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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
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Mechatronics Engineer - Biotech - London
A start-up Biotech company, based in Central London, is currently hiring for a Mechatronics Engineer to join them and help accelerate the design, development, building, and testing of a novel Diagnostics technology, working to ISO 13485 Medical Devices standards.
Due to the early stage of this organisation, there is still the potential of acquiring equity.
Meaning your success will have a direct impact on your future.
Your focus will be accelerating the design, development, building and testing of the hardware of this new Diagnostics Medical Device, working alongside some excellent Medical Devices Physicists, Scientists, Electronics Engineers, and Design Engineers.
This work will be working on the design and implementation of Mechatronics Systems, using Python programming for the systems documentation and BoM.
This Biotech organisation is looking for a Mechatronics Engineer who has worked on hardware development of a Medical Devices, Biotech System or Life Sciences Technologies, that have ideally been based around pumps, fluidics or microfluidics.
Due to the size of this company, you will be exposure to other areas of the business, including third-party meetings and attending Biotech, Medical Devices and Science conferences and trade shows.
Due to this, it would be ideal if you have worked for a start-up or scale-up Medical Devices company previously or worked for a Medical Devices/Scientific Design Consultancy and know what it's like to wear multiple hats when needed.
It is expected that you would hold a degree and masters in a related Medical Devices, Biomedical Engineering, Mechanical Engineering, Design Engineering, Electronics Engineering, or another relevant scientific subject.
Apart from equity, you will also be rewarded with an excellent starting salary, pension, and future career development as the company grows while also working in an interesting field on a product that could help a lot of people.
As this is an exciting role, joining a start-up company right at the beginning of their story, I'm expecting a lot of interest in the role.
So, if you are interested, please apply straight away or risk missing out to someone else.
Due to the anticipated level of interest in this role, we are considering candidates with varying levels of experience, provided they process the right attitude.
Therefore, if you are interested, we recommend submitting an application promptly to avoid missing out.
Once the company identifies the right candidate, they will extend an offer, so we do not expect this role to remain open for long.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices, Biotech and Science recruitment specialists, Newton Colmore, on +44 121 268 2240 or submit an application, and a member of our team at Newton Colmore will be in touch with you. ....Read more...
Type: Permanent Location: City of London, England
Salary / Rate: Share options
Posted: 2024-03-22 14:56:01
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SENIOR MICROBIOLOGY MANAGER | HERTFORDSHIRE | Competitive SalaryAn exciting clinical-stage biopharmaceutical company are currently recruiting for a Senior Microbiology Manager to join the team based in the Hertfordshire area on a permanent basis.Reporting to the Senior Director QC & Microbiology, the core function of the role will be to lead a team of Microbiologists covering a 7 day operation.
You would be responsible for the efficient provision of QC microbiology services to production and other internal / external customers.
Key responsibilities include:
Ensuring adherence to Health & Safety policies and procedures
Managing a team of Microbiologists, carrying out performance assessments, improvement and development plans
Establishing SMART objectives for team members
Managing the QC schedule, ensuring timely delivery of results
Managing workload and capacity for the team
Ensuring adequate training levels within the team
Collation and presentation of team metrics and data
Development and implementing continuous improvement projects using LEAN
Coordination of shift activities with production counterparts
Looking after the wellbeing of the team
To be considered for the role candidates must have a BSc/MSc in a Life Sciences / Microbiology-related field, along with significant experience working in a microbiology laboratory and a detailed understanding of aseptic technique and practices.
Strong leadership experience is essential, along with regulatory / inspection involvement.
In order to apply for this role please forward your CV to melissa@blackfieldassociates.com or call Melissa on +44 (0) 2392 322 306 for further details.
STR Limited is acting as an Employment Agency in relation to this vacancy. ....Read more...
Type: Permanent Location: Hertfordshire, England
Posted: 2024-03-20 14:03:33
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Systems Engineer - Medical Devices Diagnostics - London
A start-up Medical Devices company, based in Central London, is currently hiring for a Systems Engineer to join them and help accelerate the design, development, building, and testing of a novel Diagnostics technology, working to ISO 13485 Medical Devices standards.
Due to the early stage of this organisation, there is still the potential of acquiring equity.
Meaning your success will have a direct impact on your future.
Your focus will be accelerating the design, development, building and testing of the hardware of this new Diagnostics Medical Device, working alongside some excellent Medical Devices Physicists, Scientists, Electronics Engineers, and Design Engineers.
This Medical Devices organisation is looking for a Systems Engineer who has worked on hardware development of a Medical Devices, Biotech System or Life Sciences Technology that have included mechatronics elements.
Apart from hardware development experience for systems design, Python programming, and design for manufacturing, providing systems documentation and BoM will also be important.
Due to the size of this company, you will be exposure to other areas of the business, including third-party meetings and attending Medical Devices and Science conferences and trade shows.
Due to this, it would be ideal if you have worked for a start-up or scale-up Medical Devices company previously or worked for a Medical Devices/Scientific Design Consultancy and know what it's like to wear multiple hats when needed.
It would be highly advantageous if you have also worked on microfluidic systems in the past, products that have had an element of chemistry, biochemistry, and medical products.
It is expected that you would hold a degree and masters in a related Medical Devices, Biomedical Engineering, Mechanical Engineering, Design Engineering, Electronics Engineering, or another relevant scientific subject.
Apart from equity, you will also be rewarded with an excellent starting salary, pension, and future career development as the company grows while also working in an interesting field on a product that could help a lot of people.
As this is an exciting role, joining a start-up company right at the beginning of their story, I'm expecting a lot of interest in the role.
So, if you are interested, please apply straight away or risk missing out to someone else.
Due to the anticipated level of interest in this role, we are considering candidates with varying levels of experience, provided they process the right attitude.
Therefore, if you are interested, we recommend submitting an application promptly to avoid missing out.
Once the company identifies the right candidate, they will extend an offer, so we do not expect this role to remain open for long.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices, Biotech and Science recruitment specialists, Newton Colmore, on +44 121 268 2240 or submit an application, and a member of our team at Newton Colmore will be in touch with you. ....Read more...
Type: Permanent Location: City of London, England
Salary / Rate: Equity, pension, etc.
Posted: 2024-03-20 10:46:05
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We have an exciting opportunity for a Associate Scientist to join a cutting-edge Biotech start-up company based in London.
As the Associate Scientist you will be responsible for providing cell biology and tissue culture support to the experimental biology group, as well as assisting with lab management activities.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Associate Scientist will be varied however the key duties and responsibilities are as follows:
1.
As the Associate Scientist you will provide cell biology and tissue culture support to the experimental biology group.
2.
You will assist with routine lab management tasks such as reagent procurement and stock monitoring.
3.
As the Associate Scientist you will form a critical component of the lab team, supporting and vitally contributing to the development and implementation of next generation in vitro discovery platforms.
4.
You will be working as part of a multi-disciplinary team, closely collaborating with data scientists and product engineers.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Associate Scientist we are looking to identify the following on your profile and past history:
1.
A BSc/Higher degree in immunology, cell biology or other related discipline.
2.
Proven academic or industry experience working in a laboratory, ideally with assays and tissue cultures.
3.
A working knowledge and practical experience in working aseptically.
Key Words: Biotech | Immunology | Cell Biology | Immunotherapy | T-Cells | Scientist | Tissue Culture | Lab Management | Associate Scientist | TCR | In Vitro | Experimental Biology
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: 20/03/2024
Salary / Rate: Competitive
Posted: 2024-03-20 08:29:03
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We are currently looking for a Biomedical Engineer Lead to join a leading Biotechnology company based in the Cambridgeshire area.
As the Maintenance Technician Lead you will be responsible for all aspects of the installation, maintenance, and repair of biomedical equipment throughout the R&D Laboratory.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Biomedical Engineer Lead will be varied however the key duties and responsibilities are as follows:
1.
You will arrange a work order system to perform planned maintenance, repairs, and electrical safety checks and various devices throughout the R&D laboratory.
2.
You will provide operational knowledge to staff to improve use of biomedical equipment, continuously improve the department through report management, and recommend product /system improvements.
3.
You will lead the inspection of new laboratory equipment for safe installation and operation, and readily calibrate and troubleshoot equipment.
4.
You will lead and guide junior technicians, as well as attend training to expand devices you are capable of repairing.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Biomedical Engineer Lead we are looking to identify the following on your profile and past history:
1.
Relevant degree in Biomedical Engineering, Electronics, or similar.
2.
Proven industry experience working in a clinical laboratory setting working in a maintenance technician-type role
3.
A working knowledge and practical experience working in a leadership / management position, with capability to execute projects systematically.
Key Words: Maintenance Technician | Engineering | Biomedical Engineer | Electronics | Clinical | GCLP | GLP | GMP | R&D | Research and Development | Leadership | Management | Team Leader | BSc | MSc | Biotechnology | Cambridgeshire |
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: Cambridge,England
Start: 20/03/2024
Salary / Rate: £40000 - £45000 per annum
Posted: 2024-03-20 08:01:03
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Cheminformatics Expert - Drug Discovery
Newton Colmore is working for a start-up drug discovery biotech and we are assisting them in their search for a cheminformatics expert to join their research team.
The company is seeking an experienced Cheminformatics Scientist to join their multidisciplinary team in San Diego and help setup their cheminformatics function.
As a key member of their research and development team, you will leverage your expertise in computational chemistry and data analysis to support drug discovery efforts and advance their pipeline of therapeutic candidates.
There will also be the possibility of growing a larger cheminformatics team around you, depending on the progress the company makes with their technology.
You will be Responsible for:
Develop and implement cheminformatics tools and algorithms to analyze chemical data, predict compound properties, and facilitate drug design workflows.
Collaborate with interdisciplinary teams of chemists, biologists, and computational scientists to design and optimize small molecule libraries for lead identification and optimization.
Utilize computational modelling techniques to predict molecular interactions, bioactivity profiles, and ADMET properties of drug candidates.
Maintain and enhance databases, software platforms, and data visualization tools for chemical and biological data management and analysis.
To be considered for this role you will ideally have the following;
Ideally educated to PhD-level in Computational Chemistry, Cheminformatics, Bioinformatics, or related field.
Experience in cheminformatics or computational chemistry, preferably within a start-up environment in industry.
Proficiency in programming languages such as Python, R, or Java, and experience with cheminformatics software packages (e.g., RDKit, OpenEye, ChemAxon).
Strong understanding of chemical informatics principles, molecular modeling techniques, and structure-activity relationship (SAR) analysis.
The company are open on seniority level and can tailor the role to suit the right candidate's experience level and so do get in touch even if you feel you are either too junior or senior for the role.
Newton Colmore specializes in this type of role and so we will be able to provide more opportunities to you in the future too.
The company are offering tailored packages for the right candidate that will match your expectations and experience level.
This comes with a comprehensive list of benefits along with the chance to build your own team.
To find out more, make a confidential application now and Matt Lowdon, our Head of Biotechnology and Therapeutics will be in touch with more details.
Newton Colmore is a specialist medical devices and biotechnology recruitment agency, with expertise in helping our clients find the experts they need to develop ground-breaking products, therapeutics, and services.
Partnering with an expert agency in your job search is a great way to expand your horizons.
As Specialist recruiters we develop our network every day, meaning they have access to roles and companies that you may not be aware of.
To complement this, we have deep insights into our markets and clients that will benefit you in the interview process, ensuring you can perform at your best.
To conclude the process, we have an excellent track record of negotiating offers on behalf of our clients and candidates.
....Read more...
Type: Permanent Location: San Diego, California
Salary / Rate: US$105000 - US$135000 per annum + Tailored package
Posted: 2024-03-15 11:32:00
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We have an exciting opportunity for a Bioanalytical Scientist to join a fast-growing CRO based in the Cheshire area.
As a bioanalytical scientist, you will be primarily laboratory-based, working with the team to ensure that bioanalytical assays utilising LC-MS/MS or Ligand Binding technology are performed to a GLP/GCP standard and delivered within scheduled time frames.
The team work on a broad range of molecule types including small molecules, peptides, Oligonucleotides and Proteins.
You will be involved with the development and validation of the assays and will also use the assays to analyse samples from the company's clients studies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Bioanalytical Scientist will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for the development of quantitative and qualitative methods for the analyses of drugs and biomarkers within a GLP / GCP environment.
2.
As a Scientist within the Bioanalysis team you will be carrying out LCMS/MS and HPLC methods for analysing drug metabolites as well as applying these methods in clinical and pre-clinical studies.
3.
Your role will include preparing and planning studies and reports whilst working in compliance with GLP / GCP.
Additional responsibilities will include routine MS, UPLC and bioanalytical extraction as well as method development, method validation and troubleshooting.
4.
As the Senior Scientist, you will have additional responsibilities such as supervise and mentor more junior laboratory scientists as well as some responsibility with client interaction when required.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Bioanalytical Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Life Sciences related degree such as, but not limited to, Chemistry, Biochemistry and Biotechnology.
2.
Proven industry experience of working in a bioanalytical laboratory performing quantitative analysis and experience of sample extraction techniques for biological sample analysis.
3.
Practical experience working within a regulated GLP / GCP / GxP / GMP laboratory is also essential to your application.
Key Words: Biotechnology | GCP | GMP | GxP | Life Sciences | LCMS | HPLC | Bioanalytical | Scientist | Chromatography | Drug Development | CRO | Quality | Biological Matrix | Bioanalysis Senior Scientist
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: Cheshire,England
Start: 15/03/2024
Salary / Rate: Competitive
Posted: 2024-03-15 08:55:03
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We have an exciting opportunity for a Quality Assurance Auditor to join a fast-growing CRO based in the Cheshire area.
As the Quality Assurance Auditor you will be required to give advice on the compliance and quality issues, and look for improvement opportunities to working practices to ensure the company's GLP and GCP regulations are maintained.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Auditor will be varied however the key duties and responsibilities are as follows:
1.
You will be mainly part of the busy QA team to assure management that the facility is operating in compliance with the UK GLP regulations.
This involves scheduling work within the QA team and co-ordinate activities for the QA unit.
2.
You will be required to review study plans to ensure the GLP regulations are followed, as well as audit scientific reports, to ensure that the reports fully and completely describe the data generated on studies.
3.
You will be responsible the inspection of the study procedures, laboratory processes and facilities, interacting with staff at all levels.
You will also advise upon and audit computerised system validation activities and assure validation documentation is in compliance with regulatory requirements.
4.
Additionally, as the QA Auditor, you would design and deliver GLP and GLP training to the scientific team and support the test facility manager in the planning and hosting of external client audits and government agencies.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Quality Assurance Auditor we are looking to identify the following on your profile and past history:
1.
Relevant degree in Life Sciences or a chemistry related subject (e.g.
Biochemistry)
2.
Proven industry experience working in a GLP testing facility is essential as well as experience of working in a quality role under GLP or GCP.
3.
You will need to have an eye for detail and the determination to complete tasks to a high standard within tight deadlines.
Key Words: Quality Assurance Officer | QA Officer | GLP | GCP | Documentation | Quality and Compliance | Testing | CAPA | Root Cause Analysis
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: Cheshire,England
Start: 15/03/2024
Salary / Rate: Competitive
Posted: 2024-03-15 08:51:16
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This Compliance Officer role is available within a globally renowned Chemical manufacturing company, committed to investing significantly in the successful candidate's career and personal growth.
The position offers a salary of up to £30,000 per annum, along with a profit share bonus tied to performance after nine months of employment.As a Compliance Officer, you'll be responsible for providing technical and administrative support to ensure product compliance with global chemical legislation.
This includes managing chemical-specific data and documentation for both raw materials and finished goods, fostering effective communication with various departments, and collaborating closely with the Regulatory Manager to develop and enforce departmental procedures in line with the company's policies.Compliance Officer Responsibilities
Ensure adherence to the company's safety culture and maintain health, safety, and environmental standards consistently.
Manage crucial raw material data and facilitate the introduction of new materials through the company's change management process.
Assist the regulatory manager in maintaining data for raw materials and finished products in the company's SDS authoring software.
Author and release Safety Data Sheets and label content according to established procedures.
Offer insights for customer inquiries and distribute documents to customers.
Aid the regulatory compliance manager in compiling and presenting departmental KPIs.
Generate monthly reports to monitor import volumes, sales, and inventory levels to support COMAH and REACH.
Assist the Manager in implementing the global strategy, including supporting REACH registrations, global notifications, reviewing global inventories, and handling poison centre notifications.
Please apply directly for further information regarding this Compliance officer role. ....Read more...
Type: Permanent Location: Manchester, England
Start: ASAP
Salary / Rate: £25000.00 - £30000.00 per annum + Plus Profit Share Increase
Posted: 2024-03-14 14:03:25
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Laboratory Product Process Technician required to join a successful Process and Development Engineering team testing of materials and electrical products using on site laboratory equipment and facilities.
Key skills:
Degree or HNC in Engineering subject.
Materials testing and electrical testing experience.
Microsoft Office and MS Access familiarity.
Manual and hands on practical skills
In this role you will
Manage Lab calibration
Testing new materials being investigated.
Sample contract testing.
Undertaking full electrical and material type approval testing including Type Approval Test reports.
Manage Laboratory safety procedures for all activities within the Lab.
....Read more...
Type: Permanent Location: Wrexham, Wales
Start: ASAP
Duration: Permanent
Salary / Rate: £35000 - £38000 Per Annum None
Posted: 2024-03-14 10:19:11
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We have an exciting opportunity for an R&D Manager to join a leading genetic research company based in the Cambridge area.
As the R&D Manager you will be responsible for managing and resourcing the development team for new product development projects, continuous process improvements and customer/product support functions.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the R&D Manager will be varied however the key duties and responsibilities are as follows:
1.
As the R&D Manager you will be managing a team made up of Research Assistants, Scientists and Senior Scientists, which includes setting and monitoring SMART objectives, annual appraisals and ensuring staff training records are maintained and up to date.
2.
You will have the opportunity to attend relevant scientific conferences to gain a deeper understanding of the cytogenetics industry, while keeping up to date with the newest industry technologies.
3.
As R&D Manager you will be ensuring all the documentation of the R&D team is kept up to date and adhered to correctly as per the company guidelines.
4.
You will also, naturally, nurture a positive culture of collaboration across both the R&D team, as well as with other departments of the company.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the R&D Manager we are looking to identify the following on your profile and past history:
1.
At least a BSc in a biological discipline (e.g.
Biological Science), with significant post qualification experience.
2.
Demonstrable industry experience of managing a team within an R&D setting.
3.
A working knowledge and practical experience with molecular biology techniques such as FISH, PCR, basic DNA manipulations, fluorescent labelling of DNA and work with bacteria
Key Words: R&D | Genetics | Research | Development | Cytogenetics | Manager | Biological | DNA | Analysis | FISH | PCR | Diagnostic
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: Cambridge,England
Start: 14/03/2024
Salary / Rate: £50000 - £65000 per annum
Posted: 2024-03-14 09:27:03
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Do you have a strong technical background in Analytical Science, in particular,high resolution triple quad mass spectrometry? Would you like to use these skills in a technical specialist role? If so, this opportunity could be ideal for you!
We are currently looking for an LCMS Technical Specialist to join a leading manufacturer of Analytical Instrumentation.
You will play a key part in supporting the sales team by providing your technical expertise in LCMS.
This job is remote based and will require frequent travel to customer sites around the UK as well as attending meeting at our clients location in Buckinghamshire.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the LCMS Technical Specialist will be varied however the key duties and responsibilities are as follows:
1.
You will lead the technical aspects of all projects related to LCMS, providing insights and solutions to overcome any technical challenges based on customer requirements.
2.
Provide thorough customer instrument training, supporting customers with existing queries and maintaining a professional approach at all times.
3.
There will be a significant amount of client engagement and you will support the Sales Team by attending discovery meetings, providing technical sessions, performing demonstrations, conducting sample analysis and provided customers with presentations.
4.
By supporting the Sales Team you will develop and execute campaigns to help drive sales and marketing growth.
This will include attending conferences and exhibitions to showcase products.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the LCMS Technical Specialist we are looking to identify the following on your profile and past history:
1.
Relevant scientific degree qualification, such as a BSc in Analytical Chemistry, with a focus on chromatography and mass spectrometry instrumentation.
2.
As the LCMS Technical Specialist, it is essential you have extensive experience with high resolution mass spectrometry.
3.
Candidates with commercial / sales, customer facing experience is highly desirable.
4 You must hold a clean UK driving licence and be willing to travel.
Key Words: Analytical Instrumentation | Elemental Spectroscopy | Molecular Spectroscopy | Sales | Technical Support | LCMS | High Resolution Mass Spectrometry | LC-MS/MS ....Read more...
Type: Permanent Location: Buckinghamshire,England
Start: 13/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-13 23:01:02
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We are currently looking for a R&D Manager to join a leading genetic research company based in the Cambridge area.
As the R&D Manager you will be responsible for managing and resourcing the development team for new product development projects, continuous process improvements and customer/product support functions.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the R&D Manager will be varied however the key duties and responsibilities are as follows:
1.
You will be managing a team made up of Research Assistants, Scientists and Senior Scientists, which includes setting and monitoring SMART objectives, annual appraisals and ensuring staff training records are maintained and up to date.
2.
You will have the opportunity to attend relevant scientific conferences to gain a deeper understanding of the cytogenetics industry, while keeping up to date with the newest industry technologies.
3.
You will be ensuring all the documentation of the R&D team is kept up to date and adhered to correctly as per the company guidelines.
4.
You will also, naturally, nurture a positive culture of collaboration across both the R&D team, as well as with other departments of the company.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the R&D Manager we are looking to identify the following on your profile and past history:
1.
At least a BSc in a biological discipline, with significant post qualification experience.
2.
At least 3 years experience of managing a team within the R&D setting.
3.
A working knowledge and practical experience with molecular biology techniques such as FISH, PCR, basic DNA manipulations, fluorescent labelling of DNA and work with bacteria.
.
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: Cambridge,England
Start: 13/03/2024
Salary / Rate: £50000 - £65000 per annum
Posted: 2024-03-13 17:30:07
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We are currently looking for a Maintenance Technician Lead to join a leading Biotechnology company based in the Cambridgeshire area.
As the Maintenance Technician Lead you will be responsible for all aspects of the installation, maintenance, and repair of biomedical equipment throughout the R&D Laboratory.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Maintenance Technician Lead will be varied however the key duties and responsibilities are as follows:
1.
You will arrange a work order system to perform planned maintenance, repairs, and electrical safety checks and various devices throughout the R&D laboratory.
2.
You will provide operational knowledge to staff to improve use of biomedical equipment, continuously improve the department through report management, and recommend product /system improvements.
3.
You will lead the inspection of new laboratory equipment for safe installation and operation, and readily calibrate and troubleshoot equipment.
4.
You will lead and guide junior technicians, as well as attend training to expand devices you are capable of repairing.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Maintenance Technician Lead we are looking to identify the following on your profile and past history:
1.
Relevant degree in Biomedical Engineering, Electronics, or similar.
2.
Proven industry experience working in a clinical laboratory setting working in a maintenance technician-type role
3.
A working knowledge and practical experience working in a leadership / management position, with capability to execute projects systematically.
Key Words: Maintenance Technician | Engineering | Biomedical Engineer | Electronics | Clinical | GCLP | GLP | GMP | R&D | Research and Development | Leadership | Management | Team Leader | BSc | MSc | Biotechnology | Cambridgeshire
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: Cambridge,England
Start: 12/03/2024
Salary / Rate: £40000 - £45000 per annum
Posted: 2024-03-12 17:57:02
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Fantastic new role in a leading Market Access & HEOR consultancy experiencing continued success and growth.
The company has been on a steep growth trajectory for a number of years and have placed employee wellbeing at the forefront of their development, creating a supportive, fun and dynamic work environment.
This role is a fantastic opportunity to increase team, project and client management responsibilities, and capitalise on the extensive scope for progression within a highly successful company.
The Candidate
Experience across a broad range of treatment and disease areas and high level of knowledge within economic modelling, outcomes research, and HTA.
Driven to thrive in a dynamic work environment and committed to developing professionally and personally.
Strong organisational and time management skills, as well as an ability to manage conflicting priorities.
Excellent communication and interpersonal skills applied to ensure great management of internal and external stakeholders.
The Role
Varied range of projects delivering HEOR and Market Access solutions to improve global patient access to medical innovations.
Point of contact for internal and external stakeholders to ensure team development and client satisfaction.
Highly visible role working alongside key opinion leaders within this space who are passionate about providing mentorship to support your personal and professional growth.
Proactive contributions to the team's growth through internal improvement initiatives aligned with company's overall mission.
The Company
High growth consultancy that delivers outstanding quality service offerings to pharma, biotech and medtech partners.
Energetic team driven by a mission to make a difference to the world by bringing transformative medicines to the market.
Scope for rapid progression - passionate about supporting professional development with a number of examples of individuals on ‘fast-track trajectories' within the business.
Fantastic company culture and work/life balance.
Ideally a hybrid role, going into the offices in central London one or two days per week.
Remuneration
Our client is committed to securing the services of the right candidate and is flexible with regards to the remuneration package available.
Zest Medical is working to a strict deadline so in order to be considered for this opportunity please apply now and your application will be reviewed immediately. ....Read more...
Type: Permanent Location: London, England
Posted: 2024-03-11 16:53:25
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Great opportunity to join a leading Market Access & HEOR consultancy with exciting growth plans for 2024.
The company has been on a steep growth trajectory for a number of years and have placed employee wellbeing at the forefront of their development, creating a supportive, fun and dynamic work environment.
This role is a fantastic opportunity to apply your current technical skillset, refine team and project management responsibilities, and capitalise on the extensive scope for progression within a highly successful team.
The Candidate
Experience within economic modelling, outcomes research, and/or HTA and reimbursement submissions, as well as knowledge across a range of therapeutic areas.
Project management experience - previous exposure to developing delivery processes and managing conflicting demands.
Self-motivated individual with outstanding interpersonal skills - ability to work independently as well as cohesively with the team members in an agile environment.
Driven to personally and professionally develop, as well as to support progress within junior members of the team.
The Role
Varied range of projects delivering HEOR and Market Access solutions to improve global patient access to medical innovations.
Highly visible role working alongside leading figures in this space who are passionate about investing in upskilling.
Organisational lead - delegate tasks through considered project planning to ensure quality standards are consistently met.
Internal point of contact and mentor for junior members with personal development plans.
Proactively contribute to internal initiatives to strive for company's overall mission and culture.
The Company
High growth consultancy that delivers outstanding quality service offerings to pharma, biotech and medtech partners.
Energetic team driven by a mission to make a difference to the world by bringing transformative medicines to the market.
Scope for rapid progression - passionate about supporting professional development with a number of examples of individuals on ‘fast-track trajectories' within the business.
Fantastic company culture and work/life balance.
Ideally a hybrid role, going into the offices in central London one or two days per week.
Remuneration
Our client is committed to securing the services of the right candidate and is flexible with regards to the remuneration package available.
Zest Medical is working to a strict deadline so in order to be considered for this opportunity please apply now and your application will be reviewed immediately. ....Read more...
Type: Permanent Location: London, England
Posted: 2024-03-11 16:51:49