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Are you an experienced Validation Specialist looking for a new exciting job opportunity?
We are currently looking for a Validation Specialist to join a leading pharmaceutical company based in the Caerphilly area.
As the Validation Specialist you will enhance validation practice and compliance; support improvement to validation system; streamline processes.
Identify risk areas and required mitigation to meet regulatory inspections e.g.
MHRA, FDA, Notified Body etc.
through routine compliance activities and specific validation projects.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Specialist will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for ensuring that the Site Validation Master Plan is maintained accurately and Validation Plans are implemented for all relevant aspects of Equipment, Process, Cleaning, Computer Systems, Facilities/Utilities and Analytical Method validation.
2.
Additionally, you will also be assisting with all validation activities on equipment before handover / return to system owner and updating all relevant records and schedules.
You will be responsible for arranging specialist services to maintain, calibrate and qualify specialist equipment.
3.
Technical input into all Validation Lifecycle activities as part of a cross functional team.
Provide guidance and support to other internal site departments ensuring compliance with applicable regulatory requirements (MHRA, EU, FDA, U.S., Notified Body and international), International Standards, and quality/validation regulations and guidance documents.
4.
You will also prepare and present validation reports and Key Performance Indicators for management review.
Review and monitor trends; initiate continuous improvement opportunities, communicate any matters outside the norm to the Validation Manager / Site Director of Quality.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Validation Specialist we are looking to identify the following on your profile and past history:
1.
Successful validation experience in a GMP environment (in the pharmaceutical, medical devices, consumer healthcare or semi-conductor industry) is essential for this position.
Experience working in a sterile manufacturing facility would be highly desirable.
2.
Demonstrated expertise in cGMP's, EU/FDA regulations, GAMP guidelines, assessment of risk and drafting of plans, protocols, reports and procedures.
3.
Previous team leadership experience (direct or indirect) desirable, operating in a matrix organization.
Key Words: Validation Specialist | Validation Engineer | Biotechnology | Life Science | Pharmaceutical | GMP | Manufacturing | Sterile Cleanroom | Quality Assurance
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: Caerphilly,Wales
Start: 27/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-27 11:05:09
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Are you an experienced Electrical and Instrumentation Maintenance Technician looking for a new job opportunity?
We are currently looking for an Electrical and Instrumentation Maintenance Technician to join a leading chemicals company based in the East Riding of Yorkshire area.
This role will operate on a shift rotation, you will be required to work shifts between hours 0600 - 2200 Monday to Friday.
As the Electrical and Instrumentation Maintenance Technician you will be responsible for maintenance on site in order to keep production downtime to a minimum.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Electrical and Instrumentation Maintenance Technician will be varied however the key duties and responsibilities are as follows:
1.
On-Site maintenance for issues around the plant to be resolved in time
2.
Adhere to all safety procedures when finding and solving problems on site
3.
Focus on locating solving electrical and instrumentation issues around the plant.
4.
Operate electronic management systems on a regular basis.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Electrical and Instrumentation Maintenance Technician we are looking to identify the following on your profile and past history:
1.
Minimum of a City and Guilds Certificate in Electrical and Instrumentation or equivalent plus 18th edition & Complex qualifications
2.
Proven industry experience within the chemical (or similar) industry is essential.
3.
A working knowledge and practical experience with electronic maintenance management systems and permit to work systems.
Key Words: Chemical | Electrical | Instrumentation | Engineer | Maintenance | Electronics | Manufacturing | Engineering | Technician
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: Goole,England
Start: 27/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-27 10:05:07
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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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We are currently looking for a QC Analyst to join a leading company based in the Kent area.
As the QC Analyst you will be responsible for the analysis of pharmaceutical raw materials, APIs, and finished products to ensure compliance with internal and regulatory specifications.
Daily tasks will involve general chemical analysis including stability testing, various laboratory support activities, documenting analytical data, writing reports and SOPs all in accordance with cGMP.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1.
As a QC Analyst you will be involved in Performing analytical testing using GC, HPLC, KF, FTIR and other required techniques in accordance with written procedures.
2.
You will be required to record data into appropriate records and notify the line manager of any OOS, OOT, OOE or questionable results
3.
You will create and update documents in accordance with cGMP and company procedures
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1.
Relevant degree in a chemistry or related science discipline.
2.
Proven industry experience in Pharmaceutical QC testing and GMP (ideally small molecule) and analytical testing using GC, HPLC, KF, FTIR.
3.
Experience in completing OOS investigations, deviations, CAPA, and Change Controls
Key Words: GC / HPLC / TLC / FTIR / QC / Quality Control/ QC Scientist/ GMP / API / Raw materials / Chemistry / analytical /
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: Kent,England
Start: 25/03/2024
Salary / Rate: £27000 - £29000 per annum
Posted: 2024-03-25 14:32:15
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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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We are currently looking for a Calibration Engineer to join a leading Pharmaceutical company based in the Wiltshire area.
As the Calibration Engineer you will be responsible for Maintenance, calibration, repair, and continuous development of all process and utility equipment within the mechanical, electrical, instrumentation and control remit within the Engineering Department.
This is a Monday to Friday role and is site based.
KEY DUTIES AND RESPONSIBILITIES:
Your duties will be varied however the key duties and responsibilities are as follows:
1.
As the Calibration Engineer you will conduct requalification and calibration activities in adherence to the schedule and procedures.
2.
Maintain and use GMP documentation for all aspects of the job in accordance with working in a pharmaceutical environment.
3.
Aid with Installation, Operational, and Process Qualification processes for new and existing equipment.
4.
Organise and evaluate calibration data, looking for adverse trends and identifying failures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity, we are looking to identify the following on your profile and past history:
1.
Qualification in an engineering discipline or closely related.
2.
Proven industry experience working to GMP guidelines.
3.
A working knowledge and practical experience within calibration of Pharmaceutical equipment.
Key Words: Engineer | Technician | Calibration | Pharmaceutical | GMP
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: Wiltshire,England
Start: 25/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-25 09:26:11
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We are currently looking for a Calibration Engineer to join a leading biopharmaceutical company based in the Hertfordshire area.
As the Calibration Engineer you will be responsible for Maintenance, calibration, repair, and continuous development of all process and utility equipment within the mechanical, electrical, instrumentation and control remit within the Engineering Department.
KEY DUTIES AND RESPONSIBILITIES:
Your duties will be varied however the key duties and responsibilities are as follows:
1.
Calibration of utility, process and laboratory instrumentation.
2.
Maintain and use GMP documentation for all aspects of the job in accordance with working in a pharmaceutical environment.
3.
Aid with Installation, Operational, and Process Qualification processes for new and existing equipment.
4.
Organise and evaluate calibration data, looking for adverse trends and identifying failures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity, we are looking to identify the following on your profile and past history:
1.
Qualification in at least one engineering discipline
2.
Proven industry experience in the calibration of equipment, such as pressure, temperature, flow, pH, UV, conductivity, level and weight sensors.
3.
A working knowledge and practical experience within the highly regulated manufacturing industries:
Key Words: Engineer | Technician | Calibration | Pharmaceutical | GMP
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: Hertfordshire,England
Start: 25/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-25 09:14:03
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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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We are currently looking for a Laboratory Maintenance Lead to join a leading Biopharmaceutical company based in the South of England.
As the Laboratory Maintenance Lead you will be responsible for the overall management of maintenance activities throughout the manufacturing departments.
This is a great opportunity to work in a cross functional role, leading a team, and ensure all maintenance activities are delivered in a timely manner to prevent delays to production.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Laboratory Maintenance Lead will be varied however the key duties and responsibilities are as follows:
1.
You will manage and lead the overall development of the Maintenance Team, providing expert guidance and knowledge over a range on in-house engineering activities.
2.
You will work across the companies various facilities, and take a lead role in completing non-conformance investigations relating to maintenance activities.
3.
You will coordinate with the engineering teams to ensure the smooth day-to-day running of overall maintenance across the facility.
4.
You will manage external maintenance contractors, manage housekeeping workshops, and ensure your team is complying to H&S policies and procedures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Laboratory Maintenance Lead we are looking to identify the following on your profile and past history:
1.
Relevant degree in an Engineering H&S related field, or educated to NVQ level in a relevant subject.
2.
Proven industry experience working in a maintenance role within a pharmaceutical environment.
3.
A working knowledge and practical experience with Maximo, GMP Quality Systems, and understanding engineering H&S legislation.
Key Words: Maintenance | Manager | Maintenance Manager Maintenance Team Leader | Engineering | Engineer | GMP | Pharmaceutical | Manufacturing | cGMP | QMS | Quality Systems | Regulatory Affairs | H&S | Health and Safety | Maximo | NVQ | Biopharmaceutical
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: Salisbury,England
Start: 21/03/2024
Salary / Rate: £40000 - £45000 per annum
Posted: 2024-03-21 17:33:03
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We are currently looking for a Process Engineer to join a leading Biopharmaceutical Manufacturing company based in the South of England.
As the Process Engineer you will act as the Subject Matter Expert to provide technical engineering expertise for various laboratory equipment, and systems within a manufacturing facility testing various products.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Process Engineer will be varied however the key duties and responsibilities are as follows:
1.
You will take a lead role in the Engineering department, coordinating and working within the companies Quality Systems ensuring that process equipment and utility systems within a GMP environment remain compliant.
2.
You will lead the troubleshooting and calibration of equipment, liaising with maintenance teams and perform failure investigations / root cause analysis determinations.
3.
You will act as the engineering specialist on process related projects, which will include providing input into equipment design and testing / qualifying new equipment.
4.
You will train junior engineers, and project manage the implementation of different process improvements and CAPA actions through the delivery of a variety of small projects.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Process Engineer we are looking to identify the following on your profile and past history:
1.
Relevant degree in a relevant engineering discipline or equivalent, or an engineering apprenticeship
2.
Proven industry experience in a GMP manufacturing environment
3.
A working knowledge and practical experience with troubleshooting, commissioning, and validation of equipment
Key Words: Engineering | Engineer | Troubleshooting | Validation | Equipment Validation | CAPA | QMS | Deviations | Quality Management Systems | Process Engineer | GMP | cGMP | QRM | Quality Risk Management | Biopharmaceutical | Manufacturing | SME |
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: Wiltshire,England
Start: 21/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-21 17:09:19
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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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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
-
IT Security Engineer
Location:London
HRS Consultant:Alex Colbeck
Contact Details:alex.colbeck@hyperec.com +447876145869
We are currently looking for an IT Security Engineer to join a leading energy sustainability and marine conservation company based in the London area.
As the IT Security Engineer you will be responsible for maintaining, enhancing and solidifying security protocols across the entire business.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the IT Security Engineer will be varied however the key duties and responsibilities are as follows:
1.
Proactive management of endpoint security solutions across Firewalls, switching, anti-virus, spam, and encryption protection.
2.
Own the delivery of all the Information Security elements in any IT Project, ensuring thatsecurity by designis considered at all levels.
3.
To further develop and mature the IT Security Team.
4.
Using our IT Security tool kits identify and correct any vulnerabilities/threats to the groups systems.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the IT Security Engineer we are looking to identify the following on your profile and past history:
1.
Relevant degree in a related field (Science, Engineering or similar) would be beneficial
2.
Proven hands on experience working within the IT security space is desirable.
3.
A working knowledge and practical experience with any of the following areas will be a bonus:
Microsoft 365, Active Directory, Office 365, Azure, Microsoft Defender, Azure Sentinel, Networking (LAN/WAN, Wi-Fi, Routers, Switches)
Key Words: Microsoft 365 , Active Directory , Office 365 , Azure , Microsoft Defender , Azure Sentinel , Networking , LAN , WAN , Wi-Fi , Routers , Switches , Security , Cyber
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: 14/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-14 16:41:03
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Are you an experienced Electrical Engineering Project Manager looking for a new exciting job opportunity?
We are currently looking for a Electrical Engineer Project Manager to join a leading pharmaceutical company based in Northern Ireland.
As the Electrical Engineer Project Manager you will be responsible for the planning, management, coordination and financial control of electrical projects.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Electrical Engineer Project Manager will be varied however the key duties and responsibilities are as follows:
1.
You will establish through consultation with project stakeholders the project requirements, scope of work and major project milestones, and thus determine mutually agreeable project objectives.
You will also manage and influence project stakeholder groups and coordinate automation project resource to ensure successful project delivery.
2.
You will be responsible for ensuring that LV/HV system solutions are delivered to the company within the timeframes established, agreed budget and in accordance with GAMP5 and other industry standards.
Additionally, monitor, report and escalate project issues, risks, changes and progress to project stakeholders, sponsors, and line management.
3.
As the project manager, you will lead the development of practical and cost effective electrical design solutions taking full account of the many competing factors; technical, operational and economic.
You will initiate enquiries with system vendors, evaluate technical proposals and prepare accurate and realistic budget estimates and milestone project programmes for the purpose of gaining approval to acquire capital funds by management.
4.
Additionally, you will support the tender process and supplier / contractor selection to determine the optimal economic and technical solutions for the business and support the preparation of appointment and contract documentation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Electrical Engineer Project Manager we are looking to identify the following on your profile and past history:
1.
A minimum HND in an engineering discipline is essential for the role of Project Manager.
A degree in Electrical Engineering and/or a Prince2 or Agile project management certification would be highly desirable.
2.
Proven industry experience in leading and successfully executing complex large scale electrical projects within the pharmaceutical industry is essential for this position.
You will need to have extensive experience of project delivery through the application of a comprehensive project management process too.
3.
Knowledge of LV systems including transformers, RMU's, LV Distribution, as well as experience in commissioning and qualification activities would be highly advantageous.
Key Words: Automation | Electrical | Project Manager | Engineering Management | DCS | Engineer | Pharmaceutical | Life Science | Process Safety | Prince2 | Agile | PMP | Electronics
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: Craigavon,Northern Ireland
Start: 14/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-14 10:29:05
-
Are you an experienced Procurement Co-ordinator looking for an exciting new job opportunity?
We are currently looking for a Procurement Co-ordinator to join a leading biopharmaceutical company based in the Wiltshire area on an 18 month fixed term contract.
As the Procurement Co-ordinator you will be responsible for the sourcing of all materials and services following the company's Procurement Policy.
Reporting to the Procurement Manager, you will ensure that all procurement activities adhere to the Public Contract Regulations (PCR).
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Procurement Co-ordinator will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for ensuring compliance to all procurement rules and regulations in accordance with the company Procurement Policy and related SOP's as well as undertake Invitation to Tender sourcing.
2.
You will work within the site Quality System and to current Good Manufacturing Practice (cGMP), adhering to all policies, procedures, rules, regulations and guidelines and reporting any non-compliance promptly.
3.
As the procurement co-ordinator, you will negotiate with suppliers to secure advantageous terms, mitigate risk and provide continuous supply of goods and services without compromise to quality or supply.
4.
You will also build and maintain relationships with internal stakeholders, providing support, guidance and expertise in sourcing goods and services for departmental and sites requirements.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Procurement Co-ordinator we are looking to identify the following on your profile and past history:
1.
Proven industry experience in procurement, including basic understanding of Contracts and UK Law.
2.
A degree in a relevant subject or being a Member of the Chartered Institute of Purchase and Supply is not essential for this role but desirable.
3.
Advanced MS Office skills particularly Microsoft Excel is essential, as well as excellent communication, analytical and negotiation skills.
Key Words: Procurement Co-ordinator | Buyer | Biopharmaceutical | Pharmaceutical | Logistics | Supply Chain | Purchasing
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: Wiltshire,England
Start: 14/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-14 10:25:15
-
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
-
Are you an experienced Electrical Design Draughtsman looking for an exciting new job opportunity?
We are currently looking for a Electrical Design Draughtsman to join a growing engineering company based in the Essex area.
As the Electrical Design Draughtsman you will be working alongside the automation technicians to produce the electrical wiring diagrams for the electrical control systems.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Electrical Design Draughtsman will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for generating electrical drawings and panel layouts, with supporting electrical
documentation (Bill of Materials, Component Lists, Cable Schedules, Terminal Rail Layouts etc.)
2.
You will also be assisting with the ongoing drawing transition from AutoCAD to EPLAN, working with the rest of the Automation Department to agree on methods of working and drawing standards.
3.
As the electrical design draughtsman, you will ensure all electrical drawings are updated promptly throughout the lifecycle of the project and shared with all relevant departments.
4.
Additionally, you will be maintaining a database of preferred electrical devices to ensure consistency in functional hardware from project to project.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Electrical Design Draughtsman we are looking to identify the following on your profile and past history:
1.
In-depth knowledge of EPLAN P8 and Pro Panel 3D is essential for this position.
2.
A formal Electrical Engineering Qualification is also required (e.g.
apprenticeship)
3.
Familiarity with automated production machinery or other similar capital equipment will be highly desirable.
Key Words: Electrical Design Draughtsman | Design Engineering Technician | Automation | Production | Engineer
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: Contract Location: Essex,England
Start: 13/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-13 23:38:03
-
Are you an experienced Mechanical Technician looking for an exciting new opportunity?
We are currently looking for a Mechanical Technician to join a growing engineering company based in the Essex area.
As the Mechanical Technician you will be assisting in the machining, manufacturing and build-up of enclosures, equipment and machinery on the factory floor.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Mechanical Technician will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for the fitting and assembly work on the factory floor as well as conducting trials and tests on large scale machinery.
2.
As the mechanical technician, you will also be responsible for piping, testing and fault-finding pneumatic logic circuits.
3.
Additionally, you may be required to travel to customers' sites to assemble, commission, support and service machinery.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Mechanical Technician we are looking to identify the following on your profile and past history:
1.
You will need to have good basis engineering skills, practical engineer experience and be able to interpret equipment assembly drawings for this role.
2.
Ideally some exposure to pneumatics & installation/commissioning work at customer sites.
Key Words: Mechanical Technician | Engineering | Manufacturing | Pneumatics | Equipment Assembly Technician
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: Essex,England
Start: 13/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-13 23:21:03
-
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
-
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
-
Senior Full Stack Developer- Digital Healthcare
Location:Birmingham
Salary:£60000.00 - £65000.00
HRS Consultant:Alex Colbeck
Contact Details:alex.colbeck@hyperec.com +44(0)203 910 2890
We are currently looking for a Senior Full Stack Developer to join a leading digital healthcare company based in the Birmingham area.
As the Senior Full Stack Developer you will be responsible for developing a unique, innovative platform used to provide digital healthcare to patients across the UK.
You will be involved in developing new functions and maintaining the platform across both web and mobile applications.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior Full Stack Developer will be varied however the key duties and responsibilities are as follows:
1.
Lead the development and maintenance of web and mobile applications using Vue.js, .NET Core, C#, Azure.
2.
Collaborate in the full software development lifecycle, from concept and design to testing and deployment.
3.
The focus of this role will be developing in C# and writing business logic and data tier code, but full stack capability and UI experience in Vue.js or similar front end framework would be welcome.
4.
Contribute to the Agile development process and continuous delivery frameworks, coordinate sprint rituals, understand our backlog and how to address any technical debt.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Senior Full Stack Developer we are looking to identify the following on your profile and past history:
1.
Relevant degree in an IT related subject (Computer Science, engineering or similar)
2.
Proven industry experience in the healthcare industry is highly beneficial
3.
A working knowledge and practical experience with .NET, C#, .NET Core, API development, VUE.JS, UI/UX, Testing, Azure, SQL and AI/ML
Key Words: .NET , .NETCore , dotnet , Vue.JS , C# , API , Azure , SQL , developer , full stack , UI , UX
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: Birmingham,England
Start: 13/03/2024
Salary / Rate: £60000 - £65000 per annum
Posted: 2024-03-13 13:49:12
-
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