28 Jobs für Pharmaceutical Specialist
Stellenangebote Pharmaceutical Specialist Jobs
Job gestern bei StepStone gefunden
Astra Zeneca
• München Muenchen
[. .. ] biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the worlds most serious diseases. But were more than one of [...]
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[...] the worlds leading pharmaceutical companies. SITE DESCRIPTION-Munich, Germany At Computational Pathology Munich (CPM) , we make a significant contribution to high-performance, data-driven research and development. Our team operates in a demanding, fast-paced environment where excellent collaboration, clear communication and precise organization are critical. Aufgaben We are seeking a Senior Specialist (m/f/d) , Computational Pathology Business Operations in Munich. The Senior Specialist (f/m/d) reporting to the head of Portfolio Management, acts as the operational backbone, with end-to-end accountability for core business operations spanning finance, procurement, and enterprise planning interfaces. The role partners closely with Portfolio [. .. ]
Job gestern bei StepStone gefunden
European Semiconductor Manufacturing Company
Senior Learning Development Specialist (m/f/d)
• Dresden
[. .. ] products. ESMC represents a shared commitment to strengthening the European semiconductor ecosystem. For our future fab in Dresden, we are looking for a highly motivated and committed: [...]
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[...] Senior Learning Development Specialist (m/f/d) Your mission is to establish a scalable, compliant and globally aligned learning ecosystem for our new semiconductor manufacturing site in Dresden. Working closely with our headquarters in Taiwan, you will translate global learning standards into local processes while ensuring all qualification, compliance and training requirements meet the [. .. ] of professional experience in Learning Development, Learning Operations, Training Management or a related discipline Experience building or significantly developing Learning Development structures, processes or governance Experience in manufacturing, semiconductor, automotive, pharmaceutical, medical device or another regulated industry is highly desirable Knowledge of Learning Management Systems and learning administration Experience with qualification management, quality systems or ISO-related training processes is an advantage Strong project management and stakeholder management skills Excellent communication skills in German and English High intercultural competence and enthusiasm [. .. ]
Job vor 4 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
• Unterschleißheim Unterschleissheim
Angebote von Zeitarbeitsunternehmen
[. .. ] by a company medical center, and employee discounts-all advantages that you can count on with Randstad. Its best to apply online right away and secure this job [...]
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[...] at a pharmaceutical company Applications from individuals with disabilities are warmly welcome. Aufgaben Manage and coordinate the flow of project documentation within the PIM system Ensure all project documents are accurately processed, maintained, and distributed according to project procedures Upload, track, archive, and retrieve technical and project-related documentation Monitor document revisions and [. .. ] Option of permanent employment with our business partner Candid corporate culture A wide range of employee benefits/ perks JBRT1DE. Randstad Deutschland Gmb H Co. KG sucht in Unterschleißheim eine/n Documentation Specialist (f/m/d) (ID-Nummer: 14364833) . Appcast 00374615 [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
Regulatory Affairs Manager (f/m/d)
• Ludwigshafen am Rhein
Beratungs-/ Consultingtätigkeiten Angebote von Zeitarbeitsunternehmen
Regulatory affairs
specialist at a
pharmaceutical company in Ludwigshafen wanted Are you interested? With the many benefits at our subsidiary Randstad professional solutions, such as competitive compensation and retirement plans, [...]
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[...] you certainly cant say no. If thats the case, apply today for the available position Heres another advantage: Applying with us is absolutely straightforward, requiring only [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Novartis
• AT- 7 Unterlangkampfen
Salary Range: CHF133, 700.00-CHF248, 300.00 Job Description Summary Location: Basel, Switzerland #hybrid Role Purpose: Provide
specialist knowledge and guidance on sterile and low bioburden processes, ensuring compliance with regulatory requirements. [...]
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[...] Implement, harmonize, and continuously improve aseptic standards and best practices across TRD pilot plants and all modalities (Cell and Gene Therapies, Radioligand Therapies, ADC, and New Biological Entities) . Act as a key partner in cross-[. .. ] seat at the table. Qualifications Advanced degree (Ph D, MSc, or 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 ability to influence without authority and drive change across organizational boundaries Excellent problem-solving, communication, and [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Internetwork Expert
EU Regional Training Lead (Sales Trainer)
• AT- 9 Wien
Führungs-/ Leitungspositionen
Transform Lives Through Learning At Norgine, we have been transforming patients lives for over a century. We combine
specialist expertise, entrepreneurial thinking and strong partnerships to bring life-changing medicines [...]
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[...] to patients across Europe. We are looking for an experienced EU Regional Training Lead (Sales Trainer) to shape and elevate the capabilities of our commercial teams across the region. The Opportunity As EU Regional Training Lead, (Sales Trainer) you [. .. ] compliance and regulatory standards. Skills Experience We are looking for someone who brings: Bachelors degree or equivalent experience. Fluent/ high level English and ideally German French language skills. Experience in pharmaceutical commercial roles, such as; sales roles, market access, sales management, district management, or commercial excellence/ business intelligence functions. Proven experience delivering sales training, field coaching or learning and development programmes. Strong understanding of pharmaceutical sales processes, commercial performance metrics and customer engagement models. Expertise in facilitation, coaching, presentation delivery and [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
The Biople
• AT- 2 Schweiz
As the Technical Sales
Specialist, you will lead the commercial deployment of the ORYL F1 end to end. From qualifying prospects to running the measurements and instrument demonstrations, to [...]
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[...] interacting with the scientists (drug discovery, biophysics and formulation) and be comfortable in answering their scientific questions all the way to negotiating and closing deals. The [. .. ] and qualification. We need somebody who You are a scientist first, you must be a great listener, and commercially proven. Specifically Excellent scientific foundation. MSc or Ph D in chemistry, biophysics, pharmaceutical sciences or related fields with hands-on analytical or biophysics experience. You must be comfortable answering scientific questions from scientific users. Commercial track record. You are knowledgeable in selling capital equipment, end-to-end, and understand how to interact with users and scientist as well as capex owners or R [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Carbogen AMCIS AG
Corporate Senior CSV Specialist (m/w/d)
• AT- 2 Schweiz
We are currently offering an interesting opportunity as Corporate Senior CSV
Specialist (m/f/d) for a 2 years contract, at our location in Bubendorf, Switzerland, with flexibility to be based [...]
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[...] at one of our other Swiss locations, such as Aarau or Neuland. If you are looking for a varied and exciting new professional challenge, we are happy to receive your application. Your [. .. ] At least 5 years of experience in the validation of Gx P-relevant IT systems such as ERP, LIMS, analytics systems or in process automation Sound knowledge of c Gx P requirements for pharmaceutical companies Degree in sciences (MSc/ BSc in e. g. computer science, chemistry, process engineering) or a science education with relevant professional experience A dynamic highly motivated work environment and a high value infrastructure Possibility to enhance, increase and further develop you key competences Option to work partly from home 5 [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
[. .. ] Range: 0.00-0.00 Job Description Summary Location: Schaftenau, Austria Role Purpose: Establish, lead, and continuously develop the TRD QA Sterile Operations Network, fostering accountability, learning, and collaboration. Provide [...]
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[...] specialist knowledge and guidance on sterile and low bioburden processes, ensuring compliance with regulatory requirements. Implement, harmonize, and continuously improve aseptic standards and best practices across TRD pilot plants and across all modalities (Cell and Gene Therapies, Radioligand Therapies, ADC, and New Biological Entities) . Drive continuous improvement, knowledge transfer, and [. .. ] seat at the table. Qualifications Advanced degree (Ph D, MSc, or 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 ability to influence without authority and drive change across organizational boundaries Excellent problem-solving, communication, and [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Valtria
Senior HR Operations Specialist
• AT- 2 Schweiz
[. .. ] about our work. We strive every day to ensure our clients continue choosing us. Will you join our team? Work in a high-value industry for leading and [...]
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[...] growing sectors (pharmaceutical, technology, RD, biosafety, etc. ) . Join a team of pioneering experts in Clean Rooms. Develop a career with future potential, both locally and in other countries in Europe and Latin America. Job Summary 26 July Location Experience Minimum 8 years of experience in HR Operations, International HR Administration, Shared [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
TRD QA Global Sterility Assurance
• AT- 7 Gemeinde See
Salary Range: CHF133, 700.00-CHF248, 300.00 Job Description Summary Location: Basel, Switzerland #hybrid Role Purpose: Provide
specialist knowledge and guidance on sterile and low bioburden processes, ensuring compliance with regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requirements. Implement, harmonize, and continuously improve aseptic standards and best practices across TRD pilot plants and all modalities (Cell and Gene Therapies, Radioligand Therapies, ADC, and New Biological Entities) . Act as a key partner in cross-[. .. ] seat at the table. Qualifications Advanced degree (Ph D, MSc, or 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 crossfunctional teams or networks, ideally in a matrix environment Demonstrated ability to influence without authority and drive change across organizational boundaries Excellent problemsolving, communication, and stakeholder management [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Johnson Johnson Med Tech
Manager, Health Economics Market Access (HEMA) , Mid-Sized Markets
• AT- 9 Wien
[. .. ] and local approval of regionally developed HEMA tools, translating complex messages into simple statements that can easily be articulated by the sales force Partner with sales and [...]
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[...] marketing to deliver specialist health economic and reimbursement tools to customers, spending time in the field Qualifications Who are we looking for? Advanced degree in health economics, health policy, public health, economics, healthcare management, epidemiology, outcomes research, or other relevant discipline Solid understanding of the principles of HTA and health economics Strong track record of successful engagement with clinical and non-clinical stakeholders 3 years experience in the medical devices, health care or pharmaceutical industry, an HTA or payer organization, healthcare consultancy, academic institution, research organization, or another relevant healthcare-system setting. Medtech experience in the relevant locations is preferred. Good understanding of the processes within healthcare systems and payer bodies Appetite to build on knowledge and experience of market access and health economics [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] integral to Roches mission to develop innovative and transformative meaningful medicines for patients by applying leading technical expertise to design, develop, supply, and register clinical stage products [...]
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[...] globally. The department Pharmaceutical Development is responsible for the development of parenteral drug products (Synthetic molecules and Biologics) from Phase 1 through Launch. Activities encompass formulation and manufacturing process development for parenteral drug products for all clinical stages and the market launch, the transfer of product and process to commercial manufacturing sites, commercial product [. .. ] leadership. Who You Are Educated Expert: Holds a Ph. D. in a relevant scientific or engineering discipline (or equivalent industry experience) combined with 8+ years of biopharmaceutical experience. Parenteral Regulatory Specialist: Demonstrates deep technical expertise in parenteral formulation development, endtoend pharmaceutical development, and Health Authority filing requirements. Proven People Leader: Features 5+ years of direct people management experience with a track record of coaching, recruiting top talent, and building highperforming scientific teams. Modern Leadership Champion: Embraces VACC leadership principles (Visionary, Architect, [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Triwill Group
Senior Werum PAS-X MES L2: Remote Integration Specialist
• AT- 2 Schweiz
Triwill Group, in partnership with a Swiss-based client, seeks a Senior Werum PAS-X MES L2 Support Integration
Specialist. This remote freelance role focuses on maintaining reliable manufacturing operations within [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a global pharmaceutical setting. You will provide expert MES support, troubleshoot complex production issues, and ensure seamless integration between MES and enterprise systems. Collaboration with manufacturing, quality, validation and IT teams is essential to drive compliant and J-18808-Ljbffr 00042101 [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
K- Recruiting GmbH
• AT- 2 Schweiz
QA Validation Qualification
Specialist (m/f/D) Tasks Must possess a full grasp of the duties of Qualifications (CQV) and Validation. Perform QA oversight of the Validation review and qualification activities [...]
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[...] to ensure GMP equipment, facility and/or systems are continuously maintained in a validated/qualified state. Schedule own tasks to be performed as [. .. ] like participate to Audits and inspections to demonstrate the compliance of the facility, equipment and systems with both European and US (FDA) regulations, and continuous improvement initiatives. Qualification GMP-regulated pharmaceutical, biotech, or cell gene therapy environment. 26 years Validation/ Qualification Experience The candidate should understand: IQ (Installation Qualification) OQ (Operational Qualification) PQ (Performance Qualification) Validation lifecycle Maintaining systems in a validated state. Change Control Experience Documentation Review Experience Must have experience reviewing and approving: SOPs Validation protocols Validation reports Deviations [. .. ]
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 [. .. ] Wise, Kneat, DMS, and LIMS. Support internal audits, regulatory inspections, and continuous improvement initiatives. Requirements 2-6 years experience in Validation, Qualification, CQV, or QA Validation within a GMP-regulated pharmaceutical, biotech, biologics, or cell gene therapy environment. Strong knowledge of IQ, OQ, PQ, validation lifecycle management, and maintaining a validated state. Experience reviewing and approving GMP documentation, including: SOPs Validation protocols and reports Deviations CAPAs Change Controls Working knowledge of EU GMP and FDA regulations. Fluent English; German is an [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
Novartis
Director, Global TRD QA Sterility Assurance
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
[. .. ] Operations Network, fostering accountability, learning, and collaboration. Summary Location: Schaftenau, Austria Role Purpose Establish, lead, and continuously develop the TRD QA Sterile Operations Network, fostering accountability, learning, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and collaboration. Provide specialist knowledge and guidance on sterile and low bioburden processes, ensuring compliance with regulatory requirements. Implement, harmonize, and continuously improve aseptic standards and best practices across TRD pilot plants and all modalities (Cell and Gene Therapies, Radioligand Therapies, ADC, and New Biological Entities) . Drive continuous improvement, knowledge transfer, and innovation [. .. ] seat at the table. Qualifications Advanced degree (Ph D, MSc, or 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 ability to influence without authority and drive change across organizational boundaries Excellent problem-solving, communication, and [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
K- Recruiting GmbH
Deviation Specialist
• AT- 2 Schweiz
Deviation
Specialist (m/f/D) Tasks: Responsible to own, author, record and investigate Deviations. Liaise with Subject Matter Experts (SMEs) and key stakeholders to establish the root cause (s) of deviations [...]
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[...] and the potential impact of said deviations. Ensure proper investigational tools are used to systematically define the root cause (s) and [. .. ] Support the business through ongoing change and process improvement activities. Qualification: Bachelor degree in chemistry, biotechnology, life science or related field. Previous experience in Deviations and c GMP in a regulated pharmaceutical/ API industry is a strong advantage. Knowledge of biotech. manufacturing processes and analytical methods is an advantage. Experience with Human and Organizational Performance risk management approaches is an advantage Fluency in English, both written and spoken. German is an advantage. Technical writing presentation/ communication skills are key for the role. [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The [...]
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[...] Position In Roches Pharmaceutical Research and Early Development organization (p RED) , we make transformative medicines for patients in order to tackle some of the worlds toughest unmet healthcare needs. At p RED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility, and humility, where [. .. ] INd/CTA filing and FIH readiness. Qualifications Experience Education Level: Ph D, MD, or Md/Ph D in Cardiovascular Physiology, Renal Physiology, Pharmacology, Molecular Biology, or a highly relevant life sciences discipline. Specialist Knowledge: Advanced authority on the pathophysiology of cardiorenal networks, including CKd/Nephropathy, Myocardial Remodeling Fibrosis, the Cardiorenal Axis, Genetic Rare Diseases, and Atherosclerosis Lipid Metabolism. Fluency in English (written and spoken) is required. Unwavering focus, collaborative teamwork and exceptional delivery are key behaviours that drive our mission of doing now [. .. ]
Job am 21.07.2026 bei Mindmatch.ai gefunden
Vaxcyte
Quality Assurance Specialist III, External Manufacturing
• AT- 2 Schweiz
[. .. ] business objectives. MODEL EXCELLENCE : The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary [...]
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[...] The Quality Assurance Specialist (QA) III, External Manufacturing will play a pivotal role in ensuring that all Gx P external batch records and quality records adhere to Vaxcytes quality standards and regulatory requirements. This individual will perform activities supporting dispositioning product while ensuring compliance with Quality Assurance policies and procedures, c GMPs, SOPs, and Vaxcytes Standard Requirement Documents. The ideal candidate will possess in-depth knowledge of c GMP (current Good Manufacturing Practices) and regulatory guidelines within the pharmaceutical industry. Essential Functions GMP Batch Record and Product or Program Document: reviewing executed batch records (paper and electronic) , product or program specific documents, deviation and change control review and approval, documenting batch review comments, and effectively working with cross functional team, may be the primary QA point of contact [. .. ]
Job am 18.07.2026 bei Mindmatch.ai gefunden
Bristol- Myers Squibb
Senior Specialist Compliance Process Excellence, Commercial Operations Boudry-CH R1604260 Pos. . .
• AT- 2 Schweiz
Senior
Specialist Compliance Process Excellence, Commercial Operations Boudry-CH Find out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, [. .. ] to meet business requirement. Qualifications Bachelors degree in Life Sciences or related field 3-5 years in GMP compliance Good collaboration and communication skills 3-5 years of experience in pharmaceutical environement Business Level in French and English Experience in GMP inspections and audits If you come across a role that intrigues you but doesnt perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and [. .. ]
Job am 17.07.2026 bei Mindmatch.ai gefunden
Stryker Corporation
Regulatory Affairs Specialist
• AT- 2 Schweiz
Regulatory Affairs
Specialist Applylocations: Biberist, Switzerlandtime type: Full timeposted on: Posted Todayjob requisition id: R561546Work Flexibility: Hybrid Job Title: RAQA Specialist (m/f/d) Regulatory Affairs Quality Systems Job Summary: As [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a RAQA Specialist, you will support Regulatory Affairs and Quality activities for our business across Germany, Switzerland, and Austria (GSA) , with [. .. ] degree in Engineering, Science, or a related field. Masters is a plus. 2+ years of experience in Regulatory Affairs Quality Assurance (RAQA) or a related role in a medical device, pharmaceutical, or other highly regulated industry. Practical experience in one or more of the following areas is preferred: regulatory submissions/ registrations, product registration maintenance, QMS process support, change control documentation, or regulatory compliance activities. Proficiency in English and German, with strong communication and collaboration skills. # # # Preferred Knowledge [. .. ]
Job am 11.07.2026 bei Mindmatch.ai gefunden
CTC Resourcing Solutions
QA Associate (7021)
• AT- 2 Lavamünd
[. .. ] bei sich ändernden Sachverhalten. Ein hohes Mass an Selbständigkeit und Eigeninitiative. Muttersprache Deutsch und sehr gute Kenntnisse in Englisch, schriftlich und mündlich. Quality Assurance Associate 7021 Our [...]
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[...] client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, immunological diseases, enzyme deficiency diseases, and other rare diseases. We are seeking a highly skilled Quality Assurance Associate for an initial 1 year contract position at our clients headquarters in [. .. ] documents Qualifications Experience: Relevant working/ residency permit or Swiss/ EU-Citizenship required Educational Background: Degree in a scientific field (preferably Pharmacy, Chemistry, or Biology) . Experience: Ideally, experience within a pharmaceutical company and GMP environment. 1-2 years of experience in Quality Assurance/ Quality Control 1-2 years of experience with QMS Strong enthusiasm, analytical thinking, and effective communication skills. Precise and reliable work approach with the ability to prioritize effectively. Flexibility and ability to work independently as well as in [. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
Regeneron
Sales Specialist Immunology (f/m/d) - Oberösterreich Ost, Wein-, Wald-, Mostviertel, Wien Nord
• AT- 9 Wien
As a Sales
Specialist Immunology (f/m/d) , you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Respiratory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] division at key meetings. You will identify the key people in Pneumology, understand the account context and tailor calls based on individual and [. .. ] with the ability to identify key players in Pneumology Patient first value system Bachelors degree or equivalent experience and a Pharmareferent:in qualification 5+ years of sales experience within the biotech/ pharmaceutical sector Respiratory experience is preferred Proficiency in German as well as conversational English Readiness for very frequent travel and a drivers license For this position, the Collective Bargaining Agreement for Trade (Kollektivvertrag Handel) applies; depending on qualifications and professional experience, we offer a salary above the collectively agreed minimum. Salary [. .. ]
Neu Job vor 2 Std. bei Neuvoo.com gefunden
DEC Filling Germany GmbH
IT Specialist for System Integration, Network Administrator (m/f/d)
• Hainspitz
Job Opening: IT
Specialist for System Integration, Network Administrator (m/f/d) Customized solutions. Highest quality. Innovative together DEC Filling Germany Gmb H was newly established in 2024 following its acquisition [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] by the Dec Group, but looks back on over 25 years of experience at the location under its previous name, BAUSCH Germany Gmb H. As one of the leading companies in specialized machine engineering for the pharmaceutical industry, we offer tailor-made solutions for our customers and partners. As part of the internationally active Dec Group, we specialize in the manufacture of machines and systems for liquids and serve both the domestic and international markets. As part of our continuous growth, we are expanding our team and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical specialist pro Jahr?
Als Pharmaceutical specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 28 offene Stellenanzeigen für Pharmaceutical Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Specialist Jobs?
Aktuell suchen 23 Unternehmen nach Bewerbern für Pharmaceutical Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Specialist Stellenangebote:
- Randstad Deutschland GmbH Co. KG (2 Jobs)
- Novartis (2 Jobs)
- Healthcare Businesswomens Association (2 Jobs)
- F. Hoffmann- La Roche AG (2 Jobs)
- K- Recruiting GmbH (2 Jobs)
- Astra Zeneca (1 Job)
- European Semiconductor Manufacturing Company (1 Job)
In welchen Bundesländern werden die meisten Pharmaceutical Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Specialist Jobs werden derzeit in Bayern (3 Jobs), Rheinland-Pfalz (2 Jobs) und Baden-Württemberg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Specialist Jobs?
Pharmaceutical Specialist Jobs gehören zum Berufsfeld Pharmazie.
