28 Jobs für Pharmaceutical Writer
Stellenangebote Pharmaceutical Writer Jobs
Job vor 2 Tagen bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] Canada Requisition Number: R-062453 Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose Able to function as a lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] writer on any compound independently. Leads in setting functional tactics/ strategy. Leads project-level strategy (eg, submission team, global program team, clinical team) . May represent therapeutic area (TA) head at high-level and cross-functional TA meetings and has some independent decision-making authority. Able to write and coordinate complex [. .. ] and compensation planning. Qualifications/ Requirements Education Minimum of a Bachelors Degree is required. An advanced degree (eg, Masters, Ph D, MD) is preferred. Skills/ Experience Minimum of 10 years of relevant pharmaceutical/ scientific experience is required. Minimum of 8 years of relevant clinical/ regulatory medical writing experience is required. Experience in project management and process improvement is required. A minimum of 2 years of people management experience is required. Recognizes how to best interpret, summarize, and present statistical and medical information to [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Global Medical Scientific Writer-70 part-time (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Dr. Falk Pharma is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a research-based pharmaceutical company committed to bringing innovative new medicines to patients with gastroenterological and hepatic diseases. To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Experienced Medical
Writer Regulatory Affairs Austria Location: Austria We are looking for a highly motivated and experienced Medical Writer to join a dynamic Regulatory Affairs team. In this role, you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will lead the development and review of high-quality, evidence-based regulatory documents supporting a wide range of projects. You will work closely [. .. ] verbal communication skills in English (additional languages are a plus) Strong analytical and strategic thinking abilities Ability to simplify complex scientific information into clear, actionable content Genuine interest in the pharmaceutical and medtech space Independent, proactive, and flexible working style If you are interested or know someone who might be a great fit, feel free to reach out #J-18808-Ljbffr 83450891 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Associate Director, Regulatory Medical Writing, Oncology
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] considered as a single submission. Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose Able to function as a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead writer on any compound independently. Leads in setting functional tactics/ strategy. Leads project-level strategy (eg, submission team, global program team, clinical team) . May represent therapeutic area (TA) head at high-level and cross-functional TA meetings and has some independent decision-making authority. Able to write and coordinate complex [. .. ] and compensation planning. Qualifications/ Requirements Education Minimum of a Bachelors Degree is required. An advanced degree (eg, Masters, Ph D, MD) is preferred. Skills/ Experience Minimum of 10 years of relevant pharmaceutical/ scientific experience is required. Minimum of 8 years of relevant clinical/ regulatory medical writing experience is required. Experience in project management and process improvement is required. A minimum of 2 years of people management experience is required. Recognizes how to best interpret, summarize, and present statistical and medical information to [. .. ]
Job vor 9 Tagen 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. [. .. ]
Job am 22.02.2026 bei Jobleads gefunden
Senior Medical Writer
• Berlin
[. .. ] empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. About the Role We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Key Responsibilities Prepare a wide [. .. ] teams. Mentor, train and provide constructive feedback to junior writers to support their development. What You Will Need to Succeed Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. Proven expertise in preparing at least three types of clinical, regulatory or safety documents (for example studyrelated, submissionrelated or safetyrelated documents) . Strong knowledge of the drug development lifecycle and key regulatory requirements (ICH and GVP) ; familiarity with medical device guidance (MDR 2017/ 745, ISO [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
• Wiesbaden, Hessen
[. .. ] areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Job [...]
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[...] Description The HTA Writer is responsible for providing clinical EUHTA document support to the JCA core team, ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process. Provides HTA writing expertise for multiple compounds and/or projects, expertise in HTA, oncology is a plus within a therapeutic [. .. ] quality and compliance and ensures delivery within project timelines. Familiarity with HTA dossier regulations, requirements and guidance associated with EU HTA regulations. Qualifications A minimum of 3+ years of bio-pharmaceutical industry experience in global pharma, biotech, life science, HTA agency organization delivering medicines/ therapies to a broad market across various therapeutic areas. Extensive experience in writing HTA dossiers, eg AMNOG, HAS, NICE, CDA dossier preferred. Bachelors Degree or higher in a scientific discipline. Outstanding written and oral communication skills, with [. .. ]
Job am 19.12.2025 bei Jobleads gefunden
Medical Writer (m/w/d)
• Hannover, Niedersachsen
Beratungs-/ Consultingtätigkeiten
Are you looking for a fulltime position in a global strategic consultancy as a Medical
Writer to streamline patient access to lifechanging treatments through expert guidance, innovative tools, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] impeccable delivery? We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan European specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with [. .. ] market access, medicine or related field Nativelevel proficiency in German English and extensive experience in writing scientific texts and communicate in both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Strategic structured mindset, analytical thinking, numerical understanding and problemsolving [. .. ]
Job am 12.11.2025 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 28.10.2025 bei Jobleads gefunden
Director, Medical Writing, Oncology
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] within the Medical Writing (MW) team, in close consultation and accordance with the Delivery Unit (DU) Head and in line with R D priorities and TA objectives. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Recognized expert medical writer for any document within and across TAs. Accountable for MW resource management and allocation within their portfolio (s) . Can represent MW DU Head or department at high-level and cross-functional TA meetings and has significant independent decision-making authority. Can step in for DU Head in case of [. .. ] and talent management. Qualifications/ Requirements: A university/ college degree in a scientific discipline is required. An advanced degree (eg, Masters, Ph D, MD) is preferred. Minimum of 14 years of relevant pharmaceutical/ scientific experience is required. Minimum of 12 years of relevant clinical/ medical writing experience is required. Minimum of 5 years of people management experience is required. Experience providing strategic and operational leadership to medical writing teams across all levels, with responsibility for setting vision, driving functional excellence, mentoring leaders, and [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
[. .. ] or would like to exercise your rights. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Incyte by 2x Get notified about new Medical Science Liaison jobs in Germany. Medical Science Liaison Oncology North Germany (Senior) Medical Affairs Scientist (m/w/d) Field Specialty Care: Inflammation Immunology, Gebiet: Bayern Medical Affairs Clinician-Southern Germany Austria Head of MSL Innovative Oncology DACH (m/w/d) Associate Director, Field Medical Advisor (m/w/d) Associate Director, Field Medical Advisor (m/w/d) Medical Writer/ Medical Content Manager (m/w/d) Principal Biostatistician (Medical Affairs/ HEOR-EMEA and NA Based) ) Medical Science Liaison-Germany (South) Cologne, North Rhine-Westphalia, Germany 5 days ago Medical Science Liaison Manager-NRW (m/f/d) Medical Science Liaison Oncology South West Germany Medical Science Liaison, Oncology, Germany (m/[. .. ]
Job gestern bei Neuvoo gefunden
Veristat
Principal Medical Writer
Job Description : Principal Medical
Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory [. .. ] about our core values here What we look for Bachelors degree required; science-related field preferred. Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/ biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis. Advanced knowledge of ICH and related regulatory guidelines. Excellent written English and keen attention to detail. Strong interpersonal and communication skills. Experience with Microsoft Office Suite is [. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
Dr. Falk Pharma GmbH
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Dr. Falk Pharma is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a research-based pharmaceutical company committed to bringing innovative new medicines to patients with gastroenterological and hepatic diseases. To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are [. .. ]
Job am 26.02.2026 bei Neuvoo gefunden
Veristat
Senior Medical Writer
Job Description : Senior Medical
Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory [. .. ] about our core values here What we look for Bachelors degree required; science-related field preferred. Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/ biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis; however, a minimum of 3 years of formal medical writing experience is required. Advanced knowledge of ICH and related regulatory guidelines. Excellent written English and keen attention [. .. ]
Job am 20.02.2026 bei Jooble gefunden
Evestia Clinical
• Berlin
[. .. ] where you are empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Prepare a wide range of [. .. ] regulatory documentation for clients and internal teams. Mentor, train and provide constructive feedback to junior writers to support their development. Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. familiarity with medical device guidance (MDR 2017/ 745, ISO 14155, MDCG) is advantageous. Ability to interpret and summarise complex clinical and safety data clearly and precisely. Proficiency in literature database searching and referencing software. Hybridremote working with team collaboration days in our Berlin office; fully remote [. .. ]
Job am 20.02.2026 bei Jooble gefunden
Evestia Clinical
Senior Medical Writer
• Berlin
[. .. ] empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. About the Role We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Key Responsibilities Prepare a wide [. .. ] teams. Mentor, train and provide constructive feedback to junior writers to support their development. What You Will Need to Succeed Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. Proven expertise in preparing at least three types of clinical, regulatory or safety documents (for example studyrelated, submissionrelated or safetyrelated documents) . Strong knowledge of the drug development lifecycle and key regulatory requirements (ICH and GVP) ; familiarity with medical device guidance (MDR 2017/ 745, ISO [. .. ]
Job am 20.02.2026 bei Jooble gefunden
Evestia Clinical
• Berlin
[. .. ] where you are empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Prepare a wide range of [. .. ] regulatory documentation for clients and internal teams. Mentor, train and provide constructive feedback to junior writers to support their development. Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. familiarity with medical device guidance (MDR 2017/ 745, ISO 14155, MDCG) is advantageous. Ability to interpret and summarise complex clinical and safety data clearly and precisely. Proficiency in literature database searching and referencing software. Hybridremote working with team collaboration days in our Berlin office; fully remote [. .. ]
Job am 20.02.2026 bei Jooble gefunden
Evestia Clinical
Senior/ Regulatory Medical Writer
• Berlin
[. .. ] where you are empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Prepare a wide range of [. .. ] regulatory documentation for clients and internal teams. Mentor, train and provide constructive feedback to junior writers to support their development. Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. familiarity with medical device guidance (MDR 2017/ 745, ISO 14155, MDCG) is advantageous. Ability to interpret and summarise complex clinical and safety data clearly and precisely. Proficiency in literature database searching and referencing software. Hybridremote working with team collaboration days in our Berlin office; fully remote [. .. ]
Job am 20.02.2026 bei Jooble gefunden
Evestia Clinical
• Berlin
[. .. ] where you are empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Prepare a wide range of [. .. ] regulatory documentation for clients and internal teams. Mentor, train and provide constructive feedback to junior writers to support their development. Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. familiarity with medical device guidance (MDR 2017/ 745, ISO 14155, MDCG) is advantageous. Ability to interpret and summarise complex clinical and safety data clearly and precisely. Proficiency in literature database searching and referencing software. Hybridremote working with team collaboration days in our Berlin office; fully remote [. .. ]
Job am 20.02.2026 bei Jooble gefunden
Evestia Clinical
Senior Medical Writer-Regulatory
• Berlin
[. .. ] where you are empowered to find creative solutions and make a meaningful impact on clinical development across rare disease, oncology, neurology, immunology and inflammation. We are seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Medical Writer to join our Medical Writing and Pharmacovigilance Team and take ownership of clinical, regulatory and safety writing projects. This is a fulltime, hybrid role reporting to the Head of Medical Writing and Pharmacovigilance, with one to two days per week based in our Berlin office. Prepare a wide range of [. .. ] regulatory documentation for clients and internal teams. Mentor, train and provide constructive feedback to junior writers to support their development. Established experience as a medical writer within a CRO, biotech, pharmaceutical or medical device environment. familiarity with medical device guidance (MDR 2017/ 745, ISO 14155, MDCG) is advantageous. Ability to interpret and summarise complex clinical and safety data clearly and precisely. Proficiency in literature database searching and referencing software. Hybridremote working with team collaboration days in our Berlin office; fully remote [. .. ]
Job vor 6 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
Global Medical Scientific Writer-70 part-time (m/f/d)
• Regierungsbezirk Freiburg
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Dr. Falk Pharma is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a research-based pharmaceutical company committed to bringing innovative new medicines to patients with gastroenterological and hepatic diseases. To bridge the divide from clinical research to clinical practice, we are looking for a qualified and motivated individual to translate clinical science for healthcare professionals, regulatory authorities, and other internal and external stakeholders. You are [. .. ]
Job am 13.02.2026 bei Jooble gefunden
SKC Beratungsgesellschaft mbH
Senior Medical Writer-Remote Working
• Hannover
Are you looking for a full-time position in a global strategic consultancy as a Medical
Writer We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan-European [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. Our clients in healthcare and life sciences [. .. ] in key market access disciplines Native-level proficiency in German English and extensive experience in writing scientific texts and communicate in both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS-Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Excellent organizational, agile and classic project management skills Dynamic [. .. ]
Job am 13.02.2026 bei Jooble gefunden
SKC Beratungsgesellschaft mbH
Medical Writer
• Hannover
Are you looking for a full-time position in a global strategic consultancy as a Medical
Writer to streamline patient access to life-changing treatments through expert guidance, innovative tools, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] impeccable delivery? Location: Hybrid (Office location: Hannover, Germany) Salary: Competitive, based on experience We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan-European specialist consultancy that partners with ambitious health technology developers [. .. ] access, medicine or related field Native-level proficiency in German English and extensive experience in writing scientific texts and communicate in both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS-Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Strategic structured mindset, analytical thinking, numerical understanding and problem-[. .. ]
Job am 13.02.2026 bei Jooble gefunden
SKC Beratungsgesellschaft mbH
Senior Medical Writer Remote
• Hannover
Are you looking for a full-time position in a global strategic consultancy as a Medical
Writer We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan-European [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. Our clients in healthcare and life sciences [. .. ] in key market access disciplines Native-level proficiency in German English and extensive experience in writing scientific texts and communicate in both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS-Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Excellent organizational, agile and classic project management skills Dynamic [. .. ]
Job am 13.02.2026 bei Jooble gefunden
SKC Beratungsgesellschaft mbH
Remote Senior Medical Writer
• Hannover
Are you looking for a full-time position in a global strategic consultancy as a Medical
Writer We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC) , a pan-European [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. Our clients in healthcare and life sciences [. .. ] in key market access disciplines Native-level proficiency in German English and extensive experience in writing scientific texts and communicate in both languages Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research Advanced skills in MS-Office CRM, project management, and data tools (preferred) , knowledge of La Te X is an advantage Excellent organizational, agile and classic project management skills Dynamic [. .. ]
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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 28 offene Stellenanzeigen für Pharmaceutical Writer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writer Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Pharmaceutical Writer Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Writer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Writer Stellenangebote:
- Evestia Clinical (6 Jobs)
- SKC Beratungsgesellschaft mbH (6 Jobs)
- Veristat (2 Jobs)
- Dr. Falk Pharma GmbH (2 Jobs)
- Biontech (1 Job)
In welchen Bundesländern werden die meisten Pharmaceutical Writer Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Writer Jobs werden derzeit in Niedersachsen (3 Jobs), Sachsen-Anhalt (2 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Writer Jobs?
Pharmaceutical Writer Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
