Bei Diversey steht der Mensch im Mittelpunkt – ob als Mitarbeiter oder Kunde. Wir sind stolz darauf, ein vielfältiges und globales Unternehmen zu sein, das individuelle Talente fördert und gleichzeitig den Teamgeist stärkt. Als einer von nur zwei Global Players in unserem Markt sind wir mit 8900 Mitarbeitern in über 80 Ländern tätig und bedienen rund 85.000 Kunden. Diversey vereint Chemikalien, Maschinen und Nachhaltigkeitsprogramme in einem effizienten Gesamtkonzept, das auf der Überzeugung basiert, dass Reinigung und Hygiene essentiell für ein gesundes Leben sind.

Wir sind führend in unserer Industrie und unterstützen unsere Partner in einer Vielzahl von Sektoren mit maßgeschneiderten und innovativen Hygiene- und Reinigungslösungen in folgenden Branchen: Hotel- und Gastronomie, der Lebensmittel-, Getränke- und Pharmaindustrie, im Handel, im Gesundheitswesen oder in der Gebäudereinigung.

Für die Region Graubünden suchen wir nach Vereinbarung eine engagierte, belastbare und motivierte Persönlichkeit als

Servicetechniker HORECA 100% (w/m/d) Region Graubünden

Ihre Aufgaben

• Technischer Kundenservice im professionellen Bereich, in den Anwendungen Geschirrspülen, Küchenhygiene und Textilreinigung
• Eigenständige Planung der Montagen von Dosieranlagen sowie deren Wartung
• Fachtechnische Beratung sowie rasche und selbständige Problemlösung beim Kunden
• Durchführung von Kundenschulungen
• Unterstützung der Diversey-Verkaufsorganisation bei technischen Abklärungen
• Rapportwesen gemäß Vorgaben
• Aktive Unterstützung bei der Neukundengewinnung
• Selbstständige Unterhaltung des eigenen Lagerinventars

Ihre Erfahrungen

• Abgeschlossene Berufsausbildung als Elektriker, Elektromechaniker o. Ä.
• Idealerweise Erfahrung als Servicemonteur oder -techniker
• Anwenderkenntnisse MS-Office
• Gute Deutschkenntnisse in Wort und Schrift zwingend, Italienischkenntnisse von Vorteil
• Bereitschaft Neues zu lernen, Flexibilität sowie Belastbarkeit
• Hohe Dienstleistungsorientierung mit strukturierter Arbeitsweise, gewinnende Ausstrahlung, sowie eine selbständige und qualitätsbewusste Arbeitsweise
• Wohnhaft in Graubünden oder Bereitschaft dafür, in die Region umzuziehen

Unser Angebot

• Eine anspruchsvolle und abwechslungsreiche Aufgabe in einem erfolgreichen und wachstumsstarken Unternehmen
• Viel Entwicklungspotential mit flachen Hierarchien und Wertschätzung im Team
• Ein großer Verantwortungsspielraum, in dem Sie Ihre Fähigkeiten und Ihr Fachwissen mit einbringen
• Eine intensive und strukturierte Einarbeitung  

Bei uns starten Sie sauber durch!

Wir freuen uns über Ihre Bewerbungsunterlagen (Lebenslauf, Anschreiben, Zeugnisse) inklusive Gehaltsvorstellungen und Verfügbarkeit.

Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

• Act as the primary point of contact with internal administrative functions to include Procurement, Finance, and Legal to enable the execution of the clinical activities.
• Serve as the main document control coordinator ensuring proper version control during critical document reviews and subsequent publication. 
• Assist with oversight of outside vendors, consultants, and clinical research organizations (CROs) and coordinate the needed interactions with internal vendors.
• Maintain, and continuously improve clinical veterinary operation functions. 
• Aid in developing additional tools and refining processes to ensure all clinical veterinary projects run efficiently and effectively.
• Ensure that assigned projects are properly monitored, and that data are accurate and collected uniformly among the various investigative study sites.
• Participate in regular meetings, follow-up on assigned tasks and issues, and transfer of important information to management.
• Assist in the coordination of all study activities, including start up, Investigator training, study conduct, site monitoring and close out.
• Assists Clinical Development with tasks required to conduct clinical veterinary studies during all phases of an assigned project or program.
• Assists in the authoring of clinical study protocols, amendments, deviations, and final reports as required.
• Utilize industry best practices, techniques, and standards throughout entire project execution for the timely completion of all clinical studies.
• Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

• Bachelors’ degree in STEM is required.   
• Minimum 2 years as a clinical study coordinator/monitor in the pharmaceutical industry; preferably in the veterinary pharmaceutical industry. 
• Experience conducting/monitoring studies to Good Clinical Practice and/or Good Laboratory Practice standards.
• Experience with electronic data capture platform/ eClinical software.
• Experience working with Clinical Trial Management software platforms.
• Ability to multi-task and successfully handle multiple priorities simultaneously.
• A growth mindset with a proactive approach to challenges is a plus.
• Proven proficiency in Microsoft Office and use of cloud-based applications.  Proficiency in MS Word and scientific writing is a must. 
• Strong written, verbal communication and interpersonal skills with employees at all levels of an organization.
• Strong strategic and critical thinking skills; including problem solving.

Physical Environment and Requirements

• Ability to travel overnight up to 25%.
• Ability to be able to work remotely and have reasonable infrastructure to access the internet.
• Employee must be able to occasionally lift and/or move up to 15 pounds.

Expected Salary Range :

$91,300-$108,000

The salary range displayed is the minimum and maximum annual salary of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers accessible to any and all users.  If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email hrtalentacquisition@americanregent.com.

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

CD&A - Commercial Insights Senior Manager, Primary Market Research

Live

What you will do

Let’s do this. Let’s change the world! In this vital role the Commercial Insights Senior Manager will lead insights generation activities by integrating primary market research (qualitative and quantitative) with secondary data analytics and engaging other Commercial Data and Analytics (CD&A) team members. The role reports to the Director for Commercial Insights, Inflammation.

Flexible Commuter role to Thousand Oaks, US Headquarter site. You will work on-site a minimum of 2 days a week.

Key job responsibilities:

• Leverages deep scientific or biopharma understanding to appropriately define relevant business problems and address through data and analytics approaches/projects

• Identifies key business questions that need to be addressed to meet changing business needs

• Consistently engage in thought leadership to shape brand strategy

• Influences leadership to incorporate key findings, insights and intelligence into program strategy

• Prioritize research resources to impact critical business issues and decisions

• Turn unstructured business issues/requests into appropriate action plans and projects that result in high quality, meaningful and actionable deliverables

• Plan, design and conduct key strategic and highly complex market research programs and translate the findings into strategic and tactical recommendations that help drive brand success

• Synthesize and integrate various data, research and analyses into actionable insights

• Ensuring that analyses and summaries of results are shared in the form of compelling stories that deepen customer understanding

• Stays on the leading edge of data and analytics techniques and capabilities; and leads implementation of new methodologies and best practices

• Consider alternative methodologies to collect the voice of customer, being open to emerging innovative methods without immediately jumping to standard methods

• Develop and nurture productive relationships with the cross-functional marketing team to appropriately define the business problems/business questions

• Identify, evaluate, and manage relationships with best-in-class insights vendors

• Ensure that both routine and ad-hoc projects are in compliance with all Amgen SOPs and meet service-level expectations for quality, timeliness, and budget

• Some travel required

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The market research professional we seek is a collaborative partner with these qualifications.

Basic Qualifications:

Doctorate degree and 2 years of market research and/or analytics experience

Or

Master’s degree and 3 years of market research and/or analytics experience

Or

Bachelor’s degree and 6 years of market research and/or analytics experience

Or

Associate's degree and 6 years of market research and/or analytics experience

Or

High school diploma / GED and 12 years of market research and/or analytics experience

Preferred Qualifications:

• Excellent technical skills in marketing research. Experience across a broad range of study designs and participant types

• Excellent organization and ability to integrate findings

• Ability to incorporate above-brand KBQs throughout research

• Ability to function independently

• US in-line experience

• Co-promote experience

• HCP and Consumer/DTC PMR experience

• Demonstrated exceptional strategic / critical thinking abilities and eye for business

• Demonstrated ability to dig deep and uncover the “why” beneath observed HCP behaviors (go beyond the rational)

• Excellent oral and written presentation skills with ability to explain complex concepts clearly to a variety of audiences

• Ability to work collaboratively in team-based environment

• Ability to balance multiple projects and workstreams simultaneously

• Proficient facilitation, negotiation, problem-solving and conflict resolution skills

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

• Stock-based long-term incentives

• Award-winning time-off plans and bi-annual company-wide shutdowns

• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Lonza Pharma & Biotech has an open position for a paid internship with the Biomanufacturing R&D team at our location in Bend, OR.  This is an excellent opportunity to join a challenging, dynamic, and cross-disciplinary team of scientists and engineers who focus on improving the manufacturing of biologics medicines. The position will be a 3 – 4 month term, at minimum, with a preference for a 6 month commitment.

An intern with the Mammalian Manufacturing R&D team at Lonza will be responsible for:

• Daily operations of lab scale bioreactors
• Building, setup and maintenance of bioreactors
• Making precise media solutions for bioreactor experiments
• Restocking, cleaning, and tracking inventories
• Keeping the lab running as efficiently as possible
• Maintaining accurate and precise lab records for data analysis and traceability
• Planning and executing an individual project to be presented to the team at the end of the internship

Position requirements:

• Currently studying biology, chemistry, engineering, or a related life science
• Enthusiastic about the biopharmaceutical industry and learning about industry technology
• Interest in taking ownership of project aspects
• Displays good problem solving skills
• Exhibits time management skills

Skills that will be acquired through this internship will be:

• How to work in an industrial mammalian cell culture laboratory environment
• Mammalian cell culture fundamentals
• How to collaborate with a multidisciplinary team of engineers, chemists and biologists

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As the Sr Clinical Project Lead, you will be responsible for overseeing, designing, planning, conducting, and reporting on clinical studies, supporting life cycle management activities, post-market studies and training Medical Affairs teams located remotely in the United States!

Key Responsibilities:

• Crafting and providing oversight of clinical research programs to deliver study outcomes within schedule, budget, quality/compliance and performance standards, and ensuring the studies meet scientific objectives, and are aligned with commercial needs.

• Serves as single point of contact in core teams in R&D, leads Clinical Sub-Teams, and acts as the medical/scientific consultant to marketing or research project teams and government regulatory agencies.

• Contributes to operational excellence through process improvement and knowledge sharing.

• Provides clinical functional review and expertise on the assigned projects/tasks, updates on clinical study progress and performance metrics.

• Forms relationships with key opinion leaders and applies their input to improve study design, protocols, and identified initiatives as appropriate.

• Leads the planning, conduct, and reporting of clinical studies throughout the product development and life cycle management including development of scientific publications and peer reviewed manuscripts.

• May be responsible for site or vendor selection as appropriate, post-marketing studies, and training for customer facing Medical Affairs associates worldwide.

Key Requirements/Minimum Requirements

• Bachelor’s Degree or Equivalent years of directly related experience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs)

• The ability to fluently read, write, understand, and communicate in English.

• 7 Years of Proven Experience

Travel Requirements: 20%

Relocation Assistance: No

Sponsorship Available: No

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

Job Title

Job Description

Federal Accounts Manager (AM&D) - Northeast

The Federal Accounts Manager will primarily be responsible for orchestrating the sales process from lead identification, prospect new business, maintain and grow existing government accounts and ensure sales strategies meet revenue objectives while promoting Philips ECG Solutions products and services.

 Federal Accounts Manager (AM&D)

• Build and forge strong relationships throughout the respective geographic responsibility and represent Philips ECG Solutions professionally in all client and prospect interactions to extend the One Philips Solution.

• Drive sales revenue and overall market share within the government as well as nurturing existing accounts. Serve as the primary contact with all government accounts across the territory and provide updates and sales reports to the Emerging Markets Leader regarding territory status, including forecasts, sales proposals, and business reviews. 

• Implement a government territory business plan with clearly defined strategies and objectives. Communicate the company’s competitive differentiation and value proposition to enhance sales and convert competitive accounts.

• Responsible for government Requests for Proposals (RFPs) and Requests for Information (RFIs), VISN leadership business development, VA ECG Solutions Sales with collaboration on sales with other Philips Sales Divisions.

• Travel can be up to 50% within the territory.  

You’re the right fit if:

• You have a Bachelor’s degree or equivalent experience.

• You have Three (3) or more years’ sales experience reflecting a track record of proven success within the Medical Device and / or Biotechnology arena

• You have Four(4) or more years experience working in the government arena space.  Prior Military experience preferred

• You have a demonstrated track record of consistently meeting or exceeding an annual quota of more than $1M. Good understanding of government contracts, RFPs and standard bid requests.  Advanced selling capability that showcases commitment to sales and company strategy, customer satisfaction, negotiation, and ability to close. Significant experience in negotiating and closing new business and / or budgeting. Excellent strategic selling skills (strategy development and execution). Outstanding problem-solving skills and technical aptitude with Microsoft programs (PowerPoint, Excel). Well versed on concepts, practices and procedures related to field sales

• Strong interpersonal skills with the ability to develop and maintain productive, cooperative, and interdependent working and business relationships. Exemplary presentation skills with the ability to present in front of large and small groups of people.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
• Read more about our employee benefits.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

Philips Transparency Details

Total Target Earnings is composed of base salary + target incentive. At 85% to 120% performance achievement, the Target Earning potential is $156,500 to $198,00 annually, plus company fleet/car.  Total compensation may be higher or lower dependent upon individual performance. 

Target Earnings pay is only one component of the Philips Total Rewards compensation package, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position.  For this position, you must reside in or within commuting distance to the Northeast US and near a metropolitan airport.

#LI-PH1

#LI-Remote

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

Job Title

Job Description

Federal Accounts Manager (AM&D) - West

The Federal Accounts Manager will primarily be responsible for orchestrating the sales process from lead identification, prospect new business, maintain and grow existing government accounts and ensure sales strategies meet revenue objectives while promoting Philips ECG Solutions products and services.

 Federal Accounts Manager (AM&D)

• Build and forge strong relationships throughout the respective geographic responsibility and represent Philips ECG Solutions professionally in all client and prospect interactions to extend the One Philips Solution.

• Drive sales revenue and overall market share within the government as well as nurturing existing accounts. Serve as the primary contact with all government accounts across the territory and provide updates and sales reports to the Emerging Markets Leader regarding territory status, including forecasts, sales proposals, and business reviews. 

• Implement a government territory business plan with clearly defined strategies and objectives. Communicate the company’s competitive differentiation and value proposition to enhance sales and convert competitive accounts.

• Responsible for government Requests for Proposals (RFPs) and Requests for Information (RFIs), VISN leadership business development, VA ECG Solutions Sales with collaboration on sales with other Philips Sales Divisions.

• Travel can be up to 50% within the territory.  

You’re the right fit if:

• You have a Bachelor’s degree or equivalent experience.

• You have Three (3) or more years’ sales experience reflecting a track record of proven success within the Medical Device and / or Biotechnology arena

• You have Four(4) or more years experience working in the government arena space.  Prior Military experience preferred

• You have a demonstrated track record of consistently meeting or exceeding an annual quota of more than $1M. Good understanding of government contracts, RFPs and standard bid requests.  Advanced selling capability that showcases commitment to sales and company strategy, customer satisfaction, negotiation, and ability to close. Significant experience in negotiating and closing new business and / or budgeting. Excellent strategic selling skills (strategy development and execution). Outstanding problem-solving skills and technical aptitude with Microsoft programs (PowerPoint, Excel). Well versed on concepts, practices and procedures related to field sales

• Strong interpersonal skills with the ability to develop and maintain productive, cooperative, and interdependent working and business relationships. Exemplary presentation skills with the ability to present in front of large and small groups of people.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
• Read more about our employee benefits.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

Philips Transparency Details

Total Target Earnings is composed of base salary + target incentive. At 85% to 120% performance achievement, the Target Earning potential is $156,500 to $198,000 annually, plus company fleet/car.  Total compensation may be higher or lower dependent upon individual performance. 

Target Earnings pay is only one component of the Philips Total Rewards compensation package, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position.  For this position, you must reside in or within commuting distance to Western US.

#LI-PH1

#LI-Remote

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

At Pitney Bowes, we do the right thing, the right way.

Bei Pitney Bowes können Sie das auch.

Wir schaffen dies mit besonderem Fokus auf die vier Stützpfeiler von Pitney Bowes: client. team. win. innovate.

Unsere tollen Kolleginnen und Kollegen sind das Fundament, die Inspiration und die treibende Kraft unseres Unternehmens.

Wir freuen uns auf Kolleginnen und Kollegen, die:
•    sich leidenschaftlich für den Kundenerfolg einsetzen.
•    Freude an der Zusammenarbeit haben.
•    danach streben, Erwartungen zu übertreffen.
•    mutig vorangehen auf der Suche nach hervorragenden und marktorientierten Lösungen.

Job Description:

Zur Verstärkung unseres Team von Service Technikern suchen wir einen

Mechatroniker/Servicetechniker im Außendienst (m/w/d)

für digitale Postbearbeitungs-Systeme und andere spannende technische Geräte

Wohnort: Raum Brandenburg / Berlin.

Einsatzgebiet: PLZ-Gebiete 01-19

Vollzeit (40 Std. pro Woche) und unbefristet

Diese abwechslungsreichen Aufgaben warten auf Sie:

• Ihr Start erfolgt mit einer gründlichen Einarbeitung durch unser erfahrenes Team und Produkt-Schulungen in unserem Trainingscenter in Darmstadt.
• Vernetzen Sie sich durch Ihr Firmen-iPad oder iPhone und Sie sehen, genau welche Aufgaben bei unseren Kunden auf Sie warten. Sie können sich zusätzlich jederzeit mit Ihrem Team abstimmen.
• Und wenn es mal „brennt“ und Sie nicht mehr weiterkommen, helfen Ihnen unsere Supportteams durch zielgerechte Eskalationsstufen.

Es fällt Ihnen leichter, wenn Sie

• eine technische Grundausbildung, z.B. als Mechatroniker und wertvolle Erfahrungen als Servicetechniker im Außendienst mitbringen.
• sich in der Mechanik und vor allem in Elektro- und Netzwerktechnik gut auskennen.
• Ihnen analytisches Denken Spaß macht.
• mit Freude, Respekt und offenen Augen Ihren Kunden gegenübertreten und sie beraten können.
• sich so zu organisieren wissen, dass Ihr Kunde nicht warten muss und Sie alles Notwendige dabeihaben.

Was Sie neben diesen abwechslungsreichen Aufgaben bekommen:

• Ein attraktives und marktgerechtes Gehalt
• Ford/Skoda Kombi, den Sie selbstverständlich auch privat nutzen dürfen
• Hochwertige Werkzeuge und optimale technische Ausrüstung incl. iPhone, iPad
• Schritt für Schritt Einarbeitung durch qualifizierte Kollegen
• Freiheit bei der Umsetzung Ihrer Ideen
• Ein breites Weiterentwicklungs- und Schulungsprogramm
• Kostenloses E-Learning Angebot zur persönlichen Weiterbildung
• Eine attraktive betriebliche Altersversorgung
• Persönliche Unterstützung in unserem Mitarbeiter Assistance Programm
• Ein interessanter Job in einem über 100-jährigen, innovativen und erfolgreichen Konzern
• Unbefristeter Arbeitsvertrag, 30 Tage Urlaub plus Sonderurlaub

Werden Sie Teil eines internationalen Konzerns und gestalten Sie Ihre Zukunft gemeinsam mit uns! 

Wir bei Pitney Bowes verstehen Diversität und Inklusion schon lange in all ihren Facetten als Bereicherung für unsere Teams. Chancengleichheit ist uns seit Jahrzehnten ein besonderes Anliegen, die Gleichbehandlung von Menschen ein grundlegendes Prinzip unserer Unternehmenspolitik.

Wir freuen uns über Bewerbungen von Menschen mit Behinderung.

Wenn wir Ihr Interesse wecken konnten, freuen wir uns auf Ihre Bewerbung an Birgit Correll: birgit.correll@pb.com oder direkt über unsere Karriereseite auf www.pitneybowes.com/de.

Pitney Bowes Deutschland GmbH

Poststraße 4-6

64293 Darmstadt

Germany

Unser Versprechen:

• Die Möglichkeit sich weiterzuentwickeln und Ihre Karriere voranzutreiben.
• Ein integratives Umfeld, das unterschiedliche Perspektiven und Ideen fördert.
• Herausfordernde und einzigartige Möglichkeiten, um zum Erfolg einer sich wandelnden Organisation beizutragen.
• Weltweit umfassende Benefits (PB Live Well)

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.

Moderna is seeking a Medical Science Liaison for North Germany, based in the Hamburg area, to develop key relationships with healthcare practitioners and support mRNA platform development. This role focuses on scientific engagement, clinical research support, and maintaining compliance with medical and regulatory standards. It offers the opportunity to work at the forefront of innovative medicine, collaborating with professionals in the vaccination community and other therapeutic areas.

Here's What You’ll Do:

Within 3 Months, You Will…

• Initiate and cultivate strategic peer-to-peer relationships with key healthcare practitioners (HCPs) in the vaccination community across the regions of Niedersachsen, Bremen, Schleswig-Holstein, Hamburg, and Mecklenburg-Vorpommern.

• Conduct detailed study and familiarization with Moderna’s mRNA technology platform, focusing on its application in various therapeutic areas, particularly in vaccination.

• Engage actively in presenting scientific data to healthcare professionals, tailoring the delivery to suit the audience, and ensuring clarity and compliance with scientific accuracy.

• Respond promptly and accurately to medical information requests from HCPs, ensuring all communications are in line with Moderna’s standards and regulatory guidelines.

• Start reporting any adverse events (AEs) and/or Product Quality Complaints (PQC) encountered in the field, ensuring timely and compliant documentation and communication of such incidents.

Within 6 Months, You Will…

• Develop and implement personalized HCP Engagement Plans, catering to the unique needs and interests of key healthcare practitioners in your region, in alignment with Moderna’s strategic goals.

• Expand your knowledge and understanding of clinical development processes, with a particular focus on rare diseases and vaccines, integrating this knowledge into your daily activities and discussions.

• Take an active role in coordinating and managing regional Medical Affairs initiatives, including educational programs, advisory boards, and medical conferences, fostering Moderna’s presence and reputation in the medical community.

• Work closely with physicians and other medical experts to facilitate medical education opportunities and develop advisory boards, ensuring the scientific integrity and relevance of these initiatives.

• Begin to develop training materials and content for internal stakeholders, highlighting key scientific and medical topics relevant to Moderna’s therapeutic areas.

Within 12 Months, You Will…

• Be fully integrated into the role, recognized as a key driver in medical science liaison activities and research initiatives within your region, contributing significantly to Moderna’s presence and influence in the healthcare community.

• Offer comprehensive scientific support and training to internal stakeholders, including sales and marketing teams, enhancing their understanding and ability to communicate Moderna’s scientific advancements effectively.

• Play an instrumental role in shaping and contributing to the strategic medical direction in North Germany, leveraging insights and relationships to inform company strategies and initiatives.

• Actively involve yourself in clinical trial activities, suggesting HCPs for participation in company-sponsored studies, providing scientific training at Site Initiation Visits, and ensuring clear role definition and responsibilities in collaboration with Clinical Research Associates (CRAs) and Medical Monitors.

• Continuously communicate insights gained from field interactions to the Medical Affairs Department, aiding in the refinement of medical strategies for Moderna’s therapeutic areas.

Here’s What You’ll Bring to the Table:

• Advanced scientific degree required– MD, PhD, PharmD, or MSc

• Minimum of 4 years of experience in Medical Affairs or Medical Science role

• Robust and current clinical development experience supporting drugs to treat rare diseases; prior vaccines/infectious disease(s) experience preferred

• Candidates will ideally have well-established networks, understanding of decision-making structures and active relationships with HCPs in the therapy area.

• Candidate must have a strong understanding of compliance frameworks and demonstrable ability to work compliantly in a field-based role, within the medical organization, as well as interacting with the commercial organization

• Proven ability to take initiative, determine priorities and exercise good judgment

• Ability to recognize opportunities/gaps/obstacles, then take ownership to find creative, innovative solutions that question convention, and then see them through to completion

• Accepts new challenges with curiosity and drive while remaining positive in the face of obstacles

• Strong interpersonal and relationship building skills

• Fluency in German and English

• Ability and willingness to travel up to 75% within assigned region

• Valid Driver's license

• Working knowledge of virtual presentation platforms, social media and Microsoft Office Suite (Word, PowerPoint, and Excel)

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to create your own pathway to well-being
• Free premium access to fitness, nutrition, and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
• Educational resources
• Savings and investments
• Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com.  (EEO/AAP Employer) 

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Collaboration drives Nordson’s success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find Nordson employees sharing our success by giving back in the communities around the world where we live and work.

Nordson BKG entwickelt und fertigt Präzisions-Schmelzestromkomponenten für Extrusions- und Granulierprozesse. In der Division Polymer Processing Systems sind wir einer der Marktführer im aufstrebenden Bereich Kunststoffrecycling. Im Rahmen einer Nachbesetzung suchen wir Dich als Field Service Engineer (w/m/d) für unsere europaweiten Serviceaktivitäten:

Deine Aufgaben:

• Inbetriebnahme, Reparatur und Wartung kleinerer Anlagen oder Anlagenkomponenten weltweit beim Kunden vor Ort
• Inbetriebnahme der Anlagen oder Anlagenkomponenten weltweit beim Kunden, inkl. Schulung des Kundenpersonals
• Unterstützung des Kundenunternehmens, bis die Anlage zur Zufriedenheit eingestellt ist und funktionsfähig übergeben werden kann
• Regelmäßige Wartung nach Rahmenvertrag
• Durchführung von Reparaturen im Werk
• Unterstützung der erfahrenen Kollegen
• Unterstützung des Technical Supports in reisefreien Zeiten

Dein Profil:

• Abgeschlossene Berufsausbildung als Elektroniker/in, Mechatroniker/in, Kunststoffformgeber/-in oder vergleichbar
• Einschlägige Berufserfahrung (mindestens 3 Jahre) in einem vergleichbaren Arbeitsumfeld
• Idealerweise Erfahrung mit kunststoffbearbeitenden Anlagen oder Komponenten
• Service- und Vertriebsaffinität
• Eigenverantwortliche Arbeitsweise und lösungsorientiertes Denken
• Erfahrungen im Bereich MSR Technik
• Lesen von Schaltplänen (auch R&I)
• Handwerkliches Geschick
• Gute Organisation der Arbeitsabläufe, auch unter Termindruck
• Eigenverantwortliche Arbeitsweise und lösungsorientiertes Denken
• Gute Englischkenntnisse sowie internationale Reisebereitschaft
• Durchsetzungsvermögen und Konfliktfähigkeit
• Teamfähigkeit
• Flexibilität
• Kenntnisse im Umgang mit Microsoft Office
• Führerschein Klasse B

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Nordson BKG develops and manufactures precision melt stream components for extrusion and pelletizing processes. In the Polymer Processing Systems division, we are one of the market leaders in the field of plastics recycling. For our European service organization, we are hiring a Field Service Engineer (m/f/d):

Your tasks:

• Commissioning, repair and maintenance of smaller systems or system components worldwide at the customer's site
• Commissioning of systems or system components worldwide at the customer's premises, including training of customer personnel
• Supporting the customer company until the system is adjusted to satisfaction and can be handed over in working order
• Regular maintenance in accordance with framework agreements
• Carrying out repairs at the plant
• Support of experienced colleagues
• Supporting technical support during non-travel times

Your profile:

• Completed vocational training as an electronics technician, mechatronics technician, plastics molding technician or similar
• Relevant professional experience (at least 3 years) in a comparable working environment
• Ideally experience with plastic processing systems or components
• Service and sales affinity
• Independent way of working and solution-oriented thinking
• Experience in the field of MSR technology
• Ability to read circuit diagrams (including P&I)
• Good organization of work processes, even under deadline pressure
• Independent way of working and solution-oriented thinking
• Good knowledge of English and willingness to travel internationally
• Assertiveness and ability to deal with conflict
• Ability to work in a team
• Flexibility
• Proficiency in critical tools such as Microsoft Office
• Valid driver's license

#LI-MS1

The Mosaic Company (NYSE: MOS) is the world’s leading integrated producer of concentrated phosphate and potash—two of the three most important nutrients in agriculture. We employ more than 13,000 people in six countries to serve farmers all over the world. Our Headquarters is in Lithia, Florida with operations throughout North America (U.S./Canada) and South America.

At Mosaic We Help the World Grow the Food it Needs - Apply today and join our team!

SENIOR RESEARCH & DEVELOPMENT LABORATORY TECHNICIAN

Where will you work: Onsite at New Wales, FL (3095 Hwy 640 W, Mulberry, FL 33860)

Assist process chemist in performing R&D test work. Accurately prepare, analyze, and record data on all samples as well as prepare reports and maintain database records.  Staff for this role perform critical functions related to R&D, analysis which may contain sensitive information and may involve work with materials not routinely used in the lab.  Knowledge of and proficiency in complex tasks involving hazardous materials beyond the scope of routine work usually conducted in concentrates lab.  Demonstrated cross functionality with roles at other sites and support for chemists, engineers.

What you’ll do?

• Perform calculations, review data for accuracy, prepare reports and maintain database records.
• Collect, identify, and prepare various samples for analysis.
• Perform analysis using hazardous chemicals and prescribed procedures to determine quality of product samples.
• Use and maintain various types of laboratory equipment and instruments.
• Perform miscellaneous job-related duties as assigned.
• Perform routine preventive maintenance and housekeeping on equipment and work area.

What you’ll need:

• High school/GED required. Associate degree preferred, with a major in Chemistry.
• Laboratory experience.

Benefits Offered by Mosaic:

• Medical, Dental, Vision insurance
• Paid vacation and sick time
• Tuition Reimbursement
• 401k company matching
• Optional HSA plan with company match

About JLG, an Oshkosh company

JLG began in 1969, when our founder, John L. Grove set out to resolve growing safety concerns in the construction industry. Since then we have been committed to understanding the challenges and delivering innovative solutions to the access market. We partner with customers to provide quality equipment, training opportunities and trusted support within the access industry. We are a global company, and our products—including mobile elevating work platforms, telehandlers, utility vehicles and accessories—can be found all over the world.

In this role you will be working with all platform teams from JLG at the R&D Facility. You will have the ability to assist in the design of creative solutions for New Product Development Projects. This is a hands-on role with involvement on new products within JLG. You will be working cross functionally with various engineering teams to develop the products of tomorrow.

SUMMARY:

As a R&D Fabrication Technician you will be part of the R&D Design team for Access. You will be responsible to support the fabrication shop with fabrication and material handling.  As part of the fabrication team in R&D, you will be working with equipment such as saws, welders and fabrication equipment to create parts. 

YOUR IMPACT

FABRICATION DUTIES:

• Weld complex/customized parts and weldments with foresight to avoid any technical issues
• Responsible for determining the appropriate equipment and methods required to tool, tack and weld complex parts.
• Responsible for maintaining the equipment and tools required to perform the job in your area.
• Work closely with Sr. and Lead Technicians to maintain appropriate stock of tooling table equipment, welding equipment and consumables to perform the job at hand.
• Ability to interpret an engineering drawing and 3D model to develop complex tooling setups using BluCo modular tooling to create parts and weldments.
• Maintain tooling, tooling tables, welders and measuring equipment required for fabricating activities
• Assemble and/or disassemble complex projects and mechanical structures through referencing drawings and work instructions with minimal input.
• Ability to work with Engineering team when fabricating parts
• Ability to communicate via email, phone, in person and skype conversations
• Develop and mentor fellow fabrication specialists to follow best practices and standards.
• Operate equipment to part down material to appropriate size.

MATERIALS DUTIES:

• Shuttle finished parts to the next process or workstation
• Organize weldment kits and place in orderly fashion until needed for next process
• Tag all parts when finished for next steps
• Assist in material handling throughout fabrication shop as needed
• Unload and transport raw materials to proper location with fork truck or TMH
• Place in stagging area, organized neatly
• Label materials with color code, project # (if provided) and thickness or size (sheet, bar, tubing, etc.)
• Provide paperwork to materials team, to assist with receiving of material
• Place materials on inventory rack as needed

SECONDARY DUTIES AND RESPONSIBILITIES:

• Identify and implement continuous improvement projects.
• Communicate and work cross functionally to resolve problems.
• Understand and execute directions and instructions.
• Follow through on instructions/directions and provide constructive feedback to all levels of the organization
• Plan and schedule daily activities to complete assignments in their order of priority to make effective use of time and ensure projects are being completed within identified timeline
• Responsible for maintaining a safe work environment, adhering to all safety procedures during all aspects of job performance which includes regular exposure to personal and physical hazards
• Operate heavy equipment, machinery or drive vehicles for the purpose of R&D development

MINIMUM QUALIFICATIONS:

• Technical Diploma with three (3) years of experience in engineering or equivalent*.  
• Ability to travel 5%.

STANDOUT QUALIFICATIONS: 

• Associate’s degree with three (3) years of experience in engineering or equivalent*.
• Certified Welder (CW) (internal certification required within 30 days of hire).
• Ability to read and interpret engineering drawings.
• Knowledge of automotive and mechanical terms.
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, government regulations and procedure manuals.
• Ability to adapt to a fast pace environment.
• Detail oriented.
• Verbal and written communication skills.

*Note: equivalent equates approximately four (4) years of on the job experience to one (1) year of formal education.

Oshkosh is committed to working with and offering reasonable accommodations to job applicants with disabilities. If you need assistance or an accommodation due to a disability for any part of the recruitment process, please contact our reception desk by phone at +1 (920) 502.3009 or our talent acquisition team by email corporatetalentacquisition@oshkoshcorp.com.

Oshkosh Corporation is an Equal Opportunity and Affirmative Action Employer. This company will provide equal opportunity to all individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Information collected regarding categories as provided by law will in no way affect the decision regarding an employment application.

Oshkosh Corporation will not discharge or in any manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with Oshkosh Corporation's legal duty to furnish information.

Certain positions with Oshkosh Corporation require access to controlled goods and technologies subject to the International Traffic in Arms Regulations or the Export Administration Regulations. Applicants for these positions may need to be "U.S. Persons," as defined in these regulations. Generally, a "U.S. Person" is a U.S. citizen, lawful permanent resident, or an individual who has been admitted as a refugee or granted asylum.

Career Category

Job Description

Senior Medical Science Liaison

MN, WI, N. Dakota, S. Dakota

US Medical Affairs, Bone, Therapeutic Area

Live

What you will do

Let’s do this.  Let’s change the world.  This is a field-based Senior Medical Science Liaison (MSL) position in the bone therapeutic area within the US Medical Organization. The territory will include Minnesota, Wisconsin, North and South Dakota. The Sr MSL will interact with the bone Opinion Leaders and other Healthcare Decision Makers to communicate and advance the scientific platform as aligned with Amgen's corporate goals and objectives. Accountabilities and responsibilities for the role include:

Accountabilities

• Serve as the field-based medical expert for this territory in the MSL group within the medical organization
• Communicate accurate, clear, and valued information regarding our science and products to multiple levels within the medical community and report field observations to internal stakeholders

• Support Scientific Engagement Plan (SEP) in developing local territory R&D tactics
• Engage and educate healthcare stakeholders (including APPs, fellows, and residents) by communicating clinical and scientific data, advancing the scientific platform aligned with Amgen’s corporate goals and objectives
• Educate and communicate clinical value, outcomes, and economic data to payers, providers, key stakeholders, advocacy, and access enablers
• Provide in depth clinical and pharmacoeconomic support to payers, IDNs, and formulary committees, providing feedback to key internal stakeholders on customer trends in interpreting and using value evidence, reimbursement, and payer policy. May serve as main medical point of contact at prioritized local payer, regional payer, and IDN accounts
• Respond to unsolicited inquiries consistent with the MSL compliance standards
• Provide and/or present field observations and insights to internal stakeholders
• Execute scientific engagement plan according to annual MSL goals and metrics
• Develop and implement local OL plans in line with SEP
• Support speaker training as requested and ensure the speakers are updated on new data
• Support Amgen sponsored research.  May serve as a study lead
• Liaise with potential investigators in non-sponsored clinical research and facilitate submission of investigator initiated pre-clinical and clinical proposals
• Lead and/or participate on project teams that support MSL strategies and tactics as delegated by MSL leadership
• Lead and support congress activities as aligned with strategy.  May serve as congress lead 
• Compliantly collaborate with cross-functional colleagues.  May serve as main point of contact
• Maintain clinical acumen and expertise and timely completion of assigned training.  May serve as a training lead, new hire mentor, and/or international MSL mentor/trainer
• Advance MSL value proposition, identify gaps, achieve results, and set an example for others to follow by consistently demonstrating Amgen values and leadership attributes 
• Demonstrate tact and professionalism when communicating and interacting with others

Competencies

• Plans and Organizes Work
• Builds Relationships and Impacts Others
• Achieves High Performance
• Maintains Industry and Technical Acumen
• Leverages Clinical and Therapeutic Expertise
• Effective Problem Solving and Decision Making
• Develops Personal and Professional Capabilities
• Communicates Effectively
• Demonstrates Individual Leadership and Professionalism
• Exemplifies Amgen Values

Basic Qualifications

• Doctorate degree and 2 years of MSL experience

Preferred Qualifications

• Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)
• Five years of industry experience in Scientific/Medical Affairs at a biotech or pharmaceutical company
• At least three years in a MSL role
• Managed market/payer/IDN engagement experience
• Five or more years focused on clinical practice, clinical research, or medical research.  Experience in a medically related field can include post-doctoral training (i.e., residencies and/or fellowships)

Osteoporosis and Bone Health

Salary Range

Systems & Software, a division of Harris Computer, is seeking a Director to join our Research & Development team. Reporting to the VP of Research & Development, you will lead a team of managers and software engineers responsible for product maintenance, regulatory & enhancement development, third party integrations, and customer stability.

The Director of R&D’s primary role is centered around leading a remote technical team, directly contributing to the software, collaborating with other departments, and continuously promoting best practices and the growth of technical expertise.

This is expected to be a hands-on role, where you will not just be directing the work of others but also participating in the work product.

This remote role welcomes candidates anywhere in Canada and the US. This role requires up to 20% of travel across Canada and the US. A valid passport/visa is required.

What your impact will be:

• Lead a development team and directly contribute in enhancing and maintaining a portfolio of products.
• Work closely with your managers and their teams in solving problems, debugging issues, and guiding their development efforts.
• Collaborate with management, customer service, and business analysts.
• Contribute towards providing our clients with stable and secure production environments.
• Implement and maintain R&D best practices.
• Set short & long-term goals for your team & empower them to attain those goals.
• Organize team reporting and working meetings; support managers and their teams in managing progress; manage risks and issues; correct deviations from plans; with focus on regular and timely delivery of value.
• Manage multiple requests and prioritization of your manager’s and team’s work.
• Understand the strengths and weaknesses of your managers and their teams.
• Coach your team to implement a culture of continuous improvement and performance.
• Support your team’s productivity by working across departments solving problems and clearing roadblocks.
• Promote teamwork and build trust in a safe cooperative environment.

What we are looking for:

• 10+ years of software development experience (desktop, mobile and/or web applications).
• 5+ years of leadership experience (e.g., Development Lead, Project Manager, Development Manager, etc.).
• Ability to translate Product Requirements into Technical Requirements.
• Experience with Agile and Scrum5.
• Experience with giving performance reviews.
• Experience with professional development strategy and implementation.
• Experience with solution design and architecture.
• Experience with user experience best practices.

What will make you stand out:

• Experience in the Utility sector.
• Experience with DevOps tools like Git, Ansible, Docker, etc.
• Experience in data science and/or business intelligence, especially experience with data warehousing

Location

This is a remote opportunity and can be based out of the US or Canada.

About Systems & Software:

Since 1973 it has been our unrelenting mission at Systems and Software to provide quality customer information system solutions to municipal and investor-owned utilities. To achieve that mission, we fully understand the importance of a committed, engaged group of developers, implementers and support staff. Click here (https://www.ssivt.com/) to learn more about Systems and Software!

About Harris:

Harris is a leading provider of mission critical software to the public sector in North America. As a wholly owned subsidiary of Constellation Software Inc. (“CSI”, symbol CSU on the TSX), Harris has become the cornerstone for CSI’s investment in utility, local government, school districts, public safety, and healthcare software verticals. Our success has been realized through investments in our proprietary software and market expertise. This focus, combined with acquiring businesses that build upon or complement our offerings, has helped drive our success. Harris will continue to growth through reinvestment – both in the people and products that we offer and making investments in acquiring new businesses.

Career Category

Job Description

Salary Range