39 Jobs für Drug Safety Manager
Stellenangebote Drug Safety Manager Jobs
Job vor 4 Tagen 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 [...]
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 vor 5 Tagen bei StepStone gefunden
Atotech Deutschland GmbH Co. KG
Pricing Marketing Specialist (w/m/d)
• Feucht bei Nürnberg Nuernberg
[. .. ] optimizing pricing structures, enhancing market competitiveness, and supporting the global aftermarket business through data-driven insights and strategic marketing initiatives. In this role, you will report to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Global Product Manager-After Sales Service. Safety is and remains the highest priority and must be an integral part of all activities. Ensure that all tasks are performed safely and in compliance with applicable legal requirements, company policies, and MKS HSE S standards. Demonstrate continuous transparency, collaboration, and partnership with employees, customers, and stakeholders at all levels. [. .. ] 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. JBRT1DE. Atotech Deutschland Gmb H Co. KG sucht in Feucht bei Nürnberg eine/n Pricing Marketing Specialist (w/m/d) (ID-Nummer: 14541801) 04097590 [. .. ]
Job gestern bei JobMESH gefunden
Genmab
• Bavaria Munich
Führungs-/ Leitungspositionen
[. .. ] Products Act. The role has no line management responsibility. The position leads the German affiliate Quality function and is embedded in Quality Global Affiliates, working closely with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the German General Manager and relevant global functions. The role combines strategic Quality leadership with hands-on responsibility for affiliate establishment, launch readiness and ongoing operations, exercising independent Quality judgement and the authority necessary to fulfil the designated statutory responsibilities. Responsibilities Affiliate Establishment and Collaboration Lead the Quality workstream for establishment of the German [. .. ] and authority interactions, coordinating required notifications and responses with relevant functions Exercise independent authority to place products on Quality hold, prevent supply or suspend distribution activities where product quality, patient safety or regulatory compliance may be compromised Quality Management System Establish and maintain the Genmab Germany Affiliate Quality Management System Implement applicable Global Quality procedures and develop local procedures where required Support continuous improvement of affiliate Quality processes. Quality Operations Manage deviations, CAPAs, change controls and quality risk-management activities Lead [. .. ] working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmabs vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North [. .. ]
Job vor 2 Tagen bei JobMESH gefunden
Genmab
German Affiliate Quality Director Responsible Person (RP)
• Bavaria Munich
Führungs-/ Leitungspositionen
[. .. ] Products Act. The role has no line management responsibility. The position leads the German affiliate Quality function and is embedded in Quality Global Affiliates, working closely with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the German General Manager and relevant global functions. The role combines strategic Quality leadership with hands-on responsibility for affiliate establishment, launch readiness and ongoing operations, exercising independent Quality judgement and the authority necessary to fulfil the designated statutory responsibilities. Responsibilities Affiliate Establishment and Collaboration Lead the Quality workstream for establishment of the German [. .. ] and authority interactions, coordinating required notifications and responses with relevant functions Exercise independent authority to place products on Quality hold, prevent supply or suspend distribution activities where product quality, patient safety or regulatory compliance may be compromised Quality Management System Establish and maintain the Genmab Germany Affiliate Quality Management System Implement applicable Global Quality procedures and develop local procedures where required Support continuous improvement of affiliate Quality processes. Quality Operations Manage deviations, CAPAs, change controls and quality risk-management activities Lead [. .. ] working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmabs vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
Lonza Group
• AT- 2 Lavamünd
Operational Excellence
Manager (m/f/d) 80-100 Operational Excellence Manager (m/f/d) 80-100 The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] if needed. Join our Mid-Scale Microbial Operations team in Visp and help shape the future of [. .. ] continuous improvement. This role is based on site. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Opportunities to lead high-impact transformation and continuous improvement initiatives. Professional growth through coaching, mentoring, and leadership exposure across the organization. A variety of benefits dependent on [. .. ] Lean Six Sigma methodologies to improve manufacturing performance and operational efficiency. Own the end-to-end asset improvement roadmap, accelerating operational gains, enhancing process robustness, and supporting reliable long-term drug substance supply. Partner with functional leaders across Operations, Quality, Engineering, and Technical Services to identify opportunities and establish continuous improvement objectives. Coach and support employees pursuing White Belt, Yellow Belt, and Green Belt certifications while fostering a culture of continuous improvement throughout the organization. Monitor, review, and improve operational performance [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
Incyte Corporation
Expert QA QC Release
• AT- 2 Lavamünd
Aperu Function Summary The QA QC Expert is responsible for the quality oversight of
Drug Substance batch testing and release, as well as QA oversight for Quality Control (QC) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities at the Incyte Bioplant facility in Yverdon-les-Bains. This includes batch disposition preparation, analytical method transfers/ validation, laboratory equipment qualification, and routine testing, ensuring compliance with Incyte Quality policies, c GMP, Swiss, EU, and US [. .. ] related support functions including incoming goods and vendor assessments. Foster understanding and application of c GMPs by Bioplant employees. Perform all responsibilities in accordance with company policies, procedures, applicable regulations, and safety requirements. Promote a strong culture of Quality, business integrity, and ethics. Act within compliance and legal requirements as well as company guidelines. Reporting Line Delegation to: Manager Release, QA QC. Requirements Bachelors or academic degree in a relevant field (Chemical Engineering, Bio-engineering, Bioprocessing, Pharmacy, Chemistry, Biotechnology) . Expertise in Microbiology and/or Chemical/ Biochemical. Minimum 5 years experience in a GMP environment. Demonstrated experience in QA for QC topics; experience in batch release preferred. Thorough knowledge [. .. ]
Job am 22.09.2026 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for 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 am 14.08.2026 bei Mindmatch.ai gefunden
EURAXESS Ireland
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 3 Tagen bei Jobleads gefunden
Clinical Trial Manager-single sponsor-Germany
Clinical Trial
Manager-single sponsor-Germany Updated: Today Location: Remote, Germany Job ID: 25113028 Description Clinical Trial Manager-single sponsor-Germany Syneos Health is a leading fully-integrated life sciences services organization built to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate customer success. We partner with innovators at every point 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 [. .. ] client partnerships we are currently recruiting for a Clinical Trial Manager, here in 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 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] Remote, Germany Job ID: 25113265 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 [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses 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 Excellent communication, presentation and [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Trial Managers (SMLs) sponsor dedicated in Germany
[. .. ] Get to know Syneos Health 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 [. .. ] to deliver for one another, our customers, and, most importantly, for those in need. Job Responsibilities For one of our single sponsor partnerships we are looking for a Clinical Trial Manager to join the team here in 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 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
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 [. .. ] are looking for a Site Monitoring Lead to join the team here in 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 [. .. ] 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 vor 4 Tagen bei Jobleads gefunden
Drug Safety and Complaint Manager (m/w/d)
• München, Bayern
Abgeschlossenes Studium
Flexible Arbeitszeiten
Title:
Drug Safety and Complaint
Manager (m/w/d) Company:Ipsen Pharma Gmb HAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U. S. , France and the U. K, [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Select how often (in days) to receive an alert: Are you passionate about patient
safety and ensuring that medicines are monitored to the highest standards? As a
Drug [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Case Manager, you will play a critical role in safeguarding patients by ensuring accurate and timely management of safety information throughout the product lifecycle. Working within a collaborative and highly skilled Drug Safety team, you will take ownership of adverse event case management activities while partnering closely with physicians, clinical teams, regulatory [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
CRA II-Germany
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 and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 4 Tagen bei Jobleads gefunden
[. .. ] Remote, Germany Job ID: 25112599 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 [. .. ] has been adequately performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses 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 vor 4 Tagen bei Jobleads gefunden
Lab Specialist MSAT Drug Product (f/m/d)
• Singen (Hohentwiel) , Baden- Württemberg
Lab Specialist MSAT
Drug Product (f/m/d) Join Takedas MSAT Drug Product Lab team and help advance innovative vaccine manufacturing-your hands-on DP process expertise makes the difference. How will you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] contribute: Plan and execute experiments for the drug product process, including formulation, aseptic filling, freeze drying and capping; support troubleshooting, process [. .. ] contribute to a safe and compliant working environment. Collaborate cross-functional and communicate technical results clearly in English within an international environment. In this position you will report to the Manager MSAT Lab DP What you bring to Takeda: Completed vocational training in a scientific discipline (e. g. , Laboratory Technician, MTA, BTA, CTA) with further qualification (e. g. , Chemietechniker) or several years of relevant professional experience in sterile manufacturing environments such as Vaccines, Biologics, Compounding, Aseptic Filling and/or [. .. ] technology transfer activities is advantageous. High level of accuracy and reliability in experimental execution and documentation. Strong quality and compliance mindset with a structured and independent working approach. Responsible and safety-conscious behavior in laboratory and cleanroom environments. Ability to work effectively in cross-functional teams within an international organization. Willingness to continuously develop technical knowledge and contribute to process improvement initiatives. About Us: Takeda is focused on creating better health for people and a brighter future for the world. We [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
[. .. ] Remote, Germany Job ID: 25112897 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 [. .. ] future to hire a Site Activation Specialist. Responsible for the quality deliverables at the country level; follows project requirements and applicable country rules with moderate oversight from the SSU Country Manager. Works within the forecasted submission/ approval timelines and ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time; if forecasted timelines are not reached: investigates and provides clear rationale for delays, provides support on contingency plan to mitigate impact, and escalates the [. .. ] approval submissions as required. Prepares ongoing submissions, amendments, and periodic notifications required by central and local EC and RA and other local regulatory authorities as needed within the country; includes safety notifications as required by local rules, with moderate oversight from the SSU Country Manager. May act as liaison and facilitator between investigational sites and functional leads for related tasks and/or issues. Oversee site activation end to end process at country/ site level. Country Start-Up Advisor-Acts as Subject [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Engineering Equipment Operator
[. .. ] between approximately November and May. (Port Angeles only) Operators are responsible for pre-start inspections of equipment as well as minor repairs and preventative maintenance. Operators are responsible [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for following safety rules and regulations. Education There is no substitution of education for experience for Federal Wage System (FWS) positions. Requirements Must be a U. S. Citizen or National. Appointment subject to background investigation and favorable adjudication. Males born after 12-31-59 must be registered for Selective Service. Direct Deposit participation [. .. ] weekends, holidays, overtime and shift work. Must possess and maintain a valid Class A Commercial Drivers License (CDL) with No Brake or Transmission Restrictions. Pre-employment and random alcohol and drug testing are required. You will not be appointed to the position if a verified positive test is received. Ability to lift 50 pounds You are required to wear a uniform and comply with uniform standards. A uniform allowance will be provided. You are required to complete training, obtain and maintain [. .. ] Equipment Operator Work Practices (including keeping things neat, clean, and in order) All qualified non-competitive applicants and the best-qualified Merit Promotion applicants will be referred to the hiring manager for consideration. Other Information Additional vacancies may be filled using this job announcement. Port Angeles, WA Location: Career-Seasonal appointments are permanent positions and include the same benefits as Career appointments, but do not provide work on a year-round basis. You will work for approximately 6 months in pay [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Assistant General Counsel, Legal, CEEM Region
• München, Bayern
[. .. ] the companys business while addressing legal risks and protecting the companys integrity and reputation Provides practical and timely advice on issues related to marketing claims, engagement with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] patient advocacy organizations, safety issues, regulatory strategy, publications, access, supply chain issues and life cycle management. Participates in various projects and initiatives (e. g. , workplace committees, offsite planning, strategic planning) . Drafts and negotiates a wide market access and relating to provision of drug under access programs, and general business contracts for interactions with a variety of stakeholders. As a people manager within the organization, has financial accountabilities and human resource responsibilities for assigned staff. Key Requirements: JD or LLM or law degree from a respected university Strong experience in a large law firm, biopharmaceutical company, or government agency practicing law, or the equivalent combination of education and experience Highly collaborative, with [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Assistant General Counsel, Legal, CEEM Region
[. .. ] the companys business while addressing legal risks and protecting the companys integrity and reputation Provides practical and timely advice on issues related to marketing claims, engagement with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] patient advocacy organizations, safety issues, regulatory strategy, publications, access, supply chain issues and life cycle management. Participates in various projects and initiatives (e. g. , workplace committees, offsite planning, strategic planning) . Drafts and negotiates a wide market access and relating to provision of drug under access programs, and general business contracts for interactions with a variety of stakeholders. As a people manager within the organization, has financial accountabilities and human resource responsibilities for assigned staff. Key Requirements JD or LLM or law degree from a respected university Strong experience in a large law firm, biopharmaceutical company, or government agency practicing law, or the equivalent combination of education and experience Highly collaborative, with [. .. ]
Job am 23.09.2026 bei Jobleads gefunden
Senior CRA-Germany
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 22.09.2026 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) , [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 18.09.2026 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
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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 39 offene Stellenanzeigen für Drug Safety Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Safety Manager Jobs?
Aktuell suchen 9 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:
- Genmab (2 Jobs)
- Daiichi Sankyo Europe GmbH (1 Job)
- Atotech Deutschland GmbH Co. KG (1 Job)
- Lonza Group (1 Job)
- Incyte Corporation (1 Job)
- headcount (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 (8 Jobs), Baden-Württemberg (3 Jobs) und Niedersachsen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Safety Manager Jobs?
Drug Safety Manager Jobs gehören zum Berufsfeld Arbeitssicherheit / HSE / EHS.
