40 Jobs für Drug Safety Manager
Stellenangebote Drug Safety Manager Jobs
Job am 18.08.2026 bei StepStone gefunden
Daiichi Sankyo Europe GmbH
• Pfaffenhofen an der Ilm
Work-Life-Balance
[. .. ] 2030 vision to be an innovative global healthcare company contributing to the sustainable development of society, we are shaping a healthier, more hopeful future for patients, their [...]
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[...] families, and society. Manager (m/w/d) Formulation Technology-Biologics Purpose of the function The Manager Formulation Technology-Biologics is responsible for the planning, organization and technical support of development activities in Formulation Technology for Parenteral Formulation and Process Development (e. g. lyophilization) incl. physicochemical characterization of Biologics (focus on oncology, e. g. ADCs) [. .. ] and post-approval changes) are also within the scope of this position. Aufgaben Development, optimization and upscaling of GMP-compatible manufacturing processes for lyophilization of biologics (e. g. Anti-body drug conjugates, ADCs) , incl. preparation and documentation of development activities Creation of risk analyses and statistical design of experiments (Do E) within the framework of formulation and process development of biologics Co-working with a young development team for developing and extending the department analytical capabilities with focus on physicochemical characterization of Biologics, as well as the occupational health and safety concepts for handling of high potent compounds Functional and technical management of contract manufacturing organizations (CMOs) for clinical trials material manufacturing, as well as technology transfers to in-house manufacturing sites and CMOs in Europe, incl. on-site support Supporting the team in creating and reviewing manufacturing protocols and reports [. .. ]
Neu Job vor 3 Std. bei Neuvoo.com gefunden
The BIG Jobsite
Manager (m/w/d) Formulation Technology Biologics
• Bavaria Pfaffenhofen an der Ilm
Work-Life-Balance
[. .. ] 2030 vision to be an innovative global healthcare company contributing to the sustainable development of society, we are shaping a healthier, more hopeful future for patients, their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] families, and society. Manager (m/w/d) Formulation Technology-Biologics Purpose of the function The Manager Formulation Technology-Biologics is responsible for the planning, organization and technical support of development activities in Formulation Technology for Parenteral Formulation and Process Development (e. g. lyophilization) incl. physicochemical characterization of Biologics (focus on oncology, e. g. ADCs) . [. .. ] and post-approval changes) are also within the scope of this position. Aufgaben Development, optimization and upscaling of GMP-compatible manufacturing processes for lyophilization of biologics (e. g. Anti-body drug conjugates, ADCs) , incl. preparation and documentation of development activities Creation of risk analyses and statistical design of experiments (Do E) within the framework of formulation and process development of biologics Co-working with a young development team for developing and extending the department analytical capabilities with focus on physicochemical characterization of Biologics, as well as the occupational health and safety concepts for handling of high potent compounds Functional and technical management of contract manufacturing organizations (CMOs) for clinical trials material manufacturing, as well as technology transfers to in-house manufacturing sites and CMOs in Europe, incl. on-site support Supporting the team in creating and reviewing manufacturing protocols and reports [. .. ]
Job gestern bei Mindmatch.ai gefunden
headcount
• AT- 2 Lavamünd
Regional Pharmacovigilance
Manager, Swiss-based (remote) Do you know how to keep regional pharmacovigilance running smoothly across systems, vendors and global teams? For a growing global biotech, we are looking for [...]
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[...] a handson Regional Pharmacovigilance Manager to strengthen its Global Patient Safety organisation. The role Oversee regional PV and ICSR processes Manage external PV vendors and quality follow-up Support audits, inspections and regulatory compliance Improve and harmonise PV processes across the organisation Your background Around 5 to 10 years in pharmacovigilance or drug safety Strong ICSR and global safety-database experience Experience with PV vendors, GVP requirements and inspections Relevant scientific degree and fluent English What is offered: An international biotech environment, real ownership and the opportunity to help shape regional PV operations. The package includes a competitive salary, annual bonus, equity and [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Wu Xi App Tec Group
Spray Drying Operator (contingent)
• AT- 2 Lavamünd
[. .. ] across Asia, Europe, and North America, we offer integrated, end-to-end services through our unique CRDMO (Contract Research, Development, and Manufacturing Organization) platform. Guided by our vision that [...]
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[...] every drug can be made and every disease can be treated, we are committed to advancing breakthroughs for patientsone collaboration at a time. Learn more at STA Pharmaceutical Switzerland is part of Wu Xi App Tec. The site is located in Couvet, canton Neuchatel and manufacturesoral drug products for global markets. We [. .. ] for experienced spray drying professionals and are actively creating a new team. The Spray Drying Operator is responsible for ensuring spray drying manufacturing activities comply with GMP/ c GMP regulations and safety standards. The Spray Drying Operator is accountable for adjusting equipment and process parameters to ensure production remains compliant. He/ she shall ensure the batch record and all procedures are precisely followed and data is documented following GDP. Responsibilities Prepare solutions, suspensions, or emulsions for atomization. Configure and adjust the equipment [. .. ] the set-up, operation cleaning of the equipment and processes. Ensure the production of batches in a GMP environment and work independently and efficiently according to the instructions of your manager. Perform sampling and in-process-controls on manufactured products. Participate in and support the qualification of equipment and the validation of processes. Comply with the production schedule. Generate maintenance requests in the event of equipment failure and follow up until production resumes. Analyse equipment failures and provide maintenance support in [. .. ]
Job am 14.08.2026 bei Mindmatch.ai gefunden
EURAXESS Ireland
• AT- 6 Graz
[. .. ] Duties and responsibilities Perform analytical development activities and analytical characterization of raw materials, intermediate products and final dosage forms (including stability) . Identify and characterize key material [...]
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[...] properties of active drug substance, excipients and drug product. Develop, validate and implement analytical methods to support product development and advanced manufacturing for range of products including solid, semi-solid and liquid types. Report to Analytical Science Manager, Scientific Project Lead and/or Head of Technical Operations regarding operational issues that occur during experimental execution. Oversee the transfer of methods to the manufacturing sites, ensuring their implementation to verify that products comply with quality requirements and adhere to regulatory standards. Ensure data generated from all experimental work is [. .. ] date Standard Operating Procedures (SOP) for the Analytical Science Lab Follow all agreed RCPE working procedures, including completion of all analytical test analysis, equipment log books, Standard Operating Procedures and safety procedures Completion of technical reports and contribute for scientific publications Requirements A technical or natural sciences University degree (Chemistry, Analytical Chemistry, Technical Chemistry, Pharmacy or related) with relevant experience in analytical chemistry labs (2-5 years) . Handson experience in HPLC/ UPLC as well as in UVVIS Spectroscopy method development. [. .. ]
Job am 14.08.2026 bei Mindmatch.ai gefunden
Unist
Scientist/ Senior Technician
• AT- 6 Graz
[. .. ] Duties and responsibilities Perform analytical development activities and analytical characterization of raw materials, intermediate products and final dosage forms (including stability) . Identify and characterize key material [...]
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[...] properties of active drug substance, excipients and drug product. Develop, validate and implement analytical methods to support product development and advanced manufacturing for range of products including solid, semi-solid and liquid types. Report to Analytical Science Manager, Scientific Project Lead and/or Head of Technical Operations regarding operational issues that occur during experimental execution. Oversee the transfer of methods to the manufacturing sites, ensuring their implementation to verify that products comply with quality requirements and adhere to regulatory standards. Ensure data generated from all experimental work is [. .. ] date Standard Operating Procedures (SOP) for the Analytical Science Lab Follow all agreed RCPE working procedures, including completion of all analytical test analysis, equipment log books, Standard Operating Procedures and safety procedures Completion of technical reports and contribute for scientific publications Requirements A technical or natural sciences University degree (Chemistry, Analytical Chemistry, Technical Chemistry, Pharmacy or related) with relevant experience in analytical chemistry labs (2-5 years) . Handson experience in HPLC/ UPLC as well as in UVVIS Spectroscopy method development. [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Description CRA II-Germany Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
drug development [...]
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[...] and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assess factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case [. .. ] off visits for junior CRA staff, as assigned. May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL) , or operational line manager. Qualifications Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Previous monitoring experience in Germany Must demonstrate good computer skills and be able to embrace new technologies Fluency in German and [. .. ]
Job gestern bei Jobleads gefunden
Territory Sales Manager, Interventional Oncology (North Carolina)
• Dietenhofen, Bayern
[. .. ] VMS employment in this position. These requirements vary by client and may include, but are not limited to: Proof of valid identification (photo, drivers license, SSN) , [...]
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[...] Criminal background checks, Drug screens, Immunizations (Hep B, MMR, Varicella, Influenza, Tetanus) , Annual TB testing. This role is governed by our Fleet Safety Policy. To be eligible, applicants must hold a valid drivers license in the state they reside and may not have any prior DUI/ DWI convictions or pending DUI/ DWI charges or other serious moving violations (unless such a restriction is prohibited by state/ local law) . Who we are We [. .. ]
Job gestern bei Jobleads gefunden
• Neuenburg
[. .. ] Commencement: October 2026 or at a mutually agreed date Languages Required: English (C1) and French (C1) or German (C1) . About the Role We are seeking an [...]
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[...] experienced Quality Affairs Manager to lead quality activities related to the distribution and commercialisation of medicinal products in Switzerland. The candidate will take responsibility for the maintenance and continuous improvement of the Quality Management System (QMS) , ensure compliance with Good Distribution Practice (GDP) requirements and oversee quality activities related to the storage, distribution [. .. ] driven approach. A Plus Knowledge and experience of GMP requirements. Experience with Quality Management Systems supporting clinical trial activities and GCP compliance. Experience in the CRO environment. Experience in Pharmacovigilance/ Drug Safety. #J-18808-Ljbffr 03483343 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Quality Supervisor (m/f/d)
• Weßling, Bayern
Führungs-/ Leitungspositionen
[. .. ] world around you. About the role Bavaria Medizin Technologie Gmb H (BMT) , part of Lubrizol, specializes in the design, development, and manufacturing of innovative medical devices, [...]
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[...] including the first commercial drug-coated balloon. Located near Munich, Germany, with a facility in Sibiu, Romania, BMT offers comprehensive services from R D tologisticsmanagement. They excel in catheter-based technologies and provide private label manufacturing, OEM, and contract services. BMT is dedicated to enhancing lives throughcutting-edgemedical solutions. The Quality Systems (QMS) supervisors task is to support the Quality Manager and the overall site in compliance of the Quality Management System. You will oversee operations of the Document Control and Quality Systems support team, train personnel in the relevant processes ensure resources are utilized to meet the customer and regulatory requirements and assist the Quality Manager in administrative functions associated [. .. ] (German and English) Excellent knowledge of MS Office Preferred Qualifications That Drive You Forward Detailed knowledge of QM systems and their processes/ tools/ standards High technical understanding Detailed knowledge about safety, rules, and protection of staff High level of analytical thinking High level of competence, output and integrity, excellent judgement and good interpersonal skills Advanced statistics knowledge Excellent teamwork skills Excelllent communication and leadership skills High level of reliability, integrity, and accuracy This role is based on-site in Wessling, near [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Ludwigshafen am Rhein, Rheinland- Pfalz
Work-Life-Balance
Senior
Manager, Clinical Product Supply Quality (all genders) (full-time, regular) Salary Min: 124500 Salary Max: 236500 Workday Global Grade: 19 Abb Vies mission is to discover and deliver innovative [...]
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[...] medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable [. .. ] recommendations to senior R D leadership and cross-functional governance bodies. Lead the identification, assessment, and mitigation of quality and supply risks across the product lifecycle, including risks associated with drug substance, drug product, analytical testing, manufacturing, packaging, release, distribution, and clinical supply continuity. Provide QA leadership for internal and external integration activities, including in-licensing, collaborations, acquisitions, and onboarding of third-party manufacturers, laboratories, and service providers. Lead or oversee quality assessments supporting due diligence activities. Evaluate the reasonableness, completeness, [. .. ] equivalent formal project leadership experience. Demonstrated ability to assess complex risks, challenge assumptions constructively, and determine whether proposed quality strategies, controls, timelines, and remediation plans include robust quality and patient safety plans. Strong experience with issue management, investigations, exception reports, OOS/ OOT, quality agreements, inspection readiness, audits, and product actions/ recalls. Proven ability to lead through influence, build consensus, and communicate effectively with senior leadership, cross-functional leaders, external partners, and global stakeholders. Strong strategic thinking, judgment, problem-solving, project management, [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Principal Clinical Medical Writer
[. .. ] documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Drafts and edits documents used [...]
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[...] in reporting aggregate safety and efficacy information for a molecule, such as investigators brochures and periodic safety reports (e. g. PBRERs, DSURs) Drafts and edits documents used in the preparation of regulatory filings (e. g. briefing books, CTD Module 2/ Module 5 clinical or integrated summaries) . Manages study team participation in the preparation [. .. ] the development of standard processes and templates in other departments Works effectively with cross-functional groups within Bio Marin Other tasks as assigned. EXPERIENCE: Clinical Studies Advanced understanding of the drug development process (discovery to market) , biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets. Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection. Advanced applied knowledge of: Documentation required for [. .. ] efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs) Study results reporting Integrated results reporting Management Experience: Prior administrative and/or functional management experience as a manager of a medical writer team or department in a clinical development setting preferred but not required Demonstrated leadership abilities. Demonstrated ability to plan timelines and resources for multiple documentation projects with shifting priorities. Experience with delegating and overseeing projects and tasks. Medical Writing Writing high-quality documents that support corporate [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Work with Therapeutic
Safety Teams on safety assessment activities for medical/ scientific operations Direct planning, preparation, writing and review of portions of aggregate reports Organize and direct liaison activities [...]
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[...] with affiliates and internal Amgen partners regarding products Support and provide oversight to staff regarding clinical-trial safety Review and provide input on study protocols, [. .. ] detection Present Global Safety Team recommendations to cross-functional decision-making bodies Assist with risk-management strategies, plans, risk minimization activities and regulatory inquiries Support safety-related activities for new drug applications and other regulatory filings Undertake delegated QPPV activities and maintain inspection readiness Serve as representative and point of contact for Health Authority Inspections and Internal Process Audits Requirements Doctorate degree and 2 years of industry pharmacovigilance experience, OR Masters degree and 4 years of industry pharmacovigilance experience, OR Bachelors [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Account Manager II
[. .. ] sales revenue budget and identify key customer initiatives Manage sales expenses and submit business expenses on time Maintain comprehensive knowledge of the companys business service offerings Adhere [...]
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[...] to health and safety policies and practices Take on additional duties as assigned Requirements Bachelors degree (required) ; focus within sales, business, marketing or science (preferred) 3+ years of proven industry related sales experience (required) , or 7+ years of proven industry related sales experience in lieu of degree (required) Ability to travel up to 80 of the time, with some overnight stays required Post-offer drug screen required Background check required Core Competencies Demonstrates expertise in outside sales, new business development, and account management, with a strong focus on achieving revenue and profitability goals. Proficient in managing customer relationships, resolving concerns, and negotiating contracts while adhering to industry regulations. Highest-signal resume keywords Outside Sales Account [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
[. .. ] integrated, and executed Lead communications with the USNRC, ACS, and senior NRC staff members Handle administrative tasks and support schedule planning Manage work with urgency while maintaining [...]
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[...] high quality and safety standards Review applicable regulatory and industry standards and communicate them to the design community Participate in product compliance and certification work, including testing and design reviews Interact with engineering firms and governmental agencies to obtain product certification or qualification Manage a small to medium team of senior professionals and others [. .. ] management skills PC proficiency Ability to obtain authorization for access to U. S. export-controlled information, if applicable Legally authorized to work in the United States Successful completion of a drug screen, as applicable Core Competencies Demonstrates expertise in US nuclear product licensing, regulatory compliance, and project management, with a strong focus on communication and leadership within the nuclear industry. Proven ability to develop and optimize licensing deliverables while managing teams and influencing strategic decisions. Highest-signal resume keywords Nuclear Regulated [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Manager, Circular Renewable Transformation
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
[. .. ] will be working for the worlds leading producer of renewable diesel and sustainable aviation fuel, which enables our customers to reduce their greenhouse gas emissions. We are [...]
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[...] looking for you, Manager, Circular Renewable Transformation to our Renewable Circular Transformation Team under Polymers Chemicals (OP) in Espoo, Finland or Düsseldorf, Germany. You will focus on developing and maintaining market understanding of polymers and chemicals globally, creating market assessments and competition analysis. In this job you will work closely with Public Affairs, Technology [. .. ] evolving business environment as a global leader in renewable fuels. We contribute to Nestes success by living our values every day: we care, we have courage, we cooperate. We prioritize safety at all times and in every location. We strive to create a positive and impactful work environment. Transformation brings new possibilities and fosters our courage and curiosity. As a global company, we support personal development with versatile learning and career opportunities. Collaboration is key, and we believe in flexible, smart [. .. ] information Challenge assumptions constructively, collaborate seamlessly across global teams, and deliver tangible market impact. Depending on the requirements of the position, the process may include a security clearance (with a drug test) and a potential statutory health examination based on work-related exposures. Neste (NESTE, Nasdaq Helsinki) is the worlds leading producer of renewable diesel and sustainable aviation fuel (SAF) , with production on three continents. The companys renewables production capacity is expected to reach 6.8 million tons annually in [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for
safety. NAMSA started testing medical devices before the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] U. S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industrys premier provider. We provide support for clients during every step of the product development lifecycle and [. .. ] their respective Top Accounts Responsible for adding and maintaining information in CRM software per departmental procedures. Works with Strategic Partnership group to develop and implement NAMSA multi-year agreements. Supports manager, Business Development Specialists, Strategic Partner Team, and other sales marketing professionals in developing new market opportunities in designated accounts and geographies. Prepares and delivers effective sales presentations and proposals to ensure successful outcome of sales interactions and transactions. Qualifications Technical Competencies: Bachelors degree in business, sales, marketing, or scientific discipline [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Staff AI/ ML Engineer-Controllable Biology
• Heidelberg, Baden- Württemberg
Betriebliche Altersvorsorge
[. .. ] AI methods to biological networks and sequence data from large-scale human genetic, functional genomic, and singlecell experiments. Models that control biological networks have the potential to be [...]
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[...] transformative in drug discovery, empowering us to find new lifesaving medicines. Competitive candidates will have a track record of developing SOTA deep learning models to solve challenging realworld scientific problems. You should be an outstanding scientist with indepth knowledge of modern machine learning. You can convert vaguely described biological and drug discovery challenges [. .. ] Be a standardbearer for machine learning, software engineering, code review and agentic development best practices within the organisation. Define technical strategy and roadmaps for AI/ ML products, balancing scientific needs, safety, and operational reliability. Operate in a transparent way, communicating clearly and accurately to leadership and the broader organisation. Partner with stakeholders to ensure models are explainable, safe, and relevant. Basic Qualifications Masters degree in a related field (e. g. computer science, mathematics or natural sciences) . 7+ years experience with [. .. ] years experience in software development, including code reviews, version control systems, CI/ CD pipelines, software testing, technical documentation and Agile delivery methodologies. 5+ years experience in a technical leador engineering manager role with direct reports, mentoring software engineers or machine learning practitioners. 7+ years experience with Python and Py Torch, or an equivalent machine learning framework. Experience working with biological sequence and network data, including genomics, transcriptomics, proteomics, gene regulatory networks or related biological datasets. Experience collaborating with stakeholders across multiple [. .. ]
Job am 07.09.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] Research Lead-single-client-Germany Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
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[...] class=highlight_text>drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] closely with local, regional, and global colleagues as well as external partners across Germany. Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient
safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and [. .. ] Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project
manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation [. .. ]
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Job am 07.09.2026 bei Jobleads gefunden
Clinical Research Lead-single-client-Germany
[. .. ] Research Lead-single-client-Germany Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] closely with local, regional, and global colleagues as well as external partners across Germany. Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient
safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and [. .. ] Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project
manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation [. .. ]
▶ Zur Stellenanzeige
Job am 06.09.2026 bei Jobleads gefunden
Site Head, Managing Director and VP, Head of Omics Technologies (m/f/d)
• Heidelberg, Baden- Württemberg
Führungs-/ Leitungspositionen
Betriebliche Altersvorsorge
[. .. ] and society. Find out more: Our approach to R D Position Summary This is a rare opportunity for an internationally recognised scientific leader to shape the future [...]
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[...] of omics-driven drug discovery at GSK. Based in Heidelberg, Germany, one of Europes leading life science hubs, the role combines global scientific leadership with site leadership and Managing Director responsibility. The successful candidate will lead Omics Technologies, a global organisation of approximately 75 scientists deliveringcutting-edgecapabilities across genomics, proteomics, spatial biology, computationalbiologyand emerging [. .. ] without direct authority. Strong communicationand stakeholder engagement skills, with the executive presence and credibility torepresentthe organisation internally and externally at the most senior levels. Deep commitment to scientific integrity, ethics, safety, quality, and regulatory compliance. Preferred Qualifications Significant leadership experience within pharmaceutical, biotechnology, or drug discovery R D environments, includingdemonstratedsuccess leading large, complex scientific organisations through second-line leadership structures. Experience leading technology platforms or scientific organisations focused on next-generation biology, omics technologies, data sciences, computational biology, or related discovery capabilities. Prior site leadership experience, including responsibility for operational excellence, infrastructure, employee engagement, health and safety, and organisational culture. Experience serving as a Managing Director, General Manager, Legal Entity Director, Board Member, or similar governance role with accountability for fiduciary, legal, financial, or compliance responsibilities. Experience with corporate governance, risk management, financial oversight, and executive-level board engagement. Demonstrated success attracting, retaining, and developing world-class scientific talent, including building high-performing leadership teams. Experience driving organisational [. .. ]
Job am 04.09.2026 bei Jobleads gefunden
Site Monitoring Lead (SML) sponsor dedicated in Germany
Führungs-/ Leitungspositionen
[. .. ] (SML) sponsor dedicated in Germany Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in [. .. ] healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and [. .. ] Ms) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation [. .. ]
Job am 03.09.2026 bei Jobleads gefunden
Software Engineer, Commissioner (w/m/d)
[. .. ] will partner with internal teams, customers, and engineering groups to develop, maintain, and support software systems integrated with industrial equipment. In this role, you will report to [...]
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[...] the Software Engineering Manager. This is an industrial software and automation engineering role where you install, configure, troubleshoot, and support software-controlled manufacturing equipment at customer sites, combining programming knowledge with hardware, PLC, networking, and customer-facing work. You Will Make an Impact By: Commissioning and configuring software systems during equipment installation to ensure [. .. ] Ability to diagnose and troubleshoot software, operating system, and application issues. Experience with PLC programming and industrial automation systems. Familiarity with instrumentation, sensors, actuators, and control systems. Knowledge of industrial safety standards and maintenance protocols. Strong problem-solving, communication, customer service, time management, and adaptability skills, with the ability to train and support customers and junior engineers. Strong English communication skills are required; German and Russian language skills are a plus. Preferred Skills: Basic Knowledge of Java Script and Python: Understanding [. .. ] 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 is generally only hiring candidates who reside in states where we are registered to do business. MKS is committed to working with and providing reasonable accommodations to qualified individuals with disabilities. If you need a reasonable accommodation during the application [. .. ]
Job am 03.09.2026 bei Jobleads gefunden
Fire Airtanker Base Manager
[. .. ] is a Direct-Hire advertisement. Veterans preference is not applicable to this advertisement. Learn more about this authority at: Direct Hire Authority These four Wildland Firefighter (Aviation) (Fire [...]
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[...] Airtanker Base Manager) , GW-0456-09, positions are with the US Wildland Fire Service, working in any of the following location (s) : Battle Mountain, Nevada Mountain Home, Idaho Pocatello, Idaho Winnemucca, Nevada Major Duties As a Fire Airtanker Base Manager your duties will include but are not limited to the following: [. .. ] and implements activities to accomplish DOIs multicultural organization direction. Directs and oversees air base operations in support of wildland fire suppression and serves as a subject matter expert in aviation safety and retardant aircraft limitations. Serves as the primary point of contact for airport management, contractor representatives, public affairs officials, and federal, state, tribal, and local partners regarding aviation operations. Ensures safe execution of all aviation and ground support activities, including site security, communications, aircraft movement, fueling, retardant operations, and ramp [. .. ] position. Requirements Must be a U. S. Citizen or National. Suitability for Federal employment, as determined by background investigation. Direct Deposit Required. You will be required to submit to a drug test and receive a negative drug test result prior to appointment. In addition, this position is subject to random testing for illegal drug use. This position requires the incumbent to operate a government (or private) motor vehicle as part of their official duties. Selectee must hold and maintain a valid [. .. ]
Job am 03.09.2026 bei Jobleads gefunden
Traveling Crew Supervisor (Demolition)
Führungs-/ Leitungspositionen
[. .. ] activity in the field Lead laborers, equipment operators, foremen, and other jobsite personnel Support structural demolition and selective/ interior demolition projects Help plan daily work with the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Superintendent or Project Manager Communicate job requirements, safety expectations, and production goals to the crew Make sure tools, materials, and equipment are ready for the days work Ensure equipment checks and safety inspections are completed Monitor crew productivity, work quality, and jobsite safety Keep the Superintendent or Project Manager updated on progress, issues, and jobsite needs Enforce company [. .. ] production, safety, and jobsite workflow Comfortable completing daily reports, time entry, cost codes, and safety documentation Strong communication and field leadership skills Valid drivers license Ability to pass required background, drug screen, and driving record checks Ability to work outdoors in active construction/ demolition environments Preferred qualifications: Experience with structural demolition, selective demolition, or interior demolition Experience supervising laborers, operators, foremen, drivers, subcontractors, or mixed crews Experience working around excavators, loaders, skid steers, shears, grapples, hammers, roll-offs, dump trucks, trailers, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Drug Safety Manager pro Jahr?
Als Drug Safety Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Drug Safety Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 40 offene Stellenanzeigen für Drug Safety Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Manager Jobs?
Aktuell suchen 7 Unternehmen nach Bewerbern für Drug Safety Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Drug Safety Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Safety Manager Stellenangebote:
- The BIG Jobsite (2 Jobs)
- Daiichi Sankyo Europe GmbH (1 Job)
- headcount (1 Job)
- Wu Xi App Tec Group (1 Job)
- EURAXESS Ireland (1 Job)
- Unist (1 Job)
In welchen Bundesländern werden die meisten Drug Safety Manager Jobs angeboten?
Die meisten Stellenanzeigen für Drug Safety Manager Jobs werden derzeit in Bayern (7 Jobs), Baden-Württemberg (5 Jobs) und Niedersachsen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Manager Jobs?
Drug Safety Manager Jobs gehören zum Berufsfeld Arbeitssicherheit / HSE / EHS.
