Company doctor Parking spot Health measures Employee discount Your Contact Kenny Trappl Talent Acquisition Manager J-18808-Ljbffr 88491270 [. .. ]
Job am 12.04.2026 bei Mindmatch.ai gefunden
Astrazeneca
• AT- 9 Wien
[. .. ] also active in over 100 countries. As an Austrian sales company, we set new, creative standards in market cultivation and strive for scientific leadership in the domestic [...]
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[...] market. As Brand Manager COPD Biologics you can contribute your ideas and skills with enthusiasm and competence to improve patients lives in the fields of COPD. Your tasks As Brand Manager you will drive the commercialization of two brands in Austria by developing and implementing the marketing strategy and operational marketing mix and tactics [. .. ] share digital trends within and out of pharma. Identify scale up projects from other markets, implement, and share best practices. Your profile Experience in Marketing or Sales Experience in the pharmaceutical industry is a strong plus Good strategic and analytical qualities Hands-on experience in implementing delivering marketing campaigns with digital assets/ channels. Good project management skills Excellent ability to work in a team and experience in building networks Exceptional communication skills Open mindset to break new ground to drive business [. .. ] With approximately 90, 000 people in 85 countries, our aim is simple: to unlock the power of what science can do, for people, society and the planet. From Clinical Development, Regulatory and Medical Affairs to Finance, IT, Digital, Manufacturing and Supply, the opportunities to make an impact are limitless. Our workforce reflects the diversity of the patients we serve it is embedded in everything we do. Were at our best and most creative when we seek out different perspectives, experiences and [. .. ]
Job am 06.04.2026 bei Mindmatch.ai gefunden
IQVIA
Brand Manager-Specialty Care (Immunology GI)
• AT- 9 Wien
IQVIA is recruiting a Brand
Manager to act as the brand lead for one or more specialty care brands on behalf of one of our
pharmaceutical partners. This [...]
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[...] role offers the opportunity to take ownership of brand strategy and execution for medicines promoted within specialist healthcare settings, operating in a multicountry, matrix environment. The assigned brand (s) sit within a broader partner portfolio spanning immunemediated and inflammatory diseases, including a mix of injectable biologics and oral [. .. ] and campaigns Lead multichannel/ omnichannel marketing initiatives across field, digital, congress and remote channels Ensure consistent, compliant brand storytelling across all customer touchpoints Work closely with Sales, Medical, Market Access, Regulatory, Legal/ Compliance and Operations teams Collaborate with partner stakeholders to ensure alignment and highquality execution Support field teams with approved brand materials and messaging Manage agencies and vendors, including briefing and delivery of marketing assets Own brandlevel budgets, forecasts and spend tracking Monitor performance against KPIs, including campaign effectiveness and [. .. ]
Job am 05.04.2026 bei Mindmatch.ai gefunden
IQVIA
Brand Manager Specialty Care-Rheumatology Gastroenterology
• AT- 9 Wien
IQVIA is recruiting a Brand
Manager to act as the brand lead for one or more specialty care brands on behalf of one of our
pharmaceutical partners. This [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role offers the opportunity to take ownership of brand strategy and execution for medicines promoted within specialist healthcare settings, operating in a multicountry, matrix environment. The assigned brand (s) sit within a broader partner portfolio spanning immunemediated and inflammatory diseases, including a mix of injectable biologics and oral [. .. ] and campaigns Lead multichannel/ omnichannel marketing initiatives across field, digital, congress and remote channels Ensure consistent, compliant brand storytelling across all customer touchpoints Work closely with Sales, Medical, Market Access, Regulatory, Legal/ Compliance and Operations teams Collaborate with partner stakeholders to ensure alignment and highquality execution Support field teams with approved brand materials and messaging Manage agencies and vendors, including briefing and delivery of marketing assets Own brandlevel budgets, forecasts and spend tracking Monitor performance against KPIs, including campaign effectiveness and [. .. ]
Job am 15.03.2026 bei Mindmatch.ai gefunden
Tetra Science
Senior Technical Program Manager-Vienna, Austria
• AT- 9 Wien
[. .. ] to company and team building. If you join us, you will be expected to embody its contents each day. Who You Are Tetra Science is seeking an [...]
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[...] elite Technical Program Manager dedicated to a single, high-profile account in Vienna, Austria. In this role, you will drive urgency and focus across both Tetra Science and our customer partnereveryday matters as you lead a first-of-its-kind program to productize scientific data and use cases. You are a customer-obsessed leader [. .. ] end goal of leveraging AI/ ML for improved scientific outcomes. An understanding of how scientific data underpins AI/ ML model training and deployment. Working knowledge of Gx P compliance and related regulatory frameworks (e. g. , GMP, GLP) . Ability to distill and communicate complex technical and scientific information to audiences ranging from delivery teams to VP-and C-level stakeholders. Demonstrated capability to effectively engage in customer-facing leadership conversations, influencing outcomes and maintaining alignment with strategic objectives. 5+ years of experience with public cloud (AWS, GCP, or Azure) or enterprise software environments. Join Us If Youre energized by the prospect of defining how the worlds largest pharmaceutical companies will operate in the AI era. This is more than just program management; it is industrial transformation with the potential to accelerate life-saving drug development for billions of people. 100 employer-paid benefits for all eligible employees and immediate family members Unlimited paid time off (PTO) 401K Company [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• AT- 9 Wien
[. .. ] Travel: More than 50 Requisition ID: 13617 Position Summary The Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance [...]
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[...] with applicable regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate data accuracy and subject safety required by review of regulatory documents, medical records, reported data and device storage, [. .. ] in respect to safetyrelated documents used and to safety event reporting processes. Collects local data protection requirement information and reports to CPM prior to study start. Assists the Clinical Project Manager department and studyrelated projects as requested including inhouse audits, investigator meetings, training, etc. Conducts comonitoring with Clinical Studies personnel to confirm monitoring is conducted consistently with the protocol, department SOP, WIs and monitoring plans and regulatory standards. Oversees training of newly hired Clinical Studies personnel and provides leadership performing daytoday [. .. ] degree in life sciences, nursing or other health related disciplines or a comparable qualification. Minimum two years of onsite monitoring research experience as a CRA in the medical device or pharmaceutical industry or with a CRO. High level of attention to detail and strong organizational ability paired with excellent people skills. Excellent clinical trial monitoring skills. Previous knowledge of Vascular Interventional Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to [. .. ]
Job am 09.03.2026 bei Mindmatch.ai gefunden
Rhythm Pharmaceuticals Inc.
Scientific Affairs Manager, Austria
• AT- 9 Wien
[. .. ] GSA team, you will focus on advancing medical and scientific initiatives in Rare MC4R pathway diseases. In close collaboration with the national and international Medical Affairs teams, [...]
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[...] the Scientific Affairs Manager (SAM) will provide scientific leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Austria. Responsibilities and Duties Serve as the Scientific Affairs Manager for Austria and as a member of the international Medical Affairs team. Contribute [. .. ] projects, including identification and training of sites and assistance with patient recruitment. Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements. Collaborate closely with Commercial, Regulatory, Pharmacovigilance and Market Access. Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations. Participate in local medical and cross-functional projects and initiatives. Ensure effective and compliant communication with internal and external stakeholders. Support the commercial team and HCPs with knowledge [. .. ] multidisciplinary care including patient support programs. Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways. Qualifications and Skills Advanced degree in pharmaceutical, scientific, or medical field (Pharm D, Ph D, MD) . At least 6 years of experience in a comparable role within the biopharmaceutical sector, ideally with a focus on rare diseases. Excellent communication skills and scientific expertise, especially in presenting to diverse audiences. Proven skills and ability to work in a cross [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
AOP Health
Manager Medical Information
• AT- 9 Wien
Homeoffice möglich
We are looking for an experienced and scientifically driven Medical Information
Manager to deliver a high-quality, compliant, and insight-driven Medical Information (MI) service globally. You will oversee the global [...]
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[...] medical information management system, ensuring data integrity, regulatory compliance, and operational excellence. What Your Day To Day Will Look Like Provide high-quality, evidence-based responses to medical inquiries, ensuring compliance with regulatory and legal requirements. Conduct literature searches and analyze clinical data to support accurate scientific communication. Develop, review, and maintain Medical Information content (Standard Responses, FAQs) [. .. ] Affairs teams globally. Your Qualifications And Experience Advanced degree in Life Sciences, Pharmacy, or Medicine 5+ years of experience in Medical Information, Medical Affairs, or a related function within the pharmaceutical industry. Strong scientific background with excellent analytical and medical writing skills. Experience working with global teams and external vendors. Familiarity with Veeva Medical Information systems (e. g. , Med Inquiry) is an advantage. Solid understanding of regulatory, pharmacovigilance, and data privacy requirements. Strong communication, presentation, and stakeholder management skills. High [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Regulatory Manager pro Jahr?
Als Pharmaceutical Regulatory Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Regulatory Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 249 offene Stellenanzeigen für Pharmaceutical Regulatory Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Regulatory Manager Jobs?
Aktuell suchen 47 Unternehmen nach Bewerbern für Pharmaceutical Regulatory Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Regulatory Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Regulatory Manager Stellenangebote:
- Biontech (10 Jobs)
- IQVIA (4 Jobs)
- Randstad Professional (4 Jobs)
- CHEPLAPHARM Arzneimittel GmbH (3 Jobs)
- Randstad Deutschland GmbH Co. KG (3 Jobs)
In welchen Bundesländern werden die meisten Pharmaceutical Regulatory Manager Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Regulatory Manager Jobs werden derzeit in Bayern (60 Jobs), Baden-Württemberg (21 Jobs) und Rheinland-Pfalz (21 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Regulatory Manager Jobs?
Pharmaceutical Regulatory Manager Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
