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Überblick über die Statistik des Gehaltsniveaus für "Business Analyst in "

246 € Durchschnittliches Monatsgehalt

Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Business Analyst in "

Währung: EUR USD Jahr: 2020
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Business Analyst Branche in

Verteilung des Stellenangebots "Business Analyst" in

Währung: EUR
Wie die Grafik zeigt, in gilt als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Kufstein. Den dritten Platz nimmt Lienz ein.

Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in

Währung: EUR
Wie die Grafik zeigt, in gilt als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Kufstein. Den dritten Platz nimmt Lienz ein.

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You are able to think “outside the box” and explore new avenues of analytical protein characterization. • Good understanding of Quality-by-Design (QbD) principles applied to the development of biopharmaceuticals • Advanced scientific/technical writing skills, thorough understanding of development activities and processes as well as good understanding of regulatory expectations. • Fluency in English (oral and written), knowledge of German is a plus Desirable requirements: • Ability to interpret and present scientific information critically and objectively. Strong scientific project management and leadership skills. • Strong inter-personal skills ensuring close collaboration with multiple teams on a global level, effective communication with internal and external partners, and the ability to work in international teams. 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We look for an associate with profound interest and joy in hands-on mass spectrometry-based protein, peptide and glycan analysis. You are thrilled by new analytical challenges and willing to stay on track “till the riddles are solved”. Your key responsibilities: • You design, plan, organize, perform and document scientific experiments for the characterization of therapeutic protein, their posttranslational modifications, and degradation products under minimal supervision using state of the art LC-MS instruments. • Essential tasks include generation, evaluation and interpretation of data as well as proper communication of results. You perform and document complex analytical tasks within the scope of established procedures. • You prepare technical documents including study protocols and reports or analytical procedures • You will implement new methods or optimize existing methods and processes. Furthermore, your contribution to systematically screen and implement new technologies is expected as well as your participation in general innovation and scientific network activities. • You are responsible for the maintenance and qualification of lab equipment. • You will participate in function-specific sub teams and fulfil assigned tasks and responsibilities under minimal supervision. Minimum requirements What you’ll bring to the role: Essential: • Technical expert studies with PhD in Chemistry, Pharmacy, Biology or other natural sciences and relevant experience in the biopharmaceutical industry, or Master of Science with at least 2-3 years of relevant experience or 8 years for Bachelor of Science of directly related scientific experience or equivalent. • Hands-on experience with mass spectrometric characterization of proteins/peptides/glycans is mandatory. • Theoretical and practical knowledge of state-of-the-art ESI-Q-TOF, Orbitrap or MALDI-TOF MS technologies as well as MS data processing software solutions (e.g. Xcalibur, Refiner MS, Analyst, GPMAW) is required. • Good protein chemistry knowledge and the ability to apply this knowledge to analytical challenges. • A pivotal interest in instrumental analytical approaches and the ability to obtain proficiency in new technologies in short time. You are able to think “outside the box” and explore new avenues of analytical characterization • Fluency in English (oral and written), knowledge of German is a plus Desirable requirements: • Proficient scientific/technical writing and presentation skills • Broad experience in protein/peptide/glycan separation approaches (i.e. chromatographic, various modes) • Independent, thorough and reliable working style, ability to trouble-shoot analytical equipment and processes • Understanding of development activities and processes in Biopharma and knowledge on relevant regulatory guidelines Contact: Jennifer Kriedemann, Talent Acquisition & Staffing Business Partner, 44 7525 702920 Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying Imagine what you could do here at Novartis In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development options as well as worldwide career opportunities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 46,525.22/year (on a full time basis). We also offer a potential market oriented excess payment in line with your experience and qualifications. Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Our recruitment decisions are based on selecting the best person for the job, regardless of gender, religion, age, colour, race, sexual orientation, nationality or disability. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
Project Analyst (f/m/d) Analytical Characterization
Novartis Group, Kundl, Kufstein
Project Analyst (f/m/d) Analytical Characterization Job ID 319073BR Position Title Project Analyst (f/m/d) Analytical Characterization Project Analyst (f/m/d), Analytical Characterization, Kundl, Austria Join the Novartis Biologics community and help to “reimagine medicine”. We are expanding the core of our Analytical Characterization (AC) team in Kundl, Austria – to supply cutting edge analytics and generate in-depth protein knowledge for challenging biosimilar projects or new biological entities (NBEs). Within analytical characterization in biologics development at Novartis, NBEs and biosimilars are supported from the early development phase to commercialization and up to life-cycle management activities. AC applies a wide range of physico-chemical analytical techniques with a focus on mass spectrometry to characterize the biopharmaceutical products. Be part of our highly collaborative and science oriented team and independently drive the analytical characterization strategy tasks for one of the increasing number of biosimilars and NBEs within the Novartis portfolio. Your key responsibilities: • You will take full ownership of all project related protein characterization activities of the assigned project. Thereby, you will independently represent the characterization group in global teams and manage multiple interfaces to other Novartis groups or externals. • You play a pivotal role in the design of central studies and implementation of the related documents such as Critical Quality Attribute (CQA) assessment, comparability and biosimilarity exercises. Furthermore, you provide guidance for process development by providing suitable target specifications and perform final similarity exercise for our biosimilar products. • To enable efficient execution of project tasks, you design and monitor all analytical characterization activities within assigned teams without direct manager responsibilities. This includes characterization of the API, method-development, qualification and transfer, or setting targets based on originator products for biosimilar development. • You are responsible for the overall conclusive and coherent interpretation of results as well as their proper communication to support the technical team during the development and submission phase. • During the health authority submission phase, you coordinate and compile high quality analytical registration documents. You interact with Health Authorities as part of the team where appropriate and act as technical expert in audits, inspections or due diligence exercises. Beside project related tasks, we expect you to play an active role within our scientific network community. This may i.e. include shaping wide-reaching strategy-related procedures or development guidelines and driving their implementation. • As a senior member of our research organization, we expect you to provide excellent scientific and technical guidance and to actively foster knowledge exchange. sociates in planning and performing complex analytical tasks Minimum requirements What you’ll bring to the role: Essential: • Technical expert studies with PhD in Chemistry, Pharmacy, Biology or other natural sciences and 6 years of relevant experience in the biopharmaceutical industry or equivalent. • Excellence in the relevant area (analytical characterization, laboratory and/or technical tools such as mass spectrometry), broad theoretical and scientific knowledge in other areas (i.e. manufacturing, pharmaceutical) • Good understanding of Quality-by-Design (QbD) principles applied to the development of biopharmaceuticals • Excellent scientific project management skills • Excellent knowledge on relevant regulatory guidelines and very good understanding of regulatory expectations • Advanced scientific/technical writing skills • Fluent in English (oral and written), knowledge of German is a plus Desirable requirements: • Ability to interpret and present scientific information critically and objectively. Strong scientific project management and leadership skills. • Strong inter-personal skills ensuring close collaboration with multiple teams on a global level, effective communication with internal and external partners, and the ability to work in international teams. Contact: Jennifer Kriedemann, Talent Acquisition & Staffing Business Partner, 44 7525 702920 Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying Imagine what you could do here at Novartis In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development options as well as worldwide career opportunities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 51,180.50/year (on a full time basis). In most cases, the actual salary will be higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies. Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Our recruitment decisions are based on selecting the best person for the job, regardless of gender, religion, age, colour, race, sexual orientation, nationality or disability. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
Commercial Financial Analyst (m/f/d)
INNIO Jenbacher, Jenbach, Schwaz
Your responsibilities: Developing in depth understanding of existing business policies, processes on cost accounting / labor liquidation / inter-company cross charges, etc. Supporting the team by building dashboards that provide An innovative and international working environment Flexible working time model (depending on position and role) Health We Care Program – including company sport activities Moving cost support for new employees in accordance with policy Good connections to public transport – station in direct proximity Transportation cost support in accordance with policy One of the best canteens in the area with healthy and various meals Attractive location in the heart of the alps which provides various outdoor sport and other leisure possibilities Your Responsibilities: Lead Commercial Finance related activities to ensure profitable orders growth and early cash generation Being responsible for customer risk assessment and providing guidance on risk mitigation (payment securities e.g. bank guarantee, letter of credit), defining payment terms Drive systemic financing solution and processes globally. Broaden access to financial institutions (international commercial banks, development banks/ECAs, Leasing etc.) Monthly order reporting for all product lines and perform contract audits to assure data accuracy Analysis of regional market dynamics and commercial KPIs: development of order intake and market segments, quoting activities, customer visits, profitability, cash balance, loss reasons and market share Lead simplification and system improvement initiatives to have stable, qualitative and data-driven systems in place and drive automatization of business intelligence to speed up reporting processes Drive controllership mindset and processes within Commercial team to ensure financial compliance across commercial activities & reporting Steady interaction with global sales regions and commercial leadership team Your Qualifications: Very strong professional experience in commercial finance or financial analyses Understanding of commercial and financial processes and deal structures within industrial business Very strong communication skills Excellent English and German language skills SFDC and Tableau acknowledge preferred Knowledge of INNIO business operations is preferred Legal work authorization to work in Austria is required (Non-EU-citizens: please attach the authorization form to your application The base pay is composed of the amount according to the Austrian collective agreement which is at least EUR 3.439,42 gross per month (x 14) and an over payment depending on your qualifications and experience.
Lead Finance Expert - Oracle (m/f/d)
INNIO Jenbacher, Jenbach, Schwaz
Your responsibilities: Lead Commercial Finance related activities to ensure profitable orders growth and early cash generation, Being responsible for customer risk assessment and providing guidance on risk mitigation (payment Your responsibilities: Develop in depth understanding of existing business policies, processes including chart of account setup, reporting structure, month close, sub-ledger setup, Partnering with project leaders to build This role will join the INNIO General Ledger (GL) CoE team which is part of the Accounting Team . GL CoE is a team of super users and analysts working towards General Ledger module in Oracle ERP for INNIO Group. Key responsibilities include the daily maintenance of General Ledger – Chart of Accounts values, Cross Validation rules, Security rules, loading FX rates as well as scheduling and monitoring monthly and closing automated posting jobs including revaluation etc. Successful candidate will also contribute in various improvement projects around GL area which contribute to reduce time/cost spent on various activities as well as quality of the data. What we offer: An innovative and international working environment Flexible working time model (depending on position and role) Health We Care Program – including company sport activities Moving cost support for new employees in accordance with policy Good connections to public transport – station in direct proximity Transportation cost support in accordance with policy One of the best canteens in the area with healthy and various meals Attractive location in the heart of the alps which provides various outdoor sport and other leisure possibilities Key Responsibilities: Maintenance of GL Chart of Account Values in Oracle – values creation, updates Maintenance and ownership over GL Cross Validation Rules and Security Rules in Oracle Maintenance and scheduling of daily automated posting jobs and closing posting jobs Setting up foreign currency exchange rates in Oracle Support users and conduct regular trainings on Manual Journal Entries process Month End Closing – monitoring and reporting status of Manual Journal Entries Month End Closing maintenance – opening / closing accounting periods, running month end closing automated jobs etc. ARCS Accounts Reconciliation tool – ownership, maintenance, reporting, prepare training material, conduct trainings Playing a key role in various improvements projects related to General Ledger area – testing, cooperation with IT on new functionalities Qualifications/ Requirements: Bachelor’s Degree in Accounting or Finance Strong analytical skills Proficient use of Microsoft Excel Solid work experience in GL Analyst / Superuser role Experience working with Oracle EBS would be preferred Strong oral and written communication skills in English Ability to work cross-functionally and with distributed teams Hands-on approach and autonomous in work Legal work authorization to work in Austria is required (Non-EU-citizens: please attach the authorization form to your application The base pay is composed of the amount according to the Austrian collective agreement which is at least EUR 3.439,42 gross per month (x 14) and an over payment depending on your qualifications and experience.
Project Analyst (f/m/d) Analytical Characterization
Novartis, Kundl, Kufstein
Project Analyst (f/m/d) Analytical Characterization You will be responsible for: Ensuring that all processes and procedures, tasks, responsibilities and projects are in compliance with all pharmaceutical laws, the Novartis Quality Manual and Policies as well as Industry Best Practices. In Your responsibilities: • You independently design, plan, perform and document scientific experiments for the characterization of therapeutic protein, their posttranslational modifications, degradation products and structure Your responsibilities: • You design, plan, organize, perform and document scientific experiments for the characterization of therapeutic protein, their posttranslational modifications, and degradation products under minimal Project Analyst (f/m/d) Analytical Characterization Verantwortungsgebiet Project Analyst (f/m/d), Analytical Characterization, Kundl, Austria Join the Novartis Biologics community and help to “reimagine medicine”. We are expanding the core of our Analytical Characterization (AC) team in Kundl, Austria – to supply cutting edge analytics and generate in-depth protein knowledge for challenging biosimilar projects or new biological entities (NBEs). Within analytical characterization in biologics development at Novartis, NBEs and biosimilars are supported from the early development phase to commercialization and up to life-cycle management activities. AC applies a wide range of physico-chemical analytical techniques with a focus on mass spectrometry to characterize the biopharmaceutical products. Be part of our highly collaborative and science oriented team and independently drive the analytical characterization strategy tasks for one of the increasing number of biosimilars and NBEs within the Novartis portfolio. Your key responsibilities: • You will take full ownership of all project related protein characterization activities of the assigned project. Thereby, you will independently represent the characterization group in global teams and manage multiple interfaces to other Novartis groups or externals. • You play a pivotal role in the design of central studies and implementation of the related documents such as Critical Quality Attribute (CQA) assessment, comparability and biosimilarity exercises. Furthermore, you provide guidance for process development by providing suitable target specifications and perform final similarity exercise for our biosimilar products. • To enable efficient execution of project tasks, you design and monitor all analytical characterization activities within assigned teams without direct manager responsibilities. This includes characterization of the API, method-development, qualification and transfer, or setting targets based on originator products for biosimilar development. • You are responsible for the overall conclusive and coherent interpretation of results as well as their proper communication to support the technical team during the development and submission phase. • During the health authority submission phase, you coordinate and compile high quality analytical registration documents. You interact with Health Authorities as part of the team where appropriate and act as technical expert in audits, inspections or due diligence exercises. Beside project related tasks, we expect you to play an active role within our scientific network community. This may i.e. include shaping wide-reaching strategy-related procedures or development guidelines and driving their implementation. • As a senior member of our research organization, we expect you to provide excellent scientific and technical guidance and to actively foster knowledge exchange. sociates in planning and performing complex analytical tasks Qualifikationen What you’ll bring to the role: Essential: • Technical expert studies with PhD in Chemistry, Pharmacy, Biology or other natural sciences and 6 years of relevant experience in the biopharmaceutical industry or equivalent. • Excellence in the relevant area (analytical characterization, laboratory and/or technical tools such as mass spectrometry), broad theoretical and scientific knowledge in other areas (i.e. manufacturing, pharmaceutical) • Good understanding of Quality-by-Design (QbD) principles applied to the development of biopharmaceuticals • Excellent scientific project management skills • Excellent knowledge on relevant regulatory guidelines and very good understanding of regulatory expectations • Advanced scientific/technical writing skills • Fluent in English (oral and written), knowledge of German is a plus Desirable requirements: • Ability to interpret and present scientific information critically and objectively. Strong scientific project management and leadership skills. • Strong inter-personal skills ensuring close collaboration with multiple teams on a global level, effective communication with internal and external partners, and the ability to work in international teams. Contact: Jennifer Kriedemann, Talent Acquisition & Staffing Business Partner, 44 7525 702920 Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying Imagine what you could do here at Novartis In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development options as well as worldwide career opportunities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 51,180.50/year (on a full time basis). In most cases, the actual salary will be higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies. Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Our recruitment decisions are based on selecting the best person for the job, regardless of gender, religion, age, colour, race, sexual orientation, nationality or disability. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network