With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
Internal Medical Translator/In-house Linguist (English to Japanese) Location: EMEA - Home-Based Unlock Your Potential with IQVIA Language Solutions!
Internal Medical Translator/In-house Linguist (Korean to English) Location: EMEA - Home-Based Unlock Your Potential with IQVIA Language Solutions!
Purpose As a Therapeutic Strategy Lead, you’ll develop and implement effective delivery strategies tailored to customer needs during the RFP/Bid Defense cycle. You’ll bridge the gap between sales, medical, and operational teams to ensure seamless project execution and support sales teams throughout the Business Development process.
About us Your Contribution Lead, coach, and motivate employees within respective area of responsibility, while providing direction to achieve department goals and objectivesAssist in developing department budget and investment plan(s) according to strategic goalsCultivate employee talent through training and coaching measures, while also conducting employee performance reviewsSupport the development and updating of Quality Assurance programs, policies, processes, procedures and controlsReview, analyze and report on quality discrepancies related to SCHOTT products, while developing disposition and corrective actions for product discrepanciesManage the review of batch records and avoid impacting shipment datesManage Department Training Coordinator activities and projectsManage document control activities to include, releasing, archiving, tracking and reporting of the document review process for controlled documentsLead and support the implementation of Systems and Compliance Improvements including site compliance, along with data integrity requirementsMeasure and analyze Quality System trendsOversee the internal audit function to ensure ongoing compliance to the Quality Management System (QMS)Maintain the Archive Room and document retention requirementsWrite and revise Standard Operating Procedures (SOPs) and provide training, as requiredManage the CAPA and Change-Control process to include, issuing, reviewing and approving stepsSupport all customer or registrar quality related audits and/or evaluationsUtilize quality tools, including Compliant-PRO, etc., for information, tracking and reporting purposes, as required by the Pharm Business UnitManage assigned CAPA(s) by performing root cause investigations, while defining resolution actions; implement preventive and corrective actions in a timely manner as a result of customer complaints or customer audit findingsHelp promote and implement safety/EHS directives and maintain a clean and safe workspaceAssure compliance with ISO certifications and cGMP, along with adherence to Company policies and procedures and Code of Conduct/safety guidelines Your Profile Bachelor’s Degree in Chemistry, Biology, Engineering or science related field, requiredMinimum three years of experience in Quality leadership roleSolid knowledge of ISO 9001, 14001, 15378, along with cGMP and ISOExposure to the glass forming industry and/or pharmaceutical industry, preferredThorough MS Office applications, SAP and electronic QMS systemsMulti-tasking abilitiesDecision makingDetail oriented approachForward/creative thinkingService orientedEffective communication skillsAbility to read, write and speak English language Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact usYour Profile Bachelor’s Degree in Chemistry, Biology, Engineering or science related field, requiredMinimum three years of experience in Quality leadership roleSolid knowledge of ISO 9001, 14001, 15378, along with cGMP and ISOExposure to the glass forming industry and/or pharmaceutical industry, preferredThorough MS Office applications, SAP and electronic QMS systemsMulti-tasking abilitiesDecision makingDetail oriented approachForward/creative thinkingService orientedEffective communication skillsAbility to read, write and speak English language
Balda Medical GmbH sucht in Bad Oeynhausen eine/n Quality Compliance Specialist (m/w/d) (ID-Nummer: 12744233)
About us Our Business Unit Lighting and Imaging offers challenging lighting and image transmission solutions for applications in the markets of automotive, aviation, medical devices, as well as industrial and safety engineering. With production units in Europe, North-America and the worldwide SCHOTT sales organization Lighting and Imaging is a leading supplier for fiber optic components.
Your Qualifications Bachelor in computer or electrical engineering with good mechanical skills or comparable education/training Extensive knowledge of machinery for the beverage / packaging industry and work experience of at least 2 years Analytical thinking for solving technical tasks Programmable Logic Controller’s (PLC) experience, electrical and/or mechanical Flexibility, assertiveness and organizational skills Self-confidence and friendly appearance Willingness to travel up to 90% of the time Passport or willingness to obtain a passport Benefits Innovative and international working environment Competitive wages Medical, Dental, Vision insurance offered at 30 days of employment Generous Educational Reimbursement program Company sponsored Life and Disability Insurance Paid Time Off Ten (10) Paid Holidays per year 401K with Company Match Location: Waukesha ǀ Wisconsin ǀ USA
Your Qualifications Bachelor in computer or electrical engineering with good mechanical skills or comparable education/training Extensive knowledge of machinery for the beverage / packaging industry and work experience of at least 2 years Analytical thinking for solving technical tasks Programmable Logic Controller’s (PLC) experience, electrical and/or mechanical Flexibility, assertiveness and organizational skills Self-confidence and friendly appearance Willingness to travel up to 90% of the time Passport or willingness to obtain a passport Benefits Innovative and international working environment Competitive wages Medical, Dental, Vision insurance offered at 30 days of employment Generous Educational Reimbursement program Company sponsored Life and Disability Insurance Paid Time Off Ten (10) Paid Holidays per year 401K with Company Match Location: Waukesha ǀ Wisconsin ǀ USA
BEC Medical GmbH sucht in eine/n Innovativer Qualitätsmanager / Regulatory Affairs Manager Medizinprodukte (Mensch) (ID-Nummer: 13669004)
About us Your Contribution Own and control project scopes, schedules and budgets; manage risks/issues and communicate status to stakeholdersLead cross functional execution with Production, Quality, Maintenance, Supply Chain, EHS, and Global EngineeringManage CAPEX, PO releases, FAT/SAT planning, cost tracking/forecasting and accurals; deliver fiscal year plan on time and on budgetPrepare and maintain audit ready documentation aligned to US cGMPOperate in accordance with standard cleanroom conduct consistent with ISO 14644 practices and internal QMS and site Contamination Control StrategyOwn change controls (local and global)- initiaiton, risk assessment, execution plan, verification of effectivensss and closure Lead/support validation and qualification for equipment, products, processes, etc.Integrate into operations; plan trials and downtime, coordinate line readiness/tech transfer, create/update SOPs, define PM requirements and maintenance plans, ensure spares/training are in placeSupport quality investigationsDrive continuous improvement with Lean to improve OEE, scrap rates, uptime and cycle times Mentor/train Engineers and Technicians (no direct reports); structured troubleshooting/problem solving and Best Known Methods; develop quick-reference guides/checklist, where needed Promote safety and EHS and adhere to all Company policies, procedures and guidelines Your Profile Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, Industrial/Manufacturing, Pharmaceutical or Materials) or equivalent4+ years in regulated manfuacturing Project management and CAPEX executionSix Sigma Green/Black Belt and/or PMPValidation and QMS: URS, FMEA, VMP, IQ/OQ/PQ/PV; author/review protocols/reports, managing deviations/CAPA; change controls Working knowledge of cGMP, ISO 9001, ISO 15378Knowledge and experience in leading new equipment/NPI validationsLean/CI; 5S, Kaizen, DMAIC, root cause (5-why, fishbone)Tools: SAP, MS Project, MS TEAMS, Solidworks and MinitabStrong skills in MS Office Ability to read, write and speak EnglishTeam player with upbeat approach Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact usYour Profile Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, Industrial/Manufacturing, Pharmaceutical or Materials) or equivalent4+ years in regulated manfuacturing Project management and CAPEX executionSix Sigma Green/Black Belt and/or PMPValidation and QMS: URS, FMEA, VMP, IQ/OQ/PQ/PV; author/review protocols/reports, managing deviations/CAPA; change controls Working knowledge of cGMP, ISO 9001, ISO 15378Knowledge and experience in leading new equipment/NPI validationsLean/CI; 5S, Kaizen, DMAIC, root cause (5-why, fishbone)Tools: SAP, MS Project, MS TEAMS, Solidworks and MinitabStrong skills in MS Office Ability to read, write and speak EnglishTeam player with upbeat approach
Das Unternehmen bietet Raum für Menschen, die Verantwortung übernehmen möchten und Freude daran haben, an anspruchsvollen, zukunftsorientierten Technologien mitzuwirken Weiterentwicklung eines schlanken, risikobasierten Qualitätsmanagementsystems (ISO 13485, AI Act) Sicherstellung regulatorischer Anforderungen für aktive Medizinprodukte, sterile Produkte sowie Software as a Medical Device (SaMD) Vorbereitung, Koordination und Begleitung internationaler Zulassungs- und Registrierungsprozesse (EU/MDR, USA/FDA) inkl.
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
We will consider all qualified applicants without regard to race, color, creed, religion, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity and expression (including transgender status), sexual orientation, marital status or status as a victim of domestic violence, national origin, ancestry, citizenship status, age, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, military service or veteran status, or any other classification protected by applicable local, state, and federal laws.
Senden Sie Ihre vollständigen Bewerbungsunterlagen an medcareer Ihr Spezialist für Medical & Healthcare Karrieren. ???? braunschweig@medcareer.de ?? 04941-60429-13 Wir freuen uns darauf, Sie kennenzulernen!
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Wir freuen uns auf Sie! Ihre Ansprechpartnerin bei medcareer Medical & Healthcare: Aliya Schultz ???? 04941-60429-13 ???? braunschweig@medcareer.de
Wir freuen uns auf Sie! Ihre Ansprechpartnerin bei medcareer Medical & Healthcare: Aliya Schultz ???? 04941-60429-13 ???? braunschweig@medcareer.de
Wir freuen uns auf Sie! Ihre Ansprechpartnerin bei medcareer Medical & Healthcare: Aliya Schultz ???? 04941-60429-13 ???? braunschweig@medcareer.de
Wir freuen uns auf Sie! Ihre Ansprechpartnerin bei medcareer Medical & Healthcare: Aliya Schultz ???? 04941-60429-13 ???? braunschweig@medcareer.de
Wir freuen uns auf Sie! Ihre Ansprechpartnerin bei medcareer Medical & Healthcare: Aliya Schultz ???? 04941-60429-13 ???? braunschweig@medcareer.de
Wir freuen uns auf Sie! Ihre Ansprechpartnerin bei medcareer Medical & Healthcare: Aliya Schultz ???? 04941-60429-13 ???? braunschweig@medcareer.de
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
Dann lassen Sie uns sprechen. Ich bin Jasmin Loges Recruiterin Medical & Health Care ???? Tel.: 04941-60429-15 ???? zwickau@medcareer.de Ihre Bewerbung behandele ich absolut vertraulich und melde mich schnell und persönlich bei Ihnen zurück.
mdc medical device certification GmbH sucht in Tuttlingen eine/n Projektkoordinator / Projektleiter (m/w/d) Zertifizierungsverfahren (ID-Nummer: 12216849)
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectivesDesign and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regionsBuild and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutionsConduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiativesContribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical dataOversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL DirectorAct as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentationPlan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical OfficerRepresent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencersServe as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic communityCollaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groupsFull professional proficiency in English, both spoken and writtenStrong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflowsExperience with product launches, advisory boards, and post-approval studies is highly advantageousRelevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned companyOther Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groups Full professional proficiency in English, both spoken and written Strong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflows Experience with product launches, advisory boards, and post-approval studies is highly advantageous Relevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned company Other Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
International assignments; Exclusive employee benefits/discounts; Further training and education; Medical, Dental and Vision coverage; Multiple career opportunities; Talent development; Team Events; Trust-based working time; paid vacation days, holidays and sick time Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
For our esteemed client in the pharmaceutical industry, we are looking for a Supplier Quality Engineer Packaging (m/f/d) based in Bad Homburg. Become part of a globally leading company in medical devices and pharmaceuticals and take responsibility for qualifying packaging suppliers and driving the global harmonization of packaging standards.
Proactive participation in all phases of software development from feasibility studies through design,development, testing and bug fixing and maintenanceCollaboration within the Scrum-TeamsIndependent interaction with internal framework manufacturersBased on requirements and models, definition of software architecture, design and specifications, ultimately leading to implementationParticipation in the definition of work packages, their estimation and planning in a sprint-based agile environmentAdherence to a software development process including contribution to written deliverables and documentation Degree in a software related field such as software or electrical engineering or similarHands-on experience as Software Engineer, preferred in the regulated environment such as the medical device industryYears hands- on experience with C++ and Linux from the last project or positionStrong with Linux DockersExperience with CAN busSoftware architecture would be advantageous Internal career opportunities World-renowned biotech company Ihr Kontakt Referenznummer 865145/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care.
We know: motivated and committed employees are the precondition for the success of our company. Flexible working hours; Further training and education; Medical, Dental and Vision coverage; Social Insurance System; Subsidized pension plan; paid vacation days, holidays and sick time Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
In addition, DHL offers the following: ·Paid time off: Holiday, Float Holiday, Vacation, and Sick ·Medical, Prescription, Dental, and Vision plans ·401K plan with a match ·Employee Discount plan ·Tuition Assistance Plan As the world’s leading logistics’ company, DHL offers a wide range of interesting job challenges and opportunities in our different divisions around the globe.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Wir entwickeln, fertigen und liefern unsere Premiumprodukte an die wichtigsten Hersteller in aller Welt in den Branchen Medical, Test&Measurement, Military, Robotics und wachsen seit 30 Jahren sehr dynamisch. Quality is key in unserem globalen, innovativen und stetig weiter expandierenden Unternehmen.
About us Your Contribution Achieve planned KPIs (sales, new opportunities) via sufficient order incomeElaborate Sales plans, forecasting and performance reportsPlan, direct and coordinate customer strategies and activitiesManage Key Accounts (local OEMs)Setup and execute regular customer visitation schedules and visits in CRMGenerate inquiries from customers and related quotations with support of Customer Service and other internal entitiesAuthorize quotations and pricing; perform reviews, negotiations, and contracting with customersHandle customer complaints with the support of Inside Sales and Quality departmentAssist A/R with overdue managementDocument customer knowledge in CRMFoster new growth opportunities with new customers, products, applications and projectsDrive competitive intelligence and reports to Market Intelligence teamEstablish sound market and application knowledgeContinously improve the overall customer satisfaction along the customer journeyEnsure teamwork and alignment of goals and objectives Follow Company policies and protocols, while adhering to all safety guidelines Follow Company Code of Conduct, Core Values and applicable laws and regulationsParticipate in trade shows, exhibitions and conferences, when applicable Attend both internal and external trainings Your Profile Masters Degree in Engineering, Science or Business Administration, required Minimum 5 years in Key Account Management, required Technical Sales/Marketing or Product Management of high engineesring content materials and components in an industrial Business-to-Business (B2B) environment, strongly preferredExperience in the semiconductor industry and/or quartz glass material sales, strongly desired Ability to read, write and speak English; strong oral and written communication skillsProficiency in MS Office knowledgeAbility to work in a dynamic and fast growing industryGrowth and results driven mindsetPersonable with excellent people management and teamwork skillsAbility to work in a global, matrix organization Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
WHAT YOU WILL DO Be a key influencer to our business colleagues in resolving significant or potential issuesUnderstand your customer by gathering requirement, presenting concepts and proposal, providing updates on deliverables and negotiating issue resolution when neededAct as a coordinator across projects to monitor performance to ensure delivery of quality application on timeWork with external parties in assembling the system components with standardized modulesCustomizeCommercial Off-The-Shelf (COTS)based on pre-determined parameters, and execute customizing testsEnsure works are documented according to required standards, methods and toolsAssist in the define, initiate and design of architecture in projects/ program WHAT YOU SHOULD HAVE: 8 years hands-on experience in designing and developing solutions with Java /JavaScriptWorking experience and knowledge in Software Development Life Cycle (SDLC) with relevant qualification in IT fieldPassion in developing a high quality softwareInquisitive and analytical mind Strong IT and business acumenProven ability to work in a multi-cultural and multi-functional environmentCustomer and end-user focusedExcellent oral and written communications skills WHAT YOU WILL GET FROM US Great team of IT professionals with global working exposure On-going professional and technical training and certifications Global internal job opportunities available within DPDHL A multicultural environment in modern offices Meal Card and Flexible Benefits – customized according to individual needs Choose any day for your vacation from earned public holiday (Saturday and ad hoc) Smart casual dress code everyday Unlimited Outpatient Medical Home office possibilities Sounds good? Start your application now! DHL IT Services IT Services is the internal provider of specialized IT Build services and industrialized IT Run services to Deutsche Post DHL (DPDHL) Group: Supports over 260,000 DPDHL e-mail users; Runs more than 7700 servers; Supports more than 2000 global services and applications; Processes 9 million shipment information messages per day; 200000 man days per year of development application.