Pharmacy Support Stellenangebote


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244 Jobs für Pharmacy Support


Stellenangebote Pharmacy Support Jobs


Neu Job vor 2 Std. bei StepStone gefunden Universitätsklinikum Carl Gustav Carus Dresden

Advanced Clinician Scientist (m/f/d)

• Dresden Teilzeit Work-Life-Balance [. .. ] with modern sports and fitness programs at our health center, mental health programs, and a comprehensive workplace health management program Shopping benefits: Take advantage of employee discounts [...]
MEHR INFOS ZUM STELLENANGEBOT[...] at our clinic pharmacy, exclusive corporate benefits, and other shopping portals Work-Life Balance: TU Dresden is committed to being a family-friendly university and offers a dual-career service. The School of Medicine also provides support in finding childcare options or employment opportunities for the applicants partner in the region. JBRT1DE. Universitätsklinikum Carl Gustav Carus Dresden sucht in Dresden eine/n Advanced Clinician Scientist (m/f/d) (ID-Nummer: 14548110) 03820861 [. .. ]

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Job vor 3 Tagen bei StepStone gefunden CHEPLAPHARM Arzneimittel GmbH Senior Global Science Expert (m/f/d) • Berlin, Binningen, Greifswald, Home- Office Homeoffice möglich Work-Life-Balance [. .. ] and opportunities. This includes proactively identifying potential risks, performing detailed analyses, and developing effective mitigation strategies to ensure robust and sustainable outcomes. Problem Solving Root Cause Analysis [...]
MEHR INFOS ZUM STELLENANGEBOT[...] You lead or support complex troubleshooting activities and drive thorough root cause investigations. By applying a structured and analytical approach, you identify underlying issues, develop corrective actions, and contribute to the continuous improvement of processes and scientific standards. Documentation Cross-Functional Collaboration You oversee the creation, review, and lifecycle management of critical scientific documentation, [. .. ] scientific standards and foster effective collaboration across organizational boundaries. Profil What sets you apart: Education Professional Experience You hold a Masters degree in a relevant field, such as natural sciences, pharmacy, or medicine. In addition, you bring at least seven years of relevant professional experience and have successfully applied your expertise in complex scientific and business environments. Scientific Expertise Analytical Skills You possess strong expertise in scientific evaluation, risk assessment, and problem-solving methodologies. By combining analytical thinking with a structured [. .. ]

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Job vor 3 Tagen bei StepStone gefunden medac Gesellschaft für klinische Spezialpräparate mbH

Senior Clinical Project Manager (all genders)

• Wedel bei Hamburg Homeoffice möglich Work-Life-Balance [. .. ] performance oversight throughout the study lifecycle Collaborate closely with cross-functional teams to align clinical, scientific, regulatory and operational priorities Contribute to protocol development, study planning and operational [...]
MEHR INFOS ZUM STELLENANGEBOT[...] strategies to support efficient trial execution Ensure compliance with ICH-GCP, applicable regulations and internal standards while maintaining inspection readiness Support interactions with health authorities and contribute to regulatory submissions, inspections and audits Promote a culture of collaboration, accountability and continuous improvement Profil Advanced degree in Life Sciences, Pharmacy, Medicine or a related scientific field; Ph D preferred Proven track record of successfully leading international phase IIII clinical studies Strong expertise in CRO and vendor oversight, study governance and operational risk management Sound understanding of clinical trial design, protocol development and study execution In-depth knowledge of ICH-GCP and [. .. ]

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Job vor 6 Tagen bei StepStone gefunden Aurora Europe GmbH Senior Manager, Head of Sales Force (m/f/d) • Berlin Führungs-/ Leitungspositionen [. .. ] Ideally, but not necessarily, located in Berlin or the surrounding area Fluency in German and English (written and spoken) . Education Experience: Bachelors or Masters degree in [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Life Sciences, Medicine, Pharmacy, Business Administration, or a related field. +8 years of experience in sales, inbound/outbound sales, commercial or business-related fields +5 years of leadership experience managing and developing a high-performing Key Account Management team. Preferably qualified to work in pharmaceutical sales in accordance with Section 75 of the German [. .. ] together with the Regional Key Account Managers (KAM) . 30 days of paid annual leave per calendar year Free coffee, fresh fruit, and snacks available daily in the office To support health and well-being, we offer subsidized Urban Sports Club membership. Interested? We look forward to receiving your complete online application (short cover letter, CV, and references) , including your earliest possible start date and salary expectations. Data Protection: Our privacy policy for the recruitment process can be found here: [. .. ]

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Job vor 11 Tagen bei StepStone gefunden Bausch + Lomb

Technical Responsible Person (FvP) / Senior Quality Assurance Specialist (m/f/d)

• Zug Beratungs-/ Consultingtätigkeiten [. .. ] complaints. Maintain the Quality Management System (QMS) and conduct internal audits and training management activities. Communicate with Swiss health authorities, manage regulatory activities in Switzerland, and maintain [...]
MEHR INFOS ZUM STELLENANGEBOT[...] product registrations/ licenses. Support pharmacovigilance and materiovigilance activities for the Swiss market, by handling routine activities (including literature research, reporting obligations, managing adverse event reports and participation in product recalls) . Regularly report and monitor Quality Performance Indicators (QPIs) . Qualify suppliers, service providers, and customers. Organize and conduct audits to ensure quality and compliance. Act as the responsible person for advertising. Profil University degree in Life Sciences, Pharmacy, Chemistry, or an equivalent scientific discipline. Qualified to work as Fv P as per Swiss requirements. (I-SMI. TI. 17) . Several years of experience in the pharmaceutical industry as (deputy-) Fv P, preferably in a senior position within compliance or quality; project management experience is advantageous. Strong knowledge of GMP, [. .. ]

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Job vor 13 Tagen bei StepStone gefunden Universitätsklinikum Carl Gustav Carus Dresden Research Associate/ Predoc (m/f/d) • Dresden Teilzeit Jobticket Work-Life-Balance [. .. ] scientific conferences Prepare scientific manuscripts and contribute to research reports and grant-related documentation Participate actively in the scientific activities of the Schneider Lab, the CRTD, and collaborative [...]
MEHR INFOS ZUM STELLENANGEBOT[...] research networks Support the supervision of students and contribute to shared organizational responsibilities within the laboratory Profil University degree at Masters level, in biology, molecular medicine, biomedicine, biochemistry, biotechnology, microbiology, immunology, neuroscience, bioinformatics, nutritional sciences, or a related discipline Strong interest in microbiome research, chronic liver disease, neuroimmunology, mucosal immunology, and inter-organ [. .. ] with modern fitness and exercise programs at our health center, mental health programs, and a comprehensive workplace health management program Shopping benefits: Take advantage of employee discounts at our clinic pharmacy, exclusive corporate benefits, and other shopping portals Work-life balance: Our Family Office supports you with questions regarding daycare spots, vacation programs, and caring for family members. We also offer flexible work arrangements JBRT1DE. Universitätsklinikum Carl Gustav Carus Dresden sucht in Dresden eine/n Research Associate/ Predoc (m/f/d) [. .. ]

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Job vor 14 Tagen bei StepStone gefunden Fresenius Kabi Deutschland GmbH

Senior Project Manager Biopharma Tech Ops (m/f/d)

• Bad Homburg [. .. ] risks early and develop effective mitigation strategies Provide regular updates to senior management on project status, risks, and key decisions Coordinate manufacturing, quality, regulatory, and technical stakeholders [...]
MEHR INFOS ZUM STELLENANGEBOT[...] throughout project execution Support setting up Statements of Works and aligning them with external partners and service providers Facilitate problem-solving discussions and drive resolution of complex project challenges Profil Degree in Pharmacy, Biotechnology, Life Sciences, or a related scientific discipline At least 5 years of experience in project management within the biopharmaceutical industry Proven experience managing technology transfer, manufacturing, or Tech Ops projects Strong knowledge of biopharmaceutical manufacturing processes and production equipment Demonstrated success leading cross-functional and international project teams Excellent [. .. ]

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Job am 18.08.2026 bei StepStone gefunden Daiichi Sankyo Europe GmbH Manager (m/w/d) Formulation Technology Biologics • Pfaffenhofen an der Ilm Work-Life-Balance [. .. ] for patients, their 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
MEHR INFOS ZUM STELLENANGEBOT[...] class=highlight_text>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) . The functional and technical management of contract manufacturing organizations (CMO Management) for manufacturing parenteral dosage forms in Europe and supporting the preparation of [. .. ] the preparation of regulatory submission documents; incl. NDA, and BLA. Collaboration with various international multidisciplinary project teams (incl. colleagues from Japan, US and CMOs in Europe) Profil University degree in Pharmacy or related subject, ideally with Ph D in Pharmaceutical Technology (focus on Lyophilization and Biologics) At least two years of relevant work experience in pharmaceutical industry (formulation and process development) . Previous experiences with CMO management, global CMC development, technology transfer and handling of high potent Biologics are preferrable. Experience in [. .. ]

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Job vor 5 Tagen bei Neuvoo.com gefunden Bausch + Lomb Technical Responsible Person (FvP) / Senior Quality Assurance Specialist (m/f/d) • Sachsen [. .. ] complaints. Maintain the Quality Management System (QMS) and conduct internal audits and training management activities. Communicate with Swiss health authorities, manage regulatory activities in Switzerland, and maintain [...]
MEHR INFOS ZUM STELLENANGEBOT[...] product registrations/ licenses. Support pharmacovigilance and materiovigilance activities for the Swiss market, by handling routine activities (including literature research, reporting obligations, managing adverse event reports and participation in product recalls) . Regularly report and monitor Quality Performance Indicators (QPIs) . Qualify suppliers, service providers, and customers. Organize and conduct audits to ensure quality and compliance. Act as the responsible person for advertising. University degree in Life Sciences, Pharmacy, Chemistry, or an equivalent scientific discipline. Qualified to work as Fv P as per Swiss requirements. (I-SMI. TI. 17) . Several years of experience in the pharmaceutical industry as (deputy-) Fv P, preferably in a senior position within compliance or quality; project management experience is advantageous. Strong knowledge of GMP, [. .. ]

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Job am 12.09.2026 bei JobMESH gefunden Bionorica SE (Senior) Global Brand Manager/ Team Lead (m/f/d) • Bavaria Neumarkt in der Oberpfalz Führungs-/ Leitungspositionen Homeoffice möglich Bionorica, with approximately 2200 employees worldwide, is the German market leader for pharmacy-only herbal medicines. For over 90 years, we have been unlocking the secrets of nature by combining [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the knowledge of traditional medicinal plant therapy with the forward-looking results of scientific research. For our location in Neumarkt (Oberpfalz) , we are looking for a: (Senior) Global Brand Manager/ Team Lead [. .. ] efficiency Sharing, reusing, and leading the global brand community to promote best practices Developing and implementing strategies to increase brand awareness and attractiveness Creating core creative ideas and campaigns to support our global brand strategy Defining compelling brand stories based on deep consumer insights Close collaboration with relevant country colleagues Depending on experience, qualifications and organizational needs, the role may include team leadership responsibility, contributing to the development of franchise priorities, capability building, and the successful delivery of business objectives These [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Novartis

Site MS T Head SMO-Drug Substance

• AT- 2 Lavamünd [. .. ] Technology DS organization, partnering across site functions and global teams to optimize processes, enable successful product launches and transfers, strengthen validation and compliance programs, and build the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] technical capabilities that support the future growth of the Morrisville site. In this highly visible position, you will influence site strategy, develop top talent, and help bring breakthrough therapies to patients with quality, reliability, and speed. Job Description Key Responsibilities Lead the site MS T DS organization, setting vision, priorities, and technical strategy aligned [. .. ] to resolve technical challenges and strengthen process capability. Develop technical talent, succession plans, and knowledge-sharing programs to build organizational capability. Essential Requirements Bachelors Degree Required. Masters degree in Science, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or equivalent scientific discipline preferred. Minimum 10 years of experience in manufacturing. Additional specialist experience is preferred (e. g. , pharmaceutical formulation, process development, manufacturing technology) . Proven experience driving quality and compliance in an organization. Strong working knowledge of applied statistics, quality systems and regulatory [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Novartis Quality Control Specialist II (m/f/d) • AT- 2 Schweiz [. .. ] Oversee production and testing activities to ensure compliance with c Gx P, including data integrity and e Compliance requirements. Review and approve QC testing results, production documentation, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] QC records, and AS T records. Support exception, deviation, and investigation processes, ensuring timely follow-up and appropriate documentation. Ensure QC activities are executed according to applicable GMP, Gx P, regulatory, and internal quality standards. Support batch release activities in compliance with GMP, registration, and license requirements. Contribute to audit and inspection readiness, including support during Gx P audits [. .. ] improve quality, efficiency, cost, and delivery performance. Obligatory Requirements Education as a Lab Technician or similar qualification, or a university degree in a scientific or technical field such as chemistry, pharmacy, biology, or related discipline. Professional experience in a pharmaceutical laboratory, QC, QA, analytics, or equivalent GMP-regulated environment. Strong knowledge of GMP, Gx P standards, quality control testing, quality assurance, and quality documentation. Good understanding of laboratory equipment, analytical processes, data integrity, and compliance expectations. Ability to manage ambiguity, and support [. .. ]

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Job vor 2 Tagen bei Mindmatch.ai gefunden Novartis

Process Expert (m/f/d)

• AT- 2 Schweiz [. .. ] In this role, you will play a key part in ensuring the safe, efficient, and compliant manufacture of high-quality products. As a Subject Matter Expert (SME) , [...]
MEHR INFOS ZUM STELLENANGEBOT[...] you will support manufacturing operations through equipment qualification, cleanroom management, deviation handling, and the maintenance of GMP-compliant documentation. Working closely with cross-functional stakeholders, you will drive continuous improvement initiatives, support regulatory inspections, and contribute to operational excellence in a dynamic and innovative manufacturing environment. Job Description Key Responsibilities: Ensure manufacturing of [. .. ] production environment. Demonstrate a strong awareness of quality and a proactive, self-directed work approach. Essential Requirements: Bachelors degree in a scientific or technical field such as Biotechnology, Biology, Chemistry, Pharmacy, Process Engineering, or a related discipline. Strong interest in technical processes, automation, engineering or manufacturing environments. High learning agility with the ability to quickly understand new concepts, systems, and technologies. Proactive mindset with a willingness to take initiative and seek continuous improvement opportunities. Strong problem-solving skills and a structured [. .. ]

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Job vor 4 Tagen bei Mindmatch.ai gefunden zentiva Sales Representative-Central Switzerland Ticino • AT- 2 Lavamünd [. .. ] ( i. e. SE-Physicians, Pharmacists HCP Group Member, etc. ) Ensure operational implementation of customer agreements concluded by Trade policy manager Develop cross-promotional activities within HCP groups [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to support promotion of Zentiva Visit and develop HCP customers and acquire new ones within German-speaking Swiss regions, supporting the yearly EBITDA objectives and ambitions Develop Zentiva brand and promote portfolio within defined customers groups The employee will perform other tasks under the direction of the Manager within the agreed type of work. ESSENTIAL REQUIREMENTS Business-fluent German (C1/ C2) with the ability to engage confidently with physicians, pharmacy owners, and business stakeholders. Proven success in Swiss field sales within pharmaceuticals, generics, healthcare, or a related industry. Demonstrated experience acquiring, retaining, and growing customer accounts. Strong commercial acumen with an understanding of sales performance, profitability, and customer value. Excellent CRM, pipeline management, and forecasting discipline. Valid driving licence and [. .. ]

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Job vor 4 Tagen bei Mindmatch.ai gefunden Incyte Corporation

Expert QA QC Release

• AT- 2 Lavamünd [. .. ] and reports. Approve LIMS master data changes. QA oversight for environmental and utilities monitoring programs, if needed. QA point of contact for Biologic Process Sciences SOPs and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] equipment commissioning/ qualification. Support commissioning and qualification of laboratory equipment. Lead or contribute to risk assessments. Coach QC personnel on quality compliance matters. Support the preparation of Annual Product Reviews (QC part) . Ensure QA oversight for all quality events related to QC activities. Contribute to the maintenance of Incytes Quality System. Support Health [. .. ] 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 of biotechnology processes, laboratory equipment, and c GMP/ c GDP. Familiarity with global regulatory requirements applicable to pharmaceutical manufacturing and [. .. ]

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Job vor 4 Tagen bei Mindmatch.ai gefunden Louisiana State University Omnicell Compliance Pharmacy Operations Specialist • AT- 9 Wien [. .. ] Teaching Hospital (VTH) . The role focuses on Omnicell administration, controlled substance reconciliation, and inventory coordination to ensure safe, compliant medication use across hospital workflows. Ideal candidates [...]
MEHR INFOS ZUM STELLENANGEBOT[...] will manage audits, support regulatory compliance with DEA/ Board of Pharmacy rules, and train staff in proper Omnicell usage while collaborating with clinicians and hospital teams. J-18808-Ljbffr 03697734 [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden Louisiana State University

Omnicell Compliance Specialist

• AT- 9 Wien [. .. ] the application through My Draft Applications located on your Candidate Home page. Job Posting Title: Omnicell Compliance Specialist Position Type: Professional/ Unclassified Department: LSUAM Vet Med-VTH-Admin-Non Clinical-
MEHR INFOS ZUM STELLENANGEBOT[...] class=highlight_text>Pharmacy (Andrea Gisclair (00045754) ) Work Location: Veterinary Medicine Pay Grade: Professional Hourly Job Description: This position serves as the primary Omnicell administrator within the LSU Veterinary Teaching Hospital (VTH) , playing a critical role in supporting safe, compliant, and efficient medication use across the hospital. Through oversight of automated dispensing [. .. ] and treatment records to ensure accuracy, appropriate use, and compliance with DEA, Board of Pharmacy, and hospital regulations. Generates and analyzes Omnicell reports to monitor usage trends, identify discrepancies, and support regulatory, legal, and quality improvement initiatives. Maintains accurate medication inventory within Omnicell, including timely restocking, expiration monitoring, removal of outdated medications, and par level adjustments. Troubleshoots system issues and collaborates with pharmacy leadership and technical support to ensure uninterrupted operation of dispensing systems. Supports Controlled Substance Manager (CSM) functions, including [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden Jobgether Manager, Regulatory Affairs • AT- 2 Lavamünd [. .. ] proposals, feasibility assessments, contract discussions, and technical documentation. As a senior member of the team, you will share your expertise through coaching and mentoring junior colleagues. Your [...]
MEHR INFOS ZUM STELLENANGEBOT[...] work will directly support the development and regulatory advancement of innovative medical products and clinical research programs. Accountabilities Lead and coordinate regulatory and ethics committee submissions and maintain required approvals across EMEA, Asia Pacific, and Latin America. Ensure regulatory submissions are accurately compiled, managed, tracked, and maintained in accordance with applicable requirements and timelines. [. .. ] and mentor junior regulatory affairs professionals and, where required, provide direct line management. Requirements: Bachelors degree or equivalent fouryear college education with a major concentration in medical, biological, physical, health, pharmacy, or another relevant scientific discipline. Alternatively, a twoyear college qualification or equivalent education/ training, such as a nursing or life sciences degree, combined with at least eight years of clinical research experience, including areas such as Clinical Research Associate or Regulatory Affairs roles. Minimum 57 years of experience within the [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden Zentiva Poland

Sales Representative-Central Switzerland Ticino

• AT- 2 Lavamünd [. .. ] ( i. e. SE-Physicians, Pharmacists HCP Group Member, etc. ) Ensure operational implementation of customer agreements concluded by Trade policy manager Develop cross-promotional activities within HCP groups [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to support promotion of Zentiva Visit and develop HCP customers and acquire new ones within German-speaking Swiss regions, supporting the yearly EBITDA objectives and ambitions Develop Zentiva brand and promote portfolio within defined customers groups The employee will perform other tasks under the direction of the Manager within the agreed type of work. ESSENTIAL REQUIREMENTS Business-fluent German (C1/ C2) with the ability to engage confidently with physicians, pharmacy owners, and business stakeholders. Proven success in Swiss field sales within pharmaceuticals, generics, healthcare, or a related industry. Demonstrated experience acquiring, retaining, and growing customer accounts. Strong commercial acumen with an understanding of sales performance, profitability, and customer value. Excellent CRM, pipeline management, and forecasting discipline. Valid driving licence and [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden AT33 (FCRS AT033) Novartis Pharmaceutical Manufacturing GmbH Quality Control Specialist II (m/f/d) • AT- 7 Schaftenau Salary Range: 60, 978.00-95, 800.00 Band Level 3 Job Description Summary #LI-Onsite Location: Schaftenau, Austria Relocation Support: Novartis is unable to offer relocation support: As a QC Specialist, you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] will play a key role within the QCMD team, supporting reliable laboratory operations and ensuring compliance with high quality standards. Your responsibilities will include monitoring laboratory testing activities, supporting laboratory analysts, reviewing QC analyses, handling deviations, and contributing [. .. ] improve quality, efficiency, cost, and delivery performance. Obligatory Requirements: Education as a Lab Technician or similar qualification, or a university degree in a scientific or technical field such as chemistry, pharmacy, biology, or related discipline. Professional experience in a pharmaceutical laboratory, QC, QA, analytics, or equivalent GMP-regulated environment. Strong knowledge of GMP, Gx P standards, quality control testing, quality assurance, and quality documentation. Good understanding of laboratory equipment, analytical processes, data integrity, and compliance expectations. Ability to manage ambiguity, and support [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden Incyte Corporation Specialist Quality System • AT- 2 Lavamünd [. .. ] RESPONSIBILITIES Act as a QA Admin and SME on e DMS and e QMS including Documentation, Retention/ Archiving, Training, deviation change control processes Train users on documentation [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Management and Training systems, and support other training where necessary Support actively system users in their daily tasks within the different quality systems Act as key contact point for users at the Bioplant for specific troubleshooting. Escalate unresolved topics to Global QMS team when necessary Manage the documentation change control process and Release Bioplant documentation and [. .. ] a plus Ability to make pragmatic and compliant decisions Strong result orientation and committed team member Excellent written and verbal communication skills Education Bachelors Degree in relevant field such as Pharmacy, Chemistry, Biology or Bio-engineering, Bioprocessing is a plus Trainer and/or auditor certification is a plus Delegate to: QA Specialist, QA Manager Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden Accord Healthcare Head of Quality Assurance • AT- 2 Lavamünd Führungs-/ Leitungspositionen [. .. ] quality representative towards Swissmedic, Corporate Quality, global stakeholders, and external business partners while fostering a strong culture of quality and compliance across the Swiss affiliate. The Person [...]
MEHR INFOS ZUM STELLENANGEBOT[...] University degree in Pharmacy, Life Sciences, Chemistry, or a related scientific discipline. Swissmedic-approved Fv P or eligibility to act as Fv P. 8-10+ years of Quality Assurance experience within the pharmaceutical industry, including significant experience in Switzerland. Strong knowledge of Swiss pharmaceutical regulations, GMP/ GDP requirements, and quality management systems. Proven experience with batch [. .. ] third-party quality activities. Ensure compliant management of product complaints, recalls, distribution activities, and quality metrics. Partner closely with Regulatory Affairs, Supply Chain, Pharmacovigilance, Commercial, and Global Quality teams to support business objectives while maintaining the highest quality standards. What we offer The specific salary level will be determined based on qualifications, experience, and placement within our internal, objective, and genderneutral compensation system. Ready to Make a Difference? If you are passionate about quality, compliance, and leadership and are looking to [. .. ]

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Job vor 6 Tagen bei Mindmatch.ai gefunden Rhythm Pharmaceuticals Inc. Hospital Affairs Lead, Austria • AT- 7 Innsbruck [. .. ] regional sales responsibility for our product Develop strong partnerships with health care professionals, key external experts, payers and multidisciplinary stakeholders Deliver growth in line with expectations for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Austrian affiliate Support development and expansion of comprehensive care programs and patient support programs Facilitate referral pathways between peripheral sites and prescribing centers Lead an omnichannel customer approach relevant for customer segmentation and individual customer preferences/ objectives Accountable for using CRM system for business planning Challenge current practice to deliver the best outcomes [. .. ] the highest standards of ethics, integrity and business conduct. Lead the planning (i. e. account plans) , tracking and reporting process for the territory Qualifications and Skills Academic degree (medicine, pharmacy, veterinary medicine) , MBA, Pharm D or Ph D is a plus Successfully passed the pharmaceutical sales representative examination At least 5 years sales experience with a documented tangible track record in pharma/ biotech industry in Austria Orphan/ specialty experience preferred Experience with building and maintaining strong relationships with key stakeholders (HCPs, [. .. ]

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Job vor 7 Tagen bei Mindmatch.ai gefunden IQVIA (Senior) Clinical Trial Lead (m/w/d) • AT- 9 Wien Führungs-/ Leitungspositionen [. .. ] the trial lifecycle. Use data to steer performance: Use dashboards, metrics, systems, and operational reviews to monitor progress, identify trends, ensure timely data cleaning and delivery, and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] protect milestone achievement. Support critical trial outputs: Coordinate cross-functional contributions to core trial and patient-facing documents, amendments, training updates, authority and ethics responses, safety and data monitoring activities, clinical trial reporting, TMF completeness, registry disclosure, and publication support where applicable. Improve how we work: Contribute to process optimization, cross-functional initiatives, and [. .. ] Strong working knowledge of GCP, ICH guidelines, EU Clinical Trials Regulation as applicable, SOPs, and relevant global and local requirements. Education. A Masters degree or higher in life sciences, medicine, pharmacy, or a related discipline is preferred. An equivalent combination of education and highly relevant experience may also be considered. Therapeutic and operational background Recent Phase III experience in oncology, inflammation, and/or cardiovascular, metabolic, renal (CMR) and/or eye-health indications is strongly preferred. Experience in other therapeutic areas may [. .. ]

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Job vor 7 Tagen bei Mindmatch.ai gefunden Axmed Global Health Advisory-Principal • AT- 2 Lavamünd Work-Life-Balance [. .. ] financing, and delivery models. Help evolve the organizations strategic direction by identifying new areas of opportunity and innovation in global health advisory. Requirements: Bachelors degree in Public [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Health, Life Sciences, Pharmacy, Business, or related field (Masters preferred) 8+ years of experience in consulting, global health advisory, or life sciences, with sustained exposure to LMIC settings Proven track record of leading complex, multi-stakeholder projects end-to-end Deep expertise in one or more of the following: market access, go-to-market [. .. ] Heres what we offer: Unlimited PTO : Take the time you need to recharge and maintain work-life balance. Monthly wellness allowance : Prioritize your health and wellbeing with extra support. Paid parental leave : Time off to bond with your new family member without any added stress. Flexible working hours : Enjoy the freedom to structure your workday in a way that suits your lifestyle. Annual off-site retreats : Connect with the team and build lasting relationships during our [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Pharmacy Support pro Jahr?

Als Pharmacy Support verdient man zwischen EUR 30.000,- bis EUR 45.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Pharmacy Support Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 244 offene Stellenanzeigen für Pharmacy Support Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Pharmacy Support Jobs?

Aktuell suchen 31 Unternehmen nach Bewerbern für Pharmacy Support Jobs.


Welche Unternehmen suchen nach Bewerbern für Pharmacy Support Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacy Support Stellenangebote:


  • Novartis (5 Jobs)
  • Bionorica SE (2 Jobs)
  • Incyte Corporation (2 Jobs)
  • Louisiana State University (2 Jobs)


In welchen Bundesländern werden die meisten Pharmacy Support Jobs angeboten?

Die meisten Stellenanzeigen für Pharmacy Support Jobs werden derzeit in Bayern (37 Jobs), Nordrhein-Westfalen (31 Jobs) und Berlin (23 Jobs) angeboten.


Zu welchem Berufsfeld gehören Pharmacy Support Jobs?

Pharmacy Support Jobs gehören zum Berufsfeld Apotheken.


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