148 Jobs für Technical Author
Stellenangebote Technical Author Jobs
Job vor 13 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] readout to the executive sponsor. Architect customer integrations with SAP, Microsoft, Service Now, data warehouses, identity providers and procurement systems; advise on data flows, security and scalability. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Be the trusted technical author on RFPs, RFIs, security questionnaires, DPAs and IT-security reviews. Partner closely with Account Executives on deal strategy, multi-threading and stakeholder mapping; coach AEs on technical talktracks. Feed structured prospect insights back to Product Management what we win with, where competitors outposition us, what we need next on the [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Concentrix
Infrastructure Automation Engineer-(DSC, Powershell Devops)
• Berlin, BE
[. .. ] for hybrid and cloud environments. Responsibilities Engineer and maintain production-grade Power Shell automation (functions, modules, packaging, versioning, release management) with an emphasis on reliability, maintainability, and re-use. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Design, author, and troubleshoot DSC resources and configurations (idempotent behavior; correct Get/ Test/ Set; LCM troubleshooting; drift detection and remediation) . Build and operate CI/ CD pipelines for infrastructure automation using Azure Dev Ops and/or Git Hub (PR workflows, gated builds, artifact publishing, environment promotion) . Work effectively in and with [. .. ] networking basics) , sufficient to automate and troubleshoot them. Microsoft365DSC (preferred) or demonstrable ability to ramp up quickly with prior DSC module/ resource development. Customer-facing delivery: ability to run technical workshops, capture requirements, propose architecture, and deliver/ hand over automation assets in a structured way. Nice-to-have skills Strong hands-on experience with Azure Dev Ops Pipelines and/or Git Hub Actions for Ia C and configuration pipelines (release strategies, approvals, environments) . Hybrid/on-prem platform experience relevant to [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
AT33 (FCRS AT033) Novartis Pharmaceutical Manufacturing GmbH
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
[. .. ] collaboration with Third Parties for the development of pharmaceutical packaging, drug delivery devices and drug-device combination products including the Make vs. Buy strategy in close collaboration with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] GDPD centers, Technical Research Development (TRD) and Technical Operations (Tech Ops) stakeholders across all modalities and technologies, e. g. development and supply of prefilled syringes and autoinjectors for subcutaneous injection, packagings and devices for orals, radioligand therapy and cell and gene therapy. The role establishes effective governance for outsourced work packages and cultivates [. .. ] are inline with Novartis quality standards and relevant regulatory requirements. Lead training and development of personnel on skills and capabilities required for External Partner Management. Support definition of training requirements. Author and participate in the creation and maintenance of EPM related procedures. Initiate/ drive/ support EPM related efficiency gains, e. g. automation of processes. Support internal and external audits on EPM related matters. Essential Requirements: Advanced degree in a life science or related field. Over 10 years experience in pharma/ biotech, [. .. ]
Job gestern bei Mindmatch.ai gefunden
8036 Takeda Pharmaceuticals International AG
Technology Innovation Lead, Process Equipment DP (f/m/d)
• AT- 2 Lavamünd
Job Description About the role: Champion the transformation of process and manufacturing technologies for Takedas Drug Product (DP) network by setting
technical direction, building technology visions and strategies, and enabling [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scalable execution. Provide specialist process, plant and reliability engineering expertise to ensure safe, environmentally sustainable, reliable, cost-effective, and scalable technical solutions for DP manufacturing plants. Translate site and network needs into harmonized best practices, standards, and roadmaps, ensuring solutions meet Regulatory, [. .. ] maintaining acceptable quality. Establish/ lead technology groups and Communities of Practice (Co Ps) to harmonize engineering technologies across sites and ensure sharing and application of best practices and expertise. Own/ author standards, guidelines, templates for DP process equipment technologies; drive consistent interpretation and application across the network. Establish sustained, collaborative communication with the process engineering community to understand site needs, installed standards, rationales, and local constraints. Develop nurture core competencies of site SMEs to build enduring technical capability and knowledge continuity. [. .. ]
Job gestern bei Mindmatch.ai gefunden
Lonza
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] analytical testing strategies, and ensure regulatory and GMP-compliant delivery of project milestones. This role is primarily based on site. Working together in person supports close, realtime collaboration [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20 of your time. Requests are considered on a casebycase basis, in line with business needs. What you will get: An agile career and a dynamic work culture. [. .. ] manage analytical method transfers, ensuring timely implementation of testing to meet customer and project requirements. Implement analytical testing strategies, including method suitability assessments, performance evaluation, control strategies, and specification setting. Author for quality records and c GMP documents e. g. procedures (SOPs) or source documents, reports, deviations, change requests etc. Act as QC subject matter expert during audits, inspections, and customer meetings while ensuring GMP-compliant documentation and regulatory readiness. What we are looking for: Work experience in a GMP-regulated pharmaceutical [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis
Senior Expert, Extractables Leachables-Hybrid, Global Impact
• AT- 2 Schweiz
[. .. ] Technology (Extractables and Leachables) to lead complex strategies across drug development, combining analytical science with regulatory innovation. You will collaborate with global teams, design and oversee studies, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] interpret data, and author technical and regulatory documentation to support safe, effective medicines. Hybrid work is available, with a competitive base salary and benefits. J-18808-Ljbffr 03498559 [. .. ]
Job gestern bei Mindmatch.ai gefunden
Kraken
• AT- 2 Lavamünd
[. .. ] of what arrives is a protocol, API, or primitive that someone has to turn into something the rest of the company can safely use. The opportunity Design [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and build the technical layer of the AI platform, from integration surface to production runbook. Identify capability gaps between whats possible and what the organization can safely use, then close them by evaluating vendors or building internally. Own the governed integration gateway as an engineering surface. Youll handle connector onboarding, authentication flows including OAuth [. .. ] tiered spend controls across the AI estate. Set caps by role and tier, build alerting rules, manage exception queues, run monthly reconciliation against vendor commitments, and eliminate the current single author risk in cap automation. Implement the technical controls behind policy on data handling, retention, and model eligibility. This means identity integration, SSO and SCIM, entitlement by role and tier, and workspace configuration where retention terms differ by model class. Work directly with teams to unblock them. Sit with them, understand [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Allucent
Director, Pharmacometrics
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] hepatic, TQT, ADME, DDI, BE/ BA, SAD, MAD, etc. ) and provide guidance tooptimizepharmacokinetic sampling and dosing strategies Provide strategic guidance to clients, owning deliverables and developing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical pharmacology plans Author and review PK reports and clinical pharmacology sections of regulatory documents Represent clients in regulatory interactions and contribute to business development and relationship management About You If you are a driven clinical pharmacology professional with 610 years of experience in drug development and pharmacometrics and you bring sharp analytical thinking [. .. ] Participation in our enriching Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Access to online soft-skills and technical training via internal platforms Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees J-18808-Ljbffr 03444404 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
• AT- 2 Lavamünd
[. .. ] Device Technology Solution Center is looking for a Senior Expert Engineering to lead the development of innovative drug-device combination products. We from the Device Technology Solution Center [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] drives the technical development of autoinjectors as well as novel drug delivery principles, e. g. on-body injectors, inhalers or radioligand therapy. We closely collaborate with project management, human factors engineers, packaging experts, analytical testing, quality assurance, production, external partners, regulatory experts and many more. The objective is to develop and/or integrate innovative drug delivery systems with drug formulation and author state-of-the-art technical documentation for health authorities and production. Job Description Your responsibilities include, but are not limited to: Provide technical leadership in cross-functional device development subteams for autoinjector and other drug-device combination product development projects Define design input requirements and specifications, and author, review, and [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Roche
Principal Software Development Engineer
• AT- 2 Lavamünd
[. .. ] including feasibility studies, design, implementation, unit testing, debugging, and long-term maintenance. Define, estimate, and execute development work packages within an agile team, ensuring high quality and on-time [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] delivery. Author clear subsystem/unit specifications based on software architecture guidelines and document all steps in compliance with regulatory standards. Design, implement, and review unit/ subsystem code alongside automated tests, conducting peer code reviews to optimize application design, usability, and performance. Continuously improve software workflows, share expertise with junior developers, and advise line and project management on technical solutions. Who you are You hold a degree in Computer Science, Software Engineering, Electrical Engineering, or a related field, specialising in PLC software development. You have solid experience in full-lifecycle software engineering (design, C/ C++, python, PLC structured text programming, testing, and debugging) , ideally in a regulated domain [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
• AT- 2 Schweiz
[. .. ] multidisciplinary teams, influence scientific decision-making, and drive solutions that support the delivery of high-quality medicines to patients around the world. This is an exciting opportunity to apply [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deep technical expertise while helping to redefine how we approach evolving scientific and regulatory challenges. Key Responsibilities Lead Extractables and Leachables strategies and risk assessments across complex drug development projects. Serve as the scientific expert and primary contact for multidisciplinary project teams. Design and oversee Extractables and Leachables studies with internal laboratories and external partners. Interpret analytical data, identify trends, and provide scientifically sound recommendations. Author and review technical documentation, assessments, and regulatory submission content. Drive cross-functional collaboration to solve complex scientific and operational challenges. Lead continuous improvement initiatives that enhance testing approaches, workflows, and risk assessment strategies. Essential Requirements Advanced degree in Pharmacy, Chemistry, Life Sciences, or a related scientific discipline. Strong expertise in [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
Senior Expert Science Technology
• AT- 2 Schweiz
[. .. ] multidisciplinary teams, influence scientific decision-making, and drive solutions that support the delivery of high-quality medicines to patients around the world. This is an exciting opportunity to apply [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deep technical expertise while helping to redefine how we approach evolving scientific and regulatory challenges. Key Responsibilities Lead Extractables and Leachables strategies and risk assessments across complex drug development projects. Serve as the scientific expert and primary contact for multidisciplinary project teams. Design and oversee Extractables and Leachables studies with internal laboratories and external partners. Interpret analytical data, identify trends, and provide scientifically sound recommendations. Author and review technical documentation, assessments, and regulatory submission content. Drive cross-functional collaboration to solve complex scientific and operational challenges. Lead continuous improvement initiatives that enhance testing approaches, workflows, and risk assessment strategies. Essential Requirements Advanced degree in Pharmacy, Chemistry, Life Sciences, or a related scientific discipline. Strong expertise in [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
ten23 health
• AT- 2 Lavamünd
[. .. ] support, optimization, and continuous improvement of processes used in the manufacturing of sterile parenteral products. This role includes operational oversight of aseptic production steps as well as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the scientific and technical evaluation of process data, changes, and deviations. The position holder is a recognized subject matter expert in aseptic manufacturing, supporting Production and Quality Assurance and ensuring robust, compliant, and efficient manufacturing processes. Your responsibilities will include: Serve as the subject matter expert for aseptic manufacturing processes (e. g. , filtration, [. .. ] structured root cause analyses to define and track sustainable CAPAs. Actively troubleshoot technical issues directly on the shopfloor while coaching production personnel on aseptic best practices and strict GMP compliance. Author, review, and maintain critical process documentation, including risk assessments, SOPs, manufacturing records, and the technical evaluation of process-related changes. Support equipment, cleanroom, and system qualifications, and actively oversee validation protocols, including media-fill studies and aseptic process simulations. Conduct statistical evaluations and trend analyses of critical process parameters (CPPs) [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Acadia Pharmaceuticals
Sr. Manager Quality Control, EU
• AT- 2 Lavamünd
[. .. ] stability data of DS and DP and coordinates efforts with CSPs to report and trend analytical test results in a timely manner. The position supports the quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] review of analytical technical reports and documents intended for regulatory submissions. Primary Responsibilities Review and approve analytical test results for DS and DP Review and/or author analytical method protocols, validations and analytical sections of annual product quality reviews for commercial products Review and/or author analytical transfer protocols and reports between laboratories Author stability protocols and reports Negotiate stability related agreements Actively monitor stability programs at CSPs Author and/or review analytical data summaries to support [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Roche
• AT- 2 Lavamünd
[. .. ] prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position As [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] part of Pharma Technical Operations (PT) , Pharma Technical Technology (PTT) plays a key role in leading a seamless industrialization and thorough technical product management through integrating SHE, proactive maintenance, facility fitness, performance optimization and scalable manufacturing processes and technologies in support of the manufacturing network. Product and process robustness, efficiency and reliability are [. .. ] all aspects of project deliverables Stay updated on industry trends and advancements in bioprocess technologies Collaborate with representatives from Development, Manufacturing, Quality, and Regulatory functions as required As required, review/author sections in regulatory submissions, as well as responses during Health Authority inquiries Serve as an ambassador for the function with the ability to influence stakeholders for new technology development and implementation Train and mentor team members to enhance their skills and promote professional growth Provide knowledge and training on complex [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
Senior Expert Science Technology (Analytical Operations)
• AT- 2 Schweiz
Salary Range 66, 918.00-117, 800.00 Job Description Summary Location: Schaftenau, Austria #onsite Role Purpose As a Senior Expert Science Technology, you will join Analytical Operations within
Technical Research and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development Biologics and contribute to the development of innovative biologic medicines for patients in clinical trials. In this role, you will act as a GMP Analytical Expert, representing the analytical function in global project analytical sub-teams and ensuring timely, compliant, and scientifically sound support for clinical development [. .. ] transfer, and implementation of analytical methods according to GMP standards and agreed project timelines. Design, supervise, and coordinate analytical activities while managing multiple priorities, customer needs, timelines, and resource requirements. Author, review, and approve high-quality scientific and GMP documentation such as protocols, reports, laboratory procedures, test records, release and stability documents, transfer reports, and submission-relevant documentation. Evaluate analytical data, interpret results, draw scientifically sound conclusions, and critically review data generated by others. Investigate and support resolution of quality events [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Wu Xi App Tec Group
• AT- 2 Lavamünd
[. .. ] suspensions, or emulsions for atomization. Configure and adjust the equipment and process parameters (temperatures, flow rates, pressure, atomization speed, etc. ) in accordance with your training curriculum [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and procedures. Provide technical support to operators in production activities. Precisely execute the manufacturing batch record, recording the required data in real time following GDP Master and perform the cleaning of equipment and rooms related to the various stages of production. Perform line setup, format changes and line clearances. Perform first-level maintenance (discs, nozzles, filters, seals, etc. ) . Author and revise documentation for the set-up, operation cleaning of the equipment and processes. Ensure the production of batches in a GMP environment and work independently and efficiently according to the instructions of your manager. Perform sampling and in-process-controls on manufactured products. Participate in and support the qualification [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
Vaxcyte
Senior Bioprocess Engineer II, MSAT, Proteins
• AT- 2 Lavamünd
[. .. ] The incumbent will support the microbial manufacturing operations from commercial readiness through PPQ and ongoing commercial production, onsite at contract manufacturing organizations (CMO) , with the primary [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] responsibility to provide technical and operational support of manufacturing operations that ensure robust and efficient manufacturing processes. This position will primarily be located in Visp, Switzerland, but will have responsibilities to oversee CMOs in Italy and Germany as well. This position will require the candidate to manage the highly complex microbial manufacturing processes for [. .. ] literature, industry/ regulatory guidance, and practical experience to perform work and influence CMC strategies. Recommend and implement new technology that advances knowledge and productivity within the department. Drive continuous improvement. Author and review technical reports, manufacturing documents, regulatory submissions, and publications. Present at department, project team, and senior management meetings. May present externally at scientific conferences. Support the CMOs during inspections of health authorities where necessary and ensure proper followup of any potential observation or recommendation. Requirements: Ph D in Bio/ Chemical [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Pharmadog
• AT- 2 Lavamünd
[. .. ] The incumbent will support the microbial manufacturing operations from commercial readiness through PPQ and ongoing commercial production, onsite at contract manufacturing organizations (CMO) , with the primary [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] responsibility to provide technical and operational support of manufacturing operations that ensure robust and efficient manufacturing processes. This position will primarily be located in Visp, Switzerland, but will have responsibilities to oversee CMOs in Italy and Germany as well. This position will require the candidate to manage the highly complex microbial manufacturing processes for [. .. ] literature, industry/ regulatory guidance, and practical experience to perform work and influence CMC strategies. Recommend and implement new technology that advances knowledge and productivity within the department. Drive continuous improvement. Author and review technical reports, manufacturing documents, regulatory submissions, and publications. Present at department, project team, and senior management meetings. May present externally at scientific conferences. Support the CMOs during inspections of health authorities where necessary and ensure proper follow-up of any potential observation or recommendation. Requirements: Ph D in Bio/ [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Jobsin Austria
GEELY Technical Warranty Manager (Austria)
• AT- 9 Wien
[. .. ] present not only here, but also along the Adriatic, in the Balkans, and in some other neighbouring countries. We are looking for the newest member to our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Geely team for Technical Warranty Manager position. What will be your roles and responsibilities? Responding to technical enquiries from the service network and end users in a timely manner with appropriate information and guidance. Manage warranty cases to provide customers/ dealers with a solution to any problems that might arise, with the minimum amount [. .. ] define and communicate issues to other business functions. Working collaboratively with other areas of the business and partner organisations to provide technical solutions, in a timely manner. Update existing and author new technical documents to support products and markets. Processes warranty claims on a timely basis for each dealer. Processes all warranty paperwork to ensure proper documentation. Reconciles all warranty receivables with payments through the appropriate accounting schedule. Resubmits all rejected claims promptly. Follows up on payment of outstanding claims. Tracks [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Novocure Inc.
Clinical Trial Physician, Oncology
• AT- 2 Schweiz
[. .. ] submission readiness, ensuring scientific rigor, audit preparedness, and patient-focused impact. WHAT YOULL DO As a medical leader within Clinical Development, you will: Serve as the medical expert [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and key technical contributor for a tumor-based clinical study or program evaluating the safety and efficacy of TT Fields delivered concomitantly with standard therapy in patients with cancer Drive clinical development strategy including protocol authoring, regulatory and ethics committee submissions, study initiation, investigator communication, safety and medical monitoring, data screening and analysis, and publication initiatives Author and oversee key clinical documents including study protocols and Clinical Study Reports (CSRs) , ensuring submission readiness and inspection/ audit preparedness Establish and lead physician teams and key opinion leader relationships to support study execution and overall medical strategy Partner cross-functionally with matrix teams, including R D, Innovation, regulatory, [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
u- blox AG
Senior Application Engineer
• AT- 2 Lavamünd
[. .. ] the USA, we are making a global impact. Job Description As a Senior Application Engineer you will work in a dynamic and international team within the Application [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Engineering department, providing technical support to global customers and coordinating activities with Product Development, R D, Product Management, Field Application Engineering, Sales, and Quality teams. In this role, you act as a technical product expert, ensuring customers receive the product knowledge, designin guidance, and support they need to succeed. You also serve as the [. .. ] GNSS products, with potential for expanded responsibilities and career growth. Your Responsibilities Manage customer expectations and provide high-quality on-site and remote technical support for GNSS applications and projects Author and contribute to technical product documentation, includingdatasheets, integration anduser manuals, applicationnotesand technical content for internal and external audiences. Provide customized design-in vehicles, prototype deliveries and tailored technical solutions to accelerate customer adoption ofnew technologies. Analyse non-conformities, support root-causeinvestigationsand contribute to corrective actions with the R D and [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Waters Corporation
Informatics Service Specialist II
• AT- 9 Wien
[. .. ] successful implementation and ongoing compliance of Waters Informatics solutions in regulated laboratory environments. Responsibilities Informatics Service Delivery Install, configure, and support Waters Informatics solutions (Empower, Nu Genesis, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Waters Connect) Deliver technical services across Windows Server, Oracle databases, Active Directory, networking, and infrastructure Support virtualisation and cloud environments (VMware, Citrix, AWS, Azure) Troubleshoot complex technical, system, and performance issues Maintain detailed technical documentation, including system configurations and Statements of Work Deliver customer training and postdeployment support Validation Consulting (CSV) Provide validation consulting services across the system lifecycle (SDLC) Perform gap analysis, risk assessment, and validation planning Author and review validation deliverables (Validation Plans, Test Plans, Validation Summary Reports) Support execution of IQ, OQ, PQ, UAT, and system testing Ensure compliance with Gx P, 21CFR Part11, Annex11, and Annex15 Support data integrity and change control processes Guide customers in maintaining validated systems Customer Engagement Commercial Support Act as a [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
PwC
Digital Lending Business Analyst (w/m/d) Domain Expert-Technology Consulting
• AT- 3 St. Pölten
Beratungs-/ Consultingtätigkeiten
[. .. ] the successful candidate bridges business needs and IT solutions, knows how SME lending origination actually works, and can turn regulatory and business requirements into concrete design. Beyond [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] delivery, they co-author the offers reusable assets and support business development. Clientfacing presales is done in support of the offer lead rather than owned endtoend. The candidate works closely with business stakeholders, developers, testers and project managers to ensure solutions meet business objectives and regulatory requirements. Key responsibilities in our team Domain regulation [. .. ] structured fitgap analysis. Support presales: Contribute domain credibility to pitches, proposals and client workshops, in support of the offer lead. IT business analysis delivery Gather, analyze and document functional and technical requirements related to lending products and processes. Translate business needs into clear, structured documentation (Business Requirement Documents, User Stories, Use Cases) . Collaborate with development teams to ensure alignment between technical implementation and business goals. Support functional testing and coordinate UAT (User Acceptance Testing) . Monitor project progress, identify issues [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Novartis
Senior Expert Science Technology
• AT- 7 Schaftenau
[. .. ] with global multidisciplinary teams, influence scientific decisionmaking, and drive solutions that support the delivery of highquality medicines to patients around the world. This is an exciting opportunity [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to apply deep technical expertise while helping to redefine how we approach evolving scientific and regulatory challenges. Key Responsibilities Lead Extractables and Leachables strategies and risk assessments across complex drug development projects. Serve as the scientific expert and primary contact for multidisciplinary project teams. Design and oversee Extractables and Leachables studies with internal laboratories and external partners. Interpret analytical data, identify trends, and provide scientifically sound recommendations. Author and review technical documentation, assessments, and regulatory submission content. Drive crossfunctional collaboration to solve complex scientific and operational challenges. Lead continuous improvement initiatives that enhance testing approaches, workflows, and risk assessment strategies. Essential Requirements Advanced degree in Pharmacy, Chemistry, Life Sciences, or a related scientific discipline. Strong expertise in Extractables [. .. ]
1 von 6Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Technical Author pro Jahr?
Als Technical Author verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Technical Author Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 148 offene Stellenanzeigen für Technical Author Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Technical Author Jobs?
Aktuell suchen 20 Unternehmen nach Bewerbern für Technical Author Jobs.
Welche Unternehmen suchen nach Bewerbern für Technical Author Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Technical Author Stellenangebote:
- Novartis (6 Jobs)
- Roche (2 Jobs)
- Concentrix (1 Job)
- 8036 Takeda Pharmaceuticals International AG (1 Job)
- Lonza (1 Job)
In welchen Bundesländern werden die meisten Technical Author Jobs angeboten?
Die meisten Stellenanzeigen für Technical Author Jobs werden derzeit in Berlin (32 Jobs), Bayern (22 Jobs) und Niedersachsen (22 Jobs) angeboten.
Zu welchem Berufsfeld gehören Technical Author Jobs?
Technical Author Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
