Qureos Mentor

Takeda Pharmaceuticals

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2><h1 class="jobSectionHeader">
About the role:</h1>
Takeda&rsquo;s Los Angeles Quality Control team is seeking a QC Specialist III who will serve as the primary LIMS subject matter expert (SME) for the site. In this role, you will design, configure, and optimize LIMS and related digital solutions&mdash;driving compliant, paperless, and highly efficient QC laboratory operations. You will lead end-to-end implementation of system changes and support complex QC projects, leveraging deep LabWare expertise, data analytics, and digital tools to enhance data integrity and operational excellence. 
This role is ideal for someone passionate about digital transformation in the lab environment, with strong hands-on LIMS experience and the ability to partner cross-functionally to elevate QC capabilities.<h1 class="jobSectionHeader">
How you will contribute:</h1><ul><li>
Lead the transformation of QC laboratory operations through design, configuration, and enhancement of LIMS and related QC informatics platforms.</li><li>
Apply AGILE methodologies to plan, prioritize, and manage LIMS system changes and releases.</li><li>
Serve as the primary system owner for QC LabWare LIMS, focusing on configuration, lifecycle management, data integrity, and alignment to business processes.</li><li>
Maintain deep expertise in LabWare setup, including master data structures, workflows, templates, calculations, and interface design.</li><li>
Execute full lifecycle implementation of LabWare changes&mdash;requirements, design, configuration, testing, validation, and deployment.</li><li>
Evaluate and implement LIMS functionalities and integrations that streamline QC workflows and reduce manual effort.</li><li>
Act as SME for QC systems such as LabWare, MODA, and associated digital interfaces to support system design decisions and user story development.</li><li>
Customize and optimize LIMS workflows and user interfaces to enable accurate data capture and standardized testing.</li><li>
Maximize use of LIMS and connected tools (e.g., EM, LES, equipment interfaces) to enhance performance and data integrity.</li><li>
Support data science and analytics projects through high-quality, structured data extraction from LIMS and QC systems.</li><li>
Assist with creation of analytical and reporting tools to monitor QC trends, robustness, OOS/OOT rates, and turnaround time.</li><li>
Collaborate with QC, IT, Digital, Validation, Manufacturing, and Quality Systems on LIMS enhancements, integrations, and validation strategies.</li><li>
Participate in global and local informatics forums to support harmonization of QC processes and data structures.</li></ul><h1 class="jobSectionHeader">
What your bring to Takeda:</h1>
Required:<ul><li>
Bachelor&rsquo;s degree in science, engineering, or another technical field.</li><li>
3+ years of related experience.</li><li>
Strong understanding of QC operations, GxP, and data integrity principles.</li><li>
Demonstrated hands-on proficiency in LabWare LIMS, including configuration, master data management, workflow design, and system optimization.</li><li>
Experience supporting change control, validation, and LIMS lifecycle management.</li><li>
Ability to design and implement paperless digital solutions within QC environments.</li><li>
Strong analytical background, with experience using QC/LIMS data to support decision-making.</li><li>
Ability to manage multiple system changes and projects while maintaining compliance and quality standards.</li><li>
Strong communication, collaboration, and stakeholder-influencing skills.</li><li>
Experience working in AGILE or hybrid project environments.</li></ul>
Preferred:<ul><li>
Bachelor&rsquo;s or Master&rsquo;s degree in Life Sciences, Engineering, Computer Science, or a related field.</li><li>
Advanced LabWare LIMS experience and integration knowledge.</li><li>
Experience with digital QC tools such as ELN, CDS, or MODA.</li></ul><h1 class="jobSectionHeader">
Important Considerations:</h1>
At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:<ul><li>
Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.</li><li>
Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.</li><li>
Work in a cold, wet environment.</li><li>
Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.</li><li>
Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.</li><li>
Must be able to lift, push, pull and carry up to 15 lbs.</li><li>
In general, the position requires a combination of sedentary work and walking around observing conditions in the facility.</li><li>
Must be able to work in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body</li><li>
Some Clean Room and cool/hot storage conditions.</li></ul><h1 class="jobSectionHeader">
More about us:</h1>
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
#GMSGQ #ZR1 #LI-MA1
Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
USA - CA - Los Angeles
U.S. Base Salary Range:
$86,500.00 - $135,960.00 
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.<h2 class="jobSectionHeader">
Locations</h2>
USA - CA - Los Angeles<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time
Job Exempt
Yes</div>

Quality Control Specialist III

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2>
OBJECTIVES/PURPOSE<ul><li>
Defines, develops, and leads area regulatory strategies, in close alignment with line management and Country (LOC) RA Heads, to maximize regulatory success and enabling patient access, including all aspects of submission and timely approval of investigational drugs, marketing authorizations and life-cycle management submissions and subsequent Q&amp;As from authorities. &ldquo;</li><li>
Effectively communicates (including Global Product Team (GPT) representation when relevant) the regulatory strategies, submission plans and timelines; assessment of the likelihood of success of regulatory strategies and impact assessments of trends, regulations and changes related to assigned programs.</li><li>
Liaise with cross functional stakeholders including Global Regulatory Teams (GRT) to represent GEM RA strategies</li><li>
Additionally may act as GEM RA Lead for one or more assets for entire GEM region covering from development to the life cycle maintenance activities.</li><li>
Provides strategic and tactical advice, guidance and area regulatory expertise to global leadership teams on how to achieve timely and efficient conduct of development and/or life-cycle management of assigned programs while maintaining full compliance with applicable regulatory requirements</li><li>
Leads the Submission Working Group (SWG) for submissions in the area and represents the area as needed on global and project teams for the new Mas &amp; other major submissions</li><li>
Manages or supports and oversees interactions with Health Authorities in the Area in collaboration with Area stakeholders and LOC RA teams</li><li>
May support value and access team in their interactions with Health Authorities for negotiations related to products within their responsibility (wherever applicable) &ndash; For specific areas only</li><li>
Evaluates new business development opportunities and / or participates in due diligence teams</li><li>
May act as Deputy of RA Area Head and may support RA activities for other areas as needed</li></ul>
ACCOUNTABILITIES<ul><li>
Demonstrates Takeda leadership behaviors at all times (for external need HR support to briefly highlight Takeda leadership behaviours requirements)</li><li>
Independently manages, plans, and works closely with Regional, LOC Regulatory Leads, BU Cross-functional Teams (CFT), and Global Regulatory Teams to deliver all aspects of regulatory activities throughout the product life cycle in close partnership with Global Regulatory TA Leadership and aim for a successful and timely outcome of RA applications in the area</li><li>
Oversees and accountable for working with other RA functions and/or vendor to ensure that regulatory submissions and approvals are achieved on schedule within area of responsibility</li><li>
Accountable for communications to the regulator, development teams, and GRA, other Research and Development (R&amp;D) functions, and TAU leadership.</li><li>
Provides regulatory expertise on drug development, registration and / or post-marketing compliance and life cycle management.</li><li>
Participates, as appropriate, and authors/reviews internal procedures and processes.</li><li>
Understands and interprets complex scientific issues for products of responsibility as it relates to regulatory requirements and strategy.</li><li>
Develops effective working relationships with LOC Regulatory Lead, Regional and Global Regulatory Team, cross- functional commercial Area &amp; LOC Teams; company&rsquo;s consultants and Business Partners as required.</li><li>
Actively pursues or oversees the tracking and fulfillment of post- marketing commitments.</li><li>
Presents regional regulatory strategies to leadership/senior management and shall be able to identify and share the risks and opportunities as well as probability of success of proposed strategy</li></ul>
DIMENSIONS AND ASPECTS
Technical/Functional (Line) Expertise<ul><li>
Solid regulatory experience, including knowledge of regulations and guidance applicable in the region across all phases of development and able to orient project teams in the interpretation of guidelines; an understanding of basic regulatory requirements in other regions globally (US, EU, emerging markets) is a plus.</li><li>
 Understands the essentials of evidence requirements beyond marketing authorization (i.e. in support of patient access/ tender requirement)</li><li>
Able to formulate regional regulatory strategy to achieve competitive and accelerated product approvals</li><li>
Experience of initial MA, indication/ line extension applications and/or lifecycle management and development submissions</li><li>
Experience with advanced therapeutic medical products (Cell &amp; gene therapy) will be advantageous</li></ul>
Leadership<ul><li>
Able to manage with limited supervision different types of regulatory development or lifecycle management procedures in the region in coordination with the LOC RA teams.</li><li>
Stays current with regulations / guidance in the region for impact on drug development plans, registration, and life-cycle management to maximize the positive outcomes of the regulatory applications and maintain regulatory compliance.</li><li>
Acts as an ally to support individuals as a whole and promotes an inclusive culture</li><li>
Practices active listening, encourages open dialogue, feedback, and diverse opinions</li><li>
Can speak up and is perceived as a natural, assertive authority whom peers trust for their advice</li></ul>
Decision-making and Autonomy<ul><li>
Is able to prioritize activities and execute within reasonable time with limited supervision</li><li>
Can take some tactical decisions independently</li></ul>
Interaction<ul><li>
Experience of participating or leading interaction with Health Authorities</li><li>
Communicates externally/with authorities in concise and respectful language</li><li>
Adapts to changing circumstances and is able to build and maintain relationships with Global teams and LOC RA and other CFTs</li><li>
Has their voice heard as remote participant to global or cross functional teams (GRT, GPT etc); influences meeting agendas &amp; outcomes to optimally integrate regional strategic needs</li></ul>
Complexity (Products managed, mix of businesses, internal and/or external business environment, cultural considerations)<ul><li>
Self-aware and able to function effectively while meeting the multiple challenges with a sense of energy, vitality, and confidence</li><li>
Develops concise strategic plans, understandably outlines the opportunities and risks of alternative scenarios before proposing a decision</li></ul>
EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:<ul><li>
BSc. Advanced scientific related degree preferred; BA accepted based on experience.</li><li>
A minimum of 8 years of experience in drug regulatory affairs preferably within the EU/GEM region.</li><li>
Prior experience of &lsquo;area&rsquo;/ countries will be an advantage</li><li>
Receives and gives feedback; expresses ideas, questions, and disagreement</li><li>
Fluency in English and other local languages will be an advantage</li><li>
Work in flexible hours</li></ul><h2 class="jobSectionHeader">
Locations</h2>
Dubai, UAE<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time</div>

GEM Regulatory Leads - EAMEA

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2> 
The Future Begins Here
At Takeda, we are leading digital evolution and global transformation. By building innovative solutions and future-ready capabilities, we are meeting the need of patients, our people, and the planet.
Bengaluru, the city, which is India&rsquo;s epicentre of Innovation, has been selected to be home to Takeda&rsquo;s recently launched Innovation Capability Center. We invite you to join our digital transformation journey. In this role, you will have the opportunity to boost your skills and become the heart of an innovative engine that is contributing to global impact and improvement.
At Takeda&rsquo;s ICC we Unite in Diversity
Takeda is committed to creating an inclusive and collaborative workplace, where individuals are recognized for their backgrounds and abilities they bring to our company. We are continuously improving our collaborators journey in Takeda, and we welcome applications from all qualified candidates. Here, you will feel welcomed, respected, and valued as an important contributor to our diverse team.
The Role
Our validation specialists are located at three sites in Bangalore, Mexico City and Bratislava. The teams are organized in what we call Towers, ERP, R&amp;D, Infrastructure etc. This role is intended to support the ERP Tower.
As Risk &amp; Compliance Manager, you will lead validation activities within the ERP Tower, ensuring compliance with regulatory standards and internal quality requirements. This role involves managing a team of 10+ validation specialists and collaborating across IT, QA, and business units to deliver robust, compliant solutions.
Key Responsibilities<ul><li>
Lead and manage a team of 10+ validation specialists within the ERP Tower.</li><li>
Oversee validation and qualification of IT systems and infrastructure to ensure compliance with regulatory standards and internal quality requirements.</li><li>
Define validation strategies and objectives aligned with business and compliance goals.</li><li>
Develop and maintain validation plans, protocols, and schedules; communicate expectations clearly to stakeholders.</li><li>
Identify and mitigate risks in validation processes, implementing proactive strategies for successful outcomes.</li><li>
Coordinate cross-functional teams (QA, IT, engineering, business units) for timely execution of deliverables.</li><li>
Monitor progress and performance, providing regular updates and facilitating review meetings.</li><li>
Ensure complete and accurate documentation per GxP and industry standards.</li><li>
Drive adherence to regulatory guidelines (FDA, EMA) and internal SOPs throughout the lifecycle.</li><li>
Promote continuous improvement by evaluating processes and introducing efficiency enhancements.</li><li>
Manage resource planning and prioritization in close collaboration with business stakeholders.</li></ul>
Additional Responsibilities<ul><li>
Act as the primary point of contact for ERP validation demands, ensuring timely assessment and execution of validation activities for new implementations, upgrades, and change requests.</li><li>
Plan and manage validation projects end-to-end, including scope definition, timelines, resource allocation, and stakeholder communication.</li><li>
Ensure risk-based validation approach for ERP systems, balancing compliance requirements with operational efficiency.</li><li>
Collaborate with business process owners and IT teams to align validation deliverables with system functionality and business needs.</li><li>
Maintain validation readiness for audits and inspections, ensuring documentation and processes meet regulatory expectations.</li><li>
Drive standardization of validation practices across ERP systems and related infrastructure globally.</li><li>
Support continuous improvement initiatives by introducing automation or digital tools for validation documentation and reporting.</li><li>
Provide training and guidance to team members and stakeholders on ERP validation principles and compliance requirements.</li><li>
Monitor industry trends and regulatory updates to keep validation strategies current and compliant.</li></ul>
Qualifications<ul><li>
Min 10 years of experience in a similar role</li><li>
Proven ability to develop and execute validation strategies for SAP 4/Hana implementations and rollouts , including system upgrades and migrations.</li><li>
Experience from leading or coordination cross functional teams (e.g., IT, QA, Business process owners, project managers and vendors)</li><li>
Strong experience in SAP ERP modules (e.g., Finance, Supply Chain, Manufacturing) and their integration points.</li><li>
Hands-on knowledge of SAP GxP compliance requirements, including validation of SAP cloud solutions and related infrastructure.</li><li>
Bachelors or Master's degree in a relevant scientific or engineering discipline (e.g., Computer Science, Engineering, Chemistry, Pharmacy, or related fields).</li><li>
Experience with PMP or Agile or other iterative project management methodologies is a plus</li><li>
Proven experience as an IT Project Manager, with a track record of successfully delivering IT projects on time and within budget.</li><li>
Strong understanding of project management methodologies and best practices.</li><li>
Excellent leadership, communication, and interpersonal skills.</li><li>
Exceptional problem-solving and decision-making abilities.</li><li>
Proficiency in project management tools and software.</li><li>
Ability to work collaboratively in a cross-functional team environment.</li><li>
Strong organizational skills and attention to detail.</li><li>
Excellent people management skills with experience working in global multi-cultural organizations</li><li>
Ability to balance compliance, efficiency and business needs a risk-based approach</li><li>
Good technical understanding of SAP cloud solutions</li></ul>
Benefits:
It is our priority to provide competitive compensation and a benefit package that bridges your personal life with your professional career. Amongst our benefits are:<ul><li>
Competitive Salary + Performance Annual Bonus</li><li>
Flexible work environment, including hybrid working</li><li>
Comprehensive Healthcare Insurance Plans for self, spouse, and children</li><li>
Group Term Life Insurance and Group Accident Insurance programs</li><li>
Employee Assistance Program</li><li>
Broad Variety of learning platforms</li><li>
Diversity, Equity, and Inclusion Programs</li><li>
Reimbursements &ndash; Home Internet &amp; Mobile Phone</li><li>
Employee Referral Program</li><li>
Leaves &ndash; Paternity Leave (4 Weeks) , Maternity Leave (up to 26 weeks), Bereavement Leave (5 calendar days)</li></ul>
About ICC in Takeda<ul><li>
Takeda is leading a digital revolution. We&rsquo;re not just transforming our company; we&rsquo;re improving the lives of millions of patients who rely on our medicines every day.</li><li>
As an organization, we are committed to our cloud-driven business transformation and believe the ICCs are the catalysts of change for our global organization.</li></ul>
#Li-Hybrid<h2 class="jobSectionHeader">
Locations</h2>
IND - Bengaluru<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time</div>

Risk & Compliance Manager

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2>
Portf&ouml;y Etkile&#351;im M&uuml;d&uuml;r&uuml; ve t&uuml;m ilgili payda&#351;lar ile yak&#305;n i&#351; birli&#287;i i&ccedil;inde &ccedil;al&#305;&#351;arak, sorumlu oldu&#287;u b&ouml;lgede portf&ouml;y ve marka stratejilerinin etkin saha uygulamas&#305;n&#305; y&uuml;r&uuml;tmek; sorumlu oldu&#287;u &uuml;r&uuml;nlerin bilimsel tan&#305;t&#305;m&#305;n&#305;, mevzuata ve &#351;irket politikalar&#305;na tam uyumla ger&ccedil;ekle&#351;tirmek; tan&#305;mlanan kantitatif ve kalitatif hedeflere ula&#351;mak; m&uuml;&#351;teri etkile&#351;imini ve memnuniyetini art&#305;rmak ve maksimize etmek; pazar dinamikleri, rekabet ve m&uuml;&#351;teri i&ccedil;g&ouml;r&uuml;lerini sistematik olarak toplay&#305;p analiz ederek istenen sistem ve frekansta d&uuml;zenli raporlamak.
Role Core Responsibilities &amp; Accountabilities<ul><li>
Sorumlu oldu&#287;u b&ouml;lgede portf&ouml;y ve marka stratejilerini saha uygulamalar&#305;na d&ouml;n&uuml;&#351;t&uuml;rerek etkili &#351;ekilde hayata ge&ccedil;irmek.</li><li>
&Uuml;r&uuml;n tan&#305;t&#305;m faaliyetlerini yerel mevzuat, Takeda politikalar&#305; ve sistemlerine tam uyumla; etik ve bilimsel &ccedil;er&ccedil;evede y&uuml;r&uuml;tmek.</li><li>
B&ouml;lgesel hedeflere ula&#351;mak amac&#305;yla planl&#305; ve d&uuml;zenli maksimum efektif ziyaretler planlamak ve ger&ccedil;ekle&#351;tirmek.</li><li>
Kilit m&uuml;&#351;teri ve ilgili &uuml;niteler y&ouml;netimini y&uuml;r&uuml;tmek, sa&#287;l&#305;k profesyonelleri ile g&uuml;&ccedil;l&uuml; ve s&uuml;rd&uuml;r&uuml;lebilir ili&#351;kiler geli&#351;tirmek.</li><li>
CRM sistemi &uuml;zerinden hedef hekim ve kurum segmentasyonlar&#305;n&#305; eksiksiz ve g&uuml;ncel tutmak, ziyaret kay&#305;tlar&#305;n&#305; &#351;irket kurallar&#305;na uygun olarak zaman&#305;nda ve eksiksiz &#351;ekilde yapmak.</li><li>
Pazar dinamikleri, rekabet bilgileri ve m&uuml;&#351;teri i&ccedil;g&ouml;r&uuml;lerini toplay&#305;p analiz etmek; d&uuml;zenli olarak analiz sonu&ccedil;lar&#305;n&#305; ve gerekli dinamik aksiyon plan&#305;n&#305; Portf&ouml;y Etkile&#351;im M&uuml;d&uuml;r&uuml;&rsquo;ne aktarmak.</li><li>
Dijital ve y&uuml;z y&uuml;ze etkile&#351;im kanallar&#305;n&#305; b&uuml;t&uuml;nle&#351;ik &#351;ekilde kullanarak eri&#351;imi ve etkiyi en &uuml;st d&uuml;zeye &ccedil;&#305;karmak.</li><li>
&Uuml;r&uuml;n ve terap&ouml;tik alan bilgilerini s&uuml;rekli g&uuml;ncel tutmak, fikir lideri g&ouml;r&uuml;&#351;melerinde y&uuml;ksek bilimsel de&#287;er sunmak.</li><li>
B&ouml;lgesel i&#351; planlar&#305;n&#305; maksimum verimde olu&#351;turmak, uygulamak ve belirlenen periyotlarda g&uuml;ncellemek.</li><li>
B&ouml;lge ve kurum baz&#305;nda performans analizleri yapmak, raporlamak ve gerekti&#287;inde payla&#351;mak.</li><li>
Yerel toplant&#305;lar, e&#287;itimler ve saha aktivitelerini organize ederek stratejiye uyumu ve ekip motivasyonunu sa&#287;lamak.</li><li>
M&uuml;&#351;teri odakl&#305; inovatif projeler geli&#351;tirerek etkile&#351;imi ve eri&#351;imi art&#305;rmak.</li><li>
&Ccedil;apraz fonksiyonlarla (Pazarlama, Medikal, Pazar Eri&#351;im, IPS, DD&amp;T vb.) , PTRB &ccedil;er&ccedil;evesinde yak&#305;n ve efektif i&#351; birli&#287;i i&ccedil;inde &ccedil;al&#305;&#351;mak.</li><li>
Takeda&rsquo;n&#305;n de&#287;erlerini ve liderlik davran&#305;&#351;lar&#305;n&#305; sahada &ouml;rnek &#351;ekilde temsil etmek.</li></ul>
Role Mandatory Responsibilities<ul><li>
Takeda'n&#305;n &ldquo;Bilgi G&uuml;venli&#287;i Politikas&#305;&rdquo; ve &ldquo;Teknolojinin Kabul Edilebilir Kullan&#305;m&#305; Politikas&#305;&rdquo;na uymak.</li><li>
&Uuml;r&uuml;n kalitesi ile ilgili sorunlar&#305; zaman&#305;nda Kalite Ekibine iletmek.</li><li>
Etik davran&#305;&#351;&#305; &uuml;st&uuml;n k&#305;lmak, Takeda-izm de&#287;erlerini her ko&#351;ulda yans&#305;tmak.</li><li>
Zorunlu t&uuml;m global e&#287;itimleri zaman&#305;nda tamamlamak ve politikalara tam uyum sa&#287;lamak.</li><li>
&#350;irket sistemlerini (&ouml;rn. Veeva, Concur, Dakika) do&#287;ru ve zaman&#305;nda kullanmak.</li><li>
Uyumsuzluk veya etik ihlallerini ilgili Takeda kanallar&#305;na proaktif &#351;ekilde bildirmek.</li></ul>
Nitelikler:<ul><li>
4 y&#305;ll&#305;k &uuml;niversite mezunu olmak (tercihen sa&#287;l&#305;k/bilim alan&#305;nda).</li><li>
&#304;la&ccedil; sekt&ouml;r&uuml;nde en az 2-3 y&#305;l saha deneyimi (tercihen Hematoloji terap&ouml;tik alan tecr&uuml;besi olan).</li><li>
Tercihen en az orta seviyede &#304;ngilizce bilgisi.</li><li>
MS Office ve CRM sistemlerine (&ouml;rn. Veeva) hakimiyet.</li><li>
B s&#305;n&#305;f&#305; ehliyete sahip olmak ve aktif ara&ccedil; kullanabilmek.</li><li>
Erkek adaylar i&ccedil;in askerlik hizmetini tamamlam&#305;&#351; olmak.</li><li>
Seyahat engeli bulunmamak.</li></ul>
Yetkinlikler:<ul><li>
M&uuml;&#351;teri Odakl&#305;l&#305;k: Hekimlerle g&uuml;vene dayal&#305; ili&#351;kiler kurma ve ihtiya&ccedil;lara uyum sa&#287;lama.</li><li>
Multichannel Uygulama: Dijital ve y&uuml;z y&uuml;ze etkile&#351;im kanallar&#305;n&#305; etkin y&ouml;netme.</li><li>
Analitik D&uuml;&#351;&uuml;nme: Veriye dayal&#305; karar alma ve performans iyile&#351;tirme.</li><li>
Uyum Yetene&#287;i: De&#287;i&#351;en ko&#351;ullara h&#305;zla uyum sa&#287;lama.</li><li>
&#304;leti&#351;im Yetkinli&#287;i: Etkili ve hedefe uygun ileti&#351;im kurma.</li><li>
Tak&#305;m &Ccedil;al&#305;&#351;mas&#305;: &Ccedil;apraz fonksiyonlarla i&#351; birli&#287;i geli&#351;tirme.</li><li>
Etik ve Uyum: Yasal, d&uuml;zenleyici ve etik standartlara tam uyum.</li></ul><h2 class="jobSectionHeader">
Locations</h2>
Istanbul, Turkey<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time</div>

Portföy Etkileşim Lideri Hematoloji - Istanbul Bölge

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2>
OBJECTIVES/PURPOSE<ul><li>
Supports solutions engineers on one or more software applications.</li><li>
Participates and executes technical standard analysis, implementation and evaluation of small-scale solution projects within technical area of expertise on the following areas:</li><li>
End User Support</li><li>
Hardware troubleshooting and repair</li><li>
Operating systems and software</li><li>
Tools and processes</li></ul> 
ACCOUNTABILITIES:<ul><li>
Investigates issues, analyzes solutions and implements technical changes on small projects.</li><li>
Analyses requirements, and maintains, tests, debugs and integrates application components.</li><li>
Supports on making decisions on guidelines and policies, and may look to others to help in the support of making decisions.</li><li>
Performs technical analysis and design, modifies and/or configures software and hardware solutions according to Takeda standards, typically executed in a defined project.</li><li>
Provides application software development services or related technical support in solutions maintenance or in a defined project.</li><li>
Supports the delivery of business solutions deployment to production, handle IMACD-processes of End User Equipment and IT Asset Management.</li><li>
Serve as local hands on support for the managed IT infrastructure and the End User Equipment.</li><li>
Support on meeting rooms and meeting events</li><li>
Ensures that system improvements are successfully implemented.</li><li>
Develops and maintains support documentation according to Takeda Quality Management System (QMS), Software Development Life Cycle (SDLC) and IT Project Life Cycle (ITPLC) standards, policies and procedures.</li><li>
Works under moderate guidance and direction.</li><li>
Understands key IT and Business objectives / goals and uses this knowledge within its own working field.</li></ul>
RELATED TO THIS ROLE
<ul><li>Provide regular updates on planned Initiatives and reports on Technology Operations and projects.</li><li>
Ensure data accuracy on managed services</li></ul>
DIMENSIONS AND ASPECTS
Technical/Functional (Line) Expertise<ul><li>
Operational knowledge of IT infrastructure and operations including desktop, server, operating systems, LAN/WAN, print, collaboration, and unified communication services.</li></ul>
Leadership<ul><li>
Oversee day-to-day operations and performance</li><li>
Objective performance self-evaluation</li><li>
Develop self and colleagues by available trainings and knowledge sharing.</li><li>
Support training needs identified with the business.</li><li>
Provide Voice of the Customer feedback and continuous improvement opportunities.</li></ul>
EDUCATION, BEHAVORIAL COMPETENCIES AND SKILLS:
Required:<ul><li>
Associate degree or equivalent.</li><li>
1 to 3 years of relevant experience.</li><li>
Good oral and written communications skills, with analytical and problem-solving skills.</li><li>
Ability to write and speak in the English and local language.</li><li>
Efficient time management and coordination of tasks, working in a global IT environment.</li><li>
Ability to gain working knowledge of IT solutions and grows expertise in the subject matter area.</li><li>
Professional vocational training in Computer Science.</li><li>
Work continuously to enhance own skills and take proactive ownership</li><li>
Excellent customer management skills</li></ul>
Preferred:<ul><li>
Bachelor Degree/Masters</li><li>
Working knowledge of ITIL</li><li>
Pharmaceutical industry and/or drug development business experience is a plus.</li></ul><h2 class="jobSectionHeader">
Locations</h2>
Istanbul, Turkey<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time</div>

Technology Support Technician