176 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 4 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Senior Clinical Scientist Clinical Drug Development (m f d)
• 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 4 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 gestern bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Frankfurt (Oder) , Brandenburg
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 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [...]
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 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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
• 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
• 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
• 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 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 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
Senior Risk Manager
• 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 [...]
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 [. .. ]
Job am 01.09.2025 bei Jobleads gefunden
• 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
Analytical Scientist LC-MS Method Development and Transfer (all genders)
• Wien
[. .. ] of provided process test samples Review and communicate analytical results effectively across teams Qualifications For this interesting opportunity we are looking for somebody with: Masters or Ph [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] D in Analytical Sciences, Pharmaceutical Sciences, Biochemistry or a related field Demonstrated experience in the pharmaceutical industry Strong background in HPLC and LC-MS method development/ troubleshooting Proven proficiency in technical writing (e. g. , publications, thesis, project reports) Independent planning and execution of analytical projects and result communication (reports, PPTs, etc. ) Proficiency in German and English written and spoken Strong problemsolving and analytical abilities Teamoriented with a flexible and collaborative personality Understanding of Gx P requirements Additional Information We are offering [. .. ]
Job gestern bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] and needs of access with strong influencing skills. Ensures all access activities adhere to governance compliance quality and ethical standards. Essential requirements At least 15 years of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in the pharmaceutical industry with significant senior leadership experience in market access pricing reimbursement or health policy. Advanced degree in life sciences health economics public health or related field; business qualification (e. g. MBA) is desirable. Experience in both country and regional/ global roles; strong knowledge of key European markets and HTA-based [. .. ] Evidence (RWE) Regulatory Compliance Resource Allocation 6 more Required Experience Director Key Skills Fiscal Management, Fundraising, Assisted Living, Management Experience, Hospice Care, Nonprofit Management, Operations Management, Strategic Planning, Budgeting, Grant Writing, Leadership Experience, Public Speaking Employment Type Full-Time Experience years Vacancy 1 #J-18808-Ljbffr 73203623 [. .. ]
Job gestern bei Jobleads gefunden
Global Head of Drug Product Qualification Validation (MSAT)
• Schwaderloch, Aargau
Führungs-/ Leitungspositionen
[. .. ] OPV strategy, as applicable Implement Process Capability/ Quality/ Cost Improvement Changes Enable innovation and technical strategy projects associated to DP aseptic manufacturing What were looking for : [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ph. D. in pharmaceutical sciences, pharmaceutical engineering, biochemistry, or related fields or similar qualification Proven experience and technical knowledge of equipment qualification related to aseptic drug product manufacturing processes Extensive experience and technical knowledge of process validation and current validation approaches for sterile manufacturing of biological drug products (lyophilized products, liquid in vials and [. .. ] or lean black belt certification required; experience with SAA JMP/ STATISTICA software is highly desirable. In depth knowledge of risk assessments, deviation and change management, root cause investigation analysis Excellent writing skills and documentation practices Excellent communication skills and command of English both written and oral Excellent leadership and interpersonal skills; proven ability as team player and ability to manage cross-functional teams. Excellent planning and organizing skills Every day, Lonzas products and services have a positive impact on millions of [. .. ]
Job gestern bei Jobleads gefunden
Sr. Manager, Drug Substance MSAT
• Zug
[. .. ] tools (e. g. , FMEA, gap analysis) throughout lifecycle management. Develop data management processes for operational analysis, including Annual Product Review (APR) and Continuous Process Verification (CPV) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] . Contribute to writing and reviewing CTD Module 3 sections for regulatory submissions (NDA, PAS, etc. ) . Required Qualifications Bachelors degree in life sciences/ engineering; advanced degree (MS/ Ph D) preferred. Experience Extensive experience in c GMP development and manufacturing with strong MSAT background. Deep knowledge of pharmaceutical processes, technologies, and systems; experience in process development, tech transfer, scaleup, validation, and manufacturing. Proven track record in MSAT or related fields. Experience in process validation and lifecycle management. Familiarity with CTD Module3 authorship and regulatory standards (FDA, EMA, ICH) . Expertise in at least two modalities (e. g. , [. .. ]
Job gestern bei Jobleads gefunden
Global Head of Drug Product Qualification Validation (MSAT)
• Zeihen, Aargau
Führungs-/ Leitungspositionen
[. .. ] OPV strategy, as applicable Implement Process Capability/ Quality/ Cost Improvement Changes Enable innovation and technical strategy projects associated to DP aseptic manufacturing What were looking for : [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ph. D. in pharmaceutical sciences, pharmaceutical engineering, biochemistry, or related fields or similar qualification Proven experience and technical knowledge of equipment qualification related to aseptic drug product manufacturing processes Extensive experience and technical knowledge of process validation and current validation approaches for sterile manufacturing of biological drug products (lyophilized products, liquid in vials and [. .. ] or lean black belt certification required; experience with SAA JMP/ STATISTICA software is highly desirable. In depth knowledge of risk assessments, deviation and change management, root cause investigation analysis Excellent writing skills and documentation practices Excellent communication skills and command of English both written and oral Excellent leadership and interpersonal skills; proven ability as team player and ability to manage cross-functional teams. Excellent planning and organizing skills Every day, Lonzas products and services have a positive impact on millions of [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
EMESA Compliance Analyst-temporary position (13 months)
• München, Bayern
[. .. ] effectively in a fastpaced environment, with the ability to prioritize and balance competing, timeurgent demands Strong attention to details Outstanding English written and oral communication skills, including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clear and concise writing and editorial skills and excellent listening skills. Additional languages desirable What Youll Bring: An academic degree in a relevant discipline. Advanced degree preferred Experience in a compliance function/ or other risk management discipline such as audit, fraud examination, quality control, risk analysis within a financial/ banking institution, professional services, consulting firm or international business (aerospace, transport, construction, pharmaceutical, healthcare etc. ) . We are seeking candidates with 26 years of relevant compliance experience. Comfortable with, and preferably advanced knowledge of, Microsoft Office (Power Point, Excel, Word) , Trello, exposure to business intelligence tools: Tableau, Power BI Commitment to confidentiality required Who Youll Work With: You will be part [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Research Associate
[. .. ] oncology global trials preferred Other Qualifications: Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines At least 2 years of (CRA) monitoring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in the pharmaceutical or CRO industry Experience in oncology/ hematology trials preferred Excellent communication and interpersonal skills Excellent organizational skills and ability to prioritize and multi-task Fluent in English German (writing and speaking) Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS Power Point and Outlook Travel: up to 60Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Director CMC Projects (all genders) - Fulltime, permanent
• Ludwigshafen am Rhein, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] at least 16years of relevant CMC experience, or a Ph D with at least 10 years of relevant CMC experience Strong educational foundation, with significant experience across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CMC functions Excellent scientific writing and verbal communication skills Expertise includes regulatory requirements and familiarity with relevant research instrumentation and techniques Solid knowledge of pharmaceutical sciences and the drug development process Interdisciplinary CMC experience and depth of expertise Negotiation, influencing, and leadership abilities are well developed Creative and entrepreneurial thinking to guide smart business decisions Fostering a high level of team morale within the CMC group Zusätzliche Informationen Heres how we can move mountains together [. .. ]
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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 176 offene Stellenanzeigen für Pharmaceutical Writing Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Jobs?
Aktuell suchen 18 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 (21 Jobs)
- Miltenyi Biotec B. V. Co. KG (2 Jobs)
- West Pharmaceutical Services (2 Jobs)
- Rentschler Biopharma (2 Jobs)
- Simon- Kucher Partners (2 Jobs)
- Abbott (1 Job)
In welchen Bundesländern werden die meisten Pharmaceutical Writing Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Writing Jobs werden derzeit in Bayern (31 Jobs), Nordrhein-Westfalen (28 Jobs) und Niedersachsen (23 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs?
Pharmaceutical Writing Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
