Technical Author Stellenangebote

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163 Stellenangebote

Stellenangebote Technical Author Jobs bei Neuvoo.com

Stellenangebot Technical Author Job bei Abb Vie Deutschland GmbH Co. KG

Job vom 26.10.2024 Abb Vie Deutschland GmbH Co. KG

Principal Research Scientist I (all genders) Medicinal Chemistry (permanent/ full- time)

• Münster- Sarmsheim Work-Life-Balance

MEHR

[...] molecule drug candidates. The ideal candidate will be able to lead by influence in a matrix environment and maintain a productive, collaborative, and inclusive environment. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. Responsibilities In your role, you will lead international Medicinal [...] scientific trends from internal and external sources into functional objectives Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]
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Job vom 26.10.2024 Abb Vie Deutschland GmbH Co. KG Principal Research Scientist I (all genders) Medicinal Chemistry (permanent/ full- time) • Ludwigshafen Work-Life-Balance

MEHR

[...] molecule drug candidates. The ideal candidate will be able to lead by influence in a matrix environment and maintain a productive, collaborative, and inclusive environment. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. Responsibilities In your role, you will lead international Medicinal [...] scientific trends from internal and external sources into functional objectives Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]

Stellenangebote Technical Author Jobs bei Stellenanzeigen.de

Job vom 13.10.2024 EKATO Rühr- und Mischtechnik GmbH

Technischer Redakteur (m/w/d)

• 79650, Schopfheim, Deutschland Weihnachtsgeld

MEHR

[...] Fähigkeit, Sachverhalte und Abläufe leicht verständlich, textlich und grafisch darzustellen Sehr gute Deutsch- und gute Englischkenntnisse in Wort und Schrift Sicherer Umgang mit den gängigen MS- Office- und Adobe- Programmen Wünschenswert sind Erfahrungen im Umgang mit Illustrationsprogrammen (z. B. Corel Technical Suite) sowie im Erstellen von XML- Dokumenten, z. B. mit Frame Maker oder TIM- RS Ihre Stärken: Strukturierte, gewissenhafte und [...] Kontakt: Ann- Katrin Ludwig +49 7622 29- 463 www. ekato. com . Erstellung und Optimierung von modularen Service- Anleitungen sowie entsprechender Grafiken in Zusammenarbeit mit allen prozessbeteiligten Bereichen; Anwendung und Weiterentwickelung des Redaktionsleitfadens;. . . . Dokumentationsingenieur, technische, Dokumentation, Technical, author, Technical, writer, Fachterminologie, Online- Redaktion, Präsentation, Technische, Redaktion DUBLETTEOVERRIDE 14552203 [...]
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Stellenangebote Technical Author Jobs bei Jobware

Job vom 26.10.2024 Abb Vie Deutschland GmbH Co. KG Principal Research Scientist I (all genders) Medicinal Chemistry (permanent/ full- time) Work-Life-Balance

MEHR

[...] molecule drug candidates. The ideal candidate will be able to lead by influence in a matrix environment and maintain a productive, collaborative, and inclusive environment. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. Responsibilities In your role, you will lead international Medicinal [...] scientific trends from internal and external sources into functional objectives Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]

Stellenangebote Technical Author Jobs bei Neuvoo

Job vor 2 Tagen gefunden LHH

Principal Scientist Stability- 1 year contract

• Neuchtel, Neuchtel, Switzerland

MEHR

[...] required premarket stability program in support of the change Perform change control impact assessments and document the stability assessment in change controls. Review and endorse change controls as an expanded reviewer. Initiate change controls related to stability operations Provide the technical requirements in a Master Stability Protocol, review and approve study specific protocols and/ or batch enrollment forms Responsible for the handling of annual commercial stability program for assigned products in coordination with sample management groups. Author stability sections of CTD dossiers for post- approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related [...]

Stellenangebote Technical Author Jobs bei JobMESH

Job vom 25.10.2024 Abb Vie Deutschland GmbH Co. KG Principal Research Scientist I (all genders) Medicinal Chemistry (permanent/ full- time) • Rhineland- Palatinate Work-Life-Balance

MEHR

[...] molecule drug candidates. The ideal candidate will be able to lead by influence in a matrix environment and maintain a productive, collaborative, and inclusive environment. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. Responsibilities In your role, you will lead international Medicinal [...] scientific trends from internal and external sources into functional objectives Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]

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Weitere Stellenangebote Technical Author bei JobMESH

Job vom 26.10.2024 Abb Vie Deutschland GmbH Co. KG Principal Research Scientist I (all genders) Medicinal Chemistry (permanent/ full- time) • Rhineland- Palatinate Work-Life-Balance

MEHR

[...] molecule drug candidates. The ideal candidate will be able to lead by influence in a matrix environment and maintain a productive, collaborative, and inclusive environment. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. Responsibilities In your role, you will lead international Medicinal [...] scientific trends from internal and external sources into functional objectives Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]

Stellenangebote Technical Author Jobs bei Stellen-Online.de

Job vom 30.10.2024 Abb Vie Deutschland GmbH Co. KG Principal Research Scientist I (all genders) Medicinal Chemistry (permanent/ full- time) - Vollzeit, Homeoffice • Ludwigshafen, 67059 Homeoffice möglich Work-Life-Balance

MEHR

[...] molecule drug candidates. The ideal candidate will be able to lead by influence in a matrix environment and maintain a productive, collaborative, and inclusive environment. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. Responsibilities In your role, you will lead international Medicinal [...] scientific trends from internal and external sources into functional objectives Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]
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Stellenangebote Technical Author Jobs bei Jooble

Job vom 27.10.2024 Abb Vie Deutschland GmbH Co. KG

Research Fellow/ PhD

Work-Life-Balance

MEHR

[...] medicinal chemistry, including an appreciation of modern computational and experimental tools, multidisciplinary inputs, and synthetic technologies needed to develop low dose small molecule drug candidates. Strong communication skills are essential, as the candidate must be able to tailor interactions with technical teams and represent the medicinal chemistry advances to Abb Vie leadership. In your role, you will lead international Medicinal Chemistry [...] a team of scientists through effective mentoring, guidance, and supervision Present program updates and research strategies to functional and non- functional leaders as well as potential and existing partners Maintain awareness of emerging literature and science in the field and author scientific disclosures/ publications Maintain scientific presence outside Abb Vie with appropriate publication and conference abstract submission highlighting innovative medicinal chemistry [...]
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Job vom 27.10.2024 Abb Vie Deutschland GmbH Co. KG Research Fellow (m/w/d) Work-Life-Balance

MEHR

Job vom 27.10.2024 Abb Vie Deutschland GmbH Co. KG

Research Scientist m/w/d

Work-Life-Balance

MEHR

Stellenangebote Technical Author Jobs bei Mindmatch.ai

Job vor 7 Tagen gefunden International Atomic Energy Agency Consultant Regulatory Effectiveness Conference • AT- 9 Beratungs-/ Consultingtätigkeiten

MEHR

[...] the needs of its Member States related to nuclear safety and nuclear security. The Office of Safety and Security Coordination is located in the Office of the Deputy Director General, Head of the Department. Its mission is to ensure the technical consistency and effective coordination of the IAEAs activities in the nuclear, radiation, transport and waste safety and nuclear security programmes. [...] and communication products and materials tailored for the Conference. Manage the submission process via IAEAs INDICO system, ensuring efficient tracking and handling of all submissions. Compile, analyse, and report on data related to submissions, including submission rates, acceptance rates, and author demographics for reporting purposes. Knowledge, Skills and Abilities Required Skills and Expertise Project Management Data Management Qualifications and Experience University [...]

Job vor 8 Tagen gefunden Novartis

RA CMC Manager

• AT- 7

MEHR

[...] Molecules projects/ products. Lead and implement global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/ products. Identify the required documentation and any content, quality and/ or timelines issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines. Author and/ or review high- quality CMC documentation for HA submission, applying agreed CMC global regulatory strategies, current regulatory trends and [...]

Job vor 11 Tagen gefunden Novartis RA CMC Senior Manager • AT- 7

MEHR

Job vor 12 Tagen gefunden Sandoz

Regulatory Drug Substance Manager (d/ f/m)

• AT- 7

MEHR

[...] with regulatory compliance. Lead and implement global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/ products. Identify the required documentation and any content, quality and/ or timelines issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines. Author and/ or review high- quality CMC documentation for HA submission, applying agreed global regulatory strategies, current regulatory trends and guidelines. [...]

Job vor 12 Tagen gefunden International Atomic Energy Agency Pipeline for Nuclear Fuel Cycle and Materials Professionals and Experts- Short- Term Consultancy • AT- 9

MEHR

[...] exchange, thereby building Member States capacity in all aspects of the nuclear fuel cycle. Knowledge, Skills and Abilities The Nuclear Fuel Cycle and Materials Section seeks qualified experts with the necessary knowledge and skills to provide specialized advice to: Perform technical editing of multi- author documents. Develop training courses based on existing guidance/ reference material and lectures. Develop storyboards for eLearning correlated with published documents. [...]
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Job vom 15.10.2024 Renesas Electronics Corporation

Sr System Engineer (f/m/d)

• AT- 6

MEHR

[...] team to innovate and enhance measurement procedures and protocols, drawing on a rich background in system engineering. Engage with cross- functional teams to seamlessly integrate measurement results into comprehensive system designs, contributing to the development of cutting- edge NFC applications. Author detailed technical reports documenting procedures and findings, catering to the nuanced requirements of both internal and external stakeholders. Offer expert technical guidance [...]

Job vom 02.10.2024 Novartis Farmacutica Regulatory Affairs CMC Associate Director • AT- 7 Führungs-/ Leitungspositionen

MEHR

[...] activities (planning, authoring, reviewing, coordina- tion, submission) for assigned projects/ products, while applying the global strategy into submis- sions. Identify the required documentation and any content, quality and/ or timeliness issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines. Author and/ or review high- quality CMC documentation for Health Authority submissions, estab- lishing and applying CMC global regulatory strategies, current [...]

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