24 Jobs für Drug Safety Specialist
Stellenangebote Drug Safety Specialist Jobs
Job vor 5 Tagen 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 12 Tagen bei Jobleads gefunden
Freelance Senior/ Medical Director (Neurology-Bid Defense Support)
• München, Bayern
Führungs-/ Leitungspositionen Freiberuflich
[. .. ] (FSP) solutions. Join Our Team as a Freelance Senior/ Medical Director (Neurology-Bid Defense Support) . About this role TFS Health Science is seeking a highly flexible board-certified [...]
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[...] Neurology specialist to support upcoming Bid Defense Meetings. This freelance role involves contributing expert input during proposal preparation (e. g. protocol review) and participating in the Bid Defense Meeting itself. Ideally, the successful candidate would also be available for medical monitoring support if the project is awarded although this is not a [. .. ] shaping study design, leading bid defenses and ensuring medical oversight across key projects. If you are a clinically grounded leader with a strong commercial mindset and a passion for advancing drug development, we invite you to join our global team. Key Responsibilities Strategic Leadership : Act as a key scientific advisor in bid defense meetings (BDM) , RFP responses, and proposal development, ensuring compelling and medically sound strategies. Study Design Protocol Development : Provide expert input on trial design, patient recruitment, [. .. ] A Bit More About Us Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients safety and wellbeing, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] designs, and manage design deliverables produced by external partners and consultants. Knowledge of water industry design standards, products, materials, and specifications, with the ability to ensure designs [...]
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[...] align with regulatory, safety, and organisational requirements. Demonstrated capability to translate highlevel strategic and master planning needs into clear, practical solution requirements for capital works projects, aligned with customer outcomes, regulatory expectations, and best practice. Proven experience undertaking detailed needs analysis, options assessment, and impact analysis, using datadriven approaches to support evidencebased decisionmaking and [. .. ] reasonable adjustments you may need during the interview process. If you would like to speak to a team member about our commitment to diversity and inclusion, please contact our Inclusion Specialist or Reconciliation Action Plan Advisor. Additional information We are proud to be recognized as an employer of choice for women by WORK180. We are proud members of Pride in Diversity and Australian Disability Network. We are a 2025 Circle Back Initiative Employer we commit to respond to every applicant. How [. .. ] but you will need to confirm your right to work in Australia and complete relevant preemployment checks, including verification of criminal history, drivers licence and driving history, alcohol and other drug screening. Applications close Friday 16 January 2026 Previous applicants are not required to reapply. For further information please contact the Careers team at #J-18808-Ljbffr 73258888 [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Electrical Supervisor-FIFO
Führungs-/ Leitungspositionen
[. .. ] this role, you will: Undertake project-specific tasks as appropriate and directed to you by the Superintendent. Leading a Team of Leading Hands and Electricians Lead by example [...]
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[...] for all Safety on site Report task status, including forecast outcomes with relation to time, cost, scope and quality, when required Maintain records of work-in-progress and communications in line with the project management methodology Participate in and inform project planning and auditing activities ABOUT YOU Have a great attitude Enjoy problem [. .. ] (within the last 9 months) Current Unrestricted C Class Drivers License White/ Blue Construction Card ABOUT PHE GROUP PHE MINING PHE Group is an electrical and instrumentation contractor with five specialist divisions and more than 50 years experience. From design and installation to commissioning, shutdowns and logistics, we deliver projects that last. With branches and projects across Australias key mining regions, were trusted to deliver where it matters most. With PHE Mining, our people contribute to projects that are central to [. .. ] our values. To support this, our recruitment process includes a range of checks to confirm suitability for the role and workplace. These may include police and background clearances, medical assessments, drug and alcohol testing, right-to-work verification, reference checks, and other due diligence measures. SUPPORTING A DIVERSE WORKFORCE At PHE Group, diversity is core to how we build strong teams and deliver complex projects. Our workforce reflects the reality of a modern Australia bringing together people across gender, culture, age, [. .. ]
Job gestern bei Jobleads gefunden
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 vor 7 Tagen bei Jobleads gefunden
Senior Device Specialist-Device Risk Manager
• Heidelberg, Baden- Württemberg
Are you passionate about medical devices? Are you experienced within risk management, overseeing external production, and roll out of
drug-device combination products? If so, now is your chance to join [...]
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[...] Ascendis Pharma as our new Senior Device Specialist. Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in patients lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative Trans Con technology platform to fulfill our mission of developing new therapies that demonstrate bestinclass potential to address unmet [. .. ] deviations, and input to complaints. Act as a specialist for marketed products and share your product and production knowledge whenever needed. Collaborate closely with device leads, QA, Supply Chain, RA, Safety and suppliers to maintain and roll out our products globally. Qualifications and Skills: You hold a relevant technical degree and five to eight years of experience within medical device or pharmaceutical industry. you have: Formally trained and proven track record within Medical Device Risk Management (ISO14971:2019) . You have reviewed [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Wien
Lead Recruiter Meet Life Science Pharmacovigilance,
Drug Safety Clinical Operations
Specialist Drug Safety Physician (m/f/d) Employment Type: Permanent Join a leading international organisation dedicated to improving health outcomes worldwide. This [...]
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[...] privately owned global company develops and manufactures innovative therapies using advanced biological and biotechnological processes. With a strong commitment to scientific excellence and patient care, the organisation combines the [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Specialist Benefits
Discover a more connected career This is an exciting opportunity to join the Human Resources team of Utili Quest, LLC as a Human Resources
Specialist of Benefits Leave Administration [...]
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[...] (HRS) . Utili Quest, LLC has been a leading provider of quality underground utility damage prevention for over three decades. With headquarters located in Alpharetta, Georgia just north of Atlanta, we have offices located in several states including California, Indiana, Ohio and the Eastern US from [. .. ] leading provider of specialty contracting services to the telecommunications and infrastructure industry. Connecting you to great benefits Weekly Paychecks Paid Time Off, Parental Leave, and Holidays Insurance (including medical, prescription drug, dental, vision, disability, life insurance) 401 (k) w/Company Match Stock Purchase Plan Education Reimbursement Legal Insurance Discounts on gym memberships, pet insurance, and much more What youll do Benefits Administration Acts as a subject matter expert in the management of benefit documents, workflows and employee inquiries as it relates [. .. ] its your pathway to opportunity. Our hands-on training, supportive environment, and responsive leadership connect you to work with purpose. Our commitment to you extends beyond professional development to a safety-first culture that ensures you can do what you do best, with peace of mind. Building stronger solutions together Our company is an equal-opportunity employer-we are committed to providing a work environment where everyone can thrive, grow, and feel connected. All qualified applicants will receive consideration for employment [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
• München, Bayern
Pharmacovigilance
Specialist-Hombased Progressive is seeking a dedicated Pharmacovigilance Specialist Homebased to join our team. If you have initial experience in
Drug Safety or Pharmacovigilance and are ready to take [...]
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[...] the next step with a leading biotechnology company, you might be the ideal candidate. Base pay range Pay range is provided by Progressive. Your actual pay will be based on your skills and experience discuss details with your recruiter. Responsibilities Develop a sound [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
Senior PV Literature Scientist-9-Month Contract
• Basel, Basel- Stadt
A leading multinational healthcare firm in Basel is seeking a Pharmacovigilance Scientific Information
Specialist for a 9-month contract. The ideal candidate has a relevant degree and 2+ years of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in pharmacovigilance. Responsibilities include performing literature searches, developing safety reports, and creating training materials. Strong analytical and communication skills are essential. Join a dynamic team focused on innovation in healthcare and make a significant impact on drug safety and efficacy. #J-18808-Ljbffr 71992338 [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
[. .. ] short and longterm strategy and business development initiatives. Own the full P L, including waste acceptance, renewable energy offtake and ACCU revenue, ensuring strong financial performance and [...]
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[...] sustainable growth. Champion safety, regulatory compliance and overall operational performance, embedding a culture of Zero Harm across the Business Unit. Drive Wholeof Life (WOL) asset and operational planning to optimise asset utilisation, efficiency and longterm value. Manage key external relationships, including regulators, partners and JV stakeholders, to support performance, compliance and strategic outcomes. Optimise [. .. ] EAP access, discounts on private health insurance, company discounts + much more Our Process Our recruitment process involves a number of checks including, but not limited to, criminal history, medicals, drug alcohol testing, as well as verification of qualifications, licences and righttowork status. All internal applicants will receive a notification within 2 weeks of the closing date of this advertisement. We are dedicated to improving employment outcomes and encourage applications from Aboriginal and Torres Strait Islander peoples. We also welcome candidates [. .. ] communities for generations to come. An ASX 200 listed company (ASX: CWY) , our team of more than6, 300 highly trained employees are supported by a fleet of over5, 300 specialist vehicles, working from a network of more than250 locations around Australia. Our mission is to make a sustainable future possible. To some, waste may seem like an ordinary part of everyday life but we know it has extraordinary potential. We see all waste as a resource, and use our facilities [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Executive Medical Director Clinical Development Endocrinology, Europe
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] planning, and execution of the clinical development plan, including Phase 1 to 4 clinical studies in collaboration with cross-functional project team members, including clinical operations, clinical pharmacology, [...]
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[...] biometrics, regulatory, drug safety/ pharmacovigilance. The Executive Medical Director will also partner with medical affairs, HEOR, and commercial to provide guidance on publication strategy, data generation needs, and label expansion opportunities for marketed products. Your Contributions (include, but are not limited to) : Oversight of the clinical development strategy in the endocrinology therapeutic area [. .. ] of data and identification of evidence generation needs Adhere to Neurocrine Europe quality assurance system and compliance with the relevant SOPs Requirements: The appointed candidate will be a physician with specialist experience/ qualifications in endocrinology and/or a proven track record of clinical development in endocrinology products. MD qualified, ideally with specialist medical qualification in Endocrinology and previous experience in patient care At least 8 years experience in early or late stage clinical development in the pharmaceutical industry, ideally including experience [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
• Wien
Führungs-/ Leitungspositionen
[. .. ] Operate as a scientific interface and resource to HCPs/ Customer (s) , Health Care Institutions, External Experts, and professional associations regarding assigned Abb Vie Products or Products [...]
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[...] in Development. Provide specialist medical/ scientific strategic input and operational support of core activities such as local clinical research, HCP/ Customer interactions, generation and communication of clinical and scientific data, educational initiatives and patient safety for assigned products/ therapeutic areas. Qualifications Medical Degree or Bachelors degree in a scientific discipline or higher. Experience working in a pharmaceutical industry and general knowledge on drug development and clinical research an advantage. Must possess the ability to lead with confidence and to motivate people. He/ she should have the ability to impart the vision and strategy of the company and of the department to others. A strong business orientation and acumen is desirable. A results oriented [. .. ]
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 [...]
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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
• 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 29.09.2025 bei Jobleads gefunden
Senior Specialist, Supplier Quality
• Eschweiler, Nordrhein- Westfalen
[. .. ] suppliers Ability to work under high volume production and fast changing environment Willingness to work in a cross-functional team with different time zones Able to comply with [...]
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[...] the companys safety policy at all times. #LI-AP1 #LI-HYBRID Travel Requirements 20: Up to 52 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/ 4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including [. .. ] 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. #J-18808-Ljbffr 63626627 [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
• Eschweiler, Nordrhein- Westfalen
[. .. ] suppliers Ability to work under high volume production and fast changing environment Willingness to work in a cross-functional team with different time zones Able to comply with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the companys safety policy at all times. #LI-AP1 #LI-HYBRID Travel Requirements 20: Up to 52 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/ 4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including [. .. ] 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. #J-18808-Ljbffr 63571166 [. .. ]
Job am 02.09.2025 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 [. .. ]
Neu Job vor 3 Std. bei Neuvoo.com gefunden
Singleron Biotechnologies
• Cologne
Singleron Biotechnologies is an innovative life sciences tools company dedicated to applying groundbreaking single cell analysis techniques to research, clinical diagnosis,
drug development, and health management. The company was [...]
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[...] incorporated in January 2018 and currently has offices and laboratories in Germany, US, Singapore, and China. Singleron is seeking motivated and ambitious talent in the field of single cell analysis and next generation sequencing as Laboratory Technician or Application Specialist Qualifications: Training as BTA, MTA, or hold an MSc in the life sciences Proficiency in English and German Strong communication and organization skills Good knowledge and practical experience with cell culture and tissue processing Good knowledge of and practical experience with modern molecular biology lab skills, such as nucleic acid [. .. ] plus Curiosity and willingness to learn new methods Self-motivation, team player spirit, and commitment to your tasks Responsibilities: Assistance with the organization of the laboratory, including tasks for biological safety Performing single-cell RNA-sequencing experiments Quantitative and qualitative analysis of DNA and RNA Library preparation for NGS Close collaboration with Techs support and Project Management departments Detailed documentation of experiments and data, including data entry LIMS to support project management Assistance with the organization of the laboratory, including tasks [. .. ]
Job vor 9 Tagen 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 vor 11 Tagen bei Neuvoo gefunden
Charles River
Production Maintenance Technical Specialist 1
• Kaarst, North Rhine- Westphalia
Abgeschlossenes Studium
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, [. .. ] 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 [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Charles River
Quality System Specialist-limited
• Kaarst, North Rhine- Westphalia
Abgeschlossenes Studium
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, [. .. ] 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 [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
Siegfried
Personalleitung (m/w/d)
• 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 20.11.2025 bei Neuvoo.com gefunden
Nanion Technologies
Field Applications Scientist Cell Analytics Systems (FAS for CAS) - Munich, Germany
• Munich
[. .. ] technology solutions for automated patch clamp systems and innovative in vitro systems for membrane pump/ transporter studies, bilayer recordings, contractility assessments, and cell analytics measurements. Our mission [...]
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[...] is to accelerate drug development and scientific discovery by providing high-quality instrumentation and scientific support. To support the increasing demand of Nanions products, and to provide premium customer service, Nanion is expanding the team in their headquarter in Munich, Germany, and offering a position as a Field Application Scientist (m/w/d) in full-time or part-time with at least 30 h per week. The Field Application Scientist (FAS) Pre-Sales Specialist serves as a key technical liaison between Nanions commercial and scientific teams and prospective customers. This individual will play a critical role in the pre-sales process, providing scientific and technical expertise to support instrument sales, demonstrations, and evaluations. The FAS works closely with Product Specialists, Sales Managers and R [. .. ] Other days are spent working inhouse/in the lab, managing email, planning outreach, coordinating internally, and preparing training materials. Qualifications Skills Background Required Bachelors degree in electrophysiology, biophysics, pharmacology, cardiac safety, or a related life science field. Experience in a customer-facing technical or sales support role is highly desirable. 24 years of hands-on experience with instrumentation or assays (MEA (microelectrode array) , Impedance-based instruments, live-cell imaging devices) to support customers effectively. Experience with technologies currently being used [. .. ]
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 24 offene Stellenanzeigen für Drug Safety Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Specialist Jobs?
Aktuell suchen 7 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)
- Singleron Biotechnologies (1 Job)
- Edwards Lifesciences (1 Job)
- West Pharmaceutical Services (1 Job)
- Siegfried (1 Job)
- Nanion Technologies (1 Job)
In welchen Bundesländern werden die meisten Drug Safety Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Specialist Jobs werden derzeit in Nordrhein-Westfalen (6 Jobs), Bayern (4 Jobs) und Baden-Württemberg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Specialist Jobs?
Drug Safety Specialist Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
