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דרושים Associate - Ukig

תפקיד מתכנת Associate - Ukig הוא כוכב עולה בשמיי ההייטק, כשמפתחים יכולים לבחור בין מגוון של פרויקטים מעניינים תוך כדי עבודה דינאמית ומאתגרת. בואו למצוא את המשרה הבאה שלכם כמפתחי Associate - Ukig כאן באקספוינט!
חברה
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
Israel
עיר
נמצאו 27 משרות
19.11.2025
T

Teva Associate Director Patent Attorney Israel, Tel-Aviv District, Tel Aviv

Limitless High-tech career opportunities - Expoint
Collaborate with R&D Associates to determine/develop design-around formulations. Collaborate with outside counsel to determine/develop invalidity positions to relevant patents. Determine launch strategy, including labeling carve outs, and assess risk associated...
תיאור:
How you’ll spend your day
  • Collaborate with R&D Associates to determine/develop design-around formulations.
  • Collaborate with outside counsel to determine/develop invalidity positions to relevant patents.
  • Determine launch strategy, including labeling carve outs, and assess risk associated with launch.
  • Manage European Patent Office Oppositions and similar actions in national patent offices.
  • Manage Unified Patent Court revocations.
  • Collaborate with colleagues in other teams to ensure all global issues are addressed, including manufacturing site, device, and API issues.
  • Collaborate with Regulatory Affairs Associates to support regulatory submissions.
  • Collaborate with Portfolio Team to support identification of potential generic products for Teva’s European and International markets including providing IP landscapes and IP launch scenarios.
  • Collaborate with Business Development to determine launch strategy, including labeling carve outs, and assess risk associated with launch for in-licensed generic products.
  • Collaborate with Medis to support Medis’ out-licensing of Teva’s generic products.
  • Manage outside opinion counsel to ensure high quality work product on time and within budget.
Your experience and qualifications
  • Collaborate with R&D Associates to determine/develop design-around formulations.
  • Collaborate with outside counsel to determine/develop invalidity positions to relevant patents.
  • Determine launch strategy, including labeling carve outs, and assess risk associated with launch.
  • Manage European Patent Office Oppositions and similar actions in national patent offices.
  • Manage Unified Patent Court revocations.
  • Collaborate with colleagues in other teams to ensure all global issues are addressed, including manufacturing site, device, and API issues.
  • Collaborate with Regulatory Affairs Associates to support regulatory submissions.
  • Collaborate with Portfolio Team to support identification of potential generic products for Teva’s European and International markets including providing IP landscapes and IP launch scenarios.
  • Collaborate with Business Development to determine launch strategy, including labeling carve outs, and assess risk associated with launch for in-licensed generic products.
  • Collaborate with Medis to support Medis’ out-licensing of Teva’s generic products.
  • Manage outside opinion counsel to ensure high quality work product on time and within budget.
Reports To
Sr Dir Patent

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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09.11.2025
T

Teva Regulatory Affairs Associate II Israel, Center District

Limitless High-tech career opportunities - Expoint
Collection and preparation of documents intended for submission of CMC variation packages. Evaluation of changes and support for their implementation in drug documentation for EU, US, IL market, as well...
תיאור:
How you’ll spend your day
  • Collection and preparation of documents intended for submission of CMC variation packages
  • Evaluation of changes and support for their implementation in drug documentation for EU, US, IL market, as well as monitoring the status of requests and agreed activities
  • Participation in meetings for projects within responsibility and informing other organizational units about the content of the registration file
  • Work with regulatory team and other functions to create solutions and implement agreed mitigation plans
  • Provide regulatory input throughout the product life cycle of responsible product lines and understand or raise regulatory obstacles to Head of regulatory Function
  • Preparation of responses to authorities’ requests within regulated timeframe
  • Update status through electronic systems, database and relevant forums
Your experience and qualifications
  • University degree (Pharmacist/Biologist/Chemist/ Engeneering/ Biomedical)
  • 2-3 years of experience in regulatory affairs in CMC, quality assurance and control, drug development or analytics will be an advantage
  • Experience of working with Multi-national companies in Pharmaceuticals
  • Knowledge in regulation, requirements and guidelines
  • Proficiency in written and spoken English and Hebrew
  • Ability to work in dynamic environment, multi-tasking,
  • Ability to work both individually and in the team, to cooperate on cross-country level and with different business units
  • Experience in global environment- advantage
  • Experience with sterile products
  • Experience with medical device combined product- advantage
  • Knowledge with electronic systems and databases
Reports To

Assoc Dir Regulatory Affairs

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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משרות נוספות שיכולות לעניין אותך

09.11.2025
T

Teva Associate Director Accounting Israel, Tel-Aviv District, Tel Aviv

Limitless High-tech career opportunities - Expoint
Preparation of timely and accurate quarterly financial statements according to US GAAP. Manage the yearly statutory financial statements and tax returns preparation and submission. Perform accounting and audit procedures in...
תיאור:
How you’ll spend your day
  • Preparation of timely and accurate quarterly financial statements according to US GAAP
  • Manage the yearly statutory financial statements and tax returns preparation and submission
  • Perform accounting and audit procedures in collaboration with Teva's external auditors
  • Ensure reporting processes are in line with SOX and Teva's compliance policy
  • Perform monthly balance sheet reconciliations and review of accounts, to ensure all financial transactions are properly reflected in the General Ledger
  • Providing accounting support to business units and corporate functions, as part of the period end close activities, and in accordance with regulatory requirements and corporate policies
  • Supervise work performed by Israel Accounting team members
Your experience and qualifications
  • Academic degree in Accounting. CPA – must
  • 3+ years of relevant work experience
  • Experience in employee management and development
  • Big 4 audit experience – an advantage
  • Previous experience with US GAAP reporting standards and Israeli tax filing requirements - an advantage
  • Excellent ability to work independently and proactively
  • Experience working with Oracle, SAP or similar ERP system – an advantage
  • Excellent written and verbal communication skills
  • Team player with good interpersonal skills
  • Strong English skills, written and verbal
  • Ability to work under pressure
Reports To

Sr Dir Accounting Israel

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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משרות נוספות שיכולות לעניין אותך

15.09.2025
T

Teva Associate Director Total Rewards Israel, Tel-Aviv District, Tel Aviv

Limitless High-tech career opportunities - Expoint
Design and execute Compensation cross company programs in alignment with Teva Total Rewards philosophy and approach. Lead end to end Year-End Rewards process which includes Merit, Bonus, Promotions and Equity....
תיאור:
How you’ll spend your day

This role oversees Total Rewards activities in Israel

  • Design and execute Compensation cross company programs in alignment with Teva Total Rewards philosophy and approach.
  • Lead end to end Year-End Rewards process which includes Merit, Bonus, Promotions and Equity
  • Lead the annual compensation review to provide inputs to the AOP, including benchmark approach, market competitiveness and identify special needs to support the business
  • Total Rewards focal point to advice IL HRDs / HRBPs, working closely with unions
  • Design and govern benefits programs such as medical, pension, car and more
  • Support Health & Wellbeing initiatives leveraging local and global best practice

Qualifications:

  • Mastering the C&B various methodologies, global processes and programs, as well as familiarity with the current and future trends in the Rewards arena
  • Ability to run global and complex programs and process
  • Strong quantitative analytic capabilities
  • Excellence in execution - the ability to resolve complex issues and complete multiple tasks within agreed timelines
  • Excellent Collaboration, influencing and interpersonal skills

Experience:

  • Bachelor or Master degree in Business, Economy, Statistics, Human Resources or related field
  • 7+ years experience of C&B (e.g. annual pay processes, surveys benchmark, salary review processes, benefits program design)
  • Experience in working with financial concepts (P&L, cost centre management, accruals)
  • Experience in project management and major initiatives implementation
  • Familiarity with Equity based on programs (Advantage)
Reports To

Sr Director - Total Rewards International Markets

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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משרות נוספות שיכולות לעניין אותך

15.09.2025
T

Teva Associate Director Professional Learning & Development - R&D... Israel, Tel-Aviv District, Tel Aviv

Limitless High-tech career opportunities - Expoint
Analyze and map the professional capabilities of R&D teams to assess strengths and identify gaps. Develop and implement comprehensive work plans to bridge competency gaps and enhance the skill sets...
תיאור:
How you’ll spend your day

• Analyze and map the professional capabilities of R&D teams to assess strengths and identify gaps.
• Develop and implement comprehensive work plans to bridge competency gaps and enhance the skill sets of R&D employees.
• Collaborate closely with R&D managers and the HR team to align capability development initiatives with business needs and organizational goals.
• Design targeted capability-building programs, ensuring they are aligned with the latest industry trends, technological advancements, and internal requirements.
• Monitor the progress and effectiveness of capability development initiatives, using data and feedback to continuously refine and improve strategies.
• Provide ongoing support and guidance to managers in developing their teams' skills and ensuring their professional growth aligns with R&D objectives.

Your experience and qualifications

• A bachelor's degree in a relevant field is required. A master's degree preferred.
• At least 5 years of experience in learning and development, or a related field, with a strong focus on capability mapping, skills gap analysis, and training program development.
• In-depth understanding of technical and professional capabilities development ideally within R&D environments, and the ability to analyze and develop tailored solutions to address competency gaps.
• Strong project management and organizational skills, with the ability to manage multiple initiatives and timelines effectively.
• An analytical mindset and data-driven approach, with the ability to identify gaps, develop solutions, and adapt strategies to meet evolving business needs.
• Proven ability to work cross-functionally with HR teams, managers, and other stakeholders to design and implement competency development strategies.
• Excellent written and verbal communication skills, with the ability to articulate complex concepts clearly and engage with employees at all levels.
• Fluent in English (written and verbal)
• Proven experience in global companies \ corporates


Reports To

Lital Michael

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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משרות נוספות שיכולות לעניין אותך

09.09.2025
T

Teva Associate Director Financial Risk Management Israel, Tel-Aviv District, Tel Aviv

Limitless High-tech career opportunities - Expoint
Identify and manage Teva’s FX exposure; design and execute risk management strategies to protect financial performance from market volatility. Forecast finance expenses and cashflows. Collaborate with Accounting, Tax, FP&A, and...
תיאור:
How you’ll spend your day

• Identify and manage Teva’s FX exposure; design and execute risk management strategies to protect financial performance from market volatility
• Forecast finance expenses and cashflows
• Collaborate with Accounting, Tax, FP&A, and Treasury to mitigate financial risks
• Drive automation and implement new systems and platforms
• Develop financial models, processes, and risk-management policies
• Ensure hedging accuracy, operational excellence, and compliance
• Prepare periodic reports and presentations for senior stakeholders
• Educate and train finance partners across the organization
• Participate in Corporate Finance & Financial Risk Management projects

Your experience and qualifications

• Academic degree in Economics, Accounting, Statistics, Finance or a quantitative field – must
• CPA / Advanced degree or MBA/FRM – advantage
• 4+ years’ experience in finance in multinational corporations or financial institutions (including internships) – must
• Experience in financial risk management – strong advantage
• Advanced Excel skills and passion for automating processes and leveraging AI
• Experience with data analytics tools such as Power BI, Tableau, SQL, or Python – advantage.
• Experience with Treasury systems – advantage
• Advanced presentation skills – able to communicate complex topics clearly and influence diverse audiences


Reports To

Sr. Dir Treasury

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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משרות נוספות שיכולות לעניין אותך

05.09.2025
GEH

GE HealthCare Production Associate Israel, Center District

Limitless High-tech career opportunities - Expoint
Reads and follows work procedures and schematics or receives verbal instructions regarding duties to be performed. Performs manufacturing/assembly operations and various tasks following procedures, bills of materials, work instructions, and...
תיאור:

Roles and Responsibilities:

Description: Responsibilities may include manufacturing, assembly, basic testing, packaging and shipping of products.

Essential Responsibilities

  • Reads and follows work procedures and schematics or receives verbal instructions regarding duties to be performed
  • Performs manufacturing/assembly operations and various tasks following procedures, bills of materials, work instructions, and process aid sheets
  • Maintains daily production output
  • Follows all EHS and Quality policies and procedures
  • May participate in quality control inspections
  • Works with team lead, engineers, supervisors, and managers to improve quality and process efficiency
  • Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams
  • Comply with EHS regulations and policies

Qualifications/Requirements

  • High School Diploma or local equivalent or 6 months of manufacturing experience
  • Ability to communicate, receive and understand instructions regarding duties to be performed
  • Demonstrated ability to detail and quality-minded work habits
  • Demonstrated ability to communicate with co-workers and leadership

Preferred Qualifications:

  • High School Diploma/GED or local equivalent
  • 2 or more years of related manufacturing experience
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משרות נוספות שיכולות לעניין אותך

Limitless High-tech career opportunities - Expoint
Collaborate with R&D Associates to determine/develop design-around formulations. Collaborate with outside counsel to determine/develop invalidity positions to relevant patents. Determine launch strategy, including labeling carve outs, and assess risk associated...
תיאור:
How you’ll spend your day
  • Collaborate with R&D Associates to determine/develop design-around formulations.
  • Collaborate with outside counsel to determine/develop invalidity positions to relevant patents.
  • Determine launch strategy, including labeling carve outs, and assess risk associated with launch.
  • Manage European Patent Office Oppositions and similar actions in national patent offices.
  • Manage Unified Patent Court revocations.
  • Collaborate with colleagues in other teams to ensure all global issues are addressed, including manufacturing site, device, and API issues.
  • Collaborate with Regulatory Affairs Associates to support regulatory submissions.
  • Collaborate with Portfolio Team to support identification of potential generic products for Teva’s European and International markets including providing IP landscapes and IP launch scenarios.
  • Collaborate with Business Development to determine launch strategy, including labeling carve outs, and assess risk associated with launch for in-licensed generic products.
  • Collaborate with Medis to support Medis’ out-licensing of Teva’s generic products.
  • Manage outside opinion counsel to ensure high quality work product on time and within budget.
Your experience and qualifications
  • Collaborate with R&D Associates to determine/develop design-around formulations.
  • Collaborate with outside counsel to determine/develop invalidity positions to relevant patents.
  • Determine launch strategy, including labeling carve outs, and assess risk associated with launch.
  • Manage European Patent Office Oppositions and similar actions in national patent offices.
  • Manage Unified Patent Court revocations.
  • Collaborate with colleagues in other teams to ensure all global issues are addressed, including manufacturing site, device, and API issues.
  • Collaborate with Regulatory Affairs Associates to support regulatory submissions.
  • Collaborate with Portfolio Team to support identification of potential generic products for Teva’s European and International markets including providing IP landscapes and IP launch scenarios.
  • Collaborate with Business Development to determine launch strategy, including labeling carve outs, and assess risk associated with launch for in-licensed generic products.
  • Collaborate with Medis to support Medis’ out-licensing of Teva’s generic products.
  • Manage outside opinion counsel to ensure high quality work product on time and within budget.
Reports To
Sr Dir Patent

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Show more
מגוון רחב של משרות כמו Associate - Ukig. למצוא עבודה בחברות נבחרות כבר לא יהיה חלום. Expoint מסייעת לכם למצוא את המשרות הנחשקות במגוון רחב של מדינות המובילות בעולם בהן תוכלו למצוא תפקיד מאתגר במדינה שיהיה לכם כיף לעבוד בה.