26 Jobs für Drug Safety Specialist
Stellenangebote Drug Safety Specialist Jobs
Job am 18.12.2025 bei Neuvoo gefunden
Edwards Lifesciences
• Garching, Bavaria
[. .. ] studied transcatheter heart valve worldwide. We have an opportunity to join our Clinical Safety Team in Munich Germany, on an 18-month contract. As either an experienced Medical [...]
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[...] Device or Drug Safety Specialist OR a Medical Professional with an active interest in clinical trial safety and cardiology, the successful candidate will be the Clinical Safety contact for European Clinical Trials. This position has responsibility for meeting all reporting and recording requirements of Safety Data (Adverse Events) per current industry regulations. This role is [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk profile [. .. ] of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Passing on necessary information to pharmacovigilance [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Neu Job vor 5 Std. bei Jooble gefunden
Merck Sharp Dohme Corp
• Rheinland- Pfalz
The Senior
Specialist (m/f/d) Global Regulatory Affairs will support regulatory activities related to new product registrations and life cycle management to ensure efficient new licensing, product portfolio maintenance/ improvement and [...]
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[...] regulatory compliance and will also align efforts with other ongoing projects. Countries both within and outside the EU are in scope. [. .. ] standards. Identify and communicate potential regulatory issues to management, as needed. Perform other tasks as requested by management. BACKGROUND REQUIREMENTS University degree in Veterinary Medicine Multi-year experience in a safety efficacy related regulatory position within the animal health industry Excellent communication skills Proficient in English and MS office applications Proficiency with regulatory information management systems (Veeva Vault) . Advanced level of professionalism: Result-oriented, well-structured way of working, strong interpersonal skills, sound judgement and attentiveness to details Benefits: Flexible [. .. ] inclusive and diverse workplace. People with severe disabilities and their equivalents will be given preference if they are equally qualified. Required Skills: Accountability, Accountability, Adaptability, Audits Compliance, Detail-Oriented, Documentations, Drug Regulatory Affairs, Employee Training Programs, Global Communications, Mentorship, New Product Qualification, Pharmaceutical Development, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Pharmacy Regulation, Portfolio Optimization, Process Improvements, Product Approvals, Product Portfolio Management, Product Registrations, Project Management, Regulatory Affairs Management, Regulatory Compliance, Regulatory Compliance Consulting, Regulatory Issues + 4 more Preferred Skills: Current Employees apply [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Regierungsbezirk Freiburg
Führungs-/ Leitungspositionen
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including l eading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk [. .. ] of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Passing on necessary information to pharmacovigilance [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Stryker
• Augsburg
Clinical
Specialist, Joint Replacement Insert Location Overview As a Clinical Specialist at Stryker, you will help improve orthopedic surgeries around the world and play a direct role in our mission [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of making healthcare better. In this role, you will build deep clinical and technical expertise across both robotic (Mako Smart Robotics) and [. .. ] community service, leadership organizations, or athletic teams. Additional Information This position requires the handling of instruments that may have been contaminated by blood or bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, Stryker will provide a safe working environment for all employees. Ability to lift, push, pull, and carry up to 50 lbs. Ability to stand for extended periods. Ability to manage stressful OR situations with professionalism and focus Exerting up to 50 lbs of force occasionally [. .. ] or up to 20 lbs of force constantly to move objects. Must have a valid drivers license. Fluency in written and spoken English required. Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA) , Flexible Spending Accounts (FSAs) , 401 (k) plan, Employee Stock Purchase Plan (ESPP) , basic life and AD D insurance, [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Biotest AG
Documentation and Compliance Specialist (m/w/d) Drug Safety und QPPV Office support
• Dreieich
Abgeschlossene Ausbildung
Ihre Aufgaben Aufgaben im Case Management (50 der Arbeitszeit) Initiale Priorisierung, Fallanlage und Verteilung der Verantwortlichkeiten von neuen Fällen (inklusive Fall Download der EMA und FDA Fälle) Fallbearbeitung inklusive Kodierung, [...]
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[...] Narrative schreiben, Qualitätskontrolle und Versenden von Rückfragen an den Melder alle Fallkategorien Einreic [. .. ]
Job am 22.01.2026 bei Jooble gefunden
Charles River Laboratories, Inc.
• Frankfurt am Main
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 will [...]
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[...] 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 08.09.2025 bei Jobleads gefunden
Chief Medical Officer
Führungs-/ Leitungspositionen
[. .. ] the role of Chief Medical Officer (CMO) . The role The CMO is the senior clinical leader for the AFP, responsible for shaping the AFPs approach to [...]
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[...] supporting the health, safety and wellbeing of our people. The role has a broad range of responsibilities across the organisation providing clinical representation both internally and across various external forums. The CMO is responsible for the strategic clinical leadership, oversees health governance, and ensures AFP members operate under evidence based, ethical and compliant medical [. .. ] medical clearances Develop, oversee and provide advice on medical standards, in accordance with inherent requirements, including assessments of fitness for role, international deployment, recruit entry, pre and post deployment, and specialist roles. Serve as the AFPs senior clinical representative for internal and external committees and boards, representing the AFP at interdepartmental government meetings relating to health issues impacting on AFP members. Provide medical guidance to all areas of the AFP in support of AFP business objectives Provide Medical review services for Professional Standards including, for example, advice regarding prohibited drugs, pharmaceutical products, and alcohol and positive drug screen results. Act as a liaison with service providers when medical repatriations are required and give timely and expert advice to members unwell on posting overseas or on their return. All AFP appointees must ensure that the achievement of outcomes is in accordance with the regulatory framework, the AFP Code [. .. ]
Neu Job vor 5 Std. bei Jobleads gefunden
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Head [...]
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[...] of Global Safety Product Leads-Risk Label Management (m/f/d) . Responsibilities Team management of a group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Global pharmacovigilance product responsibility for the medicinal products Monitoring of the [. .. ] of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Passing on necessary information to pharmacovigilance [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Neu Job vor 5 Std. bei Jobleads gefunden
Automation Account Manager (Maternity cover)
• Frankfurt, Hesse
Overview This role is a maternity cover position within a dynamic and high-performance Automation sales team. As a Automation
Specialist Account Manager at Waters, your responsibilities include the design [...]
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[...] and implementation of a strategic sales plan that drives sales of our full range of automation products and services. In addition to bringing a proven track record in sales, the desired candidate should be a driven and dynamic individual and a fast learner, as well as an avid networker with good communication skills, capable of thinking strategically yet excellent in tactical implementation of programs. Penetrate key accounts in the Biopharma drug development space and related clinical research, CROs, Biotech accounts and to a smaller extent, Academia and Industrial accounts. Proactively manage new account acquisition, the sales funnel and maximize lead to opportunity as well as opportunity to order conversion Present and sell Andrew Alliance products and strategies. Manage sales targets which [. .. ] global leader in analytical instruments, separations technologies, and software, serving the life, materials, food, and environmental sciences for over 65 years. Our Company helps ensure the efficacy of medicines, the safety of food and the purity of water, and the quality and sustainability of products used every day. In over 100 countries, our 7, 600+ passionate employees collaborate with customers in laboratories, manufacturing sites, and hospitals to accelerate the benefits of pioneering science. Diversity and inclusion are fundamental to our core [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Ershausen/ Geismar, Thüringen Thueringen
Overview Permitting and Compliance
Specialist will be responsible for maintaining and managing day-to-day health,
safety, emergency response, environmental compliance, and security activities in support of terminal operations in [...]
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[...] the Lower River Region. Responsibilities The position provides quick and efficient responses to EHS and Terminal management when called upon for assistance with minimal supervision. Provide technical support for health, safety, training and industrial hygiene issues for [. .. ] adapt to changing priorities People-oriented supportive and fairness-focused Team-oriented cooperative and collaborative The successful candidate will be required to pass the Company and Customer required background check/ Drug screening. Equal Opportunity Employer Statement: We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, veteran status, disability or any other federal, state or local protected class. #J-18808-[. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Area Manager, Fleet Safety
Overview Position Summary. . . What youll do. . . Are you a seasoned professional with a passion for fleet
safety and a knack for coaching drivers to success? [...]
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[...] Join our team as an Area Manager, Fleet Safety, and make a substantial impact by supporting Walmart transportation offices with your expertise in DOT regulations and driver training. About Walmart Transportation: Our transportation team is crucial in ensuring the safe and efficient [. .. ] are listed, there are no preferred qualifications. 1 or More Degreed Certifications (Associate Safety Professional; Certified Safety Professional; Certified Industrial Hygienist; Graduate Safety Practitioner) or Non-degreed certifications (Safety Management Specialist; Occupational Hygiene and Safety Technician; Safety Trained Supervisor; North American Transportation Management Institute Certified Director of Safety; North American Transportation Management Institute Certified safety Supervisor; Safety Management Specialist; Certified Safety Manager; Safety Director; Licensed Safety Professional; Certified Safety and Health Manager; Construction Health and Safety Technician) , Microsoft Office Suite; Share Point and One Drive Primary Location 100 Walton Way, Smyrna, DE 19977-3757, United States of America Walmart and its subsidiaries are committed to maintaining a drug-free workplace and has a no tolerance policy regarding the use of illegal drugs and alcohol on the job. This policy applies to all employees and aims to create a safe and productive work environment. #J-18808-Ljbffr 78670546 [. .. ]
Job am 08.01.2026 bei Jobleads gefunden
Clinical Specialist, Joint Replacement-Bangor, Maine Maine
• Augsburg, Bayern
Clinical
Specialist, Joint Replacement Insert Location As a Clinical Specialist at Stryker, you will help improve orthopedic surgeries around the world and play a direct role in our mission [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of making healthcare better. In this role, you will build deep clinical and technical expertise across both robotic (Mako Smart Robotics) and manual [. .. ] community service, leadership organizations, or athletic teams. Additional Information This position requires the handling of instruments that may have been contaminated by blood or bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, Stryker will provide a safe working environment for all employees. Ability to lift, push, pull, and carry up to 50lbs. Ability to stand for extended periods. Ability to manage stressful OR situations with professionalism and focus. Exerting up to 50lbs of force occasionally and/or up to 20lbs of force constantly to move objects. Must have a valid drivers license. Fluency in written and spoken English required. Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA) , Flexible Spending Accounts (FSAs) , 401 (k) plan, Employee Stock Purchase Plan (ESPP) , basic life and AD D insurance, [. .. ]
Job am 22.12.2025 bei Jobleads gefunden
Biological Safety Specialist
Biological
Safety Specialist Join to apply for the Biological Safety Specialist role at NAMSA. Overview Who we are: NAMSA pioneered the industry and was the first independent company in the [...]
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[...] world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U. S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry, providing support to clients throughout every step of the product development lifecycle and beyond, facilitating market access (e. g. , EU, US, China, Japan, and the rest of the world) . Our values: Act with integrity in everything [. .. ]
Job am 26.10.2025 bei Jobleads gefunden
• 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 [...]
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[...] 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 09.10.2025 bei Jobleads gefunden
HSE Head
• Rasch, Bayern
Summary The HSE Head will be responsible for all HSE compliance aspects of a dynamic Radioligand Therapy (RLT)
drug product manufacturing plant. Summary The HSE Head will be responsible [...]
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[...] for all HSE compliance aspects of a dynamic Radioligand Therapy (RLT) drug product manufacturing plant. About The Role Key Responsbilities: As a member of the site leadership team, lead the creation of an injury-free work environment that protects employees [. .. ] the implementation and execution of the HSE roadmap defined by the company, working closely with all functions within the site and the broader Novartis organization. Function as the Site Radiation Safety subject matter expert and collaborate with operations and technical teams to safely manage radioactive materials from raw materials to finished product and waste disposal. Maintain knowledge of and ensure strict adherence to all applicable regulatory compliance standards including Radiation Safety, Governance, Business Continuity Emergencies Management and Environmental Health and Safety. [. .. ] Senior level Employment type Employment type Full-time Job function Job function Management and Manufacturing Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Novartis Deutschland by 2x Senior Specialist Health Safety (m/f/d) Health and Safety Manager Data Centers (w/m/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 65378195 [. .. ]
Job am 02.09.2025 bei Jobleads gefunden
• 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 [...]
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[...] 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 gestern bei Neuvoo.com gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
Führungs-/ Leitungspositionen
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk profile [. .. ] of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Passing on necessary information to pharmacovigilance [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks Team management of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] group of Global Safety Product Leads including l eading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk [. .. ] of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Passing on necessary information to pharmacovigilance [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
Waters Corporation
Automation Account Manager (Maternity cover)
• Frankfurt, Hessen
Overview This role is a maternity cover position within a dynamic and high-performance Automation sales team. As an Automation
Specialist Account Manager at Waters, your responsibilities include the design [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and implementation of a strategic sales plan that drives sales of our full range of automation products and services. In addition to bringing a proven track record in sales, the desired candidate should be a driven and dynamic individual and a fast learner, as well as an avid networker with good communication skills, capable of thinking strategically yet excellent in tactical implementation of programs. Penetrate key accounts in the Biopharma drug development space and related clinical research, CROs, Biotech accounts and to a smaller extent, Academia and Industrial accounts. Proactively manage new account acquisition, the sales funnel and maximize lead to opportunity as well as opportunity to order conversion Present and sell Andrew Alliance products and strategies. Manage sales targets which [. .. ] global leader in analytical instruments, separations technologies, and software, serving the life, materials, food, and environmental sciences for over 65 years. Our Company helps ensure the efficacy of medicines, the safety of food and the purity of water, and the quality and sustainability of products used every day. In over 100 countries, our 7, 600+ passionate employees collaborate with customers in laboratories, manufacturing sites, and hospitals to accelerate the benefits of pioneering science. Diversity and inclusion are fundamental to our core [. .. ]
Job vor 4 Tagen bei Neuvoo gefunden
Mindlance
Clinical-LTSS Service Care Manager-J01031
[. .. ] care management experience; Prior experience with social work, geriatrics, gerontology, pediatrics, or human services. RN or LCSw/LCSW-A preferred For Arkansas Total Care plan-This position is designated as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety sensitive in Arkansas and requires a drivers license, child and adult maltreatment check (before hire and recurring) , and a drug screen (at time of hire and recurring) . Must reside in AR or border city. Travel:. required Responsibilities Evaluates the needs of the member, the resources available, and recommends and/or facilitates the plan for the best outcome Assists with developing ongoing long-term care plans/ service plans and works to identify providers, specialist, and/or community resources needed for long-term care Coordinates as appropriate between the member and/or family/ caregivers and the care provider team to ensure identified services are accessible to members Provides resource support to members and their families/ caregivers for various needs ( employment, housing, participant direction, independent [. .. ]
Job am 09.01.2026 bei Neuvoo gefunden
GULP experts united
IRT Specialist/ IRT Expert (m/f/d)
• Biberach, Baden- Württemberg
We are currently looking for a dedicated individual to fill the position of IRT
Specialist/ IRT Experte (m/f/d) at a renowned pharmaceutical company based in Biberach. Heres what we [...]
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[...] offer Attractive salary and long-term job security through group affiliation Up to 30 days vacation per year Contribution to company pension scheme after end of probationary period Extensive social benefits, including Christmas and [. .. ] representative in cross-organizational and cross-functional study and project teams and have deep expertise in the technical implementation of IRT concepts and clinical study design related to compliance and drug safety. You will also contribute to the continuous development of IRT concepts by bringing in new approaches and solutions to keep systems state of the art. You will ensure that all work is performed with patient safety in mind and in compliance with GMP and GCP as well as US, EU [. .. ]
Job am 14.12.2025 bei Neuvoo gefunden
West Pharmaceutical Services
Operator, Supply Chain, Warehouse (m/f/d) ESW
• Aachen, North Rhine- Westphalia
[. .. ] and customer shipments Loading onto trucks and sea containers using the necessary load securing measures, including logging Posting via SAP (MM module) Education Successfully completed training as [...]
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[...] a warehouse logistics specialist Work Experience Several years of professional experience in the warehouse/ shipping sector Preferred Knowledge, Skills and Abilities Valid industrial truck drivers license Class B drivers license, digital driver card for truck transport desirable Good PC and SAP skills (MM module) desirable Knowledge of hazardous goods packaging desirable Teamwork skills and resilience desirable Willingness to work as a stand-in High level of quality and safety awareness West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other [. .. ] permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening. #LI-MF1 72575997 [. .. ]
Job am 13.12.2025 bei Neuvoo gefunden
Nuvisan GmbH
Scientist (m/w/d) In Vitro Genetic Toxicology, Scientist (m/w/d) In Vitro Genetic Toxicology bei Nuvisan GmbH softgarden
• 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 customer-oriented collaboration High level of ability for routine and project work within [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
Siegfried
Teamleitung Einkauf (m/w/d)
• Hamelin, Lower Saxony
Führungs-/ Leitungspositionen
[. .. ] and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers value chain. [. .. ] way through to manufacturing services, ranging from preclinical R D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products. What we do in Hameln Hameln is a renowned contract manufacturer which supplies both national and international pharmaceutical companies. It has over 450 employees who produce sterile medicinal products, mainly for use in hospitals and intensive care facilities. Main activities Contract manufacture of parenteral solutions and suspensions aseptic or terminally sterilized in ampoules and vials Specialist in the production of complex preparations such as anesthetics, flammable and oxygen-sensitive liquids and cold chain products Special features Successful transfers and establishment of new products in sterile production Batch size: up to 3500 liters Clean room area: 4000 m Batch manufacture and filling of sterile products, from visual [. .. ]
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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 26 offene Stellenanzeigen für Drug Safety Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Specialist Jobs?
Aktuell suchen 13 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:
- Dr. Falk Pharma GmbH (4 Jobs)
- Siegfried (2 Jobs)
- Merck Sharp Dohme Corp (1 Job)
- Stryker (1 Job)
- Biotest AG (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 (3 Jobs), Niedersachsen (3 Jobs) und Baden-Württemberg (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Specialist Jobs?
Drug Safety Specialist Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
