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Physicist - Scientific Systems - Cambridge
A recently established and growing defence company, located in Cambridge, is currently seeking a couple of Physicists to contribute to the invention and development of cutting-edge technologies used in various capacities to ensure the security of defence, aerospace, telecommunications, and other sectors where security is of paramount importance.
You will collaborate with a team of experts, including electronics, engineering, design, embedded systems, and other physicists, to develop these systems.
Working alongside this expert team will offer you continuous opportunities for skill development.
Given the diverse range of systems and technologies you will work on, we welcome physicists from various fields, such as microfluidics, sensors, optics, acoustics, electromagnetics, thermal physics, and other complex domains.
Ideally, you should be proficient in analytical, numerical, and finite element simulations, as well as hands-on engineering physics for building systems.
With a variety of projects and disciplines to engage in, your work will remain engaging and challenging.
The company is dedicated to enhancing your skills and knowledge, ensuring you are well-equipped to work on cutting-edge technologies and innovate new systems.
As the world increasingly adopts smart technologies and artificial intelligence devices, you may also have the opportunity to work on Machine Learning and AI technologies.
If you have experience or an interest in these fields, it will be advantageous.
Previous experience in defence, aerospace, or telecommunications is not mandatory; we welcome physicists from all sectors.
Given the sectors you will be working in, the ability to obtain Security Clearance is essential.
Typically, this requires being a British citizen without a criminal record or having lived and paid taxes in the UK for more than five consecutive years.
In addition to career development and involvement in complex and innovative projects, you will receive an attractive starting salary, regular pay reviews, bonuses, complimentary meals, free parking, a generous company pension, gym membership, wellness programs, healthcare, dental benefits, and other exceptional perks that are competitive with any UK company.
Due to the complex and inventive nature of the work, we anticipate significant interest in this role.
If you are interested, we recommend submitting your application now to avoid missing out.
For further information, please do not hesitate to call Andrew Welsh, Director of Medical Devices Recruitment and Scientific Recruitment Specialist at Newton Colmore, on +44 121 268 2240, or submit an application, and a member of our Newton Colmore team will contact you.
Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors. ....Read more...
Type: Permanent Location: Cambridge, England
Salary / Rate: Negotiable
Posted: 2024-04-02 13:11:00
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Product Design Mechanical Engineer - Medical Device - Warwick
A growing Medical Devices company, located in Warwick, is currently seeking an experienced Product Design Mechanical Engineer to contribute to the development of various Medical Devices.
As part of a team of engineering experts, including physicists, electronics engineers, scientists, and other specialists in Medical Devices, you will play a pivotal role in working on a range of projects aimed at creating life-saving and life-improving Medical Devices.
We are specifically looking for candidates with experience in Medical Devices, preferably in the areas of product design and product development.
However, individuals from the life sciences sector with experience working under strict regulations will also be considered.
The ideal candidate would have a few years of industry experience and might be seeking their second role to advance their career.
While a relevant degree in Mechanical Engineering or a related field is preferred, it is not essential if you have substantial experience as a Mechanical Design Engineer in the Medical Devices sector.
In return for your contributions, you will receive a competitive salary, regular salary reviews, bonuses, a pension plan, life assurance, and other outstanding benefits typically associated with larger organizations.
This is a fantastic opportunity to join a growing company that places a strong emphasis on staff development and career advancement.
Due to the anticipated high level of interest, we encourage interested candidates to apply promptly to avoid missing out.
For further information, please feel free to contact Andrew Welsh, Director of Medical Devices Recruitment and Scientific Recruitment Specialist at Newton Colmore, on +44 121 268 2240.
Alternatively, you can submit an application, and a member of our team at Newton Colmore will reach out to you.
Newton Colmore Consulting specializes in recruiting within the Medical Devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors. ....Read more...
Type: Permanent Location: Warwick, England
Salary / Rate: Negotiable
Posted: 2024-04-02 13:10:32
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Regulatory Affairs and Quality Assurance Assistant - Medical Devices - Cambridge
Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company's Quality Assurance and Regulatory Affairs Manager.
The team provide quality assurance and regulatory affairs advise on the creation of new products and the improvement of existing technologies.
It would be highly advantageous if you have knowledge of design processes, but it's not essential.
This team does not just fill out quality assurance and regulatory documents; this is a team where they will be very involved with the R&D team, providing vital advice on the creation of medical devices, and ensuring the team operates within the FDA 510k, ISO 13485, and FDA 21 CFR Part 820 standards.
It would be ideal if you have both quality assurance and regulatory affairs knowledge.
However, people have moved into this role from either regulatory affairs or quality assurance background, but with a general knowledge in the other side.
It is essential that you have medical devices knowledge, especially ISO 13485 and FDA 510k knowledge.
Although writing submissions will not be a major part of your role, you will relay information to the teams responsible for this, so ideally you will have done this in the past or at least assisted.
Ideally, you will have QMS experience.
If you do have this knowledge, I would advise making it clear on your CV as this is highly desirable in this role.
The products this company has been developing are industry-changing and will improve the lives of people around the world.
It is expected that you would hold a 1st or 2:1 degree within an engineering or sciences discipline along with some experience within regulatory affairs or quality assurance.
Although experience working within a medical devices R&D or design team is more important than education.
This is a growing company; due to this, they offer career progression, excellent salary, benefits package, the chance to work on life-improving devices, and share options.
If you have regulatory affairs knowledge in the medical devices sector and are looking for a challenging role, then apply now.
I expect a lot of interest in this role, and the company are looking to recruit quickly.
So, if you are interested in this role, I suggest applying immediately or risk missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application, and one of our team at Newton Colmore Consulting will contact you. ....Read more...
Type: Permanent Location: Cambridge, England
Salary / Rate: Negotiable
Posted: 2024-04-02 13:08:30
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Quality Engineer - Cambridge - Medical Devices
We are currently looking for a Quality Engineer for a growing Medical Devices organisation based in Cambridge.
The company work on a range of different Medical Devices, providing a variety of projects and tasks in your role.
You will collaborate various Medical Devices experts, including Mechanical Engineers, Physicists, Electronics Engineers, Software Engineers, and other professionals.
Your primary focus will be on Quality Assurance of Medical Devices to ISO 13485 standards, although knowledge of EN 60601 would also be advantageous.
Your responsibilities will include creating technical files and testing documentation.
If you have experience of Design Assurance, this would also enhance your approach to this work.
We would expect you to have a degree that led you into a Medical Devices Quality Engineering career.
However.
if you have another route into a Medical Devices role, we would still be keen to hear from you.
In addition to working on various Medical Devices, you will be rewarded with an excellent starting salary, a bonus, a generous pension, life assurance, healthcare, and other excellent benefits.
Given the anticipated interest in this role, if you are looking for a new opportunity, I suggest making an application now to avoid missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you. ....Read more...
Type: Permanent Location: Cambridge, England
Salary / Rate: Negotiable
Posted: 2024-04-02 13:07:53
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Quality Assurance Specialist - Cambridge
A growing Medical Devices company based in Cambridge is currently looking for a new Quality Assurance Specialist to assist in the development of the QMS system for ISO 13485 standards.
They are open to candidates from alternative sectors, allowing for ISO 13485 standards training.
You will also be creating and managing technical files for several Medical Devices lines, including Class I, Class IIa and Class IIb Medical Devices.
You'll collaborate with a number of Medical Devices experts, but you will be the sole person focusing on Quality Assurance duties.
However, you will receive Quality Assurance assistance from the parent company's Quality Assurance Manager.
Due to this, we are open to candidates who only have a couple of years of experience of ISO 9001 or QMS, but also keen to hear from people with more experience.
This is an excellent opportunity for someone a couple of years into their career and looking for more responsibility to lead the development of a QMS system, or for someone who is looking for a route into the Medical Devices sector under ISO 13485 standards.
Due to the active work in setting up the QMS system, you will need to be in the office daily; however, over time there should be the opportunity for hybrid working.
It is expected that you would hold a degree in a subject that has led you into a Quality Assurance, Quality Engineering, or Design Assurance role.
Apart from having a Quality Assurance background, it would also be highly advantageous if you have a good understanding of Regulatory Affairs.
Part of your role will involve working alongside the manufacturing teams for these medical devices.
Due to this, it would be highly beneficial if your Medical Devices Quality Assurance experience came from a Quality Engineering background, although this is not essential.
I anticipate a lot of interest in this role, so if you are interested, I suggest making an application now or risk missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you. ....Read more...
Type: Permanent Location: Cambridge, England
Salary / Rate: Negotiable
Posted: 2024-04-02 13:07:17
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Electronics Engineer - Medical Devices - Cambridge
Due to the expanding nature of Medical Devices, Wearable Technologies, Robotics, Artificial Intelligence, and other advanced technologies, we are looking for someone to work on the invention of new Medical Devices.
Based in Cambridge, you will be collaborating with engineers and scientists on the development of industry-changing, life-saving, and life-improving medical devices.
Technologies are developing all the time, and this organisation needs to stay at the forefront of technological breakthroughs.
Due to this, they need experienced Electronics Engineers who are happy to work across several different projects.
We ideally need someone who has past experience with Medical Devices within ISO 13485 or EN 60601 standards.
While working on brand-new technologies, you will be problem-solving and thinking up exciting new ways of approaching problems on projects.
This will keep your role very interesting, meaning it is unlikely that you will ever get bored in this role.
Apart from past experiences as an Electronics Engineer in Medical Devices, it is expected that you would hold a degree in an Electronics Engineering field that led you into this line of work.
You will be rewarded with an excellent starting salary, bonus, pension, gym membership, free lunches, and other excellent benefits.
I expect a lot of interest in this role, so if you are interested, I would suggest making an application now or risk missing out.
For more general information, please feel free to call Andrew Welsh, Director of Medical Devices Recruitment and Scientific Recruitment Specialists Newton Colmore, on 0121 268 2240 or make an application, and one of our team at Newton Colmore will contact you.
Please note we will not be able to discuss the role specifics until we have a copy of your CV. ....Read more...
Type: Permanent Location: Cambridge, England
Salary / Rate: Negotiable
Posted: 2024-04-02 13:05:22
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Research & Development Scientist
Warrington
£33'000 - £37'000 Basic + Technical Development + Progression + Renewable Energy Industry + ‘Immediate Start'
Join us on the Renewable Energy revolution and become a master in scaling up and commercialising Electrochemical Cells.
Have the chance to work on exciting projects that will positively impact the Environment.
The role as a Research and Development Scientist will enable you to join a rapidly ambitious commercial team working alongside industry specialists.
Take control of your career and become an industry pioneer.
You will be challenged and have the chance to change your life.
Be given an unrivalled growth opportunity for your hard work and loyalty.
Hit the ground running as a Research and Development Scientist and pave the way for the latest Green production strategies to reach the renewable sphere.
Your Role As a Research & Development Scientist Will Include:
* Reporting to the COO
* Design & Assemble Electrochemical Cells to Test operational variables
* Optimise Cell performance with a focus on Scale-up and Commercialisation.
* Develop & apply process control strategies to optimise Electrochemical Cell Operation
* Ensure consistent process efficiency and quality of products.
* Develop experimental protocols related to the characterisation of Electrochemical Properties.
* Ensure progress reports are completed on a regular basis.
* Comply with COSHH & Risk Assessments.
* Represent the business at relevant events and conferences.
The Successful Research & Development Scientist Will Have:
* Educated to MSc / PhD Chemical / Electrochemical / Fuel Cells
* Design experience in Electrochemical cell & Battery flow Cell design.
* Experience of electrochemical/battery material development (electrodes and electrolytes) and cell testing.
* An understanding of how small start-up teams operate
* Commutable To Warrington
To discuss further please call James on: 07458160082
Keywords: Research and Development Scientist, Fuel Cell Scientist, Scientist, Post Doctoral Researcher, Research Scientist, Hydrogen Scientist, Chemical Scientist, Fuel Cell Designer, Chemical Doctorate, Hydrogen Production, Renewable Engineering, Renewable Energy, Energy Transition, Power Generation, Warrington, Liverpool, Manchester, England, ....Read more...
Type: Permanent Location: Warrington, England
Start: ASAP
Salary / Rate: £32000.00 - £36000.00 per annum + Pension + Training + Progression
Posted: 2024-04-02 09:36:26
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Cleanroom Technician required to join an existing technical team as part of the internal Electrical Engineering Division with multiple Cleanrooms.
You will be responsible for helping maintain equipment and report problems with the operation of the cleanrooms, from contributing to lab waste management, user requests, restocking, sample management and general housekeeping and safety in the cleanrooms.
The ideal candidate will be educated to GCSE level 4 / NVQ level 2 or equivalent with Mathematics, English and a science subject or have an equivalent level of practical experience.
As you will be joining an existing team, it is essential that you are a team player with good communication, interpersonal and organisational skills.
IT literacy is a bonus, the ideal candidate will have previous experience in a Cleanroom or laboratory environment with health and safety knowledge of hazardous materials, electricity, machinery, pressurised systems and the safe use of chemicals. ....Read more...
Type: Permanent Location: Aylesbury, England
Start: ASAP
Duration: Permanent
Salary / Rate: £28000 - £33000 Per Annum None
Posted: 2024-03-28 15:24:42
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Are you looking for a career in research? Do you have experience working in a Lab?Service Care Solutions are working with our established client to recruit Research Assistant to support a The Laboratory Team in the Surrey area.
The successful candidate will primarily work and provide support to the labs for making agar media and using autoclaves.The contract duration is for 6 months with the likelihood of extension.
This is a full-time placement with 37.5 hours available.
Part-time applications of 3 Days or more will also be considered.
Shifts: Monday to Friday, 09:00 - 17:00Location: SurreyPay: £16.00 p/h LTDBonus: £150 Sign-Up BonusJob Purpose - Laboratory Research Assistant Key Responsibilities:
Molecular Techniques:
Perform qPCR, PCR, and DNA extraction procedures with precision and accuracy.
Maintain proper documentation and records of molecular experiments conducted.
Assist in the development and optimisation of molecular protocols as required.
Laboratory Support:
Prepare agar media and other necessary solutions with attention to detail and adherence to protocols.
Operate and maintain laboratory equipment including autoclaves, ensuring proper functionality and cleanliness.
Assist in inventory management, including ordering and restocking of laboratory supplies and reagents.
Quality Assurance:
Adhere to established quality control procedures to ensure the reliability and reproducibility of experimental results.
Monitor laboratory conditions and equipment calibration to maintain compliance with standard operating procedures.
Collaboration and Communication:
Collaborate effectively with fellow research team members, providing support and assistance as needed.
Communicate experimental procedures, results, and any issues encountered with supervisors and team members in a clear and timely manner.
Safety and Compliance:
Follow laboratory safety protocols and guidelines to ensure a safe working environment for all personnel.
Maintain awareness of regulatory requirements and ensure compliance with relevant health and safety standards.
Qualifications and Skills:
Bachelor's degree in a relevant scientific field or equivalent laboratory experience.
Benefits
Four weekly payroll runs
£250 training allowance
Excellent pay rates
Exceptional referral bonuses
Specialists mental health consultants offering single point of contact
Frequent notifications for upcoming opportunities via text and email
Ltd & PAYE payment options available
Nationwide provider of mental health staff to over 40 different NHS trusts offering mental health services and over 200 local authorities.
FREE DBS disclosures provided via fast track online services
FREE Occupational Health Check and Immunisations
Are you happy with your current agency?
£150 Agency Switch Bonus
£250 Welcome Bonus
Up to £750 Referral Bonus
....Read more...
Type: Contract Location: Surrey, England
Start: ASAP
Salary / Rate: Up to £16.00 per hour + £250 bonus
Posted: 2024-03-27 12:12:55
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We are currently looking for a QA Document Controller to join a leading Biotechnology company based in the North of the UK.
As the QA Document Controller you will be responsible for assisting in the development and on-going management of the companies Quality Management Systems.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Document Controller will be varied however the key duties and responsibilities are as follows:
1.
Responsible for the development and implementation of the Quality Management System (QMS), carrying out day to day activities such as CAPAs, deviations, change controls and supplier qualification.
2.
Make sure that the CMO batch documentation are compliant to GXP standards, including the review of GMP documentation.
3.
You will work closely with the Quality Specialist, and assist in regulatory inspections and customer audits.
4.
You will generate, retrieve, manage, and follow-up quality documents generated both internally and generated by vendors in the QMS.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QA Document Controller we are looking to identify the following on your profile and past history:
1.
Relevant degree in a relevant life sciences discipline
2.
Proven industry experience working in a GxP environment - (GMP, GLP, GDP preferred)
3.
A working knowledge and practical experience with document / Quality Management Systems, and Electronic Document Management Systems
Key Words: QA | Quality Assurance | QMS | Quality Management Systems | Clinical | GMP | GxP | Biotechnology | QDM | Quality Document Management Systems | Electronic Document Management Systems | Drug Discovery | CAPA | Deviations |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: United Kingdom,United Kingdom
Start: 26/03/2024
Salary / Rate: £26000 - £30000 per annum
Posted: 2024-03-26 18:16:03
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Fugro is now seeking a Geotechnical Senior Engineer to join the Offshore Site Investigation and Reporting team based in Wallingford, Oxfordshire, UK.
This is an exceptional opportunity to work as part of a global team on site characterisation, independently managing multiple offshore site investigations projects including engineering analyses and production of technical reports.The Geotechnical Senior Engineer will work with the Head of Department to support the professional development of team members.
Whilst this role is predominantly office based, some travel and offshore site work will also be required, typically 30 days per year working onboard vessels as Trainer and/or Consultant.
Who We're Looking For
You would like exposure to a wide variety of geotechnical projects on a global scale;
You would like to work for the world's leading geo-data company;
You are looking for a company who offers excellent learning and development opportunities;
You want to work with the latest cutting-edge technology.
What We'll Offer YouBenefits for this role include a competitive salary accompanied by an attractive package including contributory pension scheme, life assurance, 24 days annual leave, private medical insurance and a subsidised canteen/restaurant.
Hybrid working options available.Apply for this ad Online! ....Read more...
Type: Permanent Location: Wallingford, England
Posted: 2024-03-26 14:22:36
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Principal GNSS Scientist required to join our GNSS team and help lead the research and development of ADAS technology.
As a GNSS Positioning Technologies Principal Scientist you will work to set a new standard for positioning technologies working with cross functional internal teams including Automotive, C++, Signal Processing and navigation specialisms.
Experience
GNSS measurement engine and full GNSS signal processing chain knowledge.
Matlab analysis skills.
Synthetic aperture processing.
GNSS simulators.
Relevant academic or industrial experience.
Kalman filters and other probabilistic estimation techniques.
Multi-sensor fusion techniques, including tight and deep coupling for GNSS-INS.
RTK, PPP, multi-constellation positioning or Multipath mitigation methods.
Responsibilities
Technical ownership of new research and development ideas.
Contribute to the software development lifecycle on the development ADAS software and tools.
Propose, lead and participate in R&D initiatives inspiring the next generation of ground breaking technologies. ....Read more...
Type: Permanent Location: Girton, England
Start: ASAP
Duration: Permanent
Salary / Rate: £60000 - £90000 Per Annum None
Posted: 2024-03-26 10:44:53
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Principal GNSS Scientist required to join our GNSS team and help lead the research and development of ADAS technology.
As a GNSS Positioning Technologies Principal Scientist you will work to set a new standard for positioning technologies working with cross functional internal teams including Automotive, C++, Signal Processing and navigation specialisms.
Experience
GNSS measurement engine and full GNSS signal processing chain knowledge.
Matlab analysis skills.
Synthetic aperture processing.
GNSS simulators.
Relevant academic or industrial experience.
Kalman filters and other probabilistic estimation techniques.
Multi-sensor fusion techniques, including tight and deep coupling for GNSS-INS.
RTK, PPP, multi-constellation positioning or Multipath mitigation methods.
Responsibilities
Technical ownership of new research and development ideas.
Contribute to the software development lifecycle on the development ADAS software and tools.
Propose, lead and participate in R&D initiatives inspiring the next generation of ground breaking technologies. ....Read more...
Type: Permanent Location: St Paul's, England
Start: ASAP
Duration: Permanent
Salary / Rate: £60000 - £90000 Per Annum None
Posted: 2024-03-26 10:44:47
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We have an exciting new opportunity for a Study Manager Team Lead to join a leading international CRO based in the North Yorkshire area.
As the Study Manager Team Lead you will be responsible for directly line managing a team of Study Managers for regulatory and non-regulatory small molecule bioanalytical studies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Study Manager Team Lead will be varied however the key duties and responsibilities are as follows:
1.
As the Study Manager Team Lead you will directly line manage a team of study managers to ensure the successful execution of small molecule bioanalytical studies.
2.
You will collaborate with cross-functional teams, including sponsors and clients, to plan and coordinate study activities, acting as departmental lead for bioanalytical activities conducted on assigned studies.
3.
As the Study Manager Team Lead you will oversee LC-MS/MS method development and troubleshooting including reviewing protocols, study plans, SOPs or reports as required.
4.
You will document and complete any quality documentation (quality issue, CAPA, deviation, change control) as appropriate and within required time frames.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Study Manager Team Lead we are looking to identify the following on your profile and past history:
1.
Hold a degree in a Chemistry based subject or equivalent (e.g.
Biochemistry)
2.
Proven industry experience in study management leading small molecule bioanalytical studies.
3.
A working knowledge and practical experience using LC-MS/MS.
Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: North Yorkshire,England
Start: 25/03/2024
Salary / Rate: £45000 - £60000 per annum
Posted: 2024-03-25 09:44:03
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We are currently looking for a GLP Study Director to join a leading CRO company based in the Oxfordshire area.
As the GLP Study Director you will be responsible for overseeing GLP studies, executing sample preparation for analysis using various techniques and tools, and collaborating closely with the Laboratory Manager and team to ensure timely project delivery.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the GLP Study Director will be varied however the key duties and responsibilities are as follows:
1.
To apply your experience using chromatographic techniques using HPLC, IC,GC and LC for the analysis of various analytical samples.
2.
Conducting the design of study plans, method validation, method development and to ensure timely project delivery, setting and maintaining high personal standards for study quality.
3.
Oversee GLP studies in strict adherence to guidelines, ensuring compliance with standard operating procedures, and maintaining accurate data records.
4.
Taking an active role in the up-skilling and supervision of Analysts whilst effectively communicating with management to ensure the constant development of the overall Analytical function / team.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the GLP Study Director we are looking to identify the following on your profile and past history:
1.
Relevant degree in Analytical Chemistry OR relevant disciplines
2.
Proven industry experience in working in a CRO GLP environment.
Experience working across agrochemical, biocide, industrial chemical and animal health industries is advantageous
3.
A working knowledge and practical experience with chromatographic techniques such as HPLC, IC, GC, LC.
Key Words: Analytical Chemistry | GLP Studies | Laboratory Equipment | Sample Preparation | Chromatographic Techniques | Project Delivery | Standard Operating Procedures | Data Records | Calibration | Preventive Maintenance | SOP | Study Director | Method Validation | Method Development | CRO | HPLC | LC | GC | Oxfordshire
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Oxfordshire,England
Start: 25/03/2024
Salary / Rate: Competitive
Posted: 2024-03-25 09:36:08
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Post-Doctoral Researcher Chemist (Battery Materials)
Location: Godmanchester, Cambridgeshire
Salary: £39,000 + Excellent Benefits
Job Type: Full Time, Permanent
The Client:
Our client, a leading firm focused on accelerating research translation into marketable products.
The Role:
As a Post-Doctoral Researcher Chemist, you will contribute to developing energy storage materials, characterising and testing novel materials for batteries within a multidisciplinary team.
Duties:
* Contribute creatively to brainstorming sessions, studies, and project meetings.
* Assist in formulating electrode and electrolyte material inks and pastes, including solvent screening and microscopy studies.
* Characterize battery materials using electrochemical analysis techniques, including EIS.
* Fabricate and test coin cell devices with novel battery materials, interpreting data and making recommendations.
* Accurately record practical work to document new Intellectual Property (IP) and contribute to patent drafts.
* Initiate, deliver, and document high-quality studies to achieve R&D targets.
* Ensure compliance with health, safety, and environmental policies.
* Foster key working relationships with line managers, project teams, device scientists, and external partners.
* Coordinate activities and disseminate results with relevant teams.
Requirements:
Essential:
* PhD in chemistry, material science, physics, or related field, or equivalent industrial/academic experience.
* Strong knowledge and practical experience in electrochemical techniques or battery technologies.
* Familiarity with Windows and Microsoft Office.
Desirable:
* Experience in high-tech R&D or manufacturing.
* Additional background in organic, inorganic, or interface chemistry, and relevant analytical techniques.
* Understanding of structure-property relationships in functional materials.
* Interest in synthesis and evaluation of functional materials in device formats.
* Experience with Intellectual Property (IP) generation and patent filing.
Benefits:
* Competitive Salary
* Pension scheme
* 27 days holiday plus bank holidays
* Paid time off for voluntary work
* Employee Assistance Programme
* Flexi-time scheme and work-from-home opportunities
* Private health and dental care, life assurance, income protection insurance
Apply now for this exceptional opportunity to contribute to cutting-edge research and further enhance your career.
Important Information: We endeavour to process your personal data in a fair and transparent manner.
In applying for this role, Additional Resources will be acting in your best interest and may contact you in relation to the role, either by email, phone or text message.
For more information see our Privacy Policy on our website.
It is important you are aware of your individual rights and the provisions the company has put in place to protect your data.
If you would like further information on the policy or GDPR please contact us.
Additional Resources Ltd is an Employment Business and an Employment Agency as defined within The Conduct of Employment Agencies & Employment Businesses Regulations 2003.
Keywords: Materials Scientist, Research Scientist, Scientist, Battery Materials, Battery Technology, Battery
....Read more...
Type: Permanent Location: Godmanchester, England
Start:
Duration:
Salary / Rate: £39000 - £39000 Per Annum
Posted: 2024-03-22 17:11:33
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We are currently looking for a Regional Sales Specialist to join a Global Life Science company covering the London territory.
As the Regional Sales Specialist you will maintain the company's CRM database for the territory in terms of all activity and customer contacts, customer information and sales opportunities, strictly on a regular basis.
This is a remote role which requires around 80% travel to both clients and customers, with frequent visits to the Head Office in Milton Keynes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Regional Sales Specialist will be varied however the key duties and responsibilities are as follows:
1.
The Regional Sales Specialist will interact professionally with all other field personnel that will from time to time be actively supporting you in the territory e.g.
Technical/Market Specialists, Service Engineers, Sales/Technical Managers.
2.
You will fully comply to and operate within the pricing and discount directives set in place by the company whilst operating within the operational guidelines for quotations.
3.
Another responsibility will be to attend and fully represent the company at any trade or media event e.g.
exhibitions, which you may from time to time be asked to attend.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Regional Sales Specialist we are looking to identify the following on your profile and past history:
1.
It is essential to have a strong understanding of the Pharmaceutical or Clinical Market industry along with relevant Sales experience.
2.
The ideal candidate will effectively organise themselves to maximise time in front of a customer via in person and remote meetings.
They will also be a motivated individual with the drive to succeed.
Key Words: Sales Specialist | Analytical | HPLC | GC | Spectroscopy | MS | Mass Spectroscopy | Chromatography | Analytical Instrumentation | BD Executive | Business Development | Regional Sales |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: London,England
Start: 22/03/2024
Salary / Rate: Competitive
Posted: 2024-03-22 15:43:03
