31 Jobs für Drug Safety Specialist
Stellenangebote Drug Safety Specialist Jobs
Job vor 7 Tagen bei Jobware gefunden
ABDA- Bundesvereinigung Deutscher Apothekerverbände e. V.
• 10557 Berlin
Teilzeit
Flexible Arbeitszeiten Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] der systematischen Überwachung, Erkennung und Abwehr von Arz-neimittelrisiken Deine Organisationsfähigkeit, Kommunikationsstärke und Teamfähigkeit sowie der sichere Umgang mit Microsoft 365-Anwendungen runden Dein Profil ab. Pharmakovigilanz-Referentin Mitarbeiterin Arzneimittelsicherheit [...]
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[...] Drug Safety Specialist Pharmacovigilance Officer Medical Information Specialist 95702413 [. .. ]
Job vor 8 Tagen bei Jobware gefunden
ABDA- Bundesvereinigung Deutscher Apothekerverbände e. V.
Referentin (m/w/d) Arzneimittelinformation und -sicherheit
• 10557
Teilzeit
Flexible Arbeitszeiten Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] der systematischen Überwachung, Erkennung und Abwehr von Arz-neimittelrisiken Deine Organisationsfähigkeit, Kommunikationsstärke und Teamfähigkeit sowie der sichere Umgang mit Microsoft 365-Anwendungen runden Dein Profil ab. Pharmakovigilanz-Referentin Mitarbeiterin Arzneimittelsicherheit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Drug Safety Specialist Pharmacovigilance Officer Medical Information Specialist 94972900 [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
• Ramstein- Miesenbach, Rheinland- Pfalz
[. .. ] position. A non-disclosure agreement must be signed. Duties will require frequent unescorted entry into and temporary work within Sensitive Compartmented Information Facility (a windowless, air-conditioned secure vault) [...]
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[...] . Drug Testing: This position has been designated by the Air Force as a Testing Designated Position (TDP) under the Air Force Civilian Drug Demand Reduction Program. Employee must pass initial and periodic short notice drug testing. Illegal drug use by employees in sensitive positions presents a clear threat to the mission of the Air Force, national security, and public safety. The employee may be required to travel in military and/or commercial aircraft to perform temporary duty assignments. Duties are performed in a normal office setting. Work is primarily sedentary, normally performed at a desk in a fourth-floor office building. Offices are adequately lighted, heated, and ventilated. Employee is [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Clinical Supplies Quality Auditor (GMP Release)
• Luzern
nemensis ag in Luzern, Switzerland, is seeking a dedicated
Specialist Clinical Supplies Quality to ensure GMP-compliant processes in clinical
drug supply. The ideal candidate holds a relevant university degree and [...]
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[...] has 2-3 years of experience in a GMP-regulated setting. Responsibilities include batch record review, inspection of packaging components, and regulatory review, all while maintaining rigorous quality standards. This role offers an opportunity to work in a dynamic team committed to patient safety. #J-18808-Ljbffr 94874978 [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Ingelheim am Rhein, Rheinland- Pfalz
[. .. ] evidence plans (clinical, RWE, epidemiology) to support differentiation, regulatory success, and market access, while driving publication planning and scientific material creation Collaborate crossfunctionally across the Innovation Unit, [...]
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[...] Clinical Development, Operations, Safety, Epidemiology, Marketing, Market Access, Communications, and Patient Engagement, to ensure alignment and execution of medical strategies Craft and deliver compelling, scientifically robust medical narratives, communication strategies and promotional materials, ensuring alignment with strategic objectives Engage with key opinion leaders, scientific societies, and external partners to shape the medical landscape and integrate actionable insights into strategic decisions Build globallocal Medical Affairs collaborations to ensure knowledge transfer, launch readiness, and regional alignment Requirements Medical Doctor (e. g. , endocrinologist, internal medicine, obesity specialist, primary care physician) with a specialty in obesity medicine and experience in Obesity and Liver Health Longterm experience in the pharmaceutical industry, including several years in Medical Affairs as a Medical Advisor or Medical Manager in a global or international role Deep understanding of drug development, clinical trial design, data analysis, and interpretation, with expertise in introducing new medicines or expanding indications at a global level (e. g. , Obesity, Liver, or Cardiometabolic Health) Strategic thinker with strong crossfunctional collaboration skills, a clear understanding of medicomarketing processes, and the ability to lead impactful crossregional medical [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Quality Auditor (a) 100
• Luzern
[. .. ] Period 03.08.2026 31.07.2027, with option for extension About Our Client For our client, a globally active pharmaceutical company with a strong focus on clinical research and
drug [...]
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[...] supply, we are looking for a dedicated Specialist Clinical Supplies Quality (f/m/d) . The organisation is renowned for its rigorous quality standards, innovative pipeline, and a collaborative culture that places patient safety at the heart of every decision. Responsibilities GM Pcompliant batch record review and formal release of clinical finished goods Incoming inspection and release of label stock and primary packaging components Verification of printed and applied labels as part of the finished goods release process Review of regulatory filings in connection [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Gössendorf, Steiermark
[. .. ] clinical governance five core practices (clinical standards, medical standards, performance measurement, education, and scientific research) . To plan, coordinate, deliver, and evaluate the pharmaceutical care service, be [...]
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[...] responsible provision of drug therapy for purpose of achieving definite therapeutic outcome that improve the patient quality of life, wellbeing and health promotion (educational activities) , Pharmaceutical supply management, scientific research and preventive care services to provide life enhancing renal care. Key Responsibilities Definition of Reporting Lines The pharmacist is accountable to the Direct [. .. ] make a positive difference in patients medical management. Engage and actively participate in dietetic research led by the pharmaceutical care department. Pharmaceutical Supplies Manage pharmaceutical supplies with ensure both Medications Safety/ Product Quality (in terms of shipping, delivery, storage and preparation) , availability of the product to cover any situation of need. Coordinate with Logistics Services regarding quality availability, submit accurate reports to determine the need continuously submit accurate reports of critical pharmaceutical items ahead of time to SC. Review all [. .. ] of pharmaceutical team as applicable. Participate in self and others education, training and development including assigned pharmacist interns as applicable. Qualifications Education Bachelors degree in Doctor of Pharmacy Certified Pharmacist Specialist by the Saudi Commission for Health Specialties (SCFHS) Experience Fresh Graduate, 1-2 years clinical dietetics experience in a clinical setting or hospital is favorable. Experience in clinical specialty favorable (renal, diabetes, hypertension) Languages Fluent in Arabic and English (spoken and written) IT Skills Computer operating experience and MS Office [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Principal/ Senior Scientist, Biological Process Development
• München, Bayern
The Senior Scientist, Biological Process Development is a highly skilled and collaborative team member responsible for designing, executing, and interpreting experiments that advance
drug substance process development for the [...]
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[...] companys live biotherapeutic product (LBP) pipeline. This role spans both upstream and downstream processing activities for drug substance-from fermentation optimization and scale-up through harvest, concentration, lyophilization, and preparation for drug product manufacturing. In addition to strong bench science capabilities, the Senior Scientist will play an active role in coordinating technical activities with external contract development and manufacturing organizations (CDMOs) and specialist vendors, serving as an informed day-to-day liaison between internal development programs and the external partner network. KEY RESPONSIBILITIES Process Development Design and execute fermentation development experiments using bench-top and pilot-scale bioreactors, including operation of anaerobic culture systems appropriate for LBP organisms. Optimize culture media, seed train [. .. ] and contribute to process development reports, technical summaries, standard operating procedures (SOPs) . Ensure all in-house experimental work is conducted in compliance with applicable biosafety, EH S, and laboratory safety requirements. Participate in internal scientific reviews, cross-functional team meetings, and project updates; present data clearly and concisely to diverse audiences including non-technical stakeholders. Provide day-to-day technical guidance and mentorship to scientists and research associates within the process development group. Collaborate closely with Analytical Development, CMC, Quality, [. .. ]
Job am 05.06.2026 bei Jobleads gefunden
Position Overview The Associate Clinical
Specialist independently provides customer support of Fujifilms ES equipment in the Endoscopy department and/or specified departments. This role manages all relevant equipment and uses [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its own judgement and decision-making skills to provide troubleshooting and training for the proper handling of our equipment. This position provides on-site, hands-on [. .. ] identifying trends that influence strategic planning. Provide and maintain customer data for integration into a future database application. Attend local, regional, and national trade shows as requested. Adhere to all safety policies and procedures. Comply with all applicable U. S. Food and Drug Administration (U. S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. Qualifications High School Diploma or equivalent is required. Bachelors degree in business, marketing or related quantitative disciplines preferred. Minimum of 2 years of field sales or clinical experience desired. [. .. ]
Job am 27.05.2026 bei Jobleads gefunden
Endoscopy Associate Clinical Specialist (Upstate NY-Buffalo/ Rochester)
Position Overview The Associate Clinical
Specialist independently provides customer support of Fujifilms ES equipment in the Endoscopy department and/or specified departments. This role manages all relevant equipment and uses [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its own judgement and decision-making skills to provide troubleshooting and training for the proper handling of our equipment. This position provides on-site, handson client [. .. ] identifying trends that influence strategic planning. Provide and maintain customer data for integration into a future database application. Attend local, regional, and national trade shows as requested. Adhere to all safety policies and procedures. Comply with all applicable U. S. Food and Drug Administration (U. S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. Qualifications High School Diploma or equivalent is required. Bachelors degree in business, marketing or related quantitative disciplines preferred. Minimum of 2 years of field sales or clinical experience desired. [. .. ]
Job am 18.05.2026 bei Jobleads gefunden
• München, Bayern
About the Role You will support daily depot operations, ensuring vehicles and equipment are ready for each shift. This role involves handson work with vehicles, basic technical tasks, and maintaining [...]
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[...] safety and efficiency in a fastpaced environment. Key Responsibilities Prepare vehicles for shift start (software setup, checks, basic troubleshooting) Perform basic vehicle tasks (calibration, adjustments, EV charging setup) Ensure cleanliness of vehicles and work areas (sanitization, vacuuming, wiping) Support shift operations and follow startup/ endofshift procedures Monitor and report system or [. .. ] and ability to work independently Physically able to stand, walk, and lift up to 20 kg Additional Requirements Ability to pass background checks and driving record verification Willingness to undergo drug/ alcohol testing as required Availability to work rotating shifts, including evenings, weekends, and holidays What We Offer Longterm, stable employment Training and ongoing support Opportunity to work with modern technology in a structured environment #J-18808-Ljbffr 92068896 [. .. ]
Job am 16.05.2026 bei Jobleads gefunden
Field Service Engineer
• Kaarst, Nordrhein- Westfalen
Join to apply for the Field Customer Support
Specialist role at Charles River Laboratories 4 days ago Be among the first 25 applicants Join to apply for the Field [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Customer Support Specialist role at Charles River Laboratories Get AI-powered advice on this job and more exclusive features. For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, [. .. ] River is an early-stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our [. .. ]
Job am 09.05.2026 bei Jobleads gefunden
Depot Specialist
• Berlin
About the Role You will support daily depot operations, ensuring vehicles and equipment are ready for each shift. This role involves handson work with vehicles, basic technical tasks, and maintaining [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety and efficiency in a fastpaced environment. Key Responsibilities Prepare vehicles for shift start (software setup, checks, basic troubleshooting) Perform basic vehicle tasks (calibration, adjustments, EV charging setup) Ensure cleanliness of vehicles and work areas (sanitization, vacuuming, wiping) Support shift operations and follow startup/ endofshift procedures Monitor and report system or [. .. ] and ability to work independently Physically able to stand, walk, and lift up to 20 kg Additional Requirements Ability to pass background checks and driving record verification Willingness to undergo drug/ alcohol testing as required Availability to work rotating shifts, including evenings, weekends, and holidays What We Offer Longterm, stable employment Training and ongoing support Opportunity to work with modern technology in a structured environment #J-18808-Ljbffr 91134116 [. .. ]
Job am 02.05.2026 bei Jobleads gefunden
What is Retin-A Cream Made Use Of For-
• München, Bayern
[. .. ] stop the growth of acne marks. It is important to note that Retin-A cream may originally create some skin irritation and dry skin as the skin adapts [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to the drug. However, with routine use and proper moisturization, these side effects typically go away, and also the skin ends up being less prone to acne breakouts. Decreasing Wrinkles and also Great Lines Retin-A cream is likewise commonly used to minimize the appearance of wrinkles as well as fine lines. As [. .. ] to be related to tidy, completely dry skin in the evening, as sunlight can weaken its performance. It is important to comply with the guidelines supplied by your health care specialist and also not to use greater than the prescribed quantity. Safety and security and Safety measures While Retin-A cream is usually safe and also well-tolerated, depanten gel articulatii there are a couple of precautions to remember. It is not suggested for usage while pregnant or while breastfeeding, as the impacts on the coming child are still unknown. It is [. .. ]
Job am 27.02.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] symptoms like itching, soreness, and also irritation. How Does Nystatin Triamcinolone Cream Work? Nystatin triamcinolone cream works through the mixed actions of its two energetic ingredients. Nystatin [...]
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[...] is an antifungal drug that works by interrupting the cell wall surfaces of the fungis, which ultimately results in their death. It targets details parts of the fungal cell wall surfaces, called ergosterols, and prevents their synthesis. By doing so, nystatin prevents the development and also spread of the fungi, enabling the body to [. .. ] problem. When combined, nystatin and also triamcinolone give an extensive treatment for fungal infections with an included benefit of decreasing swelling as well as advertising recovery. Benefits as well as Safety measures Nystatin triamcinolone lotion supplies numerous benefits for individuals suffering from fungal infections and also inflammatory skin conditions: Effective therapy: The combination of nystatin as well as triamcinolone gives a powerful therapy alternative for fungal infections. It targets the underlying reason for the infection while reducing swelling and also promoting [. .. ] and well-tolerated, there are specific preventative measures that need to be thought about: Consultation with a health care professional: It is very important to consult with a health care specialist, such as a dermatologist, prior to making use of nystatin triamcinolone lotion. They will evaluate the condition as well as identify if this medication is suitable for the particular case. Ideal use: It is essential to adhere to the recommended dosage and directions given by the medical care expert. Overuse [. .. ]
Job am 27.02.2026 bei Jobleads gefunden
How Much Weight Can You Shed with Water Pills-
• München, Bayern
[. .. ] a safe choice. Prior to diving into the topic, it is important to note that water tablets ought to just be made use of under the guidance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of a healthcare specialist. Self-medicating or misusing diuretics can cause electrolyte discrepancies, dehydration, and also various other hazardous adverse effects. Constantly speak with your medical professional before taking into consideration any type of weight loss strategy. The Mechanism of Water Tablets Water tablets function by enhancing the excretion of water and also salt [. .. ] pills as component of your weight administration plan, consult with your medical professional or a registered dietitian. They can provide individualized referrals based upon your details demands and also objectives. Safety And Security Factors To Consider and Side Effects As stated previously, the misuse of water pills can have unfavorable effects on your health and wellness. It is vital to recognize the possible threats prior to considering their usage for weight loss. Some typical negative effects of diuretics include: Dehydration Dizziness [. .. ] women, people with kidney problems, and those with a background of gout or diabetic issues. Always divulge your complete case history to your doctor prior to starting any kind of drug. Final thought Water tablets, or diuretics, are mainly meant for individuals with certain medical conditions and also except weight-loss purposes. While they can briefly lower water weight, they do not result in substantial fat loss. Incorrect use of water pills can result in dehydration and various other wellness issues. [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
• Berlin
[. .. ] als auch Projektarbeit Sehr gute Deutsch und Englischkenntnisse English Version Scientist (m/f/d) In Vitro Genetic Toxicology RESPONSIBILITIES Scientific management strategy : Planning, controlling, and monitoring toxicological assessments [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of drug candidates, impurities, metabolites, and chemicals with a focus on genotoxicity. Definition of the in vitro toxicology strategy in close coordination with the companys research and development goals Regulatory responsibility : Study management in accordance with GLP, preparation and review of study documentation for regulatory submissions, active participation in inspections, and [. .. ] Customer business development : Building and maintaining customer relationships, assisting with quotations and pricing, identifying new business opportunities, and actively contributing to Nuvisans growth External visibility : Representing Nuvisan at specialist conferences, participating in scientific and regulatory working groups, and publishing study results QUALIFICATIONS Ph D in toxicology, pharmacology, life sciences, or a related field Practical experience in in vitro and genetic toxicology, ideally in a leadership role as a study or team leader; experience in an industrial or CRO environment is [. .. ] Experience with modern in vitro methods, in silico models, data interpretation, and biostatistics Qualification for project management in accordance with the German Genetic Engineering Act (Gen TG) and the Genetic Engineering Safety Ordinance (Gen TSV) Experience in personnel management, team development, and resource planning Cost awareness, ability to manage budgets, and interest in actively developing new business areas Strong communication skills, negotiating skills, strategic thinking, intercultural competence, and enjoyment of customeroriented collaboration High level of ability for routine and project work within the [. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
Terumo
QA Ops Qualification Validation Specialist (m/f/d)
Job Summary As a QA Operations
Specialist, you ensure that daily operations across manufacturing, quality control, engineering and warehousing are fully compliant with GMP and internal procedures. You will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] act as a key QA partner on the shop floor, providing guidance, performing document reviews, and supporting quality events such as deviations, CAPAs and change controls. In addition, [. .. ] Support real-time batch review and preparation of batch documentation packages Ensure QA compliance during qualification and validation activities Perform cleanroom release activities for GMP manufacturing Oversee quality aspects of drug product manufacturing (formulation, aseptic filling, lyophilisation, inspection and packaging) Manage abnormal and rejected materials, including SAP handling (blocking/ unblocking, master data updates) Support deviations, CAPAs, change controls and other quality events Contribute to the review and improvement of SOPs, risk assessments and batch documentation Perform electronic data review ensuring data [. .. ] to contributing to society through healthcare. A dynamic and international GMP-regulated CDMO environment The opportunity to work close to operations and have direct impact on product quality and patient safety A collaborative culture focused on continuous improvement and learning Opportunities to develop within Quality, Manufacturing and global operations A workplace where innovation, quality and integrity are at the core of everything we do 95986528 [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
GULP experts united
• Biberach, Baden- Württemberg
Ensure the highest quality standards in pharmaceutical packaging with us Adherence to strict GMP guidelines is the foundation of our success and the
safety of patients worldwide. For our [...]
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[...] packaging department, we are seeking a dedicated and detail-oriented individual to oversee operational processes and ensure compliance with our quality standards. From managing the SOP system and conducting GMP walkthroughs to supporting regulatory inspections, you will assume significant responsibility. Contribute your quality awareness and strengthen our team as a Production Support Compliance Specialist (m/f/d) . Heres what we offer Attractive salary and long-term job security through affiliation with a large corporation. Up to 30 days of vacation per year Company pension scheme contribution after the end of the probationary period Extensive social benefits, including Christmas and holiday pay Reimbursement of [. .. ] on existing guidelines. Furthermore, you will collaborate on the electronic documentation of training courses in the relevant system (LOS) . They assist in conducting GMP inspections to ensure GMP-compliant drug packaging. Furthermore, you will be involved in the preparation, coordination, execution and follow-up of internal and external (official) inspections. Your responsibilities also include conducting the logbook review in accordance with the applicable process guidelines. Your profile Completed vocational training in natural sciences or pharmaceuticals with many years of relevant [. .. ]
Job vor 10 Tagen bei Neuvoo gefunden
Charles River
Associate BD Manager RMS (m/w/d) - Benelux area
• Sulzfeld, Bavaria
For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new
drug therapies. When you join our family, you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, [. .. ] assigned regionfor all Charles River product and services into accounts in a designated geographical region. This position requires frequent domestic and international travel. YOUR RESPONSIBILITIES: Work closely with both the specialist sales staff and management teams to increase market share of both in-house and outsourced revenue spend at assigned accounts or within a geographical territory. Meet or exceed overall revenue targets and business objectives. With direction and support from management and peers, generateaccount-specific sales strategies to sell all company [. .. ] River is an early-stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
Commonwealth of Virginia
Food Safety Specialist #00429
• Hanover, Lower Saxony
Homeoffice möglich
Job Duties The Virginia Department of Agriculture and Consumer Services is seeking a self-motivated person to become part of our Food
Safety team. This position is responsible for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] evaluation of food processes and the enforcement of the Virginia Food and Drink Law and related federal and state regulations. Duties include evaluating the condition of food processing facilities relative to food safety; assisting new and existing food processing technologies and food labeling [. .. ] The selected individual will be responsible for obtaining and maintaining a commissioner with Pocket Credentials as an official of the Department of Health and Human Services, U. S. Food and Drug Administration (FDA) , and within 18 months of hire will be responsible for becoming and maintaining Standardized for Retail inspections credentials. Must have (or be eligible for) and maintain a valid drivers license and have a driving record that reflects a sense of responsibility for highway safety. HS Diploma/ GED [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
Charles River Laboratories, Inc.
Associate BD Manager RMS (m/w/d) - Benelux area
• Sulzfeld, Baden- Württemberg
For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new
drug therapies. When you join our family, you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, [. .. ] assigned regionfor all Charles River product and services into accounts in a designated geographical region. This position requires frequent domestic and international travel. YOUR RESPONSIBILITIES: Work closely with both the specialist sales staff and management teams to increase market share of both in-house and outsourced revenue spend at assigned accounts or within a geographical territory. Meet or exceed overall revenue targets and business objectives. With direction and support from management and peers, generateaccount-specific sales strategies to sell all company [. .. ] River is an early-stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our [. .. ]
Job vor 14 Tagen bei Neuvoo gefunden
NVision Quantum Technologies GmbH
Field Product Specialist (Hyperpolarization/ NMR) (m/f/d)
• Ulm, Baden- Württemberg
Homeoffice möglich
Your mission We are seeking an experienced Field Product
Specialist to serve as the primary interface between Engineering and Science. This multidisciplinary role requires a deep understanding of both [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] fields to ensure the reliable operation of our Preclinical Polaris. You will be responsible for the seamless transition from hyperpolarization physics to high-quality diagnostic doses, translating scientific needs into technical [. .. ] and maintain SOPs for NMR analysis and quality control Support validation activities and analyze system performance to ensure long-term stability and reproducibility Ensure field activities comply with applicable regulations, safety standards, and quality requirements Training Implementation Develop and deliver user training and documentation for the Preclinical Polaris Lead technical onboarding for researchers and clinical staff, enabling effective system use in daily practice Support Site Acceptance Testing (SAT) to ensure systems meet performance expectations at installation Cross-functional Collaboration Act as [. .. ] a unique approach-leveraging organic molecules to change lives for the better. Our platform spans from quantum signal enhancement that enables metabolic imaging today to quantum computing that could transform drug discovery tomorrow. Headquartered in Ulm, Germany, and backed by leading investors from the United States and Europe, we are now entering a phase of global commercialization and expansion. With our POLARIS product line, we are extending the capabilities of standard MRIs to enable real-time metabolic imaging, transforming how diseases [. .. ]
Job am 03.06.2026 bei Neuvoo gefunden
AMDT
Senior Talent Acquisition Specialist (m/f/d)
• Landau, Rhineland- Palatinate
[. .. ] on ownership, pragmatically improves processes, and delivers measurable results: closed requisitions, reduced time-to-fill, higher quality of hire, and lower dependency on external agencies. As a Senior Talent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Acquisition Specialist, you will be the key operational driver of recruiting and ensure that hiring works reliably and at scale. Your Tasks Full operational ownership of open requisitions: independently managing and successfully filling roles across multiple departments Reducing time-to-fill through efficient processes, clear prioritization, and consistent stakeholder management Hands-on [. .. ] of production processes through strong end-point management, where it consistently records and monitors changes to configurations, programming and project statuses in production. This minimizes downtime, increases efficiency, quality and safety standards, and saves costs as well as resources. As a modular solution, octoplant can be linked to different automation technologies and devices, regardless of the manufacturer. AMDT was formed in 2022 from the merger of the two established market leaders AUVESY Gmb H and MDT Software Inc. The company is headquartered [. .. ] age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. AMDT maintains a drug-free workplace. 93482210 [. .. ]
Job am 29.05.2026 bei Neuvoo gefunden
Charles River
IT Specialist
• Kaarst, North Rhine- Westphalia
Work-Life-Balance
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new
drug therapies. When you join our family, you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. Job Overview The IT Specialist I is responsible for providing exceptional end user support to the highest level and standards to the business. Job Description The position holder will need to prioritize: User requirements Basic break/ fix and root cause analysis Life-cycle replacement of devices Performs voice over internet protocol, and network software configuration, [. .. ] identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. About Charles River Charles River is an early-stage contract research organization (CRO) . We have built upon our foundation of laboratory animal medicine and science to develop [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Drug Safety Specialist pro Jahr?
Als Drug Safety Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Drug Safety Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 31 offene Stellenanzeigen für Drug Safety Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Specialist Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Drug Safety Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Drug Safety Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Safety Specialist Stellenangebote:
- Charles River (2 Jobs)
- Terry Soot (2 Jobs)
- Siegfried (2 Jobs)
- Terumo (1 Job)
In welchen Bundesländern werden die meisten Drug Safety Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Specialist Jobs werden derzeit in Bayern (7 Jobs), Baden-Württemberg (4 Jobs) und Nordrhein-Westfalen (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Specialist Jobs?
Drug Safety Specialist Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
