46 Jobs für Pharmacy Support
Stellenangebote Pharmacy Support Jobs
Neu Job vor 2 Std. bei StepStone gefunden
CHEPLAPHARM Arzneimittel GmbH
• Berlin, Binningen, Greifswald
Work-Life-Balance
[. .. ] business objectives. You manage and coordinate regulatory submissions, variations, renewals, and approvals across the product portfolio. You develop and implement regulatory strategies, including risk assessments and change [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] management initiatives. You support all regulatory processes within the team, ensuring timely execution and proactive risk management across the entire regulatory scope. You take over the supervision, coordination and support of regulatory processes/ applications within the team. You collaborate closely with internal stakeholders, external partners, and authorities to ensure smooth and timely execution. You lead cross-functional initiatives, contribute to process improvements, and present regulatory updates to senior management. Profil A Masters degree in a relevant field, i. e. generally in the natural sciences, pharmacy or medicine You bring at least 7 years of relevant professional experience. You have strong knowledge of international regulatory requirements and submission processes. You demonstrate strong analytical and strategic thinking, with the ability to manage complex regulatory topics. You are a strong communicator with experience in cross-functional collaboration and [. .. ]
Job vor 12 Tagen bei StepStone gefunden
Universitätsklinikum Carl Gustav Carus Dresden
Postdoctoral Research Associate Position (m/f/d) - Surgical AI
• Dresden
Teilzeit
Jobticket Work-Life-Balance
[. .. ] in clinical surgery, interdisciplinary oncology, and translational research Ability to time-manage and lead research projects independently, ability to mentor junior researchers, ability to identify and communicate the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] need for support Collaborative and curious mindset with an interest in clinical or translational applications at the intersection of disciplines, in particular clinical surgery/ surgical oncology and data science/ AI Excellent English communication skills, willingness to learn/ knowledge of German is a plus Wir bieten at the Department of Visceral, Thoracic and Vascular [. .. ] 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 Postdoctoral Research Associate Position (m/f/[. .. ]
Job vor 12 Tagen bei StepStone gefunden
MED- EL Medical Electronics
• Innsbruck
[. .. ] of strategic partnerships with manufacturers, distributors, and other relevant market partners Analysis of the market, competition, target groups, and regulatory developments Development and implementation of new sales [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and marketing strategies Support for product launches, go-to-market activities, and market expansion Monitoring of relevant trends in Healthcare and Consumer Health Acquisition of new customers and development of long-term business relationships Derivation of strategic recommendations for the further development of the business area Profil Completed degree in pharmacy, life sciences, healthcare management, or a comparable qualification, as well as experience in business development, sales, key account management, or product management, ideally in the pharmaceutical/ healthcare sector Knowledge of regulatory requirements in the pharmaceutical sector is an advantage Very good German skills and business-fluent English skills Proficient in [. .. ]
Job vor 12 Tagen bei StepStone gefunden
Universitätsklinikum Carl Gustav Carus Dresden
Postdoc (m/f/d) - Child and Adolescent Psychiatry and Psychotherapy
• Dresden
Teilzeit
Jobticket Work-Life-Balance
[. .. ] coordinates perception, action, and cognitive control. The project will investigate how neural oscillations interact across time and frequency, how information flows between brain regions, and how transient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] EEG brain states support adaptive behaviour. The position is ideal for candidates who are excited by the interface of experimental psychology, cognitive neuroscience, computational EEG analysis, and translational neurotechnology. The project asks, which dynamic EEG states are meaningful markers of cognitive control, and how could such markers inform future adaptive neurofeedback, neuromodulation, or closed-[. .. ] 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, retirement provision, and caring for family members. We also offer flexible working hours to support a genuine balance between family and professional life JBRT1DE. Universitätsklinikum Carl Gustav Carus [. .. ]
Job vor 14 Tagen bei StepStone gefunden
Daiichi Sankyo Europe GmbH
• Pfaffenhofen an der Ilm
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] disciplinary leadership for the group. Plan, lead, and implement product development projects within the Formulation Technology Research Laboratories (FTRL) . Establish manufacturing processes, control strategies, and formulation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] designs. Provide technical support for Life Cycle Management (LCM) of commercialized products. Lead manufacturing technology transfer activities, primarily to Daiichi Sankyo Europe and CDMOs in the EU, as well as pivotal formulation development. Oversee CTM manufacturing activities at Daiichi Sankyo manufacturing sites and/or CDMOs in the EU. Support and prepare regulatory submissions for [. .. ] group. Drive talent development, foster employee engagement, and support team growth. Lead the training and supervision of pharmaceutical interns in accordance with local regulations (Approbationsordnung) . Profil Ph. D. in Pharmacy, Engineering, Life Sciences, or a related discipline, or a Masters degree with equivalent professional experience. Extensive experience (preferably 10+ years) in formulation research, CMC development, or related functions within the pharmaceutical industry, ideally in a global organization. Proven expertise in formulation development, product development, and analytical activities. In-depth knowledge [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• München Muenchen
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in [. .. ]
Job vor 14 Tagen bei JobMESH gefunden
TÜV SÜD Produkt Service GmbH
• Bavaria Munich
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in [. .. ]
Job am 25.07.2026 bei Mindmatch.ai gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• Munich, BY
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in [. .. ]
Job am 22.07.2026 bei Neuvoo.com gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• Bavaria Munich
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in [. .. ]
Job vor 4 Tagen bei JobMESH gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d)
• Bayern
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in [. .. ]
Job vor 4 Tagen bei Stellen-Online.de gefunden
TÜV SÜD Produkt Service GmbH
• Deutschland, 99986 Oppershausen
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification:The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) :University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in assessing [. .. ]
Job vor 14 Tagen bei Stellen-Online.de gefunden
TÜV SÜD Produkt Service GmbH
Product Reviewer (IVD Clinical Review/E-ICR) (w/m/d) - Vollzeit
• München, 80333
Flexible Arbeitszeiten Betriebliche Altersvorsorge
[. .. ] reports in line with notified body quality processes Collaborate with cross-functional experts such as product reviewers, QMS auditors, software experts, and other technical specialists in multidisciplinary assessment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams Internal Support in product classification Oversight and assessment of various European national databases for Field Safety Notice Records Qualification: The role requirements are based on IVDR expectations for notified body personnel and the internal qualification framework for E-ICR (Expert for IVD Clinical Review) : University degree in medicine, pharmacy, biochemistry, genetics, biology, biomedical science, biotechnology, laboratory medicine, or another relevant scientific discipline Minimum of 4 years of professional experience in the in vitro diagnostic medical device sector, medical devices, medicine, or laboratory medicine At least 2 years of practical experience in planning, conducting, or monitoring performance studies, or in [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Octapharma Austria
• AT- 9 Wien
[. .. ] Provide strategic oversight for study concepts, clinical protocols and key development deliverables Drive innovative clinical development approaches, including novel trial designs and realworld evidence generation Partner with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Affairs to support global regulatory strategies and health authority interactions Collaborate across Clinical Development, Clinical Operations, Medical Affairs, Biometrics, Regulatory Affairs and Business Unit functions to ensure successful program execution Build strong relationships with external experts, investigators, key opinion leaders and regulatory authorities Qualifications Completed degree in Medicine, Pharmacy, Life Sciences or another relevant scientific discipline (MD, Pharm D or Ph D preferred) Experience in pharmaceutical or CRO clinical development, including a minimum of 10years in clinical research Strong expertise in protocol development, clinical study design, clinical study reports and clinical development planning Demonstrated experience with regulatory interactions, including FDA Type B/ [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
Qualified Person (QP/ Sachkundige Person) (m/w/d)
• AT- 7 Schaftenau
[. .. ] in full compliance with the Austrian Medicines Act (AMG) , the Marketing Authorization, and current GMP requirements. Job Description This role is based in Schaftenau, Austria. Novartis [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] can offer relocation support for this role: we look forward your application Major Accountabilities: Certify and release secondary packed finished dosage form batches for commercial supply, ensuring compliant technical and market release decisions. Act as Qualified Person in accordance with AMBO 2009 and EU GMP Annex 16, covering medicinal products for human and veterinary [. .. ] and productrelated projects, trainings, audits, and inspections to strengthen compliance, inspection readiness, and quality culture. Obligatory Requirements: Qualification as a Qualified Person in accordance with AMBO 2009. University degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or an equivalent scientific discipline. At least 2 years of experience as Qualified Person in the pharmaceutical or biopharmaceutical industry in Quality Assurance and/or Quality Control department. Thorough knowledge of c GMP requirements and applicable quality standards. Demonstrates accountability, sound decisionmaking, teamwork, results orientation, customer focus, [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
• AT- 7 Schaftenau
Salary Range: 66, 918.00-117, 800.00 Job Description Summary #LI-Hybrid Location: Schaftenau, Austria Relocation
Support: This role is based in Schaftenau, Austria. Novartis is unable to offer relocation support: please [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] only apply if accessible. What if your expertise could help shape the future of medicines and ensure patient safety worldwide? As Senior Expert Science Technology (Extractables and Leachables) (m/f/d) , you will play [. .. ] content. Drive cross-functional collaboration to solve complex scientific and operational challenges. Lead continuous improvement initiatives that enhance testing approaches, workflows, and risk assessment strategies. Essential Requirements Advanced degree in Pharmacy, Chemistry, Life Sciences, or a related scientific discipline. Strong expertise in Extractables and Leachables assessment within a regulated industry environment. Hands-on experience with advanced chromatographic and mass spectrometry analytical techniques. Proven ability to lead complex scientific projects and manage multiple priorities effectively. Excellent scientific writing skills with experience creating [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Bridge Bio Pharma
Senior Director, Medical Affairs, International
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] a pivotal role in advancing Bridge Bios pipeline across Europe. You will operate at the scientific forefront of rare disease innovation, translating cutting-edge science into impactful medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies that support successful launches and long-term patient benefit. In this regional role, you will serve as a trusted scientific and strategic partner across regions and functions, shaping how we engage with healthcareprofessionals (HCPs) , patient organizations, and other stakeholders in rare diseases. You have a proven track record of working in [. .. ] Zug Office. Involves 3050 travel to represent the company at medical conferences and industry meetings, with occasional weekend engagements. Who You Are University degree in the field of life sciences, pharmacy, medicine, dentistry or veterinary medicine Minimum of 10-15 years of experience in Local, Regional and Global medical affairs roles in biotech or pharma; Proven track record of successful launches, evidence generation, publications, external medical communication, and collaboration with scientific opinion leaders Expertise in rare diseases is critical, or extensive [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Novartis
• AT- 7 Schaftenau
[. .. ] perform and document scientific experiments; handle several activities at a time Documentation of the studies in electronic documentation systems according to defined standards Evaluate and interpret results, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] propose and actively support the design of next experiments supervise project related activities; perform complex tasks without having established procedures of downstream processes. Work according to appropriate standards for quality, ethics, health, safety, environment protection, and information security, lead initiatives to ensure continuous improvement; all activities have to be aligned with organizational workflows and [. .. ] participate in sub-teams and contribute to overall TRD strategies and goals and support decision-making. Skills/ Experience Completed studies in Biotechnology, Process Engineering, Biology, Biochemistry, Pharmaceutical Technology, Technical Chemistry, Pharmacy, ideally with several years of industry experience Experience in Downstream Processing, in particular with chromatography systems, e. g. ÄKTA systems Hands-on experience with statistical discovery software (e. g. JMP) . Proficiency in programming languages such as Python, R, or SQL is a plus Excellent problem-solving skills and the [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Jobgether
Solutions Consultant (with Pharma/ Life Sciences expertise)
• AT- 2 Schweiz
Beratungs-/ Consultingtätigkeiten
[. .. ] technical capabilities, you will collaborate with cross-functional teams to design tailored solution strategies, deliver impactful product demonstrations, and guide proof-of-concept initiatives. You will engage with senior stakeholders, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support business development efforts, and contribute valuable market insights that influence product evolution. This role offers the opportunity to work in a global, collaborative environment focused on innovation, customer success, and digital transformation within the healthcare sector. Accountabilities Lead technical discovery sessions with prospective customers to understand business objectives, existing technology [. .. ] Ability to adapt quickly to changing customer needs and evolving industry trends while maintaining strong attention to detail. Commitment to continuous learning and professional development. Bachelors degree in Life Sciences, Pharmacy, Marketing, Communications, or a related discipline. Relevant certifications in project management, digital marketing, or content management are considered an advantage. Upper-intermediate (B2) level of English or higher. Benefits Competitive salary with regular performance and career development reviews. Opportunities for professional growth within an experienced, international team. Clear career progression [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Bavarian- Nordic
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] product and batch readiness, manufacturing documentation, raw material quality oversight, stability-related QA activities, and product disposition preparation. Acting as a key partner to Manufacturing, QC, Supply Chain, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] MSAT, Fv P Support, Compliance, and Technical Quality, you will help ensure seamless execution, effective prioritization of quality-related risks, and strong cross-functional collaboration. Leading a team of eight (Sr) QA Specialists, you will foster a high-performing, quality-focused environment while driving operational excellence, inspection readiness, and continuous improvement across QA operations. [. .. ] a collaborative and pragmatic leader who can balance operational priorities, compliance requirements, and stakeholder needs while driving quality excellence. Besides this, we are looking for someone who brings:A degree in Pharmacy, Life Sciences, Biotechnology, Chemistry, Engineering, or a related scientific discipline Proven experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, ideally supporting manufacturing operations Strong knowledge of GMP, batch disposition, deviation management, change control, CAPA, and inspection readiness Experience leading and developing high-performing teams in a complex, cross-[. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
Director, Global TRD QA Sterility Assurance
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
[. .. ] negotiate, and handle pushback diplomatically. Political savvy-navigate informal networks and overcome barriers to secure a seat at the table. Qualifications Advanced degree (Ph D, MSc, or equivalent) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in life sciences, pharmacy, or related field Extensive experience in sterile manufacturing, quality assurance, or related areas within the pharmaceutical/ biotech industry Strong knowledge of aseptic processing, sterility assurance, and regulatory requirements (e. g. , FDA, EMA, ICH) Proven track record in leading cross-functional teams or networks, ideally in a matrix environment Demonstrated [. .. ] neurodiverse condition you require an adjustment during the recruitment process, please reach out to and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP) , in the application process. If you would like to request this, please let us [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Source Technology Limited
QA Validation Specialist (Fixed-Term Contract)
• AT- 2 Schweiz
QA Validation Specialist (Fixed-Term Contract) We are seeking an experienced QA Validation Specialist to
support a major biologics manufacturing expansion project in canton Valais. You will play a key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role in ensuring GMP equipment, facilities, and systems remain qualified, validated, and inspection-ready throughout the project lifecycle. This is a handson role requiring strong expertise in validation, qualification, change control, and GMP documentation review. The [. .. ] including: SOPs Validation protocols and reports Deviations CAPAs Change Controls Working knowledge of EU GMP and FDA regulations. Fluent English; German is an advantage. Degree in Engineering, Biotechnology, Chemistry, Biology, Pharmacy, or related discipline preferred, though equivalent industry experience will also be considered. Candidate Profile Able to hit the ground running in a critical project phase. Comfortable working independently and managing priorities. Strong attention to detail and quality mindset. Effective communicator with the ability to work across Engineering, Operations, Quality, and [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
Novartis
Director, Global TRD QA Sterility Assurance
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
[. .. ] messaging, negotiate, and handle pushback diplomatically. Political savvynavigate informal networks and overcome barriers to secure a seat at the table. Qualifications Advanced degree (Ph D, MSc, or [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] equivalent) in life sciences, pharmacy, or related field Extensive experience in sterile manufacturing, quality assurance, or related areas within the pharmaceutical/ biotech industry Strong knowledge of aseptic processing, sterility assurance, and regulatory requirements (e. g. , FDA, EMA, ICH) Proven track record in leading cross-functional teams or networks, ideally in a matrix environment Demonstrated [. .. ] neurodiverse condition you require an adjustment during the recruitment process, please reach out to and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP) , in the application process. If you would like to request this, please let us [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Sandoz International GmbH
Medical Manager (d/f/m)
• AT- 2 Schweiz
[. .. ] medical/ scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies/ clinical research within the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] respective therapeutic area. Support country strategy for Non Interventional Studies/ Investigator Initiated Trial activities. Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs and reviewed/approved per local/ P3 guidelines. Ensure medical insights [. .. ] adverse events/ special case scenarios related to Sandoz products within 24 hours of receipt-Distribution of marketing samples (where applicable) What youll bring to the role: Scientific degree in Medicine, Pharmacy, (Molecular) Biology or similar, completed with a Ph D or doctoral thesis. Fluency in German and English, plus very strong proficiency in French and/or Italian. Excellent skills in presenting scientific data in German and English is essential, and French/ Italian is desirable. Previous experience in the pharmaceutical industry, ideally in [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
8558- Janssen- Cilag Pharma GmbH Legal Entity
Healthcare Relations Manager
• AT- 9 Wien
[. .. ] team located in Vienna, Austria. About the Role This role is part of the Market Access organization ensuring market access for all Johnson Johnson products in the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] hospital sector and support patient access in the outpatient sector. The focus will include various stakeholders within the healthcare system with the ultimate goal of obtaining Market Access. Tasks/ Responsibilities Conduct negotiations with buyers and decision-makers in the hospital sector. Ensure listing and market access of Johnson Johnson products in the hospital sector. [. .. ] risks. Interact with internal and external stakeholders to obtain relevant information related to upcoming changes in the healthcare system and new product applications. Skills Pharmareferentenprüfung or degree in Veterinary medicine, pharmacy or human medicine and at least five years working experience in the pharmaceutical industry in field access and/or market access. Strong communication and negotiation skills, advanced business acumen and strategic thinking, cross functional collaboration to interact with and influence key stakeholders, both internally and externally Good knowledge on the [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
Johnson Johnson Innovative Medicine
Healthcare Relations Manager
• AT- 9 Wien
[. .. ] team located in Vienna, Austria. About The Role This role is part of the Market Access organization ensuring market access for all Johnson Johnson products in the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] hospital sector and support patient access in the outpatient sector. The focus will include various stakeholders within the healthcare system with the ultimate goal of obtaining Market Access. Tasks/ Responsibilities Conduct negotiations with buyers and decision-makers in the hospital sector. Ensure listing and market access of Johnson Johnson products in the hospital sector. [. .. ] risks. Interact with internal and external stakeholders to obtain relevant information related to upcoming changes in the healthcare system and new product applications. Skills Pharmareferentenprüfung or degree in Veterinary medicine, pharmacy or human medicine and at least five years working experience in the pharmaceutical industry in field access and/or market access. Strong communication and negotiation skills, advanced business acumen and strategic thinking, cross functional collaboration to interact with and influence key stakeholders, both internally and externally Good knowledge on the [. .. ]
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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 46 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:
- Healthcare Businesswomens Association (3 Jobs)
- Novartis (3 Jobs)
- Jobsin Austria (2 Jobs)
- Jobtailor (2 Jobs)
In welchen Bundesländern werden die meisten Pharmacy Support Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacy Support Jobs werden derzeit in Bayern (4 Jobs), Sachsen (2 Jobs) und Baden-Württemberg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacy Support Jobs?
Pharmacy Support Jobs gehören zum Berufsfeld Apotheken.
