84 Jobs für Pharmaceutical Writing
Stellenangebote Pharmaceutical Writing Jobs
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Johnson Johnson Med Tech
• AT- 9 Wien
[. .. ] of the principles of HTA and health economics Strong track record of successful engagement with clinical and non-clinical stakeholders 3 years experience in the medical devices, health [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] care or pharmaceutical industry, an HTA or payer organization, healthcare consultancy, academic institution, research organization, or another relevant healthcare-system setting. Medtech experience in the relevant locations is required. . Good understanding of the processes within healthcare systems and payer bodies Appetite to build on knowledge and experience of market access and health [. .. ] Commercial Awareness Competitive Landscape Analysis Developing Others Global Market Health Economics Health Intelligence Inclusive Leadership Leadership Market Knowledge Market Opportunity Assessment Operations Management Performance Measurement Pricing Strategies Regulatory Compliance Report Writing Strategic Change Team Management J-18808-Ljbffr 03560548 [. .. ]
Job gestern bei Mindmatch.ai gefunden
State of Oregon
AVP, Quality Systems Compliance
• AT- 2 Lavamünd
[. .. ] Gx P Audit Compliance, Operational Quality Oversight of R D functions, Quality oversight and maintenance of design for medical devices combination products, the end to end (E2E) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complaints management process for pharmaceutical and device products, microbiology, analytical standards management and QMS Operations. Responsibilities Primary Responsibilities include, but are not limited to: Lead Development and Implementation of Quality Strategy and Planning on behalf of both OMS R D Report on significant quality issues to senior management Develop an annual risk-based audit plan [. .. ] processes for which their direct reports are responsible: Updating global quality manual and ensuring the QMS meets the requirements to be compliant, effective and efficient and is appropriately BT enabled Writing global quality standards and procedures Conducting internal and external Site Quality Audits, including, but not limited to, the external API sites Approval of global quality standards Approval of global quality procedures/ Approval of quality directives as required The Quality Compliance Lead chairs the following governance bodies and forums: QMS Council [. .. ]
Job gestern bei Mindmatch.ai gefunden
Johnson Johnson
Manager, Health Economics Market Access (HEMA) , Mid-Sized Markets
• AT- 2 Lavamünd
[. .. ] of the principles of HTA and health economics Strong track record of successful engagement with clinical and non-clinical stakeholders 3 years experience in the medical devices, health [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] care or pharmaceutical industry, an HTA or payer organization, healthcare consultancy, academic institution, research organization, or another relevant healthcare-system setting. Medtech experience in the relevant locations is required. . Good understanding of the processes within healthcare systems and payer bodies Appetite to build on knowledge and experience of market access and health [. .. ] Commercial Awareness, Competitive Landscape Analysis, Developing Others, Global Market, Health Economics, Health Intelligence, Inclusive Leadership, Leadership, Market Knowledge, Market Opportunity Assessment, Operations Management, Performance Measurement, Pricing Strategies, Regulatory Compliance, Report Writing, Strategic Change, Team Management J-18808-Ljbffr 03501198 [. .. ]
Job gestern bei Mindmatch.ai gefunden
8525- Cilag International Legal Entity
Digital Product Owner
• AT- 2 Lavamünd
[. .. ] product development, ensuring alignment with the companys technology strategy and standard processes. Qualifications Required: Bachelors degree in Science, Business, Engineering, or related field. 6+ years of related [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in in pharmaceutical or related industries. Experience in Product Owners roles and adoption of Agile Ways of Working Deep knowledge of Enterprise Document Management Systems and Smart Asset Optimization digital products (i. e. Meridan, Kneat, Solidworks) Preferred: Exceptional time management and prioritization abilities. Strong communication and business partner management skills. A collaborative attitude [. .. ] Skills: Applications Support, Business Requirements Analysis, Collaboration, Consulting, Customer Analytics, Data Science, Data Structures, Digital Fluency, Digital Marketing, Digital Strategy, Emerging Technologies, Global Market, Negotiation, Process Improvements, Product Development, Report Writing, Technical Credibility J-18808-Ljbffr 03498847 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Planet Pharma
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] initiatives. Build strong relationships with external experts, academic collaborators, and CRO partners. Required Qualifications Ph D or MSc in Statistics, Biostatistics, Mathematics, Bioinformatics, or a related quantitative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] discipline. Significant experience in pharmaceutical, biotechnology, or healthcare research environments. Extensive experience supporting biomarker development within clinical drug development programs. Deep understanding of statistical methodologies for biomarker research and precision medicine. Expertise in clinical trial design and analysis. Strong knowledge of regulatory expectations related to biomarker and companion diagnostic development. Advanced proficiency in statistical programming [. .. ] accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. J-18808-Ljbffr 03446195 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
8036 Takeda Pharmaceuticals International AG
Senior/ Process Scientist (f/m/d)
• AT- 2 Lavamünd
[. .. ] to the appropriate leadership or governance forum, providing a clear recommendation and scientific rationale. WHAT YOU BRING TO TAKEDA Education Bachelors or Masters degree in Chemical Engineering, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Biochemical Engineering, Biotechnology, Pharmaceutical Sciences, Life Sciences, or a related technical discipline. Ph D is an advantage. Significant Experience Significant experience in vaccine or sterile Drug Product manufacturing within a GMP environment, with demonstrated accountability for technical process ownership or leadership of complex processscience workstreams. Proven expertise in technology transfer, process validation, PPQ, CPV, process [. .. ] quality, regulatory, supply, timeline, and technicalrisk considerations. Skills Strong scientific and technical judgment, structured problem-solving, and riskbased decisionmaking. Effective stakeholder management, influencing, communication, and project leadership skills. Highquality technical writing and documentation discipline. Proficiency in data analytics, statistical methods, and digital tools; ability to use AIenabled tools appropriately to support process understanding and knowledge management. Fluent English required; additional languages are an advantage. ADDITIONAL INFORMATION International and domestic travel, typically 20 to 30, depending on assigned sites, CMOs, and project [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] Head of Quality Control in accordance with AMBO 9. Representative within internal and authorities inspections for the areas of responsibility. Essential Requirements Master or Ph D (preferred) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in natural science, engineering, pharmaceutical field or equivalent. Experience working with combination products. Minimum 2-4 years of experience in the pharmaceutical industry, preferably with experience in drug-device technical development. Strong track-record of people leadership Proven knowledge and track record in project and program planning and execution Understanding and awareness of regulatory guidelines [. .. ] level of self-motivation, systematic and conscientious way of working. Collaborative spirit, self-driven attitude, high level of learning agility, good listening skills, strategic thinker. Fluent in English (oral and writing) , German is beneficial Benefits Rewards At Novartis, were committed to reimagining medicine together-and rewarding the people who make it happen. You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https:/ /in addition to a market-competitive base salary, [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD
Associate Director, JCA Dossier Content (EU HTA)
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
Job Description Description The Associate Director, Joint Clinical Assessment (JCA) Dossier Content is a role within the Global Medical Value Capabilities (GMVC) EUCAN EEMEA Hub, responsible for developing and
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>writing product specific JCA Dossiers in accordance with the requirements of the EU Regulation on Health Technology Assessment (HTAR) . Actively engage with key stakeholders to facilitate the creation and writing of product specific JCA Dossiers Develop a clear understanding of the JCA Dossier template and associated content requirements as well [. .. ] leverages technical tools and digital solutions to streamline the creation and maintenance of the JCA Dossier Requirements Minimum 5 years experience as an HTA writer or Medical Writer for the
pharmaceutical industry, preferably in an in-house role Prior experience writing large, complex documents and dossiers in English, with required adherence to template guidance Demonstrated ability to integrate complex clinical, statistical, and methodological evidence into clear and scientifically robust text Strong working knowledge of oncology Prior experience working in a Regional [. .. ]
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Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
• AT- 2 Schweiz
[. .. ] continuous improvement and optimization of work processes. Ensure all activities comply with GMP, HSE, and applicable Novartis quality standards. Essential Requirements Masters degree in biotechnology, biochemical engineering, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] biology, chemistry, biochemistry, pharmaceutical technology, chemical engineering, or a related scientific discipline with at least 7 years of relevant industry experience; or Ph D in a relevant field with at least 4 years of relevant industry experience. Proven experience with analytical methods in an industrial or pharmaceutical setting, preferably within biotechnology or biologics development. Strong [. .. ] in analytical development, QC, or a comparable environment. Good theoretical and scientific expertise in relevant analytical technologies such as HPLC, CE, biochemical methods, or comparable techniques. Excellent scientific and technical writing skills, with the ability to prepare clear, submission-ready documentation. Strong proficiency in oral and written English, including effective presentation skills. Demonstrated collaboration and communication skills, with the ability to work effectively across functions and organizational interfaces. Ability to lead and contribute to cross-functional teams in a matrix environment. [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Roche
Digital Biomarker Scientist Parkinsons Disease/ Huntingtons Disease-Freelancer (m/f/d)
• AT- 9 Wien
Freiberuflich
[. .. ] scientific core messages for product marketing Your profile: University degree (Ph. D. or equivalent) in Life Sciences or related field with a minimum of 5 years related [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in the pharmaceutical and digital health industry Track record of writing compelling publications in high impact, peer reviewed journals Knowledge of disease etiology and symptomatology for Parkinsons and Huntingtons Disease Comprehensive understanding of the current state of drug development for Parkinsons and Huntingtons Disease In-depth knowledge of the clinical endpoint landscape and associated challenges in Parkinsons and Huntingtons Disease Overview [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
• AT- 9 Wien
[. .. ] We are seeking an experienced Clinical Project Manager to join our team at Gouya Insights Gmb H Co KG, a clinical development consulting and clinical research services [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] company supporting innovative biotech, pharmaceutical, and medical device companies. As Clinical Project Manager, you will take operational ownership of early-phase clinical studies and development projects, working at the interface between our clients, clinical sites, CROs, specialist vendors, and internal clinical development experts. You will translate clinical development strategies into operational execution, coordinate cross-functional [. .. ] development strategies into executable clinical programs and studies. Our expertise spans clinical and regulatory strategy, study design and scientific advice, clinical operations, CRO and vendor oversight, study conduct, and medical writing. A particular strength of Gouya Insights is our ability to operate at the interface between clinical development strategy and execution. We coordinate sponsors, investigators, sites, CROs, specialist vendors, and clinical experts to deliver operationally feasible, highquality clinical studies. Our international team combines scientific and clinical development expertise with handson operational [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Roche Holding AG
Digital Biomarker Scientist Parkinsons Disease/ Huntingtons Disease-Freelancer (m/f/d)
• AT- 9 Wien
Freiberuflich
[. .. ] scientific core messages for product marketing Your profile: University degree (Ph. D. or equivalent) in Life Sciences or related field with a minimum of 5 years related [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in the pharmaceutical and digital health industry Track record of writing compelling publications in high impact, peer reviewed journals Knowledge of disease etiology and symptomatology for Parkinsons and Huntingtons Disease Comprehensive understanding of the current state of drug development for Parkinsons and Huntingtons Disease In-depth knowledge of the clinical endpoint landscape and associated challenges in Parkinsons and Huntingtons Disease Overview [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] Health Authority communications Lead strategy and execution for INDs, CTAs, NDA/ BLA submissions, MAA filings, amendments, annual reports, and post-marketing commitments Align Clinical, Nonclinical, CMC, Biostatistics, Quality, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Medical Writing teams for major submissions Oversee regulatory documentation for scientific excellence and compliance Drive submission readiness for marketing applications and commercial launch Collaborate on study design, endpoint selection, statistical considerations, global registration strategies, protocols, and major clinical program decisions Provide regulatory guidance for oncology development programs, including rare cancers and orphan [. .. ] 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 and device development Extensive experience interacting directly with FDA [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Medical Consultant
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Jobticket
[. .. ] focus is to provide medical consultation and scientific background for campaigns and projects. It also advises clients and agency members, ensuring the best possible services related to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] high science, medical writing, compliance, and healthcare marketing. Execution of Service: Ensure the professional and timely execution of all requested services, maintaining a high level of scientific expertise and healthcare marketing proficiency. Key responsibilities: Develop a thorough understanding of clients business, brands, and indications. Ensure compliance with health industry standards, company policies, and HWG [. .. ] mindset. Ability to work under time pressure. Above-average commitment. Solution-oriented with a focus on successful results. Diplomatic skills. Benefits/ what we offer: Exciting and varied projects with TOP pharmaceutical companies in diverse sectors and specialist areas. Healthcare communication that is engaging and surprising. Collegial interdisciplinary cooperation at eye level with medical, creative, and consultant team members. Appreciation, recognition, and a strong hands-on mentality within the team. Comprehensive induction with a personal contact person. Global networking and local sovereignty. [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
• Starnberg, Bayern
Führungs-/ Leitungspositionen
[. .. ] responsibility? Then we look forward to hearing from you Excellence beyond manufacturing-thats what we stand for as Aenova, one of the worlds leading contract manufacturers and developers [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for the pharmaceutical industry with 4, 000 employees at 15 sites. Our site in Starnberg is the headquarters of the Aenova Group. Your key responsibilities Serve as a strategic advisor and staff function to the CEO on corporate messaging, reputation management, and stakeholder engagement Define and execute the global Corporate Communication strategy aligned [. .. ] growth strategy, and corporate priorities Build and maintain strong relationships with external PR agencies, communications advisors, and creative partners in the pharmaceutical, biotech, and life sciences industries Lead the development, writing, and publication of the companys annual report, ensuring alignment with corporate strategy, performance, innovation pipeline, sustainability commitments, longterm value creation, and regulatory requirements Drive communication initiatives supporting leadership visibility, corporate transformation, and cultural development to strengthen employee engagement, transparency, and alignment with corporate goals Collaborate with HR to support employer [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
In Vitro Scientist
• Braunschweig, Niedersachsen
[. .. ] the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development [. .. ] of novel testing protocols and overall assay development. Maintain cell lines. Prepare test solutions in accordance with directions. Meticulously maintain precise records in accordance with good laboratory practices. Assist in writing of reports. Follow all PSL safety requirements. Oversees all laboratory assays and day to day procedures. Creates and maintains lab assay schedule. Leads training of In Vitro Scientists. Other duties as assigned. Qualifications B. S. degree or equivalent experience in laboratory animal medicine, toxicology, animal science, or biology is preferred. [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] collaboration with physicians, institutions, and key industry stakeholders. Job requirements Essential 5+ years of experience in B2B marketing, HCP marketing or lead generation, , ideally within the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] German healthcare, international pharmaceutical or Health Tech/ Saa S sectors. Proven track record of developing a B2B marketing function or inbound funnel Proven track record of managing a B2B website and executing multi-channel campaigns (Print, SEA) . Highly analytical mindset: ROI attribution modelling, funnel KPI interpretation, data-driven channel optimisation. Strong writing and editing skills, with an ability to create content that resonates with a business audience/ physicians. Strong project management: juggling multiple campaigns and stakeholders simultaneously in a fast, pilot-driven environment. Native-level German and professional fluency in English (C1) . Desirable Strong command of multi-channel HCP marketing: digital [. .. ]
Job gestern bei Jobleads gefunden
AVP, Quality Systems Compliance
• Luzern
[. .. ] Gx P Audit Compliance, Operational Quality Oversight of R D functions, Quality oversight and maintenance of design for medical devices combination products, the end to end (E2E) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complaints management process for pharmaceutical and device products, microbiology, analytical standards management and QMS Operations. Responsibilities Primary Responsibilities include, but are not limited to: Lead Development and Implementation of Quality Strategy and Planning on behalf of both OMS R D Report on significant quality issues to senior management Develop an annual risk-based audit plan [. .. ] processes for which their direct reports are responsible: Updating global quality manual and ensuring the QMS meets the requirements to be compliant, effective and efficient and is appropriately BT enabled Writing global quality standards and procedures Conducting internal and external Site Quality Audits, including, but not limited to, the external API sites Approval of global quality standards Approval of global quality procedures Approval of quality directives as required The Quality Compliance Lead chairs the following governance bodies and forums: QMS Council [. .. ]
Job gestern bei Jobleads gefunden
• Lavamünd, Kärnten Lavamuend
[. .. ] product development, ensuring alignment with the companys technology strategy and standard processes. Qualifications Required: Bachelors degree in Science, Business, Engineering, or related field. 6+ years of related [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in in pharmaceutical or related industries. Experience in Product Owners roles and adoption of Agile Ways of Working Deep knowledge of Enterprise Document Management Systems and Smart Asset Optimization digital products (i. e. Meridan, Kneat, Solidworks) Preferred: Exceptional time management and prioritization abilities. Strong communication and business partner management skills. A collaborative attitude [. .. ] Skills: Applications Support, Business Requirements Analysis, Collaboration, Consulting, Customer Analytics, Data Science, Data Structures, Digital Fluency, Digital Marketing, Digital Strategy, Emerging Technologies, Global Market, Negotiation, Process Improvements, Product Development, Report Writing, Technical Credibility #J-18808-Ljbffr 03494932 [. .. ]
Job gestern bei Jobleads gefunden
Software Engineering/ Development: Senior PHP Cloud Developer
• Bielefeld, Nordrhein- Westfalen
[. .. ] ecosystem Develop dynamically rendered pages using JS and AJAX data Optimization of application performance and implementation of backend security controls SQL database experience including schema design, table [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] normalization, and the writing of efficient queries Core Requirements: Bachelors degree, computer science preferred, or equivalent combination of education and experience Solid understanding and effective use of sessions Demonstrated experience in technical project management Experience in troubleshooting legacy systems and moving them forward including contributing to the quality assurance process by working to resolve [. .. ] will be discussed with you during the interview process. Canfield Imaging Systems is a division of Canfield Scientific, Inc. , the largest provider of photographic documentation resources and services for pharmaceutical research. #J-18808-Ljbffr 03487383 [. .. ]
Job gestern bei Jobleads gefunden
Senior Product Specialist:Compliance Quality for Regulated Industries-Digital Manufacturig (f/m/d) (Walldorf, DE, 69190)
• Walldorf, Baden- Württemberg
[. .. ] revalidation of DM. Support or implementation of supplier and customer audits and preparation of all required documents Operational transformation of International Organization for Standardization (ISO) content into [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] International Society for Pharmaceutical Engineering (ISPE) GAMP related format Constantly evaluate internal processes and solution capabilities regarding Gx P compliance Develop and deliver on a product vision and roadmap for DM, including AI in a regulated environments What you bring 4+ years experience in consulting, product engineering or management of computerized system validation in regulated [. .. ] MES; SAP DM or related SAP products are a plus Proven expertise in implementing AI in regulated environments. Experience with risk-based validation approaches Strong analytical, planning, coordination, and technical writing skills, with the ability to manage complex activities High affinity for IT solutions and ability to translate complex technical topics into clear, understandable content Fluent English; German is a plus Meet your team The Digital Manufacturing unit is a global, diverse team successfully delivering Cloud/Edge solutions to SAP customers [. .. ]
Job gestern bei Jobleads gefunden
Director, Global Medical Safety Lead
• Genf
Führungs-/ Leitungspositionen
[. .. ] Collaborate closely with Clinical Development, Regulatory Affairs, Medical Affairs and other stakeholders to ensure patient safety remains central to decision making. Key Requirements: MD, MBBS or equivalent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical degree. Significant pharmaceutical or biotechnology industry experience, including substantial experience within Pharmacovigilance/ Drug Safety. Demonstrated expertise in safety signal management, benefit-risk assessment and aggregate safety reporting. About Planet Pharma: Planet Pharma is an American parented Employment Business/ Agency that provides global staffing services with its head-quarters in Chicago and our EMEA [. .. ] accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. #J-18808-Ljbffr 03486925 [. .. ]
Job gestern bei Jobleads gefunden
AVP, Quality Systems Compliance
• Lavamünd, Kärnten Lavamuend
[. .. ] Gx P Audit Compliance, Operational Quality Oversight of R D functions, Quality oversight and maintenance of design for medical devices combination products, the end to end (E2E) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complaints management process for pharmaceutical and device products, microbiology, analytical standards management and QMS Operations. Responsibilities Primary Responsibilities include, but are not limited to: Lead Development and Implementation of Quality Strategy and Planning on behalf of both OMS R D Report on significant quality issues to senior management Develop an annual risk-based audit plan [. .. ] processes for which their direct reports are responsible: Updating global quality manual and ensuring the QMS meets the requirements to be compliant, effective and efficient and is appropriately BT enabled Writing global quality standards and procedures Conducting internal and external Site Quality Audits, including, but not limited to, the external API sites Approval of global quality standards Approval of global quality procedures/ Approval of quality directives as required The Quality Compliance Lead chairs the following governance bodies and forums: QMS Council [. .. ]
Job gestern bei Jobleads gefunden
Digital Products Quality Engineering Lead (all genders)
• Darmstadt, Hessen
Führungs-/ Leitungspositionen
[. .. ] bring at least 10 years of combined experience in software development or engineering, digital transformation, software quality assurance or control, and software quality management, ideally in a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] life-science or pharmaceutical environment. You have experience managing or supervising teams and building quality engineering capabilities through coaching, mentoring, and competency development. You have a strong command of the software product lifecycle, change management, Agile product development, Dev Ops, Lean, Plan-Do-Check-Act, software test automation, cloud platforms, and risk-based quality [. .. ] actions. You are experienced in design reviews, verification activities, reviewing software engineering artifacts and testing evidence, managing defects, maintaining product traceability, and supporting audits or inspections. You communicate clearly in writing and verbally, are confident using tools such as Word, Excel, Power Point, Share Point, and project-planning applications, and are willing to travel globally when required. What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director, JCA Dossier Content (EU HTA)
• Lavamünd, Kärnten Lavamuend
Führungs-/ Leitungspositionen
Job Description Description The Associate Director, Joint Clinical Assessment (JCA) Dossier Content is a role within the Global Medical Value Capabilities (GMVC) EUCAN EEMEA Hub, responsible for developing and
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>writing product specific JCA Dossiers in accordance with the requirements of the EU Regulation on Health Technology Assessment (HTAR) . Actively engage with key stakeholders to facilitate the creation and writing of product specific JCA Dossiers Develop a clear understanding of the JCA Dossier template and associated content requirements as well [. .. ] leverages technical tools and digital solutions to streamline the creation and maintenance of the JCA Dossier Requirements Minimum 5 years experience as an HTA writer or Medical Writer for the
pharmaceutical industry, preferably in an in-house role Prior experience writing large, complex documents and dossiers in English, with required adherence to template guidance Demonstrated ability to integrate complex clinical, statistical, and methodological evidence into clear and scientifically robust text Strong working knowledge of oncology Prior experience working in a Regional [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Writing pro Jahr?
Als Pharmaceutical Writing verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Writing Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 84 offene Stellenanzeigen für Pharmaceutical Writing Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Pharmaceutical Writing Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Writing Stellenangebote:
- Planet Pharma (2 Jobs)
- Novartis (2 Jobs)
- Johnson Johnson Med Tech (1 Job)
- State of Oregon (1 Job)
- Johnson Johnson (1 Job)
- 8525- Cilag International Legal Entity (1 Job)
In welchen Bundesländern werden die meisten Pharmaceutical Writing Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Writing Jobs werden derzeit in Niedersachsen (14 Jobs), Bayern (8 Jobs) und Baden-Württemberg (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs?
Pharmaceutical Writing Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
