Jobs in Iceland as a Foreigner 2023 – Apply Now

Jobs in Iceland as a Foreigner: Are you thinking about working as a foreigner in Iceland? The kingdom of fire and ice offers a one-of-a-kind combination of breathtaking landscapes, a high standard of living, and a robust economy. This post will walk you through the steps of looking for work, navigating the labor market, and learning the prerequisites for working in Iceland.

Jobs in Iceland as a Foreigner 2023

Front End Developer

Skills

• Experience creating high-quality user interfaces with HTML, CSS, Bootstrap, and JavaScript.
• 2-3 years of expertise with Vue.js, Angular, or React (preference for Vue.js and Angular).
• Experience with web component libraries like Ionic, Vuetify, Tailwind, and others is preferred.
• Knowledge of ES6.
• Extensive experience developing custom general-purpose modules and components that enhance the fundamental Vue or Angular elements and modules.
• Integrating Restful APIs and external web services to provide good performance on mobile and desktop platforms.
• Knowledge of code versioning systems such as Git.

Process Engineer – Engineering Support

We are searching for many Engineering resources to join our Life Sciences team to support important projects for diverse pharmaceutical companies in Massachusetts and Southern New Hampshire (or other places based on interest). Candidates with a solid understanding of GMPs and expertise in providing engineering support in highly regulated pharmaceutical/biotech facilities are preferred.

Responsibilities

• Responsibilities will revolve around providing operational assistance for GMP manufacturing facilities.
• Equipment support and troubleshooting.
• Small project management and quality control.
• Understanding of the Manufacturing Systems Lifecycle methodology.
• CAPAs, deviations, and change control methods must be understood.

Qualifications

• 2+ years’ experience working in a GMP or highly regulated engineering setting is required.
• Ability to work independently on projects with client stakeholders in Validation, Quality, Manufacturing, and Maintenance, as well as other relevant individuals.
• Motivated, well-organized, and displays professional initiative.
• Takes responsibility for assignments and can work both independently and as part of a team.
• Capability to work in a fast-paced, demanding workplace.
• Excellent organizational skills, as well as the capacity to manage several activities at the same time.

Read More: How To Find A Job In Iceland 2023

Project Manager

We are searching for Project Managers and Project Coordinators to work on a variety of projects across the country. You will be expected to direct and manage MEP/CSA (Tool Install and Basebuild) project development from start to finish, as well as manage projects from start to finish- setting up a bid process or time/materials budget, tool shipping and receiving, tool set, install, and start-up.

Responsibilities

• Define project scope, goals, and deliverables in partnership with senior management and stakeholders to support business goals.
• Contact buying, trades, installation superintendents, and facilities management.
• Effectively and clearly convey project expectations to team members and stakeholders.
• Estimate the resources and manpower required to complete the project.
• Budget plans should be written and submitted, and any further budget modifications should be recommended.
• Identify and reduce project team challenges and conflicts; identify and manage project dependencies and critical path
• Using appropriate tools, plan and schedule project deadlines and milestones.
• Maintain a record of project milestones and deliverables.
• Create and provide progress reports, proposals, necessary documentation, and presentations.
• Proactively manage project scope changes, detect potential crises, and develop contingency measures.
• Members of the project team and contractors should be coached, mentored, motivated, and supervised.
• Conduct project lessons learned and collaborate to develop recommendations distinguishing project parts that were effective and those that were not
• Create best practices and tools for project management and execution.

Qualifications

• Experience in the semiconductor/microelectronics industry is preferred.
• Knowledge of Microsoft Office and the Windows Suite of Software.
• The ability to learn, comprehend, and apply new technologies is required.
• Strong customer service skills are required.
• It is critical to be able to prioritize and execute activities successfully in a high-pressure setting.
• Excellent time management and budgeting abilities.

Computer Systems Validation

We are searching for a seasoned Quality/Validation resource to join our Life Sciences team in Boston, MA to serve a pharmaceutical customer. This person will be largely responsible for aiding the Quality group with specification review and approval, user acceptability testing, and so on (particularly for Manufacturing Execution Systems – MES).

Ideal candidates will have prior experience preparing and reviewing CSV protocols, reports, and procedures for GMP controls and computerized systems, as well as reviewing and approving change controls and auditing CSV documentation for compliance with current corporate, FDA, and regulatory requirements. Candidates with a solid understanding of GMPs and expertise in providing engineering support in highly regulated pharmaceutical/biotech facilities are preferred.

Responsibilities

• Understand and execute Computer System Validation, System Development Life Cycle (SDLC), and other pharmaceutical equipment/system commissioning/validation (IQ/OQ/PQ) protocols in accordance with Good Engineering Practices, GAMP, local SOPs, industry best practices, and other industry related guidance documents.
• Assess the impact of modifications to cGMP equipment/systems and techniques, and develop the necessary Validation Plan to guarantee that the validated status is maintained following changes.
• Experience in technical writing and report development for automated system testing approaches.
• Validation protocol and summary report evaluation expertise.
• Strong knowledge of the Software Development Lifecycle and QA techniques.
• Responsible for serving as a quality contact and key Subject Matter Expert (SME) for complicated deviations in engineering, facilities, automation, manufacturing, and validation systems, processes, and equipment.
• Complex deviation investigations involving manufacturing process equipment, utilities, automation, validation, and engineering are supported and reviewed.
• Collaborate closely with Operations, Facilities, Manufacturing, Automation, Validation, and Engineering to handle outstanding issues caused by equipment failures, issues, and deviation record reviews.
• Lead the QA review and deviation assessments; this includes risk assessments, root cause analysis investigations, tracking, follow-up, closeout, and reporting/trending.

Qualifications

• 5+ years of demonstrated expertise in the pharmaceutical sector in cGMP automation/computerized systems, quality, and compliance domains.
• Comprehensive knowledge of industry standards and best practices for computer system validation.
• Experience validating equipment controlled by PLCs, BAS/BMS systems, DeltaV, and other common automated system platforms is preferred.

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