14 Jobs für Technical Author
Stellenangebote Technical Author Jobs
Job vor 10 Tagen bei Mindmatch.ai gefunden
Bachem Holding AG
• AT- 2 Schweiz
Bachem Holding AG sucht eine/n
Technical Author R D (a) für die Erstellung von GMP-relevanten Dokumenten in der Wirkstoffproduktion. Die Position erfordert exakte Arbeitsweise, Deutsch als Muttersprache und exzellente Englischkenntnisse. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Sie arbeiten in einem GMP-regulierten Umfeld, arbeiten eng mit Produktion, Qualitätssicherung, Regulatory Affairs und R D zusammen und tragen durch Ihre Arbeit zu einem reibungslosen [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Anteris Technologies
• AT- 2 Schweiz
[. .. ] Define applicable regulatory requirements under the EU Medical Device Regulation, MDR (EU) 2017/ 745, and provide clear guidance to cross-functional project teams. Lead the preparation, review, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] submission of technical documentation and other materials required to support CE marking, clinical investigations, substantial modifications, and product registrations. Serve as a primary regulatory contact with Notified Bodies, Competent Authorities, Ethics Committees, and other European regulatory stakeholders. Coordinate responses to questions and requests for additional information through approval or resolution. Provide regulatory support [. .. ] renewals, licenses, and regulatory maintenance activities across European and other international markets. Maintain complete, accurate, and audit-ready regulatory documentation, including records required for Notified Body assessments and regulatory inspections. Author, review, and approve regulatory procedures, work instructions, and other controlled documents. Monitor changes in European regulations, guidance, standards, and regulatory practices; assess potential business impact and communicate requirements to appropriate stakeholders. Provide regulatory leadership, mentorship, and strategic guidance to colleagues and project teams. Skills, Knowledge, Experience Qualifications Bachelors degree in [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Wu Xi App Tec Group
• AT- 2 Schweiz
[. .. ] 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 3 Tagen bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
• AT- 7 Schaftenau
[. .. ] 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. Job Description 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 3 Tagen bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
[. .. ] strategies across the drug development lifecycle, integrating analytical science, materials science and regulatory innovation to support high-quality medicines worldwide. You will collaborate with global teams, design studies, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] interpret data, author technical documentation, and drive continuous improvement while benefiting from hybrid working options and a J-18808-Ljbffr 00762534 [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
PVH (Tommy Hilfiger/ Calvin Klein)
• AT- 2 Schweiz
[. .. ] in development and implementation of an efficient Computerized Systems Validation Program for automated equipment, processes, and information management systems for the Laboratory and Manufacturing Operations. Contribute with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Customer QA and Technical Unit in harmonizing and implementing specifications. Contribute in change management and deviation tracking processes, including leading or contributing to CAPA. May contribute to developing procedures and/or protocols. More information about our One Source services: One Source Laboratory Solutions Perkin Elmer Periodic Reviews Works closely with Lifecycle Compliance team to [. .. ] harmonization projects by identifying specification discrepancies across the installed base at Customer site. Processes Changes, Temporary Changes, Deviations, and CAPA related with periodic review findings. Computerized Systems Validation Participate as author or executor to new system validation projects, partnering with Customer CSV team. Contributes to changes and investigations as a member of cross-functional teams. Preferred Characteristics Strong background and understanding of FDA regulations. Knowledge of c GMP and validation regulations and requirements. Knowledge of Good Clinical practice (GCP) , Good pharmaco [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
Perkin Elmer
Computerized System Validation Specialist
• AT- 2 Schweiz
[. .. ] in development and implementation of an efficient Computerized Systems Validation Program for automated equipment, processes, and information management systems for the Laboratory and Manufacturing Operations. Contribute with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Customer QA and Technical Unit in harmonizing and implementing specifications. Contribute in change management and deviation tracking processes, including leading or contributing to CAPA. May contribute to developing procedures and/or protocols. More information about our One Source services: One Source Laboratory Solutions Perkin Elmer Periodic Reviews Works closely with Lifecycle Compliance team to [. .. ] harmonization projects by identifying specification discrepancies across the installed base at Customer site. Processes Changes, Temporary Changes, Deviations, and CAPA related with periodic review findings. Computerized Systems Validation Participate as author or executor to new system validation projects, partnering with Customer CSV team. Contributes to changes and investigations as a member of cross-functional teams. Preferred Characteristics Strong background and understanding of FDA regulations. Knowledge of c GMP and validation regulations and requirements. Knowledge of Good Clinical practice (GCP) , Good pharmaco [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
K- Recruiting GmbH
• AT- 2 Schweiz
Deviation Specialist (m/f/D) Tasks: Responsible to own,
author, record and investigate Deviations. Liaise with Subject Matter Experts (SMEs) and key stakeholders to establish the root cause (s) of deviations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and the potential impact of said deviations. Ensure proper investigational tools are used to systematically define the root cause (s) and contributing factor (s) (e. g. , Fault Tree [. .. ] processes and analytical methods is an advantage. Experience with Human and Organizational Performance risk management approaches is an advantage Fluency in English, both written and spoken. German is an advantage. Technical writing presentation/ communication skills are key for the role. Demonstrated previous experience is a strong advantage. Structured, focused and well-organised working attitude. Open-minded for new ideas and suggestions; agile, highly motivated and dynamically driven. Requirements: Start : 03.08.2026 Duration : 6 months Capacity : 5 days [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
Novocure Inc.
• 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 am 25.07.2026 bei Mindmatch.ai gefunden
Suma Medtec
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] design initiatives across the full product life cycle. Main Responsibilities Drive device development projects across all design stages, collaborating with subject matter experts to complete deliverables following [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] applicable Design Controls. Author key Design History File documents (DIR, Design V V reports, etc. ) and complete phase reviews. Draft or collaborate on applicable Risk Management and Human Factors documentation, improving product design and user interactions (RM Plan, FMEA, URRA, Task/ Comparative Analysis, etc. ) . Ensure that medical device RM and Usability considerations are documented according to applicable standards (e. g. , ISO 14971, IEC 62366) . Collaborate with manufacturers as technical lead, planning assemblies required for testing, clinical trial, or commercial production. Support Post Market Surveillance activities and determine necessary updates to product design, Risk File, and Usability based on collected feedback. Support Regulatory Affairs in preparing medical device submissions (e. g. , US FDA 510 (k) , EU Technical Documentation [. .. ]
Job am 23.07.2026 bei Mindmatch.ai gefunden
Physics World
Experimental Physicist (EP-DI-2026-29-LD)
• AT- 2 Schweiz
[. .. ] but have already demonstrated some years of post-doctoral experience in experimental particle physics. Experience in data analysis and online/ offline software. Demonstrated competence in detector hardware and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experimental instrumentation. Technical competencies Knowledge and application of electromagnetic radiation propagation and interaction with matter. Physics analysis and experimental particle physics. Particle detectors and interaction of particles with matter. Behavioural competencies Learning and Sharing Knowledge: keeping up-to-date with developments in own field of expertise and readily absorbing new information. Building Relationships: [. .. ] CV (English or French) . A copy of your Ph D Degree. A list of up to ten most-important publications indicating where you have been a principal contributor or co-author, indicating your contribution to each publication in a couple of lines. A one-page cover letter, giving your motivation in applying for this position. A research statement (of maximum two pages) , including research interests and plans in the context of CERNs scientific programme. Any document you consider relevant to [. .. ]
Job am 23.07.2026 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 [. .. ]
Job am 21.07.2026 bei Mindmatch.ai gefunden
Vaxcyte
Staff Engineer, Drug Substance, MSAT
• AT- 2 Schweiz
[. .. ] Engineer. The incumbent will support conjugation manufacturing operations from commercial readiness through PPQ and ongoing commercial production, onsite at contract manufacturing organizations (CMO) . The primary responsibility [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is to provide technical and operational support of manufacturing operations to ensure robust and efficient processes. This position will be located primarily in Visp, Switzerland. This role requires management of the highly complex conjugation manufacturing processes for Vaxcytes vaccine portfolio. This is an opportunity to join an outstanding team, supporting late-stage clinical manufacture, [. .. ] Leverage literature, regulatory guidance, and practical experience to inform work and influence CMC strategies. Recommend and implement new technology to advance knowledge and productivity within the department; drive continuous improvement. Author and review technical reports, manufacturing documents, regulatory submissions, and publications. Present at department, project teams, and senior management meetings; may present externally at scientific conferences. Support CMOs during health authority inspections and ensure proper follow-up of any observations or recommendations. Requirements Ph D in Bio/ Chemical Engineering or Microbiology/ Chemistry/ [. .. ]
Job am 11.07.2026 bei Mindmatch.ai gefunden
Takeda
Research Scientific Associate Director-Process Development
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] (AD, DP, QA, RA, Manufacturing, MSci) to ensure successful delivery. Act as a Lead and SME for process development, optimization, characterization, Qb D and tech transfer activities. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Collaborate on and review technical documents including protocols and reports, risk assessments and provide input for master batch records, changes, and deviations. Author and revise submission documents. Drive and further develop the way statistical/ mechanistic/ hybrid modelling, data science exchange supports the PD team and revolutionizes the quality and speed of drug substance development. Strategize and drive the internal PD software tool set to make process development more efficient. Coach and develop staff, [. .. ]
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 14 offene Stellenanzeigen für Technical Author Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Technical Author Jobs?
Aktuell suchen 13 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:
- Healthcare Businesswomens Association (2 Jobs)
- Anteris Technologies (1 Job)
- Wu Xi App Tec Group (1 Job)
- Perkin Elmer (1 Job)
- K- Recruiting GmbH (1 Job)
- Bachem Holding AG (1 Job)
In welchen Bundesländern werden die meisten Technical Author Jobs angeboten?
Die meisten Stellenanzeigen für Technical Author Jobs werden derzeit in Schleswig-Holstein (0 Jobs), Thüringen (0 Jobs) und Baden-Württemberg (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Technical Author Jobs?
Technical Author Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
