Expoint – all jobs in one place
המקום בו המומחים והחברות הטובות ביותר נפגשים

דרושים Quality Control Lead Analyst Biochemistry Cell Biology ב-Msd ב-אירלנד

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Quality Control Lead Analyst Biochemistry Cell Biology ב-Ireland והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו Msd. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
חברה (1)
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
Ireland
עיר
נמצאו 11 משרות
29.06.2025
MSD

MSD Quality Control Lead Analyst Biochemistry Cell Biology Ireland

Limitless High-tech career opportunities - Expoint
Develop and coach the Quality Control team and drive a high-performance organisational culture that accommodates rapid growth and highly dynamic expectations, ensuring attainment of site operational and development goals. Perform...
תיאור:

Job Description

Bring energy, knowledge, innovation to carry out the following:

  • Develop and coach the Quality Control team and drive a high-performance organisational culture that accommodates rapid growth and highly dynamic expectations, ensuring attainment of site operational and development goals.
  • Perform a variety of routine Biochemistry and Cell Biology analytical testing techniques and associated documentation; including but not limited to ELISA, PCR, Bioassays and Cell Culture, water and cleaning validation sample testing and compendial methods in compliance with GMP requirements.
  • Perform advanced assays requiring precise analytical skills and an understanding of biological and chemical principles.
  • Complete special project/protocol testing in a timely manner under direction of Project Leads and/or Area Lead.
  • Contribute to a team setting within the laboratory and project activities and potentially with other work teams to increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.
  • Provide support and expertise for the preparation of regulatory submissions, inspection readiness, health authority inspections including interaction with inspectors, responses to inspection observations, and monitoring of follow up actions.
  • Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation.
  • Champion site metrics to ensure targets are achieved, met and counter measures in place when applicable.
  • Consistently deliver on specific area Key Performance Indicators.
  • Operate to the highest standards of Safety, Quality, and Compliance.
  • Provide immediate feedback to others at any time to reinforce good safety and improvement behaviours and acts.
  • Provide coaching for the team members as part of the continuous improvement mindset.
  • Role model the behaviours that creates a culture of dignity and respect.
  • Responsible for being a designee for the people lead as required
  • Lead projects as required

What skills you will need:

In order to excel in this role, you will more than likely have:

  • A degree qualification in Science/Quality/Technical disciplines.
  • Minimum 4 years’ experience in the biotechnology and/or pharmaceutical industry, (preferably both) •
  • Leadership skills and experience managing daily activities.
  • Preferably Lean Six Sigma experience.
  • Excellent written and oral communication skills.
  • Strong understanding of cGMP requirements for manufacturing and/or systems and compliance.
  • Required to work on their own initiative in a constructive manner in addition to working as part of a team.
  • Excellent time management and organisational skills.
  • Strong understanding of biochemical and cell biology methodology (ELISA, SDS-Page, Bio-Assays, PCR, and compendial assays, e.g. pH, Appearance, TOC etc) and strong technical skills.
  • Strong understanding of GMP, ICH, USP and global compendia regulations and guidance's, particularly as related to analytical method development and validation.
  • Experience with continuous quality/process improvement tools (As defined by the site, e.g. DMAIC, Lean QA, 5S etc).
  • Excellent trouble shooting and problem solving skills.
  • Ability to think logically and be proactive under pressure.
  • Flexible and self-motivated.
  • Ability to challenge the status quo with a continuous improvement mindset.
  • Promoting a culture where diversity and inclusion is part of the DNA

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,please apply today.

Current Contingent Workers apply


Not Applicable

Analytical Instrumentation, Analytical Instrumentation, Animal Husbandry, Assay, Biochemical Assays, Biological Analysis, Cell-Based Assays, Cell Cultures, Cell Physiology, Chemical Analysis, Clinical Data Interpretation, Communication, Equipment Maintenance, GMP Compliance, Hazardous Waste Disposal, Hazardous Waste Management, Hazardous Wastes, Inventory Management, Laboratory Safety, Mammalian Cell Culture, Management Process, Microbiological Analysis, Personal Initiative, Polymerase Chain Reaction (PCR), Qualitative Testing {+ 5 more}


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more
29.06.2025
MSD

MSD Associate Director – Site Procurement Lead Dundalk Ireland

Limitless High-tech career opportunities - Expoint
Lead strategic sourcing and project execution using the Sourcing Management Process (SMP). Drive supplier performance, cost reduction, and risk mitigation initiatives. Manage supplier relationships, including performance reviews and continuous improvement....
תיאור:

Job Description

is responsible fordriving procurement strategy and execution to support site operations and growth. You will lead key sourcing initiatives, manage supplier relationships, and partner with internal and external stakeholders to deliver value, innovation, and compliance.

Key Responsibilities

  • Lead strategic sourcing and project execution using the Sourcing Management Process (SMP).

  • Drive supplier performance, cost reduction, and risk mitigation initiatives.

  • Manage supplier relationships, including performance reviews and continuous improvement.

  • Support new product introductions from early design through to launch.

  • Ensure compliance with procurement policies and regulatory requirements.

  • Champion supplier diversity and working capital improvements.

  • Collaborate with cross-functional teams and global/regional partners to align procurement goals with business needs.

  • Provide procurementexpertise


  • , Engineering, Science, Supply Chain, ora relatedfield

  • 5+ years of procurement and project management experience in aGMP manufacturingenvironment.

  • Experience working with senior leaders on large-scale change initiatives.

  • Proven ability to influence sourcing decisions during early product development.

  • Excellent negotiation, communication, and stakeholder engagement skills.

  • Strong project management capabilities and a continuous improvement mindset.

Current Contingent Workers apply

Language(s) Job Description:

hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more

משרות נוספות שיכולות לעניין אותך

29.06.2025
MSD

MSD Production Lead – Operations Ballydine Co Tipperary Ireland

Limitless High-tech career opportunities - Expoint
Lead and develop a high-performing. Drive operational excellence byidentifyingand implementing process improvements using Lean tools (e.g., Value Stream Mapping, 5S). Ensure compliance with Good Manufacturing Practices (GMP), environmental, health, safety,...
תיאור:

Key Responsibilities

  • Lead and develop a high-performing

  • Drive operational excellence byidentifyingand implementing process improvements using Lean tools (e.g., Value Stream Mapping, 5S).

  • Ensure compliance with Good Manufacturing Practices (GMP), environmental, health, safety, and labor regulations.

  • Manage production schedules, inventory, costs, and performance metrics to meet business targets.

  • Support strategic development of first-line leaders, equipping them with the tools and skills to lead effectively.

  • optimizeworkflows.

  • Serve as the primary contact for union-related matters and ensure adherence to trade union agreements.

Bring

  • Honours degree in Engineering or Science.

  • Proven experience inGMPmanufacturing.

  • Demonstrated leadership experience, including managing other leaders.

  • Strong knowledge of regulatory standards and compliance.

  • Experience with Lean and Six Sigma methodologies.

  • for talent development and team growth

Current Contingent Workers apply

Language(s) Job Description:

hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,


Not Applicable

Aseptic Operations, Aseptic Operations, Business, Communication, Cost Management, Decision Making, Good Manufacturing Practices (GMP), Improvement Projects, Interpersonal Relationships, Lean Manufacturing, Lean Six Sigma Process Improvement, Management Process, Manufacturing Processes, Manufacturing Quality Control, Packaging Processes, People Leadership, Pharmaceutical Manufacturing, Pharmaceutical Systems, Prioritization, Process Improvements, Production Operations, Production Ramp Up, Production Scheduling, Productivity Improvements, Quality Management {+ 4 more}


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more

משרות נוספות שיכולות לעניין אותך

29.06.2025
MSD

MSD Director Quality Ireland, Cork

Limitless High-tech career opportunities - Expoint
Ensure the highest Compliance standards. Ensure supply of high-quality product in line with testing schedules. A Integral Member of the Site Quality leadership team (QLT) and the Site Leadership Team...
תיאור:

Job Description

The Laboratory Operations Leader will provide strategic and operational leadership to the Laboratories to test quality pharmaceutical products in meeting the four Manufacturing Division priorities of: Compliance, Supply, Strategy and Profit Plan.

The Laboratory Operations Leader is responsible to mould the culture to one that supports a High-Performance Organisation.

personal accountability and responsibility, continuous self- development and colleague collaboration in an open and trusting environment where all colleagues are comfortable to voice their opinions The Laboratory Operations Leader is responsible for prioritization of proposed mitigation plans and/or acceptance of Quality Risks identified as part of the Quality Risk Management Process under the remit of decision maker roles and responsibilities (as required)

Primary activities/responsibilities:

  • Ensure the highest Compliance standards.
  • Ensure supply of high-quality product in line with testing schedules. A Integral Member of the Site Quality leadership team (QLT) and the Site Leadership Team (SLT) on key operational and strategic priorities
  • Work as a key member of the Site Extended leadership team (ELT)
  • Provide sound financial stewardship, management, and control.
  • Lead a cross-functional management team providing ongoing coaching and support, including the identification and development of key talent.
  • Drive performance and management of individuals and team.

What Qualifications you will need:

  • Degree or 3rd level qualification (Science, Engineering, Quality).
  • Desirable project management qualification such as Project
  • Management Professional etc.
  • Desirable Lean Six Sigma Green belt or higher

So, if you are ready to:

Current Contingent Workers apply


Not Applicable

Analytical Method Development, Analytical Method Development, Analytical Thinking, Aseptic Manufacturing, cGMP Compliance, Change Management, Coaching, Decision Making, Driving Continuous Improvement, Financial Management, Financial Performance Management, Management Process, Mitigation, Motivation Management, People Leadership, Pharmaceutical Quality Control (QC), Pharmaceutical Systems, Quality Assurance Processes, Quality Management, Quality Risk Assessment, Regulatory Compliance, Regulatory Experience, Regulatory Requirements, Risk Mitigation Strategies, Six Sigma {+ 4 more}


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more

משרות נוספות שיכולות לעניין אותך

29.06.2025
MSD

MSD Associate Director Bioprocess Lead Ireland, Dublin

Limitless High-tech career opportunities - Expoint
Imbibe the product related features/benefits including scientific information thereto, so as to effectively communicate with the medical doctors and handle product related customer queries. Utilize customer focused selling techniques (CSSP),...
תיאור:

Job Description

THERAPY MANAGER

Therapy Manager is responsible for Efficiently manage the therapy area by effectively reaching out to customers and increases product awareness, answer queries and introduce new products. Also responsible for Customer Focus and have industry knowledge and schedule and plan the frequency of calls and personally visit the targeted doctors as per agreed coverage list.

WHAT YOU WILL DO

  • Imbibe the product related features/benefits including scientific information thereto, so as to effectively communicate with the medical doctors and handle product related customer queries
  • Utilize customer focused selling techniques (CSSP), continually assessing the knowledge of the customer and strategize to maintain high customer confidence and customer knowledge of companyproducts.
  • Maintain current, approved protocol (CSSP) and promotional materials to be included in sales presentation/ detailing.
  • Contact customers on regular basis and deliver informative sales presentations based on customers need.
  • Explore opportunities to develop new business in the assigned therapy area.
  • Achieve and exceed the sales targets on a consistent basis through effective implementation of the sales promotion strategies and scientific initiatives.
  • Constantly update the knowledge of disease and product area so as to facilitate scientific discussion with stakeholders to enhance productivity levels as expected by the Company.
  • Carry out Product Visibility and such ancillary or incidental activities related to the Products of the Company or Products of any other Company as may be decided from time to time, in accordance with any arrangement or agreement entered by the Company with such other Company.
  • Explore opportunities to develop new business avenues for assigned therapy area and territory.
  • Tactically plans to generate tertiary demand generation.
  • Plans and executes field working as per approved tour programs and reports into data management system at regular intervals as per company expectations.
  • Takes follow-up initiatives on feedback and customer service requirements.
  • Handles special product campaigns, new product launch campaigns as per Company’s plans.
  • Covers the Nursing homes, clinics and hospitals as per agreed coverage requirements.
  • Assists in the collection of receivables, as per company policy.
  • Work collectively with other team colleagues in arranging speakers, displays, special programs and CMEs to meet the educational needs of customers.

WHAT YOU MUST HAVE

  • Degree in Sciences / B Pharm
  • Pediatric Vaccine experience is a must.
  • 2 to 7 year’s relevant sales experience
  • Proven experience in articulating data-driven findings to various audience levels and translating these findings into actionable recommendations.
  • Relevant experience in therapeutic segment
  • Must have vaccine knowledge and selling experience at corporate hospitals with Peads,
  • B. Science / B. Pharmacy

WHAT YOU CAN EXPECT

  • You will be a part of highly motivated sales team that seek to innovate in order to improve lives.

Current Contingent Workers apply


Not Applicable


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more

משרות נוספות שיכולות לעניין אותך

28.06.2025
MSD

MSD Site Services Shift Lead Maintenance Technician Ireland

Limitless High-tech career opportunities - Expoint
Act as the escalation point of contact for all out of hours Site Services related issues. Act as Site shift ERT lead and ensure all ERT Daily and weekly checks...
תיאור:

Job Description

Bring energy, knowledge, innovation to carry out the following:

  • Act as the escalation point of contact for all out of hours Site Services related issues.
  • Act as Site shift ERT lead and ensure all ERT Daily and weekly checks are performed.
  • Be the first point of contact in relation to Quality event s related to site services.
  • Shift lead will be a Site Standard Owner for selected Safety Standards and SOPs ensuring that the department is compliant with global standards.
  • Manage all EM (Environmental Monitoring) sampling actives out of hours.
  • Support the implementation of both sustainability and CI project on an ongoing basis.
  • Ensure that all relevant maintenance activities are carried out as per site policies, schedules and procedures and in-line with site work schedule.
  • Ensure complete execution on time of the Preventive Maintenance on Site Services equipment.
  • Ensure all Site Services equipment is available and operational at all times.
  • Conduct area safety Audits, document and report all noncompliance on Enablon.
  • Conduct area Quality Audits, document and report all noncompliance on site reporting system.
  • Responsible for the correct closure of all safety permits at the end of each shift.
  • Mange all WWT systems operations out of hours.
  • Responsible for the creation and of GMP documentation related to the Site Services including WI, SOPs and Forms.
  • Clock works super user. Review and create CM based on clock works reports.
  • Act as Site service area owner managing the Permit to Work system and conducting vendor review assessments
  • Delivery of ILT training on select equipment in support of site training curricula.
  • Perform contractor evaluation for all works carried out on equipment and areas owned by the site services team.
  • Support all site commissioning and qualification activities
  • Implementation of MPS working principles including 8 Step problem solving.
  • Support all vendor visits related to Site Services.
  • Collaborate with relevant hubs to deliver the site objectives.

What skills you will need:

In order to excel in this role, you will more than likely have:

  • Trade Certificate, City & Guilds or equivalent in Mechanical / Electrical / Instrumentation discipline.
  • Level 7 Engineering degree desirable.
  • At least 4-5 years’ experience in a similar leadership role within the pharmaceutical industry.
  • Good knowledge of Systems including HVAC, Steam, water, Process gases, clean steam, Water for Injection, Chilled water systems, CTUs Wastewater system and fire systems.
  • Strong computer skills
  • Excellent communication, interpersonal, and team-working skills.
  • Good understanding of the operation of automated and control systems
  • Ability to work independently and as a member of a team in a dynamic, fast-paced environment.

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,please apply today.

Current Contingent Workers apply


Not Applicable

Building Automation Systems, Building Automation Systems, Computerized Maintenance Management Systems (CMMS), Consumer Complaint, Customer Experience Management, Electrical System Troubleshooting, Environmental Monitoring, Environmental Monitoring Systems, GMP Compliance, HVAC Engineering, HVAC Maintenance, HVAC Systems, Hydraulic Systems, Instrumentation Systems, Instrument Calibrations, Interpersonal Communication, Maintenance Strategy, Management Process, Manufacturing Equipment, Mechanical Troubleshooting, Operational Efficiency, People Management, Pneumatic Systems, Preventive Maintenance, Prioritization {+ 5 more}


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more

משרות נוספות שיכולות לעניין אותך

28.06.2025
MSD

MSD Associate Director QA Lead - Drug Product Dundalk Ireland

Limitless High-tech career opportunities - Expoint
Act as site QA responsible for onsite quality monitoring of DP manufacturing andparticipatein GMP production activities. Monitor the construction quality of GMP production and support CQVactivitiesas necessary. Create department SOPs...
תיאור:

Job Description

Associate Director. In this role, you will be pivotal in ensuring our GMP production quality system meets all regulatory, cGMP, and company requirements. Yourwill uphold ourhigh standards

Your Core Responsibilities

  • Act as site QA responsible for onsite quality monitoring of DP manufacturing andparticipatein GMP production activities.

  • Monitor the construction quality of GMP production and support CQVactivitiesas necessary.

  • Create department SOPs in collaboration with functional departments, ensuring alignment with corporate policies.

  • Audit quality documents to ensure data integrity andprovideQA guidance.

  • Support site GMP Readiness preparation activities, including the internal self-inspection program.

  • Establish and manage the DP QA team, providing online support and ensuring performance management requirements are met.

  • Review and approve manufacturing-generated documents, ensuring compliance with regulatory standards.

  • Liaise with cross-functional teams for DP release and prepare necessary documentation for QP release.

Who You Are

You are ready if you have:

  • Qualification Degree in Biopharmaceutical Science or other related science discipline.

  • Knowledge of legislative, regulatory, market and data integrity requirements.

  • Relevant experience in vaccine/biopharma or similar pharma/science background.

  • track recordin people management, problem-solving, and interpersonal skills.

  • Proven ability to lead continuous improvement initiatives to enhance quality standards and operational efficiency within the QA team.

  • Aprocesses and address issues promptly.

  • Strong leadership skills, including strategic planning, innovation, and talent development, with a commitment to diversity, equity, and inclusion.

  • Strong communicationskills with the ability to work in a matrix environment.

Current Contingent Workers apply

Language(s) Job Description:

hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,


Not Applicable


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more

משרות נוספות שיכולות לעניין אותך

Limitless High-tech career opportunities - Expoint
Develop and coach the Quality Control team and drive a high-performance organisational culture that accommodates rapid growth and highly dynamic expectations, ensuring attainment of site operational and development goals. Perform...
תיאור:

Job Description

Bring energy, knowledge, innovation to carry out the following:

  • Develop and coach the Quality Control team and drive a high-performance organisational culture that accommodates rapid growth and highly dynamic expectations, ensuring attainment of site operational and development goals.
  • Perform a variety of routine Biochemistry and Cell Biology analytical testing techniques and associated documentation; including but not limited to ELISA, PCR, Bioassays and Cell Culture, water and cleaning validation sample testing and compendial methods in compliance with GMP requirements.
  • Perform advanced assays requiring precise analytical skills and an understanding of biological and chemical principles.
  • Complete special project/protocol testing in a timely manner under direction of Project Leads and/or Area Lead.
  • Contribute to a team setting within the laboratory and project activities and potentially with other work teams to increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.
  • Provide support and expertise for the preparation of regulatory submissions, inspection readiness, health authority inspections including interaction with inspectors, responses to inspection observations, and monitoring of follow up actions.
  • Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation.
  • Champion site metrics to ensure targets are achieved, met and counter measures in place when applicable.
  • Consistently deliver on specific area Key Performance Indicators.
  • Operate to the highest standards of Safety, Quality, and Compliance.
  • Provide immediate feedback to others at any time to reinforce good safety and improvement behaviours and acts.
  • Provide coaching for the team members as part of the continuous improvement mindset.
  • Role model the behaviours that creates a culture of dignity and respect.
  • Responsible for being a designee for the people lead as required
  • Lead projects as required

What skills you will need:

In order to excel in this role, you will more than likely have:

  • A degree qualification in Science/Quality/Technical disciplines.
  • Minimum 4 years’ experience in the biotechnology and/or pharmaceutical industry, (preferably both) •
  • Leadership skills and experience managing daily activities.
  • Preferably Lean Six Sigma experience.
  • Excellent written and oral communication skills.
  • Strong understanding of cGMP requirements for manufacturing and/or systems and compliance.
  • Required to work on their own initiative in a constructive manner in addition to working as part of a team.
  • Excellent time management and organisational skills.
  • Strong understanding of biochemical and cell biology methodology (ELISA, SDS-Page, Bio-Assays, PCR, and compendial assays, e.g. pH, Appearance, TOC etc) and strong technical skills.
  • Strong understanding of GMP, ICH, USP and global compendia regulations and guidance's, particularly as related to analytical method development and validation.
  • Experience with continuous quality/process improvement tools (As defined by the site, e.g. DMAIC, Lean QA, 5S etc).
  • Excellent trouble shooting and problem solving skills.
  • Ability to think logically and be proactive under pressure.
  • Flexible and self-motivated.
  • Ability to challenge the status quo with a continuous improvement mindset.
  • Promoting a culture where diversity and inclusion is part of the DNA

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,please apply today.

Current Contingent Workers apply


Not Applicable

Analytical Instrumentation, Analytical Instrumentation, Animal Husbandry, Assay, Biochemical Assays, Biological Analysis, Cell-Based Assays, Cell Cultures, Cell Physiology, Chemical Analysis, Clinical Data Interpretation, Communication, Equipment Maintenance, GMP Compliance, Hazardous Waste Disposal, Hazardous Waste Management, Hazardous Wastes, Inventory Management, Laboratory Safety, Mammalian Cell Culture, Management Process, Microbiological Analysis, Personal Initiative, Polymerase Chain Reaction (PCR), Qualitative Testing {+ 5 more}


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more
בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Quality Control Lead Analyst Biochemistry Cell Biology בחברת Msd ב-Ireland. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.