20 Jobs für Drug Safety Specialist
Stellenangebote Drug Safety Specialist Jobs
Neu Job vor 4 Std. bei StepStone gefunden
Atotech Deutschland GmbH Co. KG
• Berlin
Abgeschlossenes Studium Abgeschlossene Ausbildung
[. .. ] Lösungen-kombiniert mit einem beispiellosen Vor-Ort-Support für Kunden weltweit. Für weitere Informationen über Atotech besuchen Sie uns bitte unter atotech. com. MKS Inc. in Berlin stellt ein: Health [...]
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[...] Safety Specialist/ Fachkraft für Arbeitssicherheit (m/w/d) Referenznummer: R18154 Als EHS Specialist DACH (m/w/d) übernehmen Sie eine zentrale Rolle in der Weiterentwicklung unserer Umwelt, Gesundheits und Sicherheitsstandards in der gesamten DACH Region. Sie kombinieren operative Verantwortung mit strategischem Einfluss und tragen aktiv dazu bei, unsere Sicherheitskultur nachhaltig zu stärken. [. .. ] orientation, gender identity or expression, genetic information, or any other category protected by applicable law. Hiring decisions are based on merit, qualifications and business needs. We conduct background checks and drug screens, in accordance with applicable law and company policies. MKS Inc. is generally only hiring candidates who reside in states where we are registered to do business. . Atotech Deutschland Gmb H Co. KG sucht in Berlin eine/n Health Safety Specialist/ Fachkraft für Arbeitssicherheit (m/w/d) (ID-Nummer: 13798592) [. .. ]
Job am 01.03.2026 bei StepStone gefunden
West Pharmaceutical Services Deutschland GmbH Co. KG
Senior Packaging Specialist R D EU
• Eschweiler
Homeoffice möglich
Do you believe in quality, service and team spirit? Then implement these values together with us. Make a difference as a Senior Packaging
Specialist R D EU West Pharmaceutical Services, [...]
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[...] Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products. Working by the side of its customers from concept to patient, West creates products that promote the efficiency, reliability and safety of the worlds pharmaceutical drug supply. West is headquartered in Exton, Pennsylvania, and supports its customers from locations in North and South America, Europe, Asia and Australia. Wests 2020 sales of 2.14 billion reflect the daily use of approximately 112 million of its components and devices which are designed to improve the delivery of [. .. ]
Job am 28.02.2026 bei StepStone gefunden
West Pharmaceutical Services Deutschland GmbH Co. KG
• Eschweiler
Absolventen, Einsteiger, Trainees
Do you believe in quality, service and team spirit? Then implement these values together with us. Make a difference as a Junior
Specialist, Technology Engineering Support West Pharmaceutical Services, Inc. [...]
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[...] is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products. Working by the side of its customers from concept to patient, West creates products that promote the efficiency, reliability and safety of the worlds pharmaceutical drug supply. West is headquartered in Exton, Pennsylvania, and supports its customers from locations in North and South America, Europe, Asia and Australia. Wests 2020 sales of 2.14 billion reflect the daily use of approximately 112 million of its components and devices which are designed to improve the delivery of [. .. ]
Job am 06.02.2026 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 [...]
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[...] 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 am 02.03.2026 bei Mindmatch.ai gefunden
Novartis
• AT- 7 Langkampfen
Führungs-/ Leitungspositionen
Summary
Drug Product Schaftenau We are the biotechnology
specialist within Novartis with decades of experience and comprehensive know-how in the entire spectrum of Biologics. Join the Manufacturing Science and Technology [...]
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[...] team in Drug Product Schaftenau as Technical Transfer Lead and participate at the frontline in bringing highly innovative, high-quality pharmaceuticals to the patients. You will lead technical transfer project teams at site and liaise efficiently with involved functions (e. g. Technical Development, Supply Chain, Production Unit, Quality Unit functions, Health, Safety Environment, Contract Development Manufacturing Organization platform, other sites) . This role will work directly with the Manufacturing, Science Technology team, and report to the Head Manufacturing Science Technology. About The Role Your responsibilities include, but are not limited to: Responsible for technology transfer activities at site level (within, inbound and [. .. ]
Job vor 3 Tagen 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 [...]
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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 am 28.02.2026 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
Technical Transfer Lead (w/m/d)
• Langkampfen, Tirol
Führungs-/ Leitungspositionen
Summary
Drug Product Schaftenau We are the biotechnology
specialist within Novartis with decades of experience and comprehensive know-how in the entire spectrum of Biologics. Join the Manufacturing Science [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Technology team in Drug Product Schaftenau as Technical Transfer Lead and participate at the frontline in bringing highly innovative, high-quality pharmaceuticals to the patients. You will lead technical transfer project teams at site and liaise efficiently with involved functions (e. g. Technical Development, Supply Chain, Production Unit, Quality Unit functions, Health, Safety Environment, Contract Development Manufacturing Organization platform, other sites) . This role will work directly with the Manufacturing, Science Technology team, and report to the Head Manufacturing Science Technology. About The Role Your responsibilities include, but are not limited to: Responsible for technology transfer activities at site level (within, inbound and [. .. ]
Job am 27.02.2026 bei Jobleads gefunden
• 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 [...]
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[...] 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 27.02.2026 bei Jobleads gefunden
What is Nystatin Triamcinolone Lotion Utilized For-
• 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 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 am 08.02.2026 bei Jobleads gefunden
Automation Account Manager (Maternity cover)
• Frankfurt, Hesse
Overview This role is a maternity cover position within a dynamic and highperformance Automation sales team. As an Automation
Specialist Account Manager at Waters, you will design and implement [...]
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[...] a strategic sales plan that drives sales of our full range of automation products and services. Responsibilities Penetrate key accounts in the Biopharma drug development space, clinical research CROs, Biotech accounts and to a smaller extent Academia and Industrial accounts. Proactively manage new account acquisition, the sales funnel and maximise leadtoopportunity and opportunitytoorder conversion. Present and sell Andrew Alliance products and strategies. Manage sales targets comprising instrument unit sales, accessories, software and service sales, [. .. ] 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 am 08.01.2026 bei Jobleads gefunden
• 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 26.10.2025 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 gestern bei Neuvoo gefunden
West Pharmaceutical Services
• Eschweiler, North Rhine- Westphalia
Work-Life-Balance
[. .. ] report recruitment activity data to support staffing metrics from the time a requisition is opened to the time candidates are identified for offer and onboarded Manage all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] background check and drug-screening processes related to new hire processing Manage all offer processes in an accurate and efficient way Ability to multitask in a high-pressure environment Analyze job descriptions and candidate profiles to determine target profile needs and appropriate match Participate in special projects and perform other duties as assigned based on business needs Abide by all regulations, policies, work procedures, instruction, and all safety rules Exhibit reliable, punctual and predictable attendance Education Bachelors Degree or equivalent work experience in Business or Human Resources discipline required Work Experience Minimum 3 years of recruiting experience in an agency, search firm or corporate setting required Preferred Knowledge, Skills and Abilities Ability to multitask in a high-pressure [. .. ]
Job am 26.02.2026 bei Neuvoo gefunden
Nuvisan GmbH
Senior Scientist/ Lab Head (m/f/d) In Vitro Genetic Toxicology, Senior Scientist/ Lab Head (m/f/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 22.02.2026 bei Neuvoo gefunden
NVision Imaging Technologies
• 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 [...]
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[...] 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 06.02.2026 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 am 27.11.2025 bei Neuvoo gefunden
Siegfried
• Hamelin, Lower Saxony
[. .. ] 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, [...]
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[...] 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 [. .. ]
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 [. .. ]
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 20 offene Stellenanzeigen für Drug Safety Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Specialist Jobs?
Aktuell suchen 9 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:
- West Pharmaceutical Services Deutschland GmbH Co. KG (2 Jobs)
- Dr. Falk Pharma GmbH (2 Jobs)
- Siegfried (2 Jobs)
- Atotech Deutschland GmbH Co. KG (1 Job)
- Novartis (1 Job)
- West Pharmaceutical Services (1 Job)
In welchen Bundesländern werden die meisten Drug Safety Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Specialist Jobs werden derzeit in Niedersachsen (5 Jobs), Nordrhein-Westfalen (5 Jobs) und Bayern (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Specialist Jobs?
Drug Safety Specialist Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
