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  • £35 - £40/hour
Are you currently looking for your next contract opportunity with an Innovative and forward-thinking design consultancy as a Senior Mechanical Design Engineer? The client we are currently working with are an established and successful consultancy looking to bring on a dynamic Senior Mechanical Design Engineer to come and join them in their Bournemouth office on a rolling contract. They are looking for someone that can hit the ground running and work on some of their more high-profile projects from the get go. The Ideal candidate will have extensive experience in the residential, commercial & retail industry. This would be an ongoing contract so offers a lot of longevity for the right candidate. Senior Mechanical Design Engineer Requirements: * Degree or HNC in building services/ mechanical engineering * Exemplary design skills within the building services environment * At least 7 years’ experience within a design role within a building services consultancy * CEng or working towards chartership * Ability to mage multiple projects at one time * Good knowledge of a variety of design software If you are interested in working with this dynamic and fast paced consultancy as a Senior Mechanical Design Engineer, then apply now
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  • £5649 - £10000/month TAX FREE + Housing + Flights + Transp
ROLE: TUNNEL Design / Tunnel Design Coordinator – South America LNGUAGES: Fluent SPANISH is Essential, Good English is preferable PROJECT: Major Water tunnel (TBM + NATM) - Global Western Contracting co. SALARY: Neg (approx 8-13K USD Year Tax Free + expat package) Level Approx 7- 20 yrs experience Education: Min BSc in Civil / Geotech / Tunnel Eng. or similar My client is a world leading Contracting company with offices globally. Highly prestigious major water tunnel, more than 20KM Long, using both TBM and Drill Blast You will be working in the design office, both on design and with a heavy emphasis coordinating designs both internally with different depts locally and Internationally and with external partners You should have a strong background in tunnel design, a mixture of both Geotechnical / Civil + Structural design experience would be ideal. Experience of working in South America on Major tunnelling, MRT, Civil or Hydropower projects would be a bonus Please contact Ben at Intec (UK) Ltd to apply or for a discrete discussion. = = = = Intec (UK) Ltd was established in 1980 by Engineers for Engineers. We deliver Global Recruitment Solutions within the Oil & Gas, Power, Nuclear, Utilities, Rail, Construction and Aerospace Sectors for Owner/Operators, Consultancies, Contractors and Sub-Contractors. Intec (UK) Ltd is an equal opportunities employer and a member of the Recruitment and Employment Confederation (REC)
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  • £4035 - £5649/month Tax free + Housing + Bonus
ROLE: Contract manager - Mining Specialist – South America (MUST HAVE MINING EXPERIENCE) LNGUAGES: Fluent SPANISH is Essential, Good English is preferable PROJECT: Major Mine facility SALARY: Neg (approx. 5-6K USD Year, Tax Free + expat package) Level Approx. 7- 20 yrs experience Education: Min BSc in Mine Eng, Geotech / Civil or similar My client is a world leading company with offices globally. They also have a large mining division You will be working in a very busy site office, being instrumental in the delivery of all parts of the contract, working with the client and sub-contractors, dealing with claims and disputes and drawing up new contracts as work demands using Intl Contract Standards Experience in either contract Management in Mining or coming through as a Mine engineer who's moved into contract management would be equally interesting A strong understanding of the mining industry is ESSENTIAL as is Fluent Spanish and good English Please contact Ben at Intec (UK) Ltd to apply or for a discrete discussion. = = = = Intec (UK) Ltd was established in 1980 by Engineers for Engineers. We deliver Global Recruitment Solutions within the Oil & Gas, Power, Nuclear, Utilities, Rail, Construction and Aerospace Sectors for Owner/Operators, Consultancies, Contractors and Sub-Contractors. Intec (UK) Ltd is an equal opportunities employer and a member of the Recruitment and Employment Confederation (REC)
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  • £112994 - £129136/annum Tax Free + Housing + Flights etc
ROLE: Tunnel Site Supervisor / Manager (including strong design experience) PROJECT: Major Water tunnel South Africa - TBM + Drill Blast LOCATION: South Africa SALARY: Neg (approx 130K-150K USD/Year Tax Free + expat package) Level - 18+ yrs experience Education: Min BSc- Eng Geology, Civil Eng, Tunnelling. Ideally Chartered Eng My client is a world leading design company with offices globally. Highly prestigious major water tunnel, more than 20KM Long, using both TBM and Drill Blast You will be supervising and managing tunnel construction. You MUST have a very strong background supervising major TBM and Drill and Blast tunnels, ideally with a strong Intl background working for respected global companies You will be responsible for managing the projects Financially, preparing budgets and targets are met and setting targets. Liaising with and negotiating with sub-contractors Responsible for Heal and Safety and Quality of material and work. Although you will not be doing the Design, You MUST have a good background in design of tunnels Please contact ben at Intec (UK) Ltd to apply or for a discrete discussion. = = = = Intec (UK) Ltd was established in 1980 by Engineers for Engineers. We deliver Global Recruitment Solutions within the Oil & Gas, Power, Nuclear, Utilities, Rail, Construction and Aerospace Sectors for Owner/Operators, Consultancies, Contractors and Sub-Contractors. Intec (UK) Ltd is an equal opportunities employer and a member of the Recruitment and Employment Confederation (REC)
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For one of my clients in the Germany we are looking for a Systems Engineer specialised in Functional Safety for coordinating Functional Safety activities in an Automotive Project.

Estimated duration of this activity would be 9-12 months.

This includes developing:

  • a Safety Plan
  • a Technical Safety Concept
  • a safety assessment plan

She/He should also:

  • Support product development to implement safety strategies and validate them
  • Support quality management to define internal processes and templates to meet ISO26262 requirements

She/He should also take the role of a Safety Manager as defined in ISO26262:

- Maintaining a Safety Plan and monitoring progress

- Planning of activities and procedures for achieving functional safety

- Implementation of project independent safety activities (eg organization specific rules, evidence of competence, evidence of quality management)

- Definition of tailored activities

- Planning of the hazard analysis and risk assessment

- Planning of development activities

- Planning of the development interface agreement (DIA)

- Development of supporting processes

- Planning of verification activities

- Planning of confirmation reviews

- Planning of analysis of dependent failures

- The provision of the confidence in the usage of software tools

The candidate should have practical experience with automotive projects applying ISO26262. She/He should also understand lighting electronics and the technical impacts to safety assessments. Ideally she/he would have worked as a safety manager.

If you're available, either immediately or in the future, send your CV to Aleksandra Wisna

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For one of our Clients in Germany we are looking for a Firmware/Software Development Engineer.

The core skills needed are as follows:

  • Development of Embedded software for our data acquisition systems mainly in area Digital Signal Processing,
  • Hardware-close programming in cooperation with the hardware designer engineers
  • Embedded software development in Linux operating system
  • Experience in wireless technologies (Ultra-Wideband, Wi-Fi)

If you are available now or will be soon, please do get in contact with Aleksandra Wisna via contact details.

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Hi,

This is Rohini with SSI, We have an immediate opening for Quality Engineer PM Consultant III with our Direct client. If you are interested please reach me with your Updated Resume

Title: Quality Engineer PM Consultant III

Duration: 9months (will extend after that)

Location: Bothell WA 98021

Responsibilities include:

  • Working in the medical industry brings much fulfilment, as well as unique challenges. As part of our HealthTech focused company, you will be responsible for successfully dealing with and managing Philips relationships with approval agencies such as the US Federal Drug Administration (FDA).
  • Project manage all aspects of CAPA activity which includes gaining the commitment of cross functional resources, scheduling CAPA team meetings, and ensuring CAPA deliverables per project timelines.
  • Represent CAPAs during audits and CAPA Review Board meetings.
  • Lead and mentor cross functional teams with the implementation of appropriate root cause analysis techniques (eg Pride problem solving).
  • Analyse quality monitoring data sources and apply statistical techniques to identify existing and potential causes of non-conformances.
  • Work effectively with all levels of management to ensure CAPA action plans can be supported and that costs/resources needed to implement the plan are available.
  • Perform periodic trend analysis and corrective action effectiveness measures of all quality system events and identify opportunities for improvement.

We are looking for:

  • A person who is excited by the unique professional challenges that our Quality Transformation presents, has strong technical competencies, and demonstrates resilience challenging, often demanding situations. We are looking for a perfectionist- a fixer who continuously strives for excellence as a way of life; not just as a job. We're looking for someone who can inspire others to adopt this mentality of prioritizing quality above all else in a relentless pursuit to improve the quality of life billions for the billions of people Philips brand touches each year.

Requirements:

  • Able to understand and analyze complex problems, including software and hardware design issues.
  • Demonstrated knowledge of tools and techniques required to perform thorough root cause analysis and develop strong investigations.
  • Strong understanding of appropriate global regulations, requirements, and standards such as 21 CFR Parts 803, 806, and 820, ISO 13485, ISO 9001 and ISO 14971.
  • Demonstrated ability to partner with the business and effectively interact with and influence employees, and managers on all levels.
  • Strong Project Management skills, including ability to project manage all CAPA activities.
  • Ability to analyze data and apply statistical techniques.
  • Excellent written and verbal communication skill
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Hi,

This is Rohini with SSI, We have an immediate opening for QA Engineer Consultant II with our Direct client. If you are interested please reach me with your Updated Resume

Title: QA Engineer Consultant II

Duration: 12months (will extend after that)

Location: North Maple Grove MN 55311

Description:
What You Will Do:

  • You will be supporting R&D integration efforts, including the remediation of Risk Files of Legacy SPNC Products. Activities include creating of Risk Management Matrix, converting from Legacy FMEA template's to Philips FMEA templates, assess risks to new risk classifications, identify gaps is previous verification and validation activities and then address gaps as needed.

What Success Looks Like:

  • Create Risk Management Matrix for Legacy products, using the PHA's, DFMEA, UFMEA and complaint history.
  • Convert Legacy UFMEA, DFMEA and PFMEA into new templates, developing language that is more patient focused.
  • Reassess Risk Classifications using new templates and identify where Risk Classifications have increased.
  • Identify gaps in verification, validation or component qualification testing occur due to a change in Risk Classification and develop and execute a plan to close gap.
  • Collaborate with Development Engineering and Design Assurance Engineering stakeholders to develop strategies and review work.
  • Tracks and reports progress and will communicate any identified risks or delays to projects.

Desired Experience:

  • B.S. of Mechanical, Chemical, Industrial, Materials or Biomedical Engineering or similar field
  • 5 years of experience working in verification and validation of Medical Devices as a Quality Engineer or Development Engineer.
  • Must have experience in applying Risk Management using a life cycle approach.
  • Working knowledge of 21 CFR 820, ISO 13485, and ISO 14971.
  • Experience creating FMEA's, writing test protocols and reports and developing engineering justifications.
  • Experience with MS Word and MS Excel.
  • Ability to travel up to 10%.
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Hi,

This is Rohini with SSI, We have an immediate opening for EU MDR R&D Engineer with our Direct client. If you are interested please reach me with your Updated Resume

Title: EU MDR R&D Engineer

Duration: 6months (will extend after that)

Location: San Diego CA 92130

Comments:

  • The position is located in the San Diego office.
  • There is 0% travel required for this position.

Update/Skills Required:

  • We are looking for someone who has familiarity with EU MDR (meaning the new EU Medical Device Regulations replacing the EU MDD) and not MDR as in "Medical Device Reporting" (complaint investigation/handling).

EU MDR R&D Engineer

Description:
In this role, you have the opportunity to

  • As the Medical Device Development Engineer for Philips IGT-Devices, you will apply your technical expertise to bring current and new products into Compliance with new EU Medical Device Regulations.
  • This is a temporary role for 6 months and may be extended.

You are responsible for

  • Coordinate with Quality/Design Assurance to evaluate post-market data
  • Generating and maintaining technical drawings and detailed design documentation
  • Identifying, optimizing, and implementing design/process changes on existing product and update Product DHF's to achieve compliance with Regulations (specifically, EUMDR, RoHS and REACH).
  • Generating test protocols, analysing test data, and generating written reports
  • Contributing to design documentation including input for the DHF and technical design reviews

You are a part of

  • The R&D team within the Image Guided Therapy Devices (IGTD) business group is a team that is driven to providing products and solutions, working collaboratively within and across business groups.

To succeed in this role, you should have the following skills and experience

  • Bachelors of Science in Engineering (Mechanical Engineering, Material Science, Plastics Engineering, or Biomedical Engineering preferred)
  • Minimum of 5 years of Medical Device Industry experience.
  • Experienced with Design Controls and Medical Device Regulations (MDD & MDR, preferably).
  • Experience with creating and managing product DHF's (familiarity with electronic DHF's - ie Windchill preferred)
  • Strong understanding of Design Controls (Product Requirements, Design Inputs, Design Outputs)
  • Experience with Solidworks and Statistical Software applications preferred
  • Knowledge of EU MDR 2017 and ISO 13485:2016 Regulations is preferred
  • Understanding of RoHS and REACH Regulations is preferred
  • Familiarity with cardiology catheterization procedures, tools, and terminology preferred
  • Ability to work in a team environment to ensure conducive working relationships.
  • Demonstrate organizational and interpersonal skills working in a cross-functional, regulated environment
  • Strong analytical skills.
  • Ability to organize and prioritize workflow in order to meet established time frames and schedules.
  • Proficiency in Microsoft Word, Excel, PowerPoint,
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Hi,

This is Rohini with SSI, We have an immediate opening for Process Engineer Consultant II with our Direct client. If you are interested please reach me with your Updated Resume

Title: Process Engineer Consultant II

Duration: 6months (will extend after that)

Location: Fremont CA 94555

Description:

  • "Experience: Minimum 12 years professional experience in the applicable role. E Education: Bachelor's/Master's degree in Engineering. Experience with drug-device combination devices preferred. Expert and technical lead with proven experience. Guide and participate in test method validation, risk assessment, requirement development, protocol and validation report writing.
  • Maintain, Validate and Release Test Systems in Production Environment, ideally in FDA regulated business. Firm understanding of IQ, OQ, PQ and Software Validation requirements and practices. Expertise in PFMEA, Gage R&R, test system and manufacturing software validation for medical devices within manufacturing environment.
  • Ability to learn and adapt to Philips QMS and work closely with Philips Engineering community on new validation methods and re-validation projects. Guide and participate in bug testing, identification, and problem solving, oversees the validation process, the QMS system and participates in the Internal Quality Audits. Write and maintain FDA level validation protocols and reports. Support quality planning activities on new and existing programs.
  • Investigate customer quality issues and requests. Interpret and implement ISO9000/13485 and FDA standards. Support internal audits. May require focus on CAPA execution in Operations."
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