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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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We are currently looking for a Director of Business Development to join a leading Advanced Therapy company based in the London area.
As the Director of Business Development you will provide strategic leadership, and direction to grow the revenue from our client's Cell Therapy and Laboratory Services and support the delivery of their strategic vision where every patient who needs them can survive and thrive.
This is will be a hybrid appointment with frequent travel required to national and international customers, as well as sites in Nottingham and London.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Director of Business Development will be varied however the key duties and responsibilities are as follows:
1.
Lead and develop a high performing team who are driven to deliver the ambitious growth plans fostering a culture of entrepreneurial growth across the team and organisation.
You will take accountability for the identification and execution of strategic partnerships that further the growth ambitions and market share.
2.
Be accountable for the delivery of a profitable pipeline of commercial income in line with agreed financial targets as well as being responsible for providing excellent market insight and intelligence in relation to cell therapies and growth opportunities.
3.
As the Director of Business Development you will also be responsible for collaborating with the delivery functions to ensure products and services are provided to the customer in line with agreed expectations, ensuring the delivery of excellent customer service that is actively sought and measured.
4.
Be responsible for providing innovative solutions to opportunities in the market through identifying new products and services in support of the development and manufacturing of new treatments.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Director of Business Development we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Life Sciences discipline (i.e Biochemistry / Biopharmaceutical Development / Advanced Therapies) with proven experience in a contract services environment for advanced therapies / biopharmaceutical development at a senior leadership level.
In doing so you would have prior experience of translating strategy and business plans into operational objectives, as well as experience of preparing, delivering and managing annual budgets and business plans
2.
Proven leadership and management capabilities to inspire, empower and motivate others and build high performing teams is required as well as a track record of undertaking research and insight into other relevant companies and building relationships and partnerships within industry.
3.
Excellent knowledge of the relevant regulatory and quality frameworks including HTA and MHRA as well as experience supporting the executive of medicinal product development
Key Words: Business Development Director / Head of Commercial Services / Head of Business Development / CDMO / Cell & Gene Therapy / Advanced Therapy / Leadership Appointment / Cell Therapy / Gene Therapy / Contract Services
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: 11/03/2024
Salary / Rate: Eexperience Dependent
Posted: 2024-03-11 12:31:02
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We are currently looking for a QC Analytical Scientist to join a leading Biopharmaceutical Manufacturing company based in the South of the UK.
As the QC Analytical Scientist you will be responsible for undertaking chemical and biochemical analyses to support the manufacture of pharmaceutical products in compliance to GMP regulations.
This is a great role for a recent graduate with a chemistry background to gain essential industry experience.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analytical Scientist will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for the testing of raw materials, finished products, in-process and stability samples.
2.
You will apply various chemical and biochemical techniques for enzyme analysis including HPLC and UPLC, Gel electrophoresis, and Western blotting
3.
You will write quality records, devise CAPAs and execute protocols and investigations (OOS procedures) to troubleshoot QC issues.
4.
You will take an active role in the training of junior staff work collaboratively with wider teams to ensure the smooth running of the Analytical QC department.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Analytical Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in a life sciences discipline relating to Chemistry, Biochemistry, Analytical Chemistry, etc.
2.
Proven industry experience working in an analytical pharmaceutical GMP environment.
3.
A working knowledge and practical experience testing raw materials and finished products using HPLC.
Key Words: Analytical | HPLC | Chemistry | Pharmaceutical | FTIR | QC | Quality Control | GMP | CAPA | OOS | OOT | Change Control | SOP | Biopharmaceutical | UPLC | Gel Electrophoresis | Graduate | BSc | MSc | CDMO | Analytical 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: Wiltshire,England
Start: 11/03/2024
Salary / Rate: £25000 - £28000 per annum
Posted: 2024-03-11 09:48:05
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Medical Devices Development Engineer - Bristol
A new start-up Medical Devices company, still offering shares/equity, is currently seeking to recruit an experienced Development Engineer.
They require you to lead the engineering progression from pilot to progression.
This role will be split between Bristol and Welwyn Garden City, so ideally, you will be based near Bristol, Welwyn City Garden, or Oxford to facilitate travel.
Overnight accommodation will be funded when required at the alternative site.
Additionally, the company will be looking to set up a single site in the long term, so flexibility regarding location in the future will be advantageous.
You will have input on the new site, as your role will be heavily involved in setting up any new manufacturing facilities.
As is typical with start-up opportunity, there is the need to wear multiple hats when necessary.
The key skill sets we are looking for include experience working as a production/manufacturing engineer and a development engineer, or in another role where you have been responsible for transferring Medical Devices from pilot to production.
A background in Medical Devices is essential as you will need to be familiar with working within ISO 13485 standards.
The Medical Devices are implantable medical devices and handheld medical devices, so any specific experience in this field would be advantageous.
Experience within a successful start-up or scale-up company would be beneficial, as your expertise will be valuable.
Alternatively, you may have acquired this experience while setting up new sites for a new product range at a larger Medical Devices company.
Apart from the split of the role between Bristol and Welwyn Garden City, there will also be meetings in London.
There is the chance of hybrid working, but this will be more ad hoc rather than a dedicated number of days per week.
This role offers an exciting and challenging opportunity and will also reward you with a shares/equity scheme, life assurance, pension, private healthcare, income protection insurance, and an employer discount scheme.
These benefits are more in line with those of a larger company.
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: Bristol, England
Salary / Rate: bonus, pension, income protection
Posted: 2024-03-08 12:01:23
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We are looking for a proven proactive and passionate Project Manager who can lead a team to deliver innovative space projects.
The Space Project Manager will have Project Management experienced of a fast-paced production environment in Aerospace, Defence, Automation and Robotics deliveries.
You will drive results leading cross functional teams.
Requirements
Satellite, Precision Engineering or Aerospace industry project management experience.
Familiar with work package systems and matrix management.
Comfortable interfacing with customers and implementing negotiated contracts.
Degree or equivalent in an engineering or technical subject.
Experience working in or closely with technical teams to understand issues and translate those to schedule and cost impacts accounting for unknown and known risks.
Able to produce and maintain a risk register and to communicate the philosophy on risk
Understanding of contracts and product assurance plans.
Responsibilities
Help build complex bespoke bids and proposals with all associated financial and contractual details.
Motivate individuals and teams to work under pressure to strict deadlines in a technical environment.
Manage projects or aspects of a project from contract commencement through development and delivery of space and ground packages, launch preparation, orbit commissioning and subsequent service delivery operations
To be responsible for all aspects of the project, or a major element of a programme, working in
Lead the development and implementation of advanced manufacturing technologies. ....Read more...
Type: Permanent Location: Aylesbury, England
Start: ASAP
Duration: Permanent
Salary / Rate: £50000 - £85000 Per Annum None
Posted: 2024-03-08 11:52:19
