8 Jobs für Pharmaceutical Writer
Stellenangebote Pharmaceutical Writer Jobs
Job vor 2 Tagen bei StepStone gefunden
Kintiga
• Hannover
Homeoffice möglich
Are you looking for a full-time position in a pan-European strategic consultancy as a Senior Medical
Writer to streamline patient access to life-changing treatments through expert guidance, innovative tools, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] impeccable delivery? Location: Hybrid with office in Hannover regular in-person presence Salary: Competitive, based on experience We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan-European specialist consultancy that partners with [. .. ] knowledge sharing, internal capability building, mentoring, and cultural development Profil Masters degree in life sciences, medicine, pharmacy, health economics, or a related field 13 years of professional experience in the pharmaceutical industry and/or market access or management consulting Good knowledge of the German healthcare system and the AMNOG process, including experience with benefit dossiers Strong skills in scientific literature research and medical writing Experience in project management, as well as conducting and moderating trainings and workshops Native level German and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Bern
Are you ready to join a world leader in the exciting and dynamic fields of the
Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking a skilled Technical CSV/ Cn Q Specialists with experience in the Life Sciences industry to support [. .. ] review, approval, revision, and archival processes Collaborate with cross-functional teams (engineering, QA, validation) to ensure document completeness and alignment Required Qualifications Proven experience min. 5 years as a Technical Writer in the Life Sciences or pharmaceutical industry Strong expertise in Gx P documentation practices Hands-on experience with validation and qualification documentation Familiarity with Kneat or similar electronic validation lifecycle management systems Excellent attention to detail and strong organizational skills Ability to manage multiple documents and deadlines in a structured manner [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel- Stadt
Global Quality Manager (m/f/d) Global Quality Manager (m/f/d) - Quality Assurance/ GMP/ GDP/ Pharma/ English. Project: For our customer a big
pharmaceutical company in Basel we are looking for a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] highly qualified Global Quality Manager (m/f/d) . About the Organization: Join IMP Quality Distribution, a critical function within Global Quality Assurance. We are responsible for maintaining the quality and compliance of Investigational Medicinal Products (IMP) throughout the clinical supply chain. [. .. ] . Proven and comprehensive experience (min. 3 years) in Quality Assurance with a strong focus on compliance. Deep knowledge of a regulated Gx P environment (GMP/ GDP) . Fluent speaker and writer in English (German is a plus) . Fluency is essential for managing critical regulatory documentation, providing authoritative guidance to European sites, and ensuring successful support during Health Authority Inspections. Nice to Haves Familiarity with Veeva vault QMS. Roche experience. PTQ experience. Experience in supplier management especially depots. Reference Nr. : [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Global Quality Manager (m/f/d) Global Quality Manager (m/f/d) Quality Assurance/ GMP/ GDP/ Pharma/ English Project: For our customer, a big
pharmaceutical company in Basel, we are looking for a highly [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] qualified Global Quality Manager (m/f/d) . Background: Join IMP Quality Distribution, a critical function within Global Quality Assurance. We are responsible for maintaining the quality and compliance of Investigational Medicinal Products (IMP) throughout the clinical supply chain. Our team [. .. ] . Proven and comprehensive experience (minimum 3 years) in Quality Assurance with a strong focus on compliance. Deep knowledge of a regulated Gx P environment (GMP/ GDP) . Fluent speaker and writer in English (German is a plus) . Fluency is essential for managing critical regulatory documentation, providing authoritative guidance to European sites, and ensuring successful support during Health Authority Inspections. Nice to Haves Familiarity with Veeva vault QMS. Roche experience. PTQ experience. Experience in supplier management especially depots. Job Details Location: [. .. ]
Job am 02.06.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] Internal training clear explanation of complex medical topics for our project management and creative team This is what we want from you Professional experience in science communication, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ideally in the pharmaceutical industry Even more ideal: knowledge and understanding of the pharmaceutical market Ability to present complex content clearly and concisely, but with an innovative approach Excellent written and spoken German and English (level for scientific texts) Willingness to learn and undergo further training in order to familiarize yourself with various indications [. .. ]
Job am 12.05.2026 bei Jobleads gefunden
Senior Medical Writer
• Hannover, Niedersachsen
[. .. ] health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. WHAT WERE LOOKING FOR [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As Senior Medical Writer at Kintiga, you will take on a leading role in the content and organizational delivery of market access projects. You will act as a key contact for clients, manage timelines and resources, and contribute to the strategic direction and quality of projects. In addition, you will support team development through [. .. ] sharing, internal capability building, mentoring, and cultural development ABOUT YOU Masters degree in life sciences, medicine, pharmacy, health economics, or a related field 13 years of professional experience in the pharmaceutical industry and/or market access or management consulting Good knowledge of the German healthcare system and the AMNOG process, including experience with benefit dossiers Strong skills in scientific literature research and medical writing Experience in project management, as well as conducting and moderating trainings and workshops Native German and excellent [. .. ]
Job am 27.03.2026 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] (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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] background knowledge in immunology and oncology. 5 years (handson) experience: working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. as a scientific and medical writer in the pharmaceutical/ biotech industry. Prior experience: drafting documents for multiple indications, preferably in Bio NTechrelevant indications. drafting alone new or updated CTPs and CSRs required for Phase IIII trials. drafting low to medium complexity variants of the following (new or updated variants) : IBs, clinical CTD modules, DSURs/ Annual Reports, [. .. ]
Job am 04.03.2026 bei Jobleads gefunden
[. .. ] skills focused on the Medical Industry, who can work on developing copy content for brand deliverables. This role would complement the design team, while working for our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] client in the pharmaceutical industry. The focus of the role will be to create promotional communication content. This role will also develop market access content. You should be recognized as a brand expert with an ability to translate the science and data into compelling promotional copy complying with medical, regulatory, legal and compliance guidelines. [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Writer pro Jahr?
Als Pharmaceutical Writer verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Writer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 8 offene Stellenanzeigen für Pharmaceutical Writer Jobs.
In welchen Bundesländern werden die meisten Pharmaceutical Writer Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Writer Jobs werden derzeit in Niedersachsen (3 Jobs), Bayern (1 Jobs) und Rheinland-Pfalz (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Writer Jobs?
Pharmaceutical Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
