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We are currently looking for a Qualified Person to join a leading Pharmaceutical company based in the South Yorkshire area.
As the Qualified Person you will be responsible for batch release of Pharmaceuticals and contributing to the management of QMS.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1.
As the Qualified Person you will review and approve batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products.
2.
You will oversee the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines.
3.
As the Qualified Person you will participating in internal and external audits of the manufacturing facilities and quality systems.
Providing expertise and guidance on regulatory requirements and quality standards to internal teams.
4.
You will investigate and resolve quality issues and deviations related to manufacturing processes and materials.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Qualified Person we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Pharmacy, Chemistry or closely related discipline and qualified QP.
2.
Proven industry experience in Pharmaceutical Manufacturing, Quality Assurance and Regulatory Compliance.
3.
A working knowledge and practical experience with activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products.
Key Words: QP, Qualified Person, Quality, Quality Assurance, QA, GMP, Manufacturing, Pharmaceuticals, South Yorkshire.
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: South Yorkshire,England
Start: 24/04/2024
Salary / Rate: £90000 - £100000 per annum
Posted: 2024-04-24 11:31:03
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We are currently looking for a Qualified Person to join a leading Pharmaceutical company based in the Staffordshire area.
As the Qualified Person you will be responsible for batch release of Pharmaceuticals and contributing to the management of QMS.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1.
As the Qualified Person you will review and approve batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products.
2.
You will oversee the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines.
3.
As the Qualified Person you will participating in internal and external audits of the manufacturing facilities and quality systems.
Providing expertise and guidance on regulatory requirements and quality standards to internal teams.
4.
You will investigate and resolve quality issues and deviations related to manufacturing processes and materials.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Qualified Person we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Pharmacy, Chemistry or closely related discipline and qualified QP.
2.
Proven industry experience in Pharmaceutical Manufacturing, Quality Assurance and Regulatory Compliance.
3.
A working knowledge and practical experience with activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products.
Key Words: QP, Qualified Person, Quality, Quality Assurance, QA, GMP, Manufacturing, Pharmaceuticals, Staffordshire.
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: Staffordshire,England
Start: 24/04/2024
Salary / Rate: £90000 - £100000 per annum
Posted: 2024-04-24 11:24:15
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Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks? Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely.
As a Regulatory Affairs Executive, your role will be instrumental in supporting the administrative backbone of the department, maintaining the precision of the regulatory database, and orchestrating the preparation and tracking of regulatory submissions across various stages.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Regulatory Affairs Executive will be varied however the key duties and responsibilities are as follows:
1.
Support the administrative needs of the regulatory department.
2.
Oversee the maintenance and accuracy of the departmental regulatory database.
3.
Manage the preparation and tracking of UK/EU regulatory submissions, including initial and post-approval stages.
4.
Ensure the meticulous archiving of regulatory submissions and approvals.
ROLE REQUIREMENTS:
To be successful in your application to this engaging role as the Regulatory Affairs Executive, we are looking to identify the following on your profile and past history:
1.
A relevant degree in an associated science subject.
2.
Proven industry experience in a similar regulatory affairs role.
3.
A working knowledge and practical experience with regulatory requirements in the UK and EU.
Key Words:
Regulatory Affairs Executive | Regulatory Database | UK Regulatory Submissions | EU Regulatory Submissions | Regulatory Archiving | Tender Support | Regulatory Strategy | CMC | Dossier Review | Variations | Regulatory Compliance | Generic Pharmaceuticals |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications for any applicant who fulfils 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: Berkshire,England
Start: 19/04/2024
Salary / Rate: Competitive
Posted: 2024-04-19 17:18:07
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We are currently looking for a Senior Analytical Development Scientist to join a leading developing Gene Therapy company based in London.
As the Senior Analytical Development Scientist you will be responsible for the driving the development of analytical assays for AAV product and process characterisation.
This opportunity would suit a Scientist with subject matter expertise in HPLC and other chromatography based analytical techniques, who also has experience analysing protein based products to support the hiring company's transition from pre-clinical and early stage to trials and commercial launch of products.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior Analytical Development Scientist will be varied however the key duties and responsibilities are as follows:
1.
You will Develop and deliver HPLC based methods for AAV product and process characterisation.
Methods of interest include but are not limited to, HPCE, cIEF, CE-SDS, MS and LCMS for large molecule characterisation.
2.
You will manage projects, supporting and up-skilling Analytical Scientists within the team, and apply industry knowledge to scope new technologies applicable for AAV product and process characterisation.
3.
You will Tech Transfer to external manufacturing partners, work closely with the CMC team and support process analytical activities to support process development, as well as R&D teams focused on new technology development.
4.
You will support the regulatory team in providing SME analytical guidance, design and write experimental plans, and ensure data is handled accordingly to strict guidelines.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Senior Analytical Development Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Biochemistry, Biochemical Engineering degree or relevant.
A PhD is not required but advantageous.
2.
Proven industry experience where you have used Chromatography based techniques as an analytical tool for the assessment of Large Molecules.
Experience of method development and troubleshooting analytical assays is highly beneficial to this role.
3.
A working knowledge and practical experience working with AAV gene therapy within a GMP analytical testing environment.
Key Words: Analytical Development | Method Development | Assay Development | MDV | Protein Characterisation | Product Characterisation | Protein Analysis | AAV | Viral Vector | Gene Therapy | GMP | QC | Quality Control | CMC | Biologics | Biopharmaceutical | C> | ATMP
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: 19/04/2024
Salary / Rate: Competitive
Posted: 2024-04-19 16:47:02
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Join a pioneering team at the forefront of cancer therapy innovation as a Protein Expression Scientist.
Based in London, this role is integral to the expansion of the biotechnology companies in-house protein expression platform, contributing to the development of life-changing antibody-drug conjugates.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Protein Expression Scientist will be varied however the key duties and responsibilities are as follows:
1.
As Protein Expression Scientist you will be designing and creating plasmids for recombinant protein expression in suspension CHO/HEK cells, including standard antibodies, alternative formats, and antigens.
2.
You will be generating stable CHO cell lines for antibody production at multi-gram scale.
3.
As Protein Expression Scientist you will be conducting antibody production using fed-batch processes in mid-scale bioreactors.
4.
Your role will also involve investigating new technologies within the protein expression domain.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Protein Expression Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in cell biology or molecular biology
2.
Proven industry experience in transient protein expression in CHO and/or HEK293 cells.
3.
A working knowledge and practical experience in the generation of antibody producing stable cell lines and large scale bioprocessing.
Key Words: Protein Expression / CHO Cells / HEK293 Cells / Recombinant Proteins / Antibodies / Bioreactors / Cell Line Generation / Bioprocessing / Antibody Production / Molecular Biology / Cell Biology / Biotechnology / Cancer Therapy / Drug Development
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: 18/04/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-04-18 09:19:03
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Are you an experienced Process Development Manager looking for an interesting new job opportunity?
We are currently looking for a Process Development Manager to join a leading chemicals company based in the Cheshire area.
As the Process Development Manager you will be responsible for liaising with internal and external customers and managing the Process Development team in order to develop and optimise new and existing products and processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Process Development Manager will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for managing the process development team and projects to develop and optimise new and existing products and processes.
2.
You will be expected to use your expertise and strong creative background to offer novel solutions, achieving desirable effects within the business.
3.
As the Process Development Manager, you will use your technical expertise creatively to generate commercially viable solutions to complex problems.
4.
Additionally, you will communicate with internal and external stakeholders from different departments and sectors to ensure projects are delivered on time.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Process Development Manager we are looking to identify the following on your profile and past history:
1.
Relevant degree in a scientific discipline and strong industrial background with experience in process development and scale-up is essential for this role.
2.
Line management and project management experience and a good understanding of Quality Assurance and Health and Safety systems is also required.
3.
A working knowledge and practical experience of protein chemistry and/or biofermentation and related technologies, with knowledge of recent developments in the field as well as understanding of Good Manufacturing Practice (GMP) is advantageous.
Key Words: Process Development Manager | Scale Up | Technology Transfer | GMP | Manufacturing | Chemicals | Pharmaceutical | Protein Chemistry | Science
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: 17/04/2024
Salary / Rate: Dependent on experience
Posted: 2024-04-17 20:30:04
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We are currently looking for a Cell Biologist to join a leading early stage, computational and AI driven drug discovery company based in the Cambridgeshire area.
As the Cell Biology Scientist you will be joining the Target Discovery team focused on functional genomics studies and you will be responsible for the development of novel cell-based assays and CRISPR screens.
This role would suit a recent PhD graduate/ Post Doctoral keen to move into a fast paced industry environment where you have the opportunity to work on novel therapeutics for rare, neural Cancers.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Cell Biology Scientist - Functional Genomics will be varied however the key duties and responsibilities are as follows:
1.
Mammalian Cell Culture of cell lines as well as neuroepithelial stem Cells (NSC) and neurosphere cultures.
2.
Help design and develop genomic screens for Target Discovery utilising CRISPR and siRNA technology approaches.
3.
Optimise and troubleshoot for target validation using a range of molecular biology and cellular biology techniques
4.
Work along side a small, dynamic team of experienced Target Discovery and Cell Biology professionals.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Cell Biology Scientist - Functional Genomics we are looking to identify the following on your profile and past history:
1.
Relevant PhD in Cell Biology, Molecular Biology or related Scientific discipline where you have hands on experience with CRISPR or siRNA technologies.
2.
Proven industry experience in developing and optimising novel cell and molecular biology approaches.
3.
A working knowledge and practical experience with in Cancer Biology and Oncology will benefit your application.
Neural Stem Cell experience is highly advantageous.
Key Words: Cell Biology | Cellular Biologist | Cell Culture | Neuroepithelial Stem Cells | 3D Cell Culture | CRISPR | CRISPR-Cas9 | siRNA | Functional Genomics | Drug Discovery | Target Discovery | Target Validation
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: Cambridgeshire,England
Start: 17/04/2024
Salary / Rate: Competitive
Posted: 2024-04-17 14:32:09
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We are currently looking for a Production Manager to join a leading Radiopharmaceutical company based in the Surrey area.
As the Production Manager you will be responsible for the management of all aspects of the Production dept.
This will include line management of the Production team, coordination of the production schedule, equipment validation and ensuring compliance with GMP.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Production Manager will be varied however the key duties and responsibilities are as follows:
1.
Managing and overseeing all aspects of the production team, including the production schedual and compliance within the department.
2.
Leading the entire production team
3.
Ensuring the efficiency of performances within first line maintenances of all products
4.
Working under a strict aseptic guidelines and GMP
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Production Manager we are looking to identify the following on your profile and past history:
1.
Relevant degree in a relevant scientific area or experiences within Radiopharmaceutical.
2.
Proven industry experience in management within Radiopharmaceutical Production.
3.
A working knowledge and practical experience with GMP and Aseptic environments
Key Words: Radiopharmaceutical / GMP / Sterile / Aseptic / PET / Production / MHRA / Fluorine
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: Surrey,England
Start: 11/04/2024
Salary / Rate: £45000 - £55000 per annum
Posted: 2024-04-11 14:32:38
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We have an exciting opportunity for a Business Development Manager to join a cutting-edge technology start-up company based in the Oxfordshire area.
As the Business Development Manager you will acting as the liaison between the organisation and external stakeholders, fostering relationships and driving income generation efforts to advance the company mission within global public health.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Business Development Manager will be varied however the key duties and responsibilities are as follows:
1.
As Business Development Manager you will serve as a liaison between the organisation and external stakeholders, fostering productive relationships and partnerships.
2.
You will write compelling grant applications, proposals, and funding requests, ensuring alignment with organisational goals and objectives.
3.
As Business Development Manager you will translate conceptual ideas into practical proposals, incorporating innovative approaches and solutions to address global health challenges, particularly in pathogen genomic networks and Antimicrobial Resistance.
4.
You will proactively follow up on new opportunity leads with global public health bodies, identifying and pursuing funding opportunities whilst also keeping informed of regulatory requirements to inform organisation strategy and decision-making.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Business Development Manager we are looking to identify the following on your profile and past history:
1.
Bachelors degree in a life science based subject (e.g.
Public Health or Biomedical Science)
2.
Proven industry experience in grant writing, proposal development, or related fields within the nonprofit, academic, or public health sectors.
3.
A working knowledge and practical experience in public health or infectious disease epidemiology.
Key Words: Business Development | Bids | Grants | Income Generation | Public Health | Bioinformatics | Rare Diseases | Grant Applications | Commercial | Funding | Social Impact | Global | Proposals | Genomics
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: 11/04/2024
Salary / Rate: Competitive
Posted: 2024-04-11 09:45:17
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We are currently looking for a CSV Analyst to join a leading European specialist pharmaceutical company based in Wales.
As the CSV Analyst you will be responsible for ensuring that IT Quality Management System, Validation documentation and all related processes, procedures and systems meet the requirements of all applicable regulations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CSV Analyst will be varied however the key duties and responsibilities are as follows:
Assist the CSV/Lead Process Analyst in continued improvement and delivery of the Global IT validation strategy and approach taking into account the relevant GxP requirements (e.g.
EU Annex 11, FDA 21 CFR Part 11, Part 820, etc.) and also other relevant regulatory requirements
Support the continuous improvement of appropriate procedures to be used in validating computerised systems.
Support project teams in the assessment of proposed new computerized systems or software for GxP impact and where GxP impact is identified provide guidance on the risk based validation approach for the system, working with key stakeholders to achieve business goals.
Acts as a quality contact and primary Subject Matter Expert (SME) for Computer System Validation (CSV) and Risk Management
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the CSV Analyst we are looking to identify the following on your profile and past history:
1.
Wide experience of the various regulatory requirements relating to Eudralex Annexe 11, FDA CFR21 Part 11, etc..
2.
Substantial experience in a validation and qualification of complex computer systems
3.
Familiarity with multiple system types such as ERP and BI, LIMS, HRIS etc
Key Words: CSV, Computer System Validation, GxP, IT Quality Management System, ERP, LIMS
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: Wales,Wales
Start: 09/04/2024
Salary / Rate: £40000 - £50000 per annum
Posted: 2024-04-09 10:48:02
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HRS are looking for a Senior Principal Scientist - C> to join a leading Diagnostics Biotechnology company based in the Bedfordshire area.
As the Senior Principal Scientist - C> you will develop a team applying your industry knowledge with adeno-associated virus (AAV), and lentivirus purification detection
This is a great opportunity to execute strategy for R&D in the cell and gene therapy space to forge growth and company advancement.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior Principal Scientist - C> will be varied however the key duties and responsibilities are as follows:
1.
You will demonstrate your expertise knowledge of AAVs and lentivirus purification, detection, production and characterisation techniques.
2.
Applying project management expertise to form new strategies to execute required work ensuring successful technology transfers to customers ensuring their synthetic polymers can be incorporated into relevant applications.
3.
You will be responsible for the line management and up-skilling of staff, work with the business's development and technical teams in early feasibility assessment and project proposals, and the Operations Team for scale-up and commercial supply.
4.
You will prepare complex technical reports and presentations, and contribute with ideas and solutions in all areas of the company's projects driving them to enable overall goals including new IP generation in the G&CT space.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as theSenior Principal Scientist - C> we are looking to identify the following on your profile and past history:
1.
Relevant PhD in Biochemistry, Chemistry, Nanotechnology or a suitably related field
2.
Extensive industry experience with product development in a C> R&D environment managing teams.
3.
Extensive working knowledge and practical experience with AAVs, lentivirus purification, detection and characterisation techniques.
Key Words: C> | Cell and Gene Therapy | ATMP | Gene Therapy | AAV | Adeno-associated virus | R&D | Research and Development | QMS | Quality Management Systems | GLP | Polymer Chemistry | PhD | Nanotechnology | Biotechnology | Diagnostics | Bedfordshire | Viral Vector | PhD | Manager | Product Development | Product Management | Senior Principal Scientist | Head of R&D | Head of Product Development
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: Bedfordshire,England
Start: 09/04/2024
Salary / Rate: £70000 - £85000 per annum
Posted: 2024-04-09 09:56:10
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Are you an experienced Electrical Control Panel Technician looking for an exciting new job opportunity?
We are currently looking for a Electrical Control Panel Technician to join a growing engineering company based in the Essex area.
As the Electrical Control Panel Technician you will work alongside the Automation Technicians to produce the electrical wiring diagrams for the electrical control systems.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Electrical Control Panel Technician will be varied however the key duties and responsibilities are as follows:
1.
You will work as part of the Automation department in building, wiring and installing control panels and check required panel components against issued wiring diagram and control panel layouts.
2.
Layout chassis plates in line with panel layouts and work with Electrical Design Draughtsman to accomplish best panel layout and design as well as assemble components on to chassis plate and fix accordingly.
3.
Mark up wiring diagrams as panel wiring completed and raising any errors detected with the Electrical Design Draughtsman and Automation Technician.
4.
Additionally, you will work with the Automation Installation electricians in installing the control panels into the production machines.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Electrical Control Panel Technician we are looking to identify the following on your profile and past history:
1.
Relevant degree or formal Electrical Engineering Qualification (e.g.
apprenticeship) is essential.
2.
Proven industry experience in a similar role, working with automated production machinery or other similar capital equipment.
3.
Experience working in a project environment in cross-functional project teams is desirable.
Key Words: Electrical Control Panel Technician | Automation | Manufacturing | Production | Engineering | Controls | Pharmaceutical
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: 08/04/2024
Salary / Rate: Dependent on experience
Posted: 2024-04-08 22:18:03
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Are you an experienced Automation Technician looking for an exciting new job opportunity?
We are currently looking for an Automation Technician to join a growing engineering company based in the Essex area.
As the Automation Technician you will work in the Electrical and Automation department, working alongside electricians and panel builders to design and build the control system and then program and commission the machines in the factory and on site.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Automation Technician will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for designing PLC based electrical control systems from design specifications and programming PLC, Touchscreen and Safety Configurable relay systems.
2.
You will be configuring Remote I/O, servo motor and inverter drives and integrating ancillary equipment into the production lines such as vision systems.
3.
As the Automation Technician, you will be fault finding electrical control systems, PLC and hardwired systems.
4.
When required, you will commission, support and service work at customers' sites.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Automation Technician we are looking to identify the following on your profile and past history:
1.
Good understanding of electrical drawings, control panel specification/design, PLC programming, touchscreens, and controls along with an understanding of vision and SCADA systems is essential.
2.
Experience of the pharmaceutical industry and/or explosive atmosphere regulations is desirable.
3.
A certain amount of travel is required to support the company's worldwide customer base.
Key Words: Automation Technician | Controls | Engineering | Pharmaceutical | Electronics | Electrical
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: 08/04/2024
Salary / Rate: Dependent on experience
Posted: 2024-04-08 22:07:03
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HRS are looking for a Head of Cell and Gene Therapy to join a leading Diagnostics Biotechnology company based in the Bedfordshire area.
As the Head of Cell and Gene Therapy you will develop a team applying your industry knowledge with adeno-associated virus (AAV), and lentivirus purification detection
This is a great opportunity to execute strategy for R&D in the cell and gene therapy space to forge growth and company advancement.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Head of Cell and Gene Therapy will be varied however the key duties and responsibilities are as follows:
1.
You will demonstrate your expertise knowledge of AAVs and lentivirus purification, detection, production and characterisation techniques.
2.
Applying project management expertise to form new strategies to execute required work ensuring successful technology transfers to customers ensuring their synthetic polymers can be incorporated into relevant applications.
3.
You will be responsible for the line management and up-skilling of staff, work with the business's development and technical teams in early feasibility assessment and project proposals, and the Operations Team for scale-up and commercial supply.
4.
You will prepare complex technical reports and presentations, and contribute with ideas and solutions in all areas of the company's projects driving them to enable overall goals including new IP generation in the G&CT space.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Head of Cell and Gene Therapy we are looking to identify the following on your profile and past history:
1.
Relevant PhD in Biochemistry, Chemistry, Nanotechnology or a suitably related field
2.
Proven industry experience in C> R&D Environment managing large teams.
3.
A working knowledge and practical experience with AAVs, lentivirus purification, detection and characterisation techniques
Key Words: C> | Cell and Gene Therapy | ATMP | Gene Therapy | AAV | Adeno-associated virus | R&D | Research and Development | QMS | Quality Management Systems | GLP | Polymer Chemistry | PhD | Nanotechnology | Biotechnology | Diagnostics | Bedfordshire | Viral Vector | PhD | Manager | Team Lead |
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: Bedfordshire,England
Start: 08/04/2024
Salary / Rate: £70000 - £80000 per annum
Posted: 2024-04-08 17:27:15
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Are you an experienced Electrical Technician looking for an exciting new job opportunity?
We are currently looking for a Electrical Technician to join a growing engineering company based in the Essex area.
As the Electrical Technician you will be responsible for working alongside existing Installation Electricians to install the electrical controls for bespoke manufacturing machines with possible site installations too.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Electrical Technician will be varied however the key duties and responsibilities are as follows:
You will install electrical controls for the company's bespoke filling machines in the factory workshop and when required assist with other tasks within the automation department, such as physical wiring inspections, installation checks and machine testing.
As the electrical technician, you will also be responsible for the factory maintenance.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Electrical Technician we are looking to identify the following on your profile and past history:
1.
Formal Electrical Engineering qualification (e.g.
apprenticeship) and familiarity with control and machine components is essential for this position.
2.
Understand electrical wiring diagrams for component identification, cable terminations and differentiation from a panel device to a field mounted device, contactors, relays, and motors.
3.
Familiar with industrial electrical installations and able to work with several types of cable management, tray, basket, trunking, conduit, and the skills to prepare and install cable management system.
Key Words: Electrical Engineering Technician | Industrial Engineer | Automation | Manufacturing
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: 08/04/2024
Salary / Rate: Dependent on experience
Posted: 2024-04-08 16:44:34
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Are you an experienced Mechanical Design Engineer looking for an exciting new job opportunity?
We are currently looking for a Mechanical Design Engineer to join a growing engineering company based in the Essex area.
As the Mechanical Design Engineer you will be responsible for producing mechanical design/drawings for mechanical systems and equipment to work within a small team of mechanical design engineers overseen by the Drawing office manager.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Mechanical Design Engineer will be varied however the key duties and responsibilities are as follows:
You will be responsible for producing mechanical design drawings and design activities including;
- layout designs
- enclosure design
- conveyor design
- ductwork design
- general mechanical design (sensor bracketry/equipment mounting etc.)
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Mechanical Design Engineer we are looking to identify the following on your profile and past history:
1.
Recognised engineering certification/apprenticeship and working knowledge in an industrial/design environment of Autodesk products, including AutoCAD (2D), Inventor (3D), Autodesk Vault (User only), although other 3D CAD software knowledge may be considered, such as SolidWorks etc.
2.
Good understanding of engineering techniques, including machining, sheet metal and fabrication as well as experience in drafting standards for BS 8888 is essential for this position.
3.
Able to interpret equipment assembly drawings and maintain the high-quality finish and output levels expected by our customers.
Key Words: Mechanical Design Engineer | Industrial | Manufacturing Engineering | AutoCAD | AutoDesk
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: 08/04/2024
Salary / Rate: Dependent on experience
Posted: 2024-04-08 16:28:03
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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
-
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
