170 Jobs für Pharmaceutical Writing
Stellenangebote Pharmaceutical Writing Jobs
Job am 05.12.2025 bei Jobleads gefunden
• Basel- Landschaft
Führungs-/ Leitungspositionen
A global healthcare company located in Switzerland is seeking a Director of Medical Writing for Oncology. This role requires extensive experience in
pharmaceutical writing and leadership capabilities, as you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] oversee projects and mentor a team of writers. You will be responsible for ensuring timely and high-quality regulatory submissions. Ideal candidates will have a strong background in medical writing, project management, and team leadership, contributing to innovative healthcare solutions. #J-18808-Ljbffr [. .. ]
Job vor 8 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Process Design Expert (m f d)
• Bergisch Gladbach
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
[. .. ] audits, team trainings, and Qualifications You hold a university degree in engineering, life sciences, economics, informatics, or a related field. You bring experience in process design, and [...]
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[...] documentation or manual writing as well as related project management-ideally within the pharmaceutical, logistics, or regulated environments. You have a strong analytical mindset and the ability to translate complex requirements into clear, actionable processes. You are a strong communicator who enjoys aligning with diverse stakeholders across functions and geographies and are comfortable with occasional business travel. Fluency in English is required; German is [. .. ]
Job vor 8 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• Bergisch Gladbach
Homeoffice möglich
[. .. ] alignment from early research through late-stage clinical development. As an integral team member of Clinical Drug Development, you communicate complex scientific data clearly and effectively in English, [...]
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[...] both in writing and speaking, and leadership by coaching, mentoring, and educating less experienced colleagues while upholding high scientific and operational standards You hold an advanced degree (Ph D, MD, Pharm D, or equivalent) in life sciences, medicine, or a related field paired with significant experience in clinical development within the pharmaceutical or biotech industry, ideally including exposure to advanced therapy medicinal products (ATMPs) and/or CAR-T therapies. You have a proven track record in protocol development, regulatory submissions (IND, CTA, BLA, MAA) , and clinical data interpretation, and are recognized as an expert in the end-to-end process of [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Solution Architect Digital Biology
• München, Bayern
[. .. ] on working with the latest GPU hardware and software. Our platform for ML/ AI and high-performance computing has already had a significant impact on the healthcare industry, [...]
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[...] serving leading pharmaceutical companies, academic medical centers, and start-ups. We are seeking an enthusiastic individual to join us in exploring new opportunities in the AI-powered digital biology revolution. As a Solution Architect, you will work as a trusted technical advisor to our customers in the pharmaceutical and techbio industries, who envision [. .. ] Architect role to gain experience in various technical areas. Document what you know and teach others. This can vary from building targeted training for partners and other Solutions Architects to writing whitepapers, blogs, and wiki articles to simply working through hard problems with a customer on a whiteboard. We make heavy use of conferencing tools, but some travel is required for this role. You are empowered to find the best way to get your job done and make our customers successful. [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Jobticket
[. .. ] focus is to provide medical consultation and scientific background for campaigns and projects. It also advises clients and agency members, ensuring the best possible services related to [...]
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[...] high science, medical writing, compliance, and healthcare marketing. Execution of Service: Ensure the professional and timely execution of all requested services, maintaining a high level of scientific expertise and healthcare marketing proficiency. Key responsibilities: Develop a thorough understanding of clients business, brands, and indications. Ensure compliance with health industry standards, company policies, and HWG [. .. ] mindset. Ability to work under time pressure. Above-average commitment. Solution-oriented with a focus on successful results. Diplomatic skills. Benefits/ what we offer: Exciting and varied projects with TOP pharmaceutical companies in diverse sectors and specialist areas. Healthcare communication that is engaging and surprising. Collegial interdisciplinary cooperation at eye level with medical, creative, and consultant team members. Appreciation, recognition, and a strong hands-on mentality within the team. Comprehensive induction with a personal contact person. Global networking and local sovereignty. [. .. ]
Job am 02.12.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
Führungs-/ Leitungspositionen
[. .. ] clinical knowledge in respective areas of Interest. Your profile Qualifications: MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
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[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase IIV trials. Experience writing protocol amendments, informed consents, and other protocolrelated documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and clinical [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] pillars Saa S solutions, Patient Services Solutions, and Consulting Services we empower life sciences companies to make smarter decisions, engage patients more meaningfully, and ultimately improve health [...]
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[...] outcomes. Our solutions support pharmaceutical partners across the entire commercial lifecycle, from launch to postmarket optimization. Your Role with us As a Senior Product Manager (f/m/d) at Temedica, youll be at the heart of shaping and shipping impactful products for our patients. Youll drive the teams momentum, ensuring that every release is highquality [. .. ] skills to truly change lives. What You Bring To The Table Core product skills: Problem discovery, user journey workflow mapping, prioritization, and datadriven decisionmaking. Execution delivery: Roadmapping, epic/ user story writing, agile rituals, and release management. Customer focus: Obsession with user needs, journey mapping, usability, and adoption growth. Leadership communication: Confident, clear communicator who can inspire teams and influence stakeholders. Business growth mindset: Experience driving product adoption, defining success metrics, and aligning with business impact. Technical domain fluency: Comfortable working with [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Essen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Stuttgart, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Dortmund, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] and clinical knowledge in respective areas of Interest Your profile MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 04.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Leipzig, Sachsen
Führungs-/ Leitungspositionen
[. .. ] knowledge in respective areas of Interest Your profile Qualifications : MD, Md/Ph. D. , in life sciences and Oncology Fellowship training is required. 3+ years of experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job am 21.09.2025 bei Jobleads gefunden
Senior Product Manager (f/m/d) (Mobile Apps)
• München, Bayern
Work-Life-Balance
[. .. ] pillars Saa S solutions, Patient Services Solutions, and Consulting Services we empower life sciences companies to make smarter decisions, engage patients more meaningfully, and ultimately improve health [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes. Our solutions support pharmaceutical partners across the entire commercial lifecycle, from launch to post-market optimization. Your Role with us As a Senior Product Manager (f/m/d) at Temedica, youll be at the heart of shaping and shipping impactful products for our patients. Youll drive the teams momentum, ensuring that every release is [. .. ] living. What you bring to the table Core product skills : Problem discovery, user journey workflow mapping, prioritization, and data-driven decision-making. Execution delivery : Roadmapping, epic/ user story writing, agile rituals, and release management. Customer focus : Obsession with user needs, journey mapping, usability, and adoption growth. Leadership communication : Confident, clear communicator who can inspire teams and influence stakeholders. Business growth mindset : Experience driving product adoption, defining success metrics, and aligning with business impact. Technical domain fluency [. .. ]
Job am 01.09.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] MUST: Have Bachelor or Master s Degree in engineering or related training background. MUST: 5+ years experience in Risk Management or Quality/ Regulatory within a regulated industry [...]
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[...] (e. g. medical, pharmaceutical, automotive, aerospace) . MUST: Demonstrable understanding and application of Design Controls per 21 CFR 820.30 and Risk Management per ISO 14971. MUST: Demonstrable understanding and application of Design, Use and Manufacture risk-related analysis methodologies, including but not limited to FMEAs, FTAs and Medical Hazard Analysis. MUST: Technical understanding [. .. ] Hands-on mindset with problem-solving skills and great attention to detail also while multitasking. MUST: Ability to work in cross-functional teams that span global operations. MUST: Have experience writing plans and reports. SHOULD: Experience with intravascular catheter or minimally invasive device design and development. SHOULD: Have knowledge of ultrasound imaging systems SHOULD: Have experience working in a startup environment. Soft Skills MUST: Strong work ethics and a team-oriented mindset. MUST: Hands-on mindset with problem-solving skills and [. .. ]
Job am 01.09.2025 bei Jobleads gefunden
Senior Risk Manager Munich, Germany
• München, Bayern
[. .. ] profile: MUST: Have Bachelor or Masters Degree in engineering or related training background. MUST: 5+ years experience in Risk Management or Quality/ Regulatory within a regulated industry [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (e. g. medical, pharmaceutical, automotive, aerospace) . MUST: Demonstrable understanding and application of Design Controls per 21 CFR 820.30 and Risk Management per ISO 14971. MUST: Demonstrable understanding and application of Design, Use and Manufacture risk-related analysis methodologies, including but not limited to FMEAs, FTAs and Medical Hazard Analysis. MUST: Technical understanding [. .. ] Hands-on mindset with problem-solving skills and great attention to detail also while multitasking. MUST: Ability to work in cross-functional teams that span global operations. MUST: Have experience writing plans and reports. SHOULD: Experience with intravascular catheter or minimally invasive device design and development. SHOULD: Have knowledge of ultrasound imaging systems SHOULD: Have experience working in a startup environment. Soft Skills: MUST: Strong work ethics and a team-oriented mindset. MUST: Hands-on mindset with problem-solving skills and [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] is strongly preferred. Substantial experience as an academic principal investigator for industrysponsored trials can be considered. Knowledge of regulatory requirements governing clinical trials and extensive experience in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development of and writing of registrationtrack clinical trial protocols and other trialrelated documents. Experience in interactions with ethics committee, regulatory authorities, and other external agencies. Previous experience providing oversight to vendor activities including CROs. Preferably board certified (or foreign equivalent) in Gastroenterology and/or Hepatology, Internal Diseases, or Pediatrics, but candidates with backgrounds in [. .. ] analyze and interpret clinical and efficacy data and develop formal written reports and presentations of those data internally and externally. Seniority level Director Employment type Contract Job function Science Industries Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr 73465512 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Frankfurt (Oder) , Brandenburg
[. .. ] oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Participate in the start-up of global clinical studies, working with Clinical Operations to ensure on schedule site activation and subject enrollment, monitoring, compliance with safety practices, policies, procedures as well as the day-[. .. ] a scientific discipline (i. e. MS, Pharm D, Ph D, MD) is preferred. A minimum of 3 years of clinical development research in oncology, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) is required. Strong knowledge in clinical development in Oncology development is required. Significant experience with clinical evaluation projects including development of protocols, case report forms, informed consent and study initiation and monitoring. Significant experience with data integrity, exploration, analysis and presentation. High-performing and energetic individual who demonstrates [. .. ]
Job gestern bei Jobleads gefunden
Regulatory Affairs Toxicologist REACH (mfd)
• München, Bayern
Jobticket
Locations : Munich Bad Kreuznach Frankfurt Berlin and Essen. Welcome to Ramboll a global leader in chemical and
pharmaceutical regulatory consultancy. We specialise in managing registration and approval procedures [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for chemicals, biocides, agrochemicals, pharmaceuticals and medical devices. With over 160 experts from various countries we provide a professional home for ambitious minds seeking a collaborative and innovative work environment. Your new role We are currently inviting dedicated and knowledgeable [. .. ] Remote Work: No Employment Type: Full-time Experience: years Vacancy: 1 Key Skills Proofreading, Adobe Acrobat, FDA Regulations, Manufacturing Controls, Biotechnology, Clinical Trials, Research Development, GLP, c GMP, Product Development, Chemistry, Writing Skills #J-18808-Ljbffr 73436869 [. .. ]
Job gestern bei Jobleads gefunden
Application Specialist (m/f/d) / SAP-/ MES-Key User (w/f/d) Pharma Production
• Pfaffenhofen an der Ilm, Bayern
[. .. ] process relationships in a regulated environment (GMP compliance) . Communication strength, teamwork ability and a confident presence in an intercultural environment. Excellent German and English language skills [...]
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[...] in speaking and writing. Proficient with MS Office (Excel, Power Point, Word) ; ideally experience with dataanalysis tools (e. g. , Power BI) . Employment Details Seniority level: Entry level Employment type: Fulltime Job function: Information Technology Industry: Pharmaceutical Manufacturing #J-18808-Ljbffr 73437456 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Digital Communication Trainee-Geneva
• Meyrin, Genf
Absolventen, Einsteiger, Trainees
[. .. ] by providing access to better treatment of immunological imbalances. For more information, visit the website: ompharma. com. Seniority level Internship Employment type Full-time Job function Marketing, Public [...]
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[...] Relations, and Writing/ Editing Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 73391520 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
QC Specialist with Project Manager skills
• Heidelberg, Baden- Württemberg
[. .. ] of tasks related to analysis to a new CMO, and ensure establishing a good collaboration environment Facilitate and support analytical performance and efficiency improvements at CMOs and [...]
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[...] internally at Ascendis Writing of regulatory documentation and followup on postapproval commitments to authorities Qualifications and Skills: You hold a relevant academic degree preferably a Master of Science degree in Chemistry, Engineering, Pharmacy or the like and several years of experience within QC and the Pharmaceutical industry. Further qualifications: Deep understanding of the processes in a QC Laboratory supporting the chemical manufacturing either from a QC laboratory or an Analytical Development Laboratory Experience with Tech Transfer of analytical methods between different sites or companies, including validation of analytical methods. Understanding of the complexity of not being [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Solutions Consultant, EMEA
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
[. .. ] is to accelerate insights, advance research, and improve patient outcomes in oncology and across life sciences. As a leader in realworld evidence (RWE) and datadriven technology, Concert [...]
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[...] AI partners with top pharmaceutical companies, healthcare providers, and research institutions to enhance patient outcomes and streamline clinical research. By leveraging evidencegeneration and artificial intelligence, we deliver unparalleled insights into treatment effectiveness, patient care, and disease progression to advance precision medicine and medical innovation. Within the Concert AI ecosystem, Tera Recon is a leading innovator in [. .. ] software and tools. This critical function is responsible for onboarding new customers by engaging executive teams in the launch, driving ongoing adoption, and managing renewals. The candidate must be proficient writing and speaking in German and English. Role Summary We will enable successful rollout of Tera Recon to customer end users, performing quarterly business reviews, training, and health checks virtually at least 3x/ year and onsite at least 1x/ year. Responsibilities Perform presales demonstrations and postsales customer training for Tera Recons [. .. ]
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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 bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 170 offene Stellenanzeigen für Pharmaceutical Writing Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Jobs?
Aktuell suchen 20 Unternehmen nach Bewerbern für Pharmaceutical Writing Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Writing Stellenangebote:
- Tubulis GmbH (22 Jobs)
- Miltenyi Biotec B. V. Co. KG (2 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- Abb Vie (2 Jobs)
- West Pharmaceutical Services (2 Jobs)
- Rentschler Biopharma (2 Jobs)
In welchen Bundesländern werden die meisten Pharmaceutical Writing Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Writing Jobs werden derzeit in Bayern (30 Jobs), Nordrhein-Westfalen (28 Jobs) und Niedersachsen (19 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs?
Pharmaceutical Writing Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
