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LEAD CRA / PRINCIPLE CRA - Netherlands, Utrecht - Growing CRO

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An excellent opportunity has arisen for a Lead CRA to join a growing CRO based near Utrecht, Amsterdam. As a Lead CRA you will oversee the daily management of trials, ensuring that projects are completed to contract, budget and on time. Working closely alongside Project Managers and CRAs, this is an interesting role that will allow development with an expanding CRO.

 COMPANY BACKGROUND:

With over 30 offices across Western, Central, Eastern Europe and the U.S. this is truly a global CRO. Due to recent bid success they are looking to recruit talented and experienced individuals to manage phase I-IV international trials.

ROLE RESPONSIBILITIES:

As a Lead CRA you will be responsible for the day-to-day running of clinical studies with operational oversight including:

• Lead monitoring team
• Deliver project on time, budget and to contract
• Investigator recruitment
• Resource allocation

Excellent role for an experienced CRA to move into more senior/operational role

SKILLS DESIRED:

• CRA monitoring background – 5 years
• International Phase I-IV project exposure
• Pharma or CRO experience
• Life Science Degree

Commutable locations: Near Utrecht, Netherlands

Salary: €55,000 - €65,000 + Benefits

Full job description and company details are available upon application, apply below. This position is being dealt with by Jack Doyle at meet, call on +44 203 178 7488 or email directly at jack@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Senior CRA, CRA, CTC, CTA, Clinical, Research, Associate, Trial, Project Management, Utrecht, Netherlands, Senior CRA, CRA, CTC, CTA, Clinical, Research, Associate, Trial, Project Management, Utrecht, Netherlands


Clinical Research Associate

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Clinical Research Associate (CRA)/6 month Contract/Immediate Start/ Homebased/UK

Clinical Research Associate (CRA)/6 month Contract/Immediate Start/ Homebased/UK

CRA/ Clinical Research Associate required in UK for December start to join a world leading CRO to work on a number of exciting studies.

Job description:
This is a home based position with the chance to work on a number of exciting studies. The chosen candidate will have a number of sites regionally to visit - allocating 3 days a week to monitor these delegated sites.

Requirements:
A good self starter; excellent communication skills; confident; strong attention to detail; highly organised.
Bachelor's Degree from a Life science, science, medical, pharmacy, healthcare related discipline.
Previous CRA II experience is essential and 2 years + monitoring. Must have a valid drivers licence .

Start Date:
ASAP

Duration:
6 Months

Key Words:
Clinical research associates/Immediate Start / home based/ 6 months/ Freelance/ UK

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
www.i-pharmconsulting.com

TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Aoife Cronin on +44 (0)20 3189 0464, or email acronin@i-pharmconsulting.com. If this role is not suitable, Aoife is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

Lead Clinical Research Associate

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Principle CRA, Cambridge, 6 Month Contract, Biotech

Principle CRA required to join a leading Biotech to work on an exciting study. This is one of the largest studies for this division of the company, spanning across 13 countries and covering 90 sites which has entered its' Interim Analysis stage. This is a 6 month office based contract at their Cambridge offices. ... Principle CRA, Cambridge, 6 Month Contract, Biotech

Principle CRA required to join a leading Biotech to work on an exciting study. This is one of the largest studies for this division of the company, spanning across 13 countries and covering 90 sites which has entered its' Interim Analysis stage. This is a 6 month office based contract at their Cambridge offices.

POSITION:
Contract - 6 months Initially, intensions for it to extended

LOCATION:
Cambridge, East Anglia, Cambridgeshire, UK

JOB DESCRIPTION:
The role is for the hands-on type of individual who enjoys working in a vibrant and busy enviornment. You will lead the study and be a point of contact for the various sites. You will be acting as a program manager and a point of contact for the various vendors involved in the study. You will be required to go monitoring once a month. This position requires you to be a point of contact between the company and the various CROs who thye have outsourced their studies to.

REQUIRED:
4+ years experience within a similar position
Strong European clinical experience
Study start up experience
Vendor management experience
Experience in Oncology, Anti fungal would be an advantage

KEY WORDS:
Vendor Manager/ Junior Project Manager /PCRA/Lead CRA/ Biotech/ Cambridge,UK/Contract

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations #CROs#. i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
www.i-pharmconsulting.com

TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Aoife Cronin on +44 #0#20 3189 0464, or email acronin@i-pharmconsulting.com. If this role is not suitable, Aoife is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


Contract Regulatory Affairs Consultant, Pharma

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Contract - Regulatory Affairs Consultant / Regulatory Affairs Manager. Pharma company in Germany. Candidate must have strong Regulatory Affairs background, full range of Regulatory Affairs maintenance skills

CONTRACT Regulatory Affairs Consultant

Note: you must be eligible to live and work in Germany before applying.

My client is a rapidly expanding international Pharmaceuticals company manufacturing and marketing a broad range of pharma products. You will enjoy a truly international environment whilst working towards a healthier world.

Experience
•Strong experience of Regulatory Affairs Registrations and Maintenance
•Line management experience welcome
•Life sciences degree



Rates, Location etc - Full details on application

APPLY NOW!
Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com
LinkedIn: http://uk.linkedin.com/in/craigedwardsmeet
Follow me on Twitter: @meet_craig

Associated keywords

Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Labeling , Labeling Regulatory Affairs, Regulatory Affairs Manager, Regulatory Affairs Senior Manager, Senior Regulatory Affairs Manager, Regulatory Affairs Management, Reg Affairs, Reg Affairs Manager, Regulatory Affairs Coordinator, Regulatory Affairs Labeling Consultant, Principal Consultant, Principal Regulatory Labeling Consultant, Regulatory Affairs Labeling Associate, Regulatory Affairs Officer, Regulatory Affairs Labeling Expert, Regulatory Affairs Labeling Specialist, Regulatory Affairs Executive Associate, Labeling , GRA, RA, Regulatory Affairs Labeling Associate, Regulatory Affairs Labeling Coordinator, RA Labeling Coordinator, Senior Regulatory Affairs Associate, Regulatory Labeling, Regulatory, Regulatory Affairs Associate, Regulatory Affairs Associate II, Regulatory Line Management, Consultant, Regulatory Affairs Associate, Regulatory Affairs Specialist, Regulatory Affairs writer, Regulatory writer, Regulatory Affairs

Contract CMC Module 3, Regulatory Affairs, Pharma

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CMC Contract - Regulatory Affairs Consultant / Regulatory Affairs CMC Manager. Pharma company in Germany. Candidate must have strong CMC Regulatory Affairs background, full range of CMC skills, module 3

CONTRACT Regulatory Affairs Consultant

Note: you must be eligible to live and work in Germany before applying.

My client is a rapidly expanding international Pharmaceuticals company manufacturing and marketing a broad range of pharma products. You will enjoy a truly international environment whilst working towards a healthier world.

Experience
•Strong experience of Regulatory Affairs CMC Module 3
•Line management experience welcome
•Life sciences degree

 

Rates, Location etc - Full details on application



APPLY NOW!
Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com
LinkedIn: http://uk.linkedin.com/in/craigedwardsmeet
Follow me on Twitter: @meet_craig

Associated keywords

Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Labeling , Labeling Regulatory Affairs, Regulatory Affairs Manager, Regulatory Affairs Senior Manager, Senior Regulatory Affairs Manager, Regulatory Affairs Management, Reg Affairs, Reg Affairs Manager, Regulatory Affairs Coordinator, Regulatory Affairs CMC Consultant, Principal Consultant, Principal Regulatory Consultant, Regulatory Affairs CMC Associate, Regulatory Affairs Officer, Regulatory Affairs CMC Expert, Regulatory Affairs CMC Specialist, Regulatory Affairs Executive Associate, CMC , GRA, RA, Regulatory Affairs CMC Associate, Regulatory Affairs Labeling Coordinator, RA Labeling CMC Coordinator, CMC Senior Regulatory Affairs Associate, Regulatory CMC , Regulatory, Regulatory Affairs Associate, Regulatory CMC Affairs Associate II, Regulatory CMC Line Management, Consultant, Regulatory Affairs Associate, CMC Regulatory Affairs Specialist, Regulatory Affairs writer, CMC Regulatory writer, Regulatory Affairs

Principal Design Control Quality Engineer

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I am seeking a talented Quality Engineer with extensive Design Control experience. This competitive position is with a cutting edge Medical Device company in Yorba Linda.

The primary activities will involve design assurance throughout product development, verification and validation activities, as well as risk management.

The candidate must have worked within a medical device regulatory environment (cGMP, iSO, FDA).

This is an urgent hire so please be in contact as soon as possible.To find out more about Real Staffing please visit www.realstaffing.com

Global Regulatory Director, Top Pharma - Switz!!

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Top Pharma!! Superb opportunity for an experienced Regulatory Affairs candidate with 10+ years experience. Based in Switzerland, this Global Regulatory Programme Director will be resopsible for Global Strategy, Phases I to IV, including Biotech Products within the Oncology Group. Line management. Regulatory Director - Global. Project your career and earn a great salary package!! This Top 10 Pharma Company is undertaking a major Product Development Project in addition to a complex group of programs. You will have significant Regulatory Affairs experience across territories and be adept in Global Regulatory Strategy. Line management of a team and supervision of sub-teams. 6+ years experience with Biologic/Biotech Products. Good working knowledge of: CTA's, VHP, IMPD's, IB's, Protocols, up-dates and End of Trial Notifications; experience in Registrations/MAA's including European Procedures, and Post Marketing. Project Management. Fluent in English required.

If you are interested in this, or any other Regulatory Affairs opportunity, please call Julian Turner Senior Manager Regulatory Affairs on 01727 811 634 or email on: jturner@keypeople.co.uk

Jr Project Manager/ Data Manager - S.E - Contract

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A unique organisation specialising in Electronic Patient Management based in the South East are seeking a Junior Project Manager to join their team on an initial 3-6 month contract basis.

The organisation is a global leader in providing wireless data collections for the life science industry. The drive for the company is to provide safer, more efficient paper-free clinical trials
A unique organisation specialising in Electronic Patient Management based in the South East are seeking a Junior Project Manager to join their team on an initial 3-6 month contract basis.

Contact Deborah Toby at Real Pharma - 0207 758 7322

The organisation is a global leader in providing wireless data collections for the life science industry. The drive for the company is to provide safer, more efficient paper-free clinical trials.

The responsibilities of the role include:

- Overseeing execution of project including budget and coordination of team

- Will be point of contact for customers and host interactive design sessions and draft technical specifications

- Being able to advise on practical and regulatory implications of certain design and implementation decisions

- Interpret client materials to assess all project deliverables and those found in sales phase

- Work closely with client’s project leadership

- Ensure customer satisfaction

- Conduct international training sessions

- Some international travel as required

Required skills and experience for the role:

- Degree in life science field

- Experience in the Pharmaceutical and Clinical Trial industry

- Previous experience managing a project

- Experience managing team

- Preferably experience with client facing activities such as meetings and presentations

- Ideally a background in Data Management but can be more along CRA line of work

- Experience with clinical software is advantageous

- Excellent communication skills, time management, presentation and organisational skills

- Previous experience working for a similar organisation in any position is advantageous

If you are interested in finding more about this position please send an updated CV to Deborah Tob and call on 0207 758 7322.

Keywords: South East,London, Clinical, Data, Project Manager, CRA, Electronic data, contract, software, Pharmaceutical, questionnaire, flow diagramsTo find out more about Real please visit www.realstaffing.com

C++ OpenGL GUI Developer - Medical Device

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Job Responsibilities:

* Develop components for web and mobile using OpenGL ES / Unity3D / Objective C.
* Work with visual and interactive designers to create visually rich content using modern shading, texturing, lighting and interactive methods.
* Analyze existing 3D functions in the product and adapt them so they are compatible with current product requirements.
* Implement 3D functionality as per design documents and specification. ... Job Responsibilities:

* Develop components for web and mobile using OpenGL ES / Unity3D / Objective C.
* Work with visual and interactive designers to create visually rich content using modern shading, texturing, lighting and interactive methods.
* Analyze existing 3D functions in the product and adapt them so they are compatible with current product requirements.
* Implement 3D functionality as per design documents and specification.
* Communicate with other team members to establish pipeline and integrate assets.
* Give regular feedback to project lead as to implementation issues and possible improvements to product design.
* Adherence to and active participation in the continuous development and improvement of all engineering team quality policies and processes.

Skills & Experience Needed:

* Deep knowledge and understanding of C++, Objective C, OpenGL ES, Java, algorithm design and program optimization. Additional skillset in J2EE, XML, HTTP, HTML, and JavaScript a big plus.
* Expert in 3D rendering algorithms (Strong 3D math skills).
* Expert in iOS and Android development.
* Expert in object oriented design and multithreaded development.
* Self-motivated with a strong desire to learn and stay abreast of latest 3D developments/standards.
* Strong working knowledge of modern software development tools including bug tracking systems, source code revision control, and automated testing and code optimization required.
* Excellent communication skills, ability to work in a fast-paced adaptive environment and strong team player required.

Pluses:

* Unity3D development experience.
* WebGL development experience.
* Experience with other scripting languages such as JavaScript, LUA and Python.
* Experience with 3D packages such as Maya.
* Understanding of scrum and agile development.

Educational Requirements / Work Experience:

* B.S. or M.S. in Computer Science or related field
* BS Degree and 5+ years of experience, or MS degree and 3+ years of experience.To find out more about Real Staffing please visit www.realstaffing.com

Clinical Study Manager - Oncology

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Clinical Study Manager- Oncology

London

£40,000 - £50,000

A Global Leading Contract Research Organisation (CRO) has a position available for a Clinical Study Manager for their outsourcing department. YOu will be working directly with one of their most important pharmaceutical clients. Clinical Study Manager - Oncology

A Global Leading Contract Research Organisation (CRO) has a position available for a Clinical Study Manager for their outsourcing department. You will be working directly with one of their most important pharmaceutical clients.

As the Clinical Study Manager with the pharma sponsor at their site in Middlesex you will be responsible for the implementation, conduct and close out of the UK Oncology trials. This position will include the matrix management of key study teams such as the regulatory and compliance and also the line management of CRAs.

My client is looking for a candidate with national clinical trial management within the field of Oncology from a CRO or Pharma background. Ideally you will have had previous line management responsibilities.

This is a great opportunity to work with one of the most successful Pharmaceutical companies gaining valuable management experience.

To apply for this positions please contact Toby Drewitt of NonStop recruitment on +44(0)20 7940 2105 or alternatively send a word copy of you CV to t.drewitt@nonstop-recruitment.com



Keywords: Clinical Project Manager, Clinical Trials Manager, Clinical Study Manager, Clinical Studies Manager, LCRA, lead CRA, Senior CRA, clinical research associate. Clinical Project Manager / Clinical Study Manager / Clinical Trial Manager/ Clinical Operation Leader/Clinical Study Manager, Clinical Studies Manager, LCRA, lead CRA, Senior CRA, clinical research associate. Clinical Project Manage/ clinical trials/ clinical study/clinical studies /pharmaceutical/ CRO/ Pharmaceuticals/ Pharma/ phase 1/ phase 2/ phase 3 / oncology

Clinical Research Associate (CRA) - SE England

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Clinical Research Associate (CRA) - Pharmaceuticals

South East England

£25,000 - £35,000


A unique opportunity is available for a CRA to work with a global Contract Research Organisation (CRO) and gain direct experience with their pharmaceutical sponsors. Clinical Research Associate (CRA)

A unique opportunity is available for a CRA to work with a global Contract Research Organisation (CRO) and gain direct experience with their pharmaceutical sponsors.

You will be working on behalf of this CRO but will be outsourced to their pharmaceutical sponsor working at their site in Berkshire. Being a part of such a successful CRO will give you the security and future career opportunity inherent in such an organisation, but the unique factor in this role is that you will be gaining direct experience of working within a pharmaceutical company.

My client is looking for candidates with a least 12 months UK monitoring experience within a pharmaceutical or clinical research organisation, a strong knowledge of ICH-GCP and a degree in life science. Candidates with regulatory experience will have a particular advantage.

To apply for this position please click on the link below or contact Toby Drewitt of Nonstop recruitment on 020 7940 2105. Alternatively you can send a work copy of CV to t.drewitt@nonstop-recruitment.com



Key words: clinical research associate, CRA, monitoring, CRA, In house CRA, clinical research, Clinical trials, clinical studies, clinical documents, Clinical research associate, ICF, CRF, clinical research organisation, Clinical report forms, clinical study, regulatory, UK, Berkshire, south east england, pharmaceutical

Controls Engineer

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Location: GA
Salary: Open
Description:

Our client is currently seeking a Process Controls Engineer to work in a team-based environment. 


This job will have the following responsibilities:

  • Promoting the utilization of regulatory and advanced controls schemes to increase the automation of the unit to improve quality, production capacity, and reduce manual intervention. 

    • Developing and documenting new strategies to troubleshoot instrumentation, diagnose operational interruptions, and maximize overall equipment effectiveness. 

    • Working with unit operation team and process engineers to identify and implement new ways to increase product yields, reduce energy usage, and optimize the value of byproducts. 

    • Coaching operations and other technical personnel on the concepts and use of control strategies. 

    • Generating new control strategies or instrument utilization projects which improve unit operations. 

    • Working in a team environment with other Process Control Engineers to maintain the overall site control system hardware and software.

      


Qualifications & Requirements:

  • B.S. in Chemical Engineering or Electrical Engineering preferred. Candidates with other degrees who have demonstrated strong process control skills will also be considered.

    At least 3 years of experience working as a process control engineer.  

    Experience in a Distributive Control System environment such as APACs, Delta V, or Siemens PCS7 is required.

    A strong knowledge of Allen Bradly PLC’s, Wonderware HMI, and TCP/IP network architecture including network domain administration a plus. 

    The ability to write and maintain various scripting languages and S88 compliant batch programs is preferred. 


Contact: kno@judge.com
This job and many more are available through The Judge Group. Find us on the web at www.judge.com

Director Safety & Pharmacovigilance

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Location: MO
Salary: 170000-215000
Description:

Director, Drug Safety and Pharmacovigilance will be responsible for assuring the medical accuracy of all clinical and post marketing adverse event filings to worldwide Regulatory Authorities such as the US Food and Drug Administration, Health Canada, European Authorities etc. received globally. Director, Drug Safety & Pharmacovigilance will also establish and maintain consistency of safety assessments within the US and outside the US. In addition, this position will work closely with the Director, Drug Safety and Pharmacovigilance EMEA, APJ and Director, Global Drug Safety to ensure regulatory compliance with all aspects of safety reporting. Position reports to the Chief Medical Officer.  Looking for a minimum of eight years clinical practical experience in a relevant clinical environment. Also a minimum of two  years of Pharmacovigilance experience in Clinical Safety or Post Marketing Safety including thorough knowledge of FDA and ICH safety reporting regulations and guidelines. Any experience at the FDA, EMEA or other global regulatory authority is a huge plus.


Contact: lmanfredy@judge.com
This job and many more are available through The Judge Group. Find us on the web at www.judge.com

Jr Project Manager/ Data Manager - S.E - Contract

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A unique organisation specialising in Electronic Patient Management based in the South East are seeking a Junior Project Manager to join their team on an initial 3-6 month contract basis.

Contact Deborah Toby at Real Pharma - 0207 758 7322

The organisation is a global leader in providing wireless data collections for the life science industry. The drive for the company is to provide safer, more efficient paper-free clinical trials.

The responsibilities of the role include:

- Overseeing execution of project including budget and coordination of team

- Will be point of contact for customers and host interactive design sessions and draft technical specifications

- Being able to advise on practical and regulatory implications of certain design and implementation decisions

- Interpret client materials to assess all project deliverables and those found in sales phase

- Work closely with client's project leadership

- Ensure customer satisfaction

- Conduct international training sessions

- Some international travel as required

Required skills and experience for the role:

- Degree in life science field

- Experience in the Pharmaceutical and Clinical Trial industry

- Previous experience managing a project

- Experience managing team

- Preferably experience with client facing activities such as meetings and presentations

- Ideally a background in Data Management but can be more along CRA line of work

- Experience with clinical software is advantageous

- Excellent communication skills, time management, presentation and organisational skills

- Previous experience working for a similar organisation in any position is advantageous

If you are interested in finding more about this position please send an updated CV to Deborah Tob and call on 0207 758 7322.

Keywords: South East,London, Clinical, Data, Project Manager, CRA, Electronic data, contract, software, Pharmaceutical, questionnaire, flow diagramsTo find out more about Real please visit www.realstaffing.com

Mechanical Design Engineer

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The ideal candidate will have the following skills:

- 3D Design (Pro Engineer)
- Design for manufacture knowledge
- Good communication skills
- Enthusiasm for career development

This is a Permanent role offering a competitive salary, based in the North West.

Tool Design Engineer

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Tool Design Engineer - Hampshire - £competitive





The Role



An exciting new opportunity has just arisen for a Tool Design Engineer to be based in the Hampshire area. Ideally they are looking to bring someone on board immediately.



The Tool Design Engineer will have a background predominantly within Aerospace.



The Candidate

* Background of Aerospace design including interiors, wings, instrumentation, undercarriages, engines, interior show models
* Experience of Aluminium and Composite Mould Tools, Intensifiers and Drill & Trim Jigs, setting and alignment gauges, machining fixtures, bonding fixtures
* CATIA 5 experience







The Salary

£competitive



How To Apply

If you would like to apply for this position, and would like the opportunity to secure the next permanent position prior to Christmas, please email your current CV and a covering letter to and/or call Lucy Heap on 0118 956 5545 for an immediate response.To find out more about Huxley Associates please visit www.huxley.com

Design Engineer - Inventor

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3D Draughtsman / Design Engineer /Dorset/ Contract

Design Engineer - Dorset - 3 Months

Huxley Associates are currently looking for a contract Design Engineer for a 3 Month contract in Dorset.

The candidate will be joining the existing design team and assist with the development and existing concept.

Essential Skills:

* AUTODESK INVENTOR (2012 Preferable)
* Experience of creating 3D drawings from concept
* Knowledge of materials and tolerances

Desirable Skills:

* Large Welded Structures
* Petro Chem / Subsea Experience
* Structural Welding

The Person

*Available for immediate start*

Rate: Market

Location:Dorset

Duration: 3 MonthsTo find out more about Huxley Associates please visit www.huxley.com

Engineering Manager role - Dorset

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Assistant Engineering Manager - Dorset - £30-37,000 + benefits



Huxley Associates are currently recruiting an Assistant Engineering Manager for theirDorsetbased client.



This position is ideal for a design engineer or senior design engineer who is looking to make the move into management.



Ideally candidates will have a strong design engineering background with good technical knowledge. The role will involve working alongside the current Engineering Manager with a view to move into this position over time.



Our client can offer fantastic career development as this role will evolve into a senior position in the business.



If you are interested in this vacancy, apply with an up to date CV.

Lead Subsea Engineer's

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I have some fantastic contract opportunities working with a leading global Oil and Gas service company who are based in Aberdeen.

Due to the company expanding and taking on new clients / projects they currently require experienced professionals in the following areas:

- Interventions Engineer (Proposals)
- Lead Subsea Engineer (Tree's and wellheads)
- Subsea Systems Engineer (Tree's / risers / tenders and bids)
- Intervention Systems Engineer (Workover risers)

They are looking for engineers with vast experience in:

- Subsea X-as Trees

- Subsea intervention systems

- Subsea risers

This is an exciting and challenging role within a company who can offer long term contracts and the best industry and project experience in this sector. Some of these roles provide the opportunity to travel internationally.

2 x Contract Mechanical Design Engineers

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Mechanical Design Engineer - Solidworks -South Wales

Huxley Associates are currently looking for 2 Mechanical Design Engineers for a large development project for a client in the South Wales Area.

Requirement 1: Skill Sets

Solidworks

3D Modeling

Plastic Injection Moulding

Requirement 2: Skill Sets

Solidworks

3D Modeling

Design of Fluid Dynamics

Heat Exchange

Both of the required contractors will be required to take part in DFMA meetings.

These contracts are for 6 Months and require the contractor to be on site for 3 Days a week, with the other 2 worked at home.

Duration: 6 Months

Rate: Market

Location:South Wales



If you feel that you are suitable for these roles or would like more information, then call 011793 88 088 for more information.To find out more about Huxley Associates please visit www.huxley.com
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