6 Jobs für Pharmaceutical Writing in Mainz
Stellenangebote Pharmaceutical Writing in Mainz Jobs
Job vor 13 Tagen bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Mainz, Germany full time Job ID: 11231 About the Role As an Associate Director Scientific/ Medical
Writing, you will play a pivotal role in advancing Bio NTechs mission to revolutionize [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medicine by ensuring the timely creation of highquality scientific and regulatory documents. Your contributions will directly impact the development and approval of novel therapeutic agents, supporting Bio NTechs efforts to address diseases with high medical needs. Collaborating within a [. .. ] (i. e. , by supporting, training, and guiding) and compliance: with relevant processes, templates, and standards. with good writing practices and the structure/ formatting requirements for scientific documents. with international pharmaceutical requirements, including applicable guidelines, regulations, and laws. Support the implementation of rolerelevant tools, guidelines, SOP documents and templates, instructions, and/or training materials. Perform with limited supervision complex medical writing tasks for programs and/or low to high complexity documents, where some adaptation of standard procedures is required. A Good [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Jobticket
[. .. ] with the following characteristics: An advanced university degree in a scientific discipline (Biology, Chemistry, Pharmacy, Biotechnology, or comparable) optional Ph D or equivalent qualification Industry experience (10+ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] years) within biotech or pharmaceutical industry, strong background in analytical CMC activities for m Abs and/or work experience in m Ab QC and/or analytical development Proven track record in analytical latestage antibody development, ideally including antibodydrug conjugates (ADCs) Demonstrated leadership and analytical project management experience Profound knowledge of relevant US and EU, EMA, FDA regulatory [. .. ] as the USP (United States Pharmacopoeia) , and Ph. Eur. (European Pharmacopoeia) Experience with preapproval activities (e. g. PAI, BLA preparation, launch activities) is a plus Fluent English and technical writing skills Experience in working in intercultural, crossfunctional teams Structured way of working, ability to understand and break down complex challenges and plan associated timelines and interdependencies Highly motivated and willingness to work in a fastpaced and fastevolving environment Your Benefits Its our priority to support you: Your flexibility: flexible hours [. .. ]
Neu Job gestern bei Jooble gefunden
Randstad Professional
• Mainz- Bingen; Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz
Angebote von Zeitarbeitsunternehmen
[. .. ] CMC contacts or subject matter experts (e. g. quality control, production, etc. ) On-time delivery of documents and contents aligned with RA CMC processes and templates for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] existing global pharmaceutical products (i. e. tech documents required for variations, geographical extensions and renewals) Manage the requests and activities together with ad-hoc external support Master s degree or equivalent with major focus on pharmaceutics, chemistry or other natural sciences Several years of industry experience in either pharmaceutical development or production, chemical development, analytical sciences, quality control, quality assurance or regulatory affairs Profound knowledge of worldwide GMP guidelines and preferably regulatory guidelines with regards to CMC Skills in CMC technical writing Proven operational experience in preparation and review of analytical and manufacturing documentation regarding scientific issues Excellent written and spoken English skills Ability to work independently in international/ multi-disciplinary project teams and to decide, prioritize and consolidate multiple tasks and complex issues Autonomous, analytical and organized working style Performance-based [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
Jobticket
[. .. ] biology, pathology or related discipline with scientific background in Oncology or Immuno-Oncology 6 to 10+ years of oncology clinical development experience as biomarker project/ program lead in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the biotech/ pharmaceutical industry Therapeutic knowledge and scientific accomplishments as evidenced by publications in peer reviewed journals in oncology or immune-oncology In depth understanding of translational medicine and biomarker mechanisms associated with immune-oncology and targeted therapies. Demonstrated experience with innovative assay development and proven ability to effectively troubleshoot and solve complex [. .. ] genuine interest and understanding of the science supporting the development programs Excellent, broad communication skills in various interpersonal settings as well as excellent organization skills and attention to details Strong writing skills as demonstrated by authorship of peer-reviewed publications and contributions to regulatory communications (e. g. , briefing documents, clinical trial protocols, marketing authorization applications) Your Benefits: It s our priority to support you: Your flexibility: flexible hours vacation account Your growth: Digital Learning Performance talent development leadership development Apprenticeships [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Biontech
Director AS T Projects Strategy
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
Jobticket
[. .. ] with the following characteristics: An advanced university degree in a scientific discipline (Biology, Chemistry, Pharmacy, Biotechnology, or comparable) optional Ph D or equivalent qualification Industry experience (10+ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] years) within biotech or pharmaceutical industry, strong background in analytical CMC activities for m Abs and/or work experience in m Ab QC and/or analytical development Proven track record in analytical latestage antibody development, ideally including antibodydrug conjugates (ADCs) Demonstrated leadership and analytical project management experience Profound knowledge of relevant US and EU, EMA, FDA regulatory [. .. ] as the USP (United States Pharmacopoeia) , and Ph. Eur. (European Pharmacopoeia) Experience with preapproval activities (e. g. PAI, BLA preparation, launch activities) is a plus Fluent English and technical writing skills Experience in working in intercultural, cross-functional teams Structured way of working, ability to understand and break down complex challenges and plan associated timelines and interdependencies Highly motivated and willingness to work in a fast-paced and fast-evolving environment Your Benefits: It s our priority to support you: [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Biontech
Associate Director Scientific/ Medical Writing
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As an Associate Director Scientific/ Medical
Writing, you will play a pivotal role in advancing Bio NTechs mission to revolutionize medicine by ensuring the timely creation of high-quality scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and regulatory documents. Your contributions will directly impact the development and approval of novel therapeutic agents, supporting Bio NTech s efforts to address diseases with high medical needs. Collaborating [. .. ] (i. e. , by supporting, training, and guiding) and compliance:-with relevant processes, templates, and standards. with good writing practices and the structure/ formatting requirements for scientific documents. with international pharmaceutical requirements, including applicable guidelines, regulations, and laws. Support the implementation of role-relevant tools, guidelines, SOP documents and templates, instructions, and/or training materials. Perform with limited supervision complex medical writing tasks for programs and/or low to high complexity documents, where some adaptation of standard procedures is required. A [. .. ]
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 in Mainz bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 6 offene Stellenanzeigen für Pharmaceutical Writing Jobs in Mainz.
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs in Mainz?
Pharmaceutical Writing Jobs in Mainz gehören zum Berufsfeld Technische Dokumentation / Redaktion.
