Pharmaceutical Writing Stellenangebote


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Regulatory Writing 845 Jobs


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Technik & Ingenieurwesen Technische Dokumentation / Redaktion


359 Stellenangebote


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Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG

Senior Director Regulatory Affairs Global Specialty/ Biosimilar Development (f/m/d)

 • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG Senior Director Regulatory Management (f/m/d) • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG

Senior Director Regulatory Affairs (f/m/d)

 • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG Senior Director Regulatory Affairs- Specialty Development (f/m/d) • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG

Global Regulatory Affairs Senior Director (f/m/d)

 • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG Pharmaceutical Regulatory Affairs Director- Global (f/m/d) • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei STADA Arzneimittel AG Job vor 5 Tagen gefunden STADA Arzneimittel AG

Global Specialty Development Senior Director Regulatory Affairs (f/m/d)

 • Darmstadt
Vergütung / Gehalt: EUR 0,- Führungs-/ Leitungspositionen Jobticket
MEHR[...] expert for all kind of global local Regulatory questions Deputy You are the Deputy of Head Global Specialty Development Who we are looking for You have a Master in Life Science, Ph. D. You have 15+ years of experience in Pharmaceutical industry and 8 + years of experience in Regulatory affairs incl. global positions You have a proven track record of [...] bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally and in writing You are a team player, proven to be successfully working in global and cross- functional environments Your focus is entrepreneur [...]
Stellenangebot Pharmaceutical Writing Job bei Abb Vie Deutschland GmbH Co. KG Job vor 8 Tagen gefunden Abb Vie Deutschland GmbH Co. KG Senior Scientist (all genders) Product Development Science Technology- Global Material and Parenteral Packaging (permanent/ full- or part- time) • Karlsruhe
Vergütung / Gehalt: EUR 0,- Work-Life-Balance
MEHR[...] accordance with design controls requirements Qualifications Senior Scientist II: Bachelors Degree or equivalent education and typically, 12 years of experience, masters degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience. Degree in Pharmaceutical Technology, Analytical Chemistry, Material Sciences, Chemistry, Physic, or related fields Senior Scientist I: Bachelors Degree or equivalent education and typically, [...] finishIn- depth knowledge of primary packaging materials, CCS, combination products and relevant regulatory requirements (e. g. , FDA, EMA, ISO etc. ) Able to mentor and guide a team of scientists Excellent oral communication skills as well as sound technical writing documentation competencies are required, experience in authoring and reviewing regulatory submissionsThe candidate must be able to work independently, respond to [...]
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Stellenangebot Pharmaceutical Writing Job bei Abb Vie Deutschland GmbH Co. KG Job vor 8 Tagen gefunden Abb Vie Deutschland GmbH Co. KG

Senior Scientist (all genders) Product Development Science Technology- Global Material and Parenteral Packaging (permanent/ full- or part- time)
Vergütung / Gehalt: EUR 0,- Work-Life-Balance
MEHR[...] accordance with design controls requirements Qualifications Senior Scientist II: Bachelors Degree or equivalent education and typically, 12 years of experience, masters degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience. Degree in Pharmaceutical Technology, Analytical Chemistry, Material Sciences, Chemistry, Physic, or related fields Senior Scientist I: Bachelors Degree or equivalent education and typically, [...] finishIn- depth knowledge of primary packaging materials, CCS, combination products and relevant regulatory requirements (e. g. , FDA, EMA, ISO etc. ) Able to mentor and guide a team of scientists Excellent oral communication skills as well as sound technical writing documentation competencies are required, experience in authoring and reviewing regulatory submissionsThe candidate must be able to work independently, respond to [...]
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Job vom 18.02.2025 Associate Director, Clinical Programming (m/w/d) Führungs-/ Leitungspositionen
MEHR[...] clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and [...] workloads. Ability to work successfully in a matrix organizational structure. Is able to identify and engage internal and external expertise as needed. Proven networking skills and ability to share knowledge and experience amongst colleagues. Fluent in English, oral and in writing. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and [...]
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Job vom 16.02.2025

Associate Director, Clinical Programming (m/w/d)

 • Frankfurt, Hesse Führungs-/ Leitungspositionen
MEHR[...] clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and [...] workloads. Ability to work successfully in a matrix organizational structure. Is able to identify and engage internal and external expertise as needed. Proven networking skills and ability to share knowledge and experience amongst colleagues. Fluent in English, oral and in writing. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and [...]
Job vom 01.02.2025 Legal Director/ Senior Legal Advisor (m/f/d) • Berlin Führungs-/ Leitungspositionen
MEHR[...] in order to pre- empt risks and allow Pfizer to gain the maximum benefit from legal advice. Actively participate in Legal Division committees. Share best practices across the Legal Division. Lead legal projects from conception to implementation. About you: Experienced pharmaceutical lawyer with strong commercial acumen. At least 8 years of experience as syndics lawyer or lawyer at a law firm. [...] industry or advising clients within the pharmaceutical industry strongly preferred. Proven ability to cultivate strong client relationships, build credibility and successfully influence leadership in a fast- paced business climate. Strategic and proactive. Anticipates needs and able to prioritize quickly. Excellent writing, communication and presentation skills. The ability to effectively manage matters with little supervision. A high level of initiative and strong [...]
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Job vom 25.01.2025

Pharmacovigilance Officer/ EU- QPPV (Reporting to the Chief Medical Officer)

 • Wuppertal, Nordrhein- Westfalen
MEHR[...] system and establishing its system master file Ensuring adherence to the GVP modules as defined by the European Commission Continuous observation of the regulatory landscape and scientific literature regarding pharmacovigilance Reviewing and amending safety information within development documents Responsible for writing and reviewing adverse event narratives and periodic reports Responsible for standard operating procedures in pharmacovigilance, regular updates and training adherence Overseeing service providers Your profile Academic degree in life science, preferably in human medicine Profound medical and pharmaceutical knowledge At least 5 years proven work experience in managing pharmacovigilance in the pharmaceutical industry including regulatory drugs in development [...]
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Job vom 11.01.2025 Director Medical Affairs C EE Führungs-/ Leitungspositionen
MEHR[...] for a Regional Medical Affairs Strategic Plan. Addressing product or patient safety issues by intervening with HCPs and within BD processes. Providing training for commercial teams and other BD personnel. Supporting legislative, market access, and reimbursement efforts. Ensuring statistical analysis, writing, reporting, publishing and presenting of portfolio level evidence, including assisting/ collaborating with HCPs, as needed Supporting implementation of Medical Information, Training and Medical Affairs Audit activities within Country/ Region Partnering with Business Development for evaluating licensing opportunities About you You are an outstanding leader with 10- 15+ years experience in the pharmaceutical or medical device industry (at least 5 years in a relevant therapeutic area) . Your ability to communicate complex issues [...]
Job vom 02.01.2025

Medical Director/ Lead Medical Director, Nephrology

 • Basel, Basel- Stadt Führungs-/ Leitungspositionen
MEHR[...] clinical experience. You have 2+ years of post- grad relevant clinical/ scientific research and/ or clinical trial experience. You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance and demonstrated experience in scientific writing (e. g. manuscripts, grants, scientific protocols) . Outstanding communication skills in both long- form scientific presentation and short- form communication [...] of healthcare. Working together, weve become one of the worlds leading research- focused healthcare groups. Our success is built on innovation, curiosity and diversity. Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10, 700 employees from over 100 countries come together at our Basel/ Kaiseraugst site, which is one of [...]
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Job vom 26.12.2024 Medical Science Liaison Austria • München, Bayern
MEHRWith its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4, 500 employees and turnover of over Euro 2bn. We are [...] or specialty care (prescription and hospital business) . Familiarity with code of conduct for pharmaceutical product compliance. Familiarity with review and approval process of promotional and educational materials. Usage of project management tools. Experience in interpretation of scientific data and writing of scientific information. Proficiency in Microsoft Office Suite, medical information systems (i. e. Veeva) and database management (i. e. CRM) [...]
Job vom 21.12.2024

Associate Director Engineering- Device Technology (m/f/d)

 Führungs-/ Leitungspositionen
MEHR[...] on medical devices related matters and provide input to health authority questions. Minimum Requirements Bachelor, Master or PhD degree in engineering or equivalent. Preferably 8+ years of experience working in development of medical device and/ or combination products; preferred in pharmaceutical area or similar. Experience of preparing for submissions and launch as well as writing design history files. Experience in developing plastic and metal components; tolerance analysis, modeling and testing. Excellent skills in English, verbal [...]
Job vom 09.12.2024 Medical Director/ Lead Medical Director, Nephrology • Basel, Basel- Stadt Führungs-/ Leitungspositionen
MEHR[...] clinical experience. You have 2+ years of post- grad relevant clinical/ scientific research and/ or clinical trial experience. You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance and demonstrated experience in scientific writing (e. g. manuscripts, grants, scientific protocols) . Outstanding communication skills in both long- form scientific presentation and short- form communication [...] of healthcare. Working together, weve become one of the worlds leading research- focused healthcare groups. Our success is built on innovation, curiosity and diversity. Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10, 700 employees from over 100 countries come together at our Basel/ Kaiseraugst site, which is one of [...]
Job vom 08.11.2024 Associate Director Engineering- Device Technology (m/f/d) • Schaftenau, Tirol Führungs-/ Leitungspositionen
MEHR[...] on medical devices related matters and provide input to health authority questions. Bachelor, Master, or PhD degree in engineering or equivalent. Preferably 8+ years of experience working in the development of medical devices and/ or combination products; preferably in the pharmaceutical area or similar. Experience of preparing for submissions and launch as well as writing design history files. Experience in developing plastic and metal components; tolerance analysis, modeling, and testing. Excellent skills in English, verbal [...]
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Weitere Job-Ideen!
Regulatory Writing 845 Jobs

Berufsfelder
Technik & Ingenieurwesen Technische Dokumentation / Redaktion


Dauer: 0,1445 s., Vers. V.2025-a-2004-Ind