46 Jobs für Pharmaceuticals Oversight
Stellenangebote Pharmaceuticals Oversight Jobs
Job am 20.01.2026 bei Jooble gefunden
KBR
• Stuttgart
[. .. ] SOF personnel, with the priority on SOF Operators and Direct Combat Support personnel: Provide neuro-musculoskeletal injury care, utilizing approved supplemental clinical privileges including the ordering of images, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] laboratory tests, pharmaceuticals, dry needling, acupuncture, joint injections and aspirations, and referrals to specialty providers. If directed by HP Program Manager and/or Coordinator, directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer (ATC) within their scope of practice. Participate in periodic meetings with HP and POTFF for reasons such [. .. ] of care. Provide input for the development and utilization of required databases. Conduct peer (record) review s for the HP Staff as directed by governing credentialing body and local medical oversight process. Assists the HP program Manager and/or Coordinator in developing and updating criteria-based job descriptions and performance standards. Assist the HP program Manager and/or Coordinator in developing and maintaining clinical practice guidelines to ensure consistency of care across all HP Training Centers ( HPTCs ) and associated [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Sobi
Global Product Safety Scientist
• München
Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty
pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere. Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100 of [. .. ] of pharmacovigilance regulations and cross-functional working Excellent written and spoken English Strong analytical and problem-solving skills Effective communication and team leadership capabilities Experience in process development, implementation, and oversight Desired: Proven delivery within a matrix safety team Personal Attributes: Problem solver with a proven delivery focus Effective team player 76628193 [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Essence Investment AG
• Leipzig
[. .. ] legal responsibility under 14 AMG for ensuring the pharmaceutical quality and regulatory compliance of all medicinal cannabis batches processed, imported, manufactured, or distributed by the company. This [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] includes batch certification, oversight of GMP/ GDP processes, and close collaboration with regulatory authorities and external partners. Responsibilities 1. Batch Certification Release-Certify and release medicinal cannabis batches in accordance with AMG, EU-GMP Part I II, and Annex 16. -Review and approve batch documentation, including BMR/ BPR, deviation reports, Co As, and stability [. .. ] and external stakeholders. Requirements-Eligibility as a Qualified Person under 14 AMG. -University degree in pharmacy or other accepted life sciences with QP recognition. -35 years of GMP experience in pharmaceuticals, ideally involving herbal medicinal products or medical cannabis. -Experience with batch certification, QMS processes, and regulatory interactions. -In-depth knowledge of EU-GMP, GDP, AMG, Bt MG, and Bt MVV. -Strong analytical and decision-making skills. -Fluent German (C1+) and strong English proficiency. Preferred Qualifications-Experience in medical cannabis import, testing, or [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
Head of Production Quality
• Ulm
Führungs-/ Leitungspositionen
Youll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. This includes Quality
oversight and support over Teva manufacturing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites, suppliers, and its Quality Compliance processes. The Quality oversight has to ensure the quality of our products, compliance with regulations, and that the products are developed, manufactured, and supplied in a timely manner, securing uninterrupted supply to internal and external customers. In addition, the [. .. ] resources. Minimum of 15 years pharmaceutical manufacturing multiples sites quality operations and leadership experience. Experience working in a large, complex matrixed environment with global processes governance structures; practical knowledge of pharmaceuticals manufacturing and/or control. Practical knowledge of Global Compliance and Regulatory requirements, Industry guidelines (e. g. ICH guidelines specifically M7, PIC/ s, PDA) , c Gx P: Good Manufacturing Practice, Good Laboratory Practice, Good Distribution Practice and other guidelines, the regulations of supervisory authorities at local and international level, specifically US FDA, [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
• Ulm
Youll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. This includes Quality
oversight and support over Teva manufacturing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites, suppliers, and its Quality Compliance processes. The Quality oversight has to ensure the quality of our products, compliance with regulations, and that the products are developed, manufactured, and supplied in a timely manner, securing uninterrupted supply to internal and external customers. In addition, the [. .. ] resources. Minimum of 15 years pharmaceutical manufacturing multiples sites quality operations and leadership experience. Experience working in a large, complex matrixed environment with global processes governance structures; practical knowledge of pharmaceuticals manufacturing and/or control. Practical knowledge of Global Compliance and Regulatory requirements, Industry guidelines (e. g. ICH guidelines specifically M7, PIC/ s, PDA) , c Gx P: Good Manufacturing Practice, Good Laboratory Practice, Good Distribution Practice and other guidelines, the regulations of supervisory authorities at local and international level, specifically US FDA, [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
Head of Quality Manufacturing, EU, India LATAM Solids LCO cluster (m/f/d)
• Ulm
Führungs-/ Leitungspositionen
[. .. ] life with work, and the opportunity to better health worldwide, together. The opportunity The role is accountable to lead and manage all quality activities in the cluster. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] This includes Quality oversight and support over Teva manufacturing sites, suppliers, and its Quality Compliance processes. The Quality oversight has to ensure the quality of our products, compliance with regulations, and that the products are developed, manufactured, and supplied in a timely manner, securing uninterrupted supply to internal and external customers. In addition, the [. .. ] pharmaceutical manufacturing multiples sites quality operations and leadership experience. Direct interaction with health authorities. Experience working in a large, complex matrixed environment with global processes governance structures; practical knowledge of pharmaceuticals manufacturing and/or control. Practical knowledge of analytical techniques and microbiological principles practical knowledge of pharmaceutical cross functional operations (e. g. , Supply Chain, Engineering) . Product and technology transfer. Critical Skills/ Capabilities: Professional : Practical knowledge of Global Compliance and Regulatory requirements, Industry guidelines (e. g. ICH guidelines specifically [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
• Ulm
Youll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. This includes Quality
oversight and support over Teva [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manufacturing sites, suppliers, and its Quality Compliance processes. The Quality oversight has to ensure the quality of our products, compliance with regulations, and that the products are developed, manufactured, and supplied in a timely manner, securing uninterrupted supply to internal and external customers. In addition, the [. .. ] resources. Minimum of 15 years pharmaceutical manufacturing multiples sites quality operations and leadership experience. Experience working in a large, complex matrixed environment with global processes governance structures; practical knowledge of pharmaceuticals manufacturing and/or control. Practical knowledge of Global Compliance and Regulatory requirements, Industry guidelines (e. g. ICH guidelines specifically M7, PIC/ s, PDA) , c Gx P: Good Manufacturing Practice, Good Laboratory Practice, Good Distribution Practice and other guidelines, the regulations of supervisory authorities at local and international level, specifically US FDA, [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
Head of Quality-Manufacturing (m/w/d)
• Ulm
Führungs-/ Leitungspositionen
Youll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. This includes Quality
oversight and support over Teva [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manufacturing sites, suppliers, and its Quality Compliance processes. The Quality oversight has to ensure the quality of our products, compliance with regulations, and that the products are developed, manufactured, and supplied in a timely manner, securing uninterrupted supply to internal and external customers. In addition, the [. .. ] resources. Minimum of 15 years pharmaceutical manufacturing multiples sites quality operations and leadership experience. Experience working in a large, complex matrixed environment with global processes governance structures; practical knowledge of pharmaceuticals manufacturing and/or control. Practical knowledge of Global Compliance and Regulatory requirements, Industry guidelines (e. g. ICH guidelines specifically M7, PIC/ s, PDA) , c Gx P: Good Manufacturing Practice, Good Laboratory Practice, Good Distribution Practice and other guidelines, the regulations of supervisory authorities at local and international level, specifically US FDA, [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Sobi
• München
Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty
pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere. Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100 of [. .. ] of pharmacovigilance regulations and cross-functional working Excellent written and spoken English Strong analytical and problem-solving skills Effective communication and team leadership capabilities Experience in process development, implementation, and oversight Desired: Proven delivery within a matrix safety team Personal Attributes: Problem solver with a proven delivery focus Effective team player 76677245 [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Essence Investment AG
Qualified Person (QP) / Sachkundige Person (Article 14 AMG)
• Gera
[. .. ] legal responsibility under 14 AMG for ensuring the pharmaceutical quality and regulatory compliance of all medicinal cannabis batches processed, imported, manufactured, or distributed by the company. This [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] includes batch certification, oversight of GMP/ GDP processes, and close collaboration with regulatory authorities and external partners. Responsibilities 1. Batch Certification Release-Certify and release medicinal cannabis batches in accordance with AMG, EU-GMP Part I II, and Annex 16. -Review and approve batch documentation, including BMR/ BPR, deviation reports, Co As, and stability [. .. ] and external stakeholders. Requirements-Eligibility as a Qualified Person under 14 AMG. -University degree in pharmacy or other accepted life sciences with QP recognition. -35 years of GMP experience in pharmaceuticals, ideally involving herbal medicinal products or medical cannabis. -Experience with batch certification, QMS processes, and regulatory interactions. -In-depth knowledge of EU-GMP, GDP, AMG, Bt MG, and Bt MVV. -Strong analytical and decision-making skills. -Fluent German (C1+) and strong English proficiency. Preferred Qualifications-Experience in medical cannabis import, testing, or [. .. ]
Job am 01.12.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] the Country Medical Director Germany is responsible for the development and execution of the German medical affairs strategy and programs that support the successful commercialization of current [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and future Jazz Pharmaceuticals products. As a strategic partner to the GM, the incumbent will lead the German Medical Affairs department and serve as the primary medical representative to internal stakeholders and external audiences. The Country Medical Director will be a key member of the German core leadership team and contribute to regional and [. .. ] for business objectives. Foster close collaboration with Market Access and Corporate/ Governmental Affairs to support scientific input into local pricing and reimbursement (P R) processes. Co-lead the development and oversight of the Launch Center of Excellence. Make high-impact medical and strategic decisions with broad organizational implications. Represent the affiliate perspective in Regional Medical Affairs Forums (such as EIMALT) , ensuring the needs of the German team are understood and addressed. Strategic Leadership in Country Medical Affairs Planning and Execution: [. .. ]
Job gestern bei Jobleads gefunden
Director CSV E-Compliance Pharmaceuticals (w/m/d)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] in collaboration with crossfunctional QA teams. Drive digital quality initiatives, automation programs, and continuous improvement efforts. Establish global validation strategies for emerging technologies, including Generative AI in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gx P environments. Governance Oversight: Maintain quality governance for global IT Quality systems (e. g. , QMS platforms, document systems, validation lifecycle tools) following SDLC principles. Ensure compliance with applicable international regulations and internal frameworks. Oversee vendor qualification, vendor management, and outsourced CSV activities. Implementation Operational Support: Lead execution of global IT Quality strategies aligned [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Wuppertal, Nordrhein- Westfalen
[. .. ] and all associated lifecycle activities (e. g. , amendments, Annual Safety Reports, End-of-Trial notifications, CSRs) while collaborating closely with clinical, regulatory, and external stakeholders You ensure daily [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] operational oversight of CTIS and act as the primary interface to approximately 30 national EU Health Authorities on behalf of the sponsor You retrieve, analyze, interpret, and manage regulatory and clinical data, assess data relevance, and ensure high-quality entries in Health Authority databases You identify emerging issues, assess their impact on [. .. ] pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination. Location: Wuppertal or Berlin Division: Pharmaceuticals Reference Code: 861261 #J-18808-Ljbffr 79965877 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director, EMN Operational Stream Lead
• Kiel, Schleswig- Holstein
Führungs-/ Leitungspositionen
Overview At Ferring
Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in the areas of reproductive and womens health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we [. .. ] enable issue resolution, and foster continuous improvement in support of company and patient needs. This is a senior level position reporting to a global organization, with international colleagues and managerial oversight out of the Headquarters. Responsibilities Lead operational performance across the External Manufacturing Network (EMN) . Head the Operational and Supplier Relationship Teams, empowering crossfunctional experts for strong supplier oversight. Align priorities, strategy, and resourcing jointly with the Supplier Relationship Team. Oversee CMO S OP and capacity planning, ensuring balanced external [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan The Opp ortunity This position works out of our Neustadt am Rübenberge site, Abbott Laboratories Gmb H in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Established Pharmaceuticals division. The Director Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan will act as the functional leader within the assigned regions for Engineering, Capital Management and responsible for overseeing the planning, execution, and governance of capital projects, ensuring alignment with Abbotts global standards, compliance with regulatory requirements, [. .. ] reporting and target setting Driving standardization and leading critical processes which span across multiple regions. Ensure Highly Protected Readiness status across the sites in the assigned regions through a critical oversight of Engineering, facilities, Utilities, critical systems Core Job Responsibilities: Implement world-class processes to manage, provide visibility, leverage and make decisions on Abbotts capital assets, including capital budget allocation and planning, capital project management and capital asset, management to improve financial and business performance. Roll out divisional Maintenance Energy Management [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Chief of Staff-RED CVRI (Cardiovascular Renal Immunology) (m/f/d)
• Nordrhein- Westfalen
[. .. ] based on internal and external insights. Operational Efficiency : Develop and coordinate functional concepts for RED CVRI, identifying opportunities to enhance operational efficiency, remove barriers, and maximize [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resource utilization. Portfolio Oversight : Collaborate with business partners to lead CVRI portfolio meetings and reviews, facilitating discussions for timely and informed decision-making. Event Coordination : Organize and contribute to key RED CVRI-wide events such as town halls and workshops to promote engagement and communication. Communication Strategy : Serve as the primary [. .. ] is committed to fair hiring practices across race, national origin, gender, age, disability, religion, and other criteria under applicable law. Location: Germany: Berlin; Germany: North Rhine Westphalia: Wuppertal-Aprath Division: Pharmaceuticals Reference Code: 859382 #J-18808-Ljbffr 79207656 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Berlin
[. .. ] based on internal and external insights Operational Efficiency : Develop and coordinate functional concepts for RED CVRI, identifying opportunities to enhance operational efficiency, remove barriers, and maximize [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resource utilization Portfolio Oversight : Collaborate closely with business partners to lead CVRI portfolio meetings and reviews, facilitating discussions that enable timely and informed decision-making Event Coordination : Organize and contribute to key RED CVRI-wide events, such as town halls and workshops, to promote engagement and communication within the organization Communication Strategy [. .. ] criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination. Location: Germany : Berlin : Berlin Germany : North Rhine Westfalia : Wuppertal-Aprath Division: Pharmaceuticals Reference Code: 859382 #J-18808-Ljbffr 79205680 [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Environmental Risk Assessment Regulatory Lead
• Berlin
Führungs-/ Leitungspositionen
[. .. ] responsibilities across GHSE, R D, Regulatory Affairs, external consultants and regulators (e. g. , governance model, workflows, timelines) . Act as ERA Subject Matter Expert, supporting MAA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams through technical oversight on study design, test monitoring, and data interpretation, as well as managing regulatory interactions, external consultants, and final ERA approvals. Support the development implementation of the global Eco-Pharmaco-Vigilance (EPV) and Pharmaceuticals in the Environment (Pi E) risk assessment and mitigation strategies, in partnership with Global Business Units (e. g. , strategic roadmap, prioritization of products) . Collaborate cross-functionally with Global Functions, Global Business Units, CSR, and Digital teams to strengthen environmental risk data collection, monitoring, and internal/ external reporting (e. g. [. .. ]
Job am 27.01.2026 bei Jobleads gefunden
Director Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] Director Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan The Opportunity This position works out of our Neustadt am Rübenberge site, Abbott Laboratories Gmb H in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Established Pharmaceuticals division. The Director Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan will act as the functional leader within the assigned regions for Engineering, Capital Management and will oversee the planning, execution, and governance of capital projects, ensuring alignment with Abbotts global standards, regulatory compliance, and delivery of [. .. ] EPD energy reporting and target setting. Driving standardization and leading critical processes which span across multiple regions. Ensure Highly Protected Readiness status across the sites in the assigned regions through oversight of engineering, facilities, utilities, and critical systems. Core Job Responsibilities Implement world-class processes to manage, provide visibility, leverage and make decisions on Abbotts capital assets, including capital budget allocation and planning, capital project management and capital asset management to improve financial and business performance. Roll out divisional Maintenance Energy [. .. ]
Job am 27.01.2026 bei Jobleads gefunden
Director Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan
• Neustadt am Rübenberge, Niedersachsen
Führungs-/ Leitungspositionen
[. .. ] Director Capital Project Engineering (m/f/d) - EMEA, Canada and Pakistan The Opportunity: This position works out of our Neustadt am Rübenberge site, Abbott Laboratories Gmb H in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Established Pharmaceuticals division. The Director Capital Project Engineering (m/f/d) EMEA, Canada and Pakistan will act as the functional leader within the assigned regions for Engineering, Capital Management and responsible for overseeing the planning, execution, and governance of capital projects, ensuring alignment with Abbotts global standards, compliance with regulatory requirements, and [. .. ] reporting and target setting Driving standardization and leading critical processes which span across multiple regions Ensure Highly Protected Readiness status across the sites in the assigned regions through a critical oversight of Engineering, facilities, Utilities, critical systems Core Job Responsibilities Implement world-class processes to manage and provide visibility into Abbotts capital assets, including capital budget allocation and planning, capital project management and capital asset management to improve financial and business performance. Roll out divisional Maintenance Energy Management Embed maturity system [. .. ]
Job am 27.01.2026 bei Jobleads gefunden
Global Pharmacovigilance QA Manager
Not Applicable Not discloses Switzerland Basel, Basel, Switzerland About Idorsia
Pharmaceuticals Ltd Headquartered near Basel, Switzerland a European biotech hub Idorsia has a highly experienced team of dedicated professionals, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] covering all disciplines from bench to bedside; QUVIVIQ (daridorexant) , a different kind of insomnia treatment with the potential to revolutionize this mounting public health concern; strong partners to maximize the value [. .. ] to verify adherence to the PV system, as defined in FDA and EMA Regulations. Perform PV QA audits of vendors across affiliate sites as applicable and of affiliates and maintain oversight of QA consultants appointed to perform PV audits on behalf of the company. Ensure audit results are formally and consistently tracked, recorded, reported, trended. Ensure corrective/ preventive actions have been identified, documented and are effective. Cooperate with the EU QPPV and national Affiliate Safety Managers (ASM) and take responsibility for [. .. ]
Job am 23.01.2026 bei Jobleads gefunden
Research Scientist Organic Analysis
• Limburg, Bayern
[. .. ] of solutions. The laboratory is equipped with a wide range of technologies, from basic to highly advanced instrumentation. Its clients are active in diverse sectors such as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] chemicals, food and pharmaceuticals. Complex analytical challenges find their answers at the VITO laboratory. In addition, as a reference laboratory, VITO is responsible within Flanders for defining how environmental measurements (e. g. water, soil, air) should be performed within a European regulatory context. To this end, VITO works closely with the Flemish government and [. .. ] priorities and manage multiple objectives in a team environment Strong project management skills, with the ability to manage multiple projects in parallel; you collaborate effectively with researchers and analysts, maintain oversight and make adjustments as needed to successfully handle challenging deadlines and technical complexity Stressresistant and capable of managing multiple projects simultaneously A flexible attitude towards rapid changes in project scope and timing Knowledge of programming and data management is a plus Able to work independently while aligning with team objectives [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
IT Service Manager-HELM Pharmaceuticals (m/f/d)
• Hamburg
Beratungs-/ Consultingtätigkeiten
Work-Life-Balance
[. .. ] and a reliable partner, all in one. Date: May 9, 2025 Location: Hamburg, DE, 20097 Business Unit: Pharma Job Function: IT/ System Engineering/ SAP Level of Experience: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Mid-Career HELM Pharmaceuticals Gmb H is seeking an IT Service Manager for its FDF Business. This dynamic environment offers significant opportunities for growth and development, providing a unique chance to shape the future of the business globally. To support this, we are looking for a motivated IT Service Manager (m/f/d) . You [. .. ] IT function within the company, developing and implementing IT strategies that support business objectives. This includes enforcing IT policies to ensure compliance and best practices. You will provide direction and oversight for IT initiatives and projects, establishing and participating in IT governance committees. You will monitor the performance of IT services, including external providers, to ensure seamless IT service delivery. You will act as the primary point of contact for all IT-related matters, collaborating with internal and external stakeholders to [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
Global Product Safety Scientist
• München, Bayern
Company Description Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty
pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere. Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100 of [. .. ] of pharmacovigilance regulations and cross-functional working Excellent written and spoken English Strong analytical and problem-solving skills Effective communication and team leadership capabilities Experience in process development, implementation, and oversight Desired: Proven delivery within a matrix safety team Personal Attributes Problem solver with a proven delivery focus Effective team player #J-18808-Ljbffr 77180198 [. .. ]
Job am 16.01.2026 bei Jobleads gefunden
European Senior Quality Director-Medical Cannabis/ Pharmaceuticals
• Berlin
Führungs-/ Leitungspositionen
European Senior Quality Director-Medical Cannabis/
Pharmaceuticals European Senior Quality Director-Medical Cannabis/ Pharmaceuticals Get AI-powered advice on this job and more exclusive features. Industry: Medical Cannabis/ Pharmaceuticals Company Overview Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] client is one of the largest medical cannabis producers, distributors, and brands in Europe. Established in 2006, the company employs over 1, 000 people globally, [. .. ] environments, navigating complexity and ambiguity while enabling business progress without compromising compliance or patient safety. This role carries direct accountability for leading and developing the European Quality leadership team, including oversight of senior leaders such as the Director of Quality. Responsibilities include setting strategic direction, closing capability gaps, implementing performance frameworks (KPIs) , and building a high-performing, accountable quality organisation. The position holds end-to-end responsibility for all European quality activities across key markets including Germany, the UK, Poland, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceuticals Oversight pro Jahr?
Als Pharmaceuticals Oversight verdient man zwischen EUR 50.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceuticals Oversight Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 46 offene Stellenanzeigen für Pharmaceuticals Oversight Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceuticals Oversight Jobs?
Aktuell suchen 11 Unternehmen nach Bewerbern für Pharmaceuticals Oversight Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceuticals Oversight Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceuticals Oversight Stellenangebote:
- Teva Pharmaceutical Industries Ltd. (5 Jobs)
- Sobi (2 Jobs)
- Essence Investment AG (2 Jobs)
- KBR (1 Job)
In welchen Bundesländern werden die meisten Pharmaceuticals Oversight Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceuticals Oversight Jobs werden derzeit in Berlin (7 Jobs), Nordrhein-Westfalen (5 Jobs) und Bayern (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceuticals Oversight Jobs?
Pharmaceuticals Oversight Jobs gehören zum Berufsfeld Pharmazie.
