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Role Overview
We are currently looking for a Field Service Engineer to join a leading Life Science company based in the Milton Keynes area.
As the Field Service Engineer you will be responsible to install, validate, maintain, and repair analytical laboratory equipment across the UK.
The role will cover the Midlands/Southeastern England/Cambridge territory with occasional travel across the UK.
Key Duties and Responsibilities
Your duties as the Field Service Engineer will be varied however the key duties and responsibilities are as follows:
1.
You will be well-versed in all HPLC products, with a focus on the pertinent Service Schedules that are offered to the companies clients.
2.
The Field Service Engineer will work as part of an experience team offering first class customer support and with time will also move onto cover LCMS single and triple Quads.
3.
You will perform installation/validation of new instrumentation (IQOQ.PQ Testing) and maintain accurate inventory of spare parts in car stock.
4.
As the Field Service Engineer you will also report of all the Service jobs using SAP in a timely manner whilst troubleshooting with 48 Hour Response times.
Role Requirements
To be successful in your application to this exciting opportunity as the Field Service Engineer we are looking to identify the following on your profile and past history:
1.
Relevant degree in a scientific discipline is ideal.
2.
Proven industry experience in HPLC / LCMS as well as a background of maintenance and troubleshooting skills in a GLP/GMP environment.
3.
Experience with other Analytical Instrumentation such as MALDI, Prep LC and SFC is beneficial but not essential.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: Cambridgeshire,England
Start: 15/11/2024
Salary / Rate: Dependent on experience
Posted: 2024-11-15 14:42:04
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Role Overview
Are you an experienced production technician / operator looking for an exciting new job opportunity?
We are currently looking for multiple Production Technicians and Operators to join a leading Pharmaceutical company based in the Hertfordshire area.
There are multiple vacancies across various production teams including; incoming materials, equipment and machine preparation, material handling/processing, sterile operations, quality control, labelling and packaging.
All production teams work 24/7 and as the Production Technician, you will be on a 4 on 4 off 12 hour shift.
As the Production Technician you will be responsible for the technical aspects of machine set-up and operation/completion of relevant documentation, whilst actively supporting process improvements and adhering to cGMP regulations.
Key Duties and Responsibilities
Your duties as the Production Technician will be varied dependent on which team you join, however the key duties and responsibilities are as follows:
1.
To adhere to cGMP and H&S standards, including hygiene, environmental control and safe working practices within the production environment.
2.
To ensure that manufacturing equipment is used in compliance with any maintenance, calibration and validation requirements.
3.
Help co-ordinate the activities of the section including the liaising with other sections when required.
4.
To develop skills which will enable reviews of SOPs, BPRs and related documentation as required by the Team Leader.
Role Requirements
To be successful in your application to this exciting opportunity as the Production Technician we are looking to identify the following on your profile and past history:
1.
Have previous work experience in a process or highly regulated industry, for e.g.
Pharmaceutical, Chemicals, Food, FMCG, Beverages etc.
2.
Experience in setting up and operating automated and semi-automated equipment in compliance with approved procedures.
3.
Demonstrated ability to understand and follow SOPs with good attention to detail.
Please note: a driving licence and access to a vehicle is required due to the location of the site.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: Hertfordshire,England
Start: 15/11/2024
Salary / Rate: includes shift allowance
Posted: 2024-11-15 14:22:03
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Job role:
To support the Senior Signal Processing Engineer in the definition and implementation of analytical tools and algorithmic methods to generate, extract, compare and contrast sub-cellular characteristics from high dimensional, datasets to support the user experience and value of the companies products.
To ensure the information embodied in the company data is robust, insightful, relevant and accessible to our end-users, acting as a first point of escalation for the test teams.
To enhance the companies product and analysis application capabilities by developing and applying machine learning algorithms and other emerging technologies.
Key Responsibilities:
Planning, developing, implementing, and testing analytical algorithms to fully exploit and demonstrate the efficacy of the companies proprietary sensing method in various bioprocessing applications.
Provide a link between the Engineering and Biology teams to support the analysis of data and ensure information is robust, relevant and accessible to users.
Work closely with the rest of the Engineering team to support testing and validation of new hardware through data analysis.
Creating and maintaining accurate documentation.
As part of a team work with the companies established external contractors and partners for the development of software/signal processing/machine learning/data visualisation solutions.
Writing Standard Operating Procedures (SOPs) and ensuring compliance with documentation standards.
Engaging in daily meetings with internal and external teams to coordinate efforts and ensure alignment.
Ensuring compliance with company policies, procedures and guidelines, together with all relevant regulatory and statutory requirements.
Where applicable work to regulatory standards throughout a software development life cycle (ISO9001).
Engaging with the companys appraisal process, and demonstrate commitment to our values, behaviours and your continuous personal development.
Performing other reasonable duties and/or projects as directed by your line manager.
If you need any more information or would like to have a chat please reach out to me on 02039102894 or mark.allen@hyperec.com ....Read more...
Type: Permanent Location: City of Edinburgh,Scotland
Start: 15/11/2024
Salary / Rate: £35000 - £44000 per annum
Posted: 2024-11-15 09:37:03
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Role Overview
We are currently looking for a Maintenance Engineer to join a leading Pharmaceutical company based in the Leicestershire area.
As the Maintenance Engineer you will be responsible for play a pivotal role in ensuring the smooth operation of maintenance activities, adhering to environmental and HS&E legislation, and contributing to the ongoing success of the companys production and facilities maintenance.
There are both day shifts (9am-5pm) and double day shifts available (6am-2pm & 2pm-10pm)
Key Duties and Responsibilities Your duties as the Maintenance Engineer will be varied however the key duties and responsibilities are as follows:
1.
Oversee maintenance activities, ensuring compliance with environmental and HS&E legislation.
2.
Support the manufacturing team with completion of Planned & Unplanned maintenance activities
3.
Assist with the coordination / completion of the weekly maintenance routines
4.
Develop and update Facilities site layout drawings in line with requirements.
Role Requirements To be successful in your application to this engaging role as the Maintenance Engineer, our client is looking to identify the following on your profile and past history:
1.
Relevant qualification in Engineering, Electrical, or a related field.
2.
Proven experience in maintenance within a production environment, within the pharmaceutical industry would be desirable.
3.
A working knowledge and practical experience with maintenance of production equipment.
Key Words:
Facilities / Maintenance / Leicestershire/ Pharmaceutical / Engineering / HS&E / Compliance / Electrical/ Mechanical/ Multi skilled / Documentation ....Read more...
Type: Permanent Location: Leicestershire,England
Start: 11/11/2024
Salary / Rate: Competitive
Posted: 2024-11-11 10:14:04
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Role Overview
We are currently looking for a Product Development Team Leader to join a leading biotechnology company based in the Manchester area.
As the Product Development Team Leader, you will be responsible for driving the design, development, and validation of in vitro diagnostic products using next-generation sequencing (NGS) technologies.
Key Duties and Responsibilities
1.
Lead and manage a team of NGS scientists and technicians, ensuring effective resource planning and skill development.
2.
Provide scientific expertise and technical leadership on all NGS projects, ensuring high-quality and timely execution.
3.
Collaborate with project managers, bioinformaticians, and regulatory affairs for effective project planning and reporting.
4.
Work with internal and external stakeholders to deliver optimised assays and workflows ready for successful product transfer.
Role Requirements:
To be successful in your application to this exciting opportunity as the NGS Product Development Team Leader we are looking to identify the following on your profile and past history:
1.
Relevant degree in a life science such as molecular biology, biochemistry, or genetics.
2.
Extensive industry experience in next-generation sequencing technologies.
3.
Proven experience in team leadership and project management within a biotechnology or molecular diagnostics setting.
Key Words: NGS | Next Generation Sequencing | Principal Scientist | Team Leader | Product Development | Biotechnology | Molecular Diagnostics | Diagnostics | Assay Development | Bioinformatics | Regulatory Submissions | Manchester | Product Transfer | In vitro | In-vitro Diagnostics
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: Manchester,England
Start: 07/11/2024
Salary / Rate: Competitive
Posted: 2024-11-07 17:00:04
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Role Overview
We are currently looking for a Research Scientist to join a leading biotechnology gene therapy company based in London.
As the Research Scientist you will be responsible for using molecular biology, in vitro and ex vivo assay set ups to conduct in-house research and pre-clinical activities to support the progression of AAV gene therapy pipeline products.
Key Duties and Responsibilities
1.
Conduct molecular biology and cloning activities to support the development of AAV vector engineering, capsid, and promoter development.
2.
Conduct molecular biology activities to support development of gene engineering technologies for complex genes and translational projects.
3.
Develop and execute qPCR, RT-PCR, and other analytical techniques for analysis of in vitro and ex vivo samples to support the product pipeline.
4.
Contribute to study and experimental design and the planning and coordinating of experimental work.
Role Requirements
1.
Relevant degree in Life Sciences or an equivalent qualification.
2.
Proven industry experience in cloning, molecular biology, and vector production.
3.
A working knowledge and practical experience with cell culture and cell-based assays.
Key Words: Research Scientist | Molecular Biology | Cellular Biology | Biotechnology | AAV Gene Therapy | Molecular Biology | Cloning | Vector Production | Cell Culture | qPCR | RT-PCR | Pre-clinical Research | London | Western blot | ELISA
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: London,England
Start: 07/11/2024
Salary / Rate: Competitive
Posted: 2024-11-07 16:54:04
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Are you an experienced MSAT Packaging Engineer looking for an exciting new job opportunity?
Role Overview
We are currently looking for a MSAT Packaging Engineer to join a leading life sciences company based in Belgium.
As the MSAT Packaging Engineer, you will be responsible for ensuring the integrity and validation of packaging processes, contributing to the development of innovative solutions that improve product quality and compliance.
Key Duties and Responsibilities
Your duties as the MSAT Packaging Engineer will be varied; however, the key duties and responsibilities are as follows:
1.
Lead closure and shipping validation projects.
2.
Execute validation tasks and ensure documentation is scientifically based and compliant with European GMP, ISO13485, and 21CFR820 standards.
3.
Conduct product impact assessments when introducing new primary packaging.
4.
Support technical investigations and other MSAT projects.
Role Requirements
To be successful in your application to this exciting role as the MSAT Packaging Engineer, we are looking to identify the following on your profile and past history:
1.
Relevant degree in Biotechnology, Chemistry, Biology, or a related field.
2.
Proven industry experience in packaging and closure integrity within the pharmaceutical or biotechnology sector.
3.
A working knowledge and practical experience with GMP and validation principles as well as fluent in both English and French.
Key Words:
MSAT / Packaging Engineer / Life Sciences / Pharmaceutical / Biotechnology / GMP / Validation / Closure Integrity / Shipping Validation / Product Quality
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from 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: Verviers,Belgium
Start: 06/11/2024
Salary / Rate: Dependent on experience
Posted: 2024-11-06 10:47:03
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We are currently looking for a Quality Control Scientist to join a leading biotechnology company based in the Oxford area.
As the Quality Control Scientist, you will be responsible for ensuring the highest standards of QC testing and laboratory management.
This is a fully on-site position.
Key Duties and Responsibilities:
Your duties as the Quality Control Scientist will be varied; however, the key duties and responsibilities are as follows:
1.
Perform QC testing following Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP).
2.
Assist with the maintenance of QC laboratory and equipment, including the generation of protocols and reports for assay transfers and validation.
3.
Review and complete documentation in accordance with cGMP, author and review SOPs, forms, Deviations, Change Controls, CAPA, and CoA reports.
4.
Lead or assist with OOS, OOT, and lab investigations as needed, and participate in regulatory inspections and submissions.
Role Requirements:
To be successful in your application to this exciting role as the Quality Control Scientist, we are looking to identify the following on your profile and past history:
1.
Relevant degree in Chemistry, Biochemistry, Microbiology, or another related science.
2.
Proven industry experience in GLP/GMP environments.
3.
A working knowledge and practical experience with QC testing, laboratory maintenance, and regulatory compliance.
Key Words: Quality Control / QC Manager / Biotechnology / cGMP / SOPs / Assay Validation / Laboratory Management / Regulatory Inspections / GLP / GMP / Chemistry / Biochemistry / Microbiology
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications for any applicant 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: Oxford,England
Start: 06/11/2024
Salary / Rate: Competitive
Posted: 2024-11-06 09:21:04
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We are currently looking for a Quality Control Analyst to join a leading biotechnology company based in the Oxford area.
As the Quality Control Analyst, you will be responsible for ensuring the highest standards of quality and compliance within the laboratory environment.
This role offers the chance to work in a dynamic setting where your contributions will directly impact the success of the companys products and services.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Business Development Manager will be varied however the key duties and responsibilities are as follows:
1. Perform QC testing of various samples according to Standard Operating Procedures (SOPs), including cell-based and ELISA-based assays.
2. Maintain various cell lines by revival and passaging at set intervals.
3. Review testing data and records of other operators and verify data for reports.
4. Perform QC sample and material receipt and maintain inventory.
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. Relevant degree in Chemistry, Biochemistry, or a related science.
2.
Proven industry experience in a laboratory setting.
3.
A working knowledge and practical experience with GMP requirements.
Key Words:
Quality Control | QC Analyst | Biotechnology | Laboratory | GMP | Cell-based Assays | ELISA | Inventory Management | SOPs | Data Review | Equipment Maintenance | Analytical Skills | Teamwork |
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: Oxford,England
Start: 06/11/2024
Salary / Rate: Competitive
Posted: 2024-11-06 09:18:04
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Do you have experience with troubleshooting and maintenance of HPLC / LCMS equipment?
We are currently looking for a Field Service Engineer to join a leading Life Science company based in the Milton Keynes area.
As the Field Service Engineer you will be responsible to install, validate, maintain, and repair analytical laboratory equipment across the UK.
The role will cover the Southeastern England/Cambridge territory with occasional travel across the UK so the ideal candidate would be based in this region.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Field Service Engineer will be varied however the key duties and responsibilities are as follows:
1.
You will be well-versed in all HPLC products, with a focus on the pertinent Service Schedules that are offered to the companies clients.
2.
The Field Service Engineer will work as part of an experience team offering first class customer support and with time will also move onto cover LCMS single and triple Quads.
3.
You will perform installation/validation of new instrumentation (IQOQ.PQ Testing) and maintain accurate inventory of spare parts in car stock.
4.
As the Field Service Engineer you will also report of all the Service jobs using SAP in a timely manner whilst troubleshooting with 48 Hour Response times.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Field Service Engineer we are looking to identify the following on your profile and past history:
1.
Relevant degree in a scientific discipline is ideal.
2.
Proven industry experience in HPLC / LCMS as well as a background of maintenance and troubleshooting skills in a GLP/GMP environment.
3.
Experience with other Analytical Instrumentation such as MALDI, Prep LC and SFC is beneficial but not essential.
Key Words: Field Service Engineer | HPLC | LCMS | MALDI | Prep LC | SFC | Maintenance | GMP | GLP | Service Schedules | Installation | Validation | Instrumentation | IQOQ | SAP | Troubleshooting |
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: St Albans,England
Start: 01/11/2024
Salary / Rate: Dependent on experience
Posted: 2024-11-01 17:22:09
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Are you an experienced Chemistry Team Leader looking for an exciting new job opportunity?
We are currently looking for a Chemistry Team Leader to join a leading pharmaceutical company based in the Hertfordshire area.
As the Chemistry Team Leader, you will be responsible for overseeing a defined section of the laboratory, ensuring that samples are taken and tested according to plan, results are checked and progressed, and that Good Manufacturing Practice (GMP) and standards are met.
This is a first-line management role, providing an excellent platform to demonstrate your leadership skills and make a significant impact.
Key Duties and Responsibilities:
Your duties as the Chemistry Team Leader will be varied; however, the key duties and responsibilities are as follows:
1.
Organise and schedule departmental work to ensure batch progression targets are met.
2.
Ensure calibration or validation of laboratory equipment and automated systems is performed.
3.
Deliver training to all members of the department and ensure all staff are working in accordance with Standard Operating Procedures and GMP.
4.
Act as a subject matter expert in relation to the work of the section and produce reports covering laboratory results.
Role Requirements:
To be successful in your application to this exciting role as the Chemistry Team Leader, we are looking to identify the following on your profile and past history:
1.
Relevant degree in Chemistry or a related field.
2.
Extensive industry experience in a laboratory setting, with demonstrated competency in managing others.
3.
A working knowledge and practical experience with cGMP/GLP and laboratory instrumentation, ideally chromatography (GC and HPLC).
Key Words:
Chemistry Team Leader / Pharmaceutical / Laboratory Management / GMP / GLP / Quality Control / Analytical Chemistry / Laboratory Supervisor / Team Leadership / Pharmaceutical Testing / Laboratory Operations
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from 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: St Albans,England
Start: 01/11/2024
Salary / Rate: Dependent on experience
Posted: 2024-11-01 15:42:11
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Are you an experienced Process Engineer looking for an exciting new job opportunity?
We are currently looking for a Process Engineer to join a leading pharmaceutical company based in the Hertfordshire area.
As the Process Engineer, you will be responsible for supporting process engineering activities for the production of biopharmaceuticals in a cGMP environment.
Key Duties and Responsibilities:
Your duties as the Process Engineer will be varied; however, the key duties and responsibilities are as follows:
1.
Providing technical expertise on cross-functional projects including process/utility improvement, technology transfer, and new product introduction.
2.
Assessing new and existing processes for reliability, quality, safety, best practices, and adherence to cGMP and regulatory requirements.
3.
Supporting installation and commissioning of new processes and equipment, monitoring effectiveness.
4.
Investigating engineering problems, troubleshooting existing processes, and determining root cause and solutions.
Role Requirements:
To be successful in your application to this exciting role as the Process Engineer, we are looking to identify the following on your profile and past history:
1.
Relevant degree in a related field.
2.
Proven industry experience in process engineering within a pharmaceutical or similar GMP environment such as the food or speciality chemicals industry.
3.
A working knowledge and practical experience with process design, commissioning, and validation.
Key Words:
Process Engineer / Pharmaceutical / GMP / Plasma-Derived Products / Process Design / Technology Transfer / Process Improvement / Commissioning / Troubleshooting / Regulatory Compliance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from 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 move. ....Read more...
Type: Permanent Location: St Albans,England
Start: 01/11/2024
Salary / Rate: Dependent on experience
Posted: 2024-11-01 15:38:04
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We are currently looking for a MSAT Packaging Engineer to join a leading life sciences company based in Belgium.
As the MSAT Packaging Engineer, you will be responsible for ensuring the integrity and validation of packaging processes, contributing to the development of innovative solutions that improve product quality and compliance.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the MSAT Packaging Engineer will be varied; however, the key duties and responsibilities are as follows:
1.
Lead closure and shipping validation projects.
2.
Execute validation tasks and ensure documentation is scientifically based and compliant with European GMP, ISO13485, and 21CFR820 standards.
3.
Conduct product impact assessments when introducing new primary packaging.
4.
Support technical investigations and other MSAT projects.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the MSAT Packaging Engineer, we are looking to identify the following on your profile and past history:
1.
Relevant degree in Biotechnology, Chemistry, Biology, or a related field.
2.
Proven industry experience in packaging and closure integrity within the pharmaceutical or biotechnology sector.
3.
A working knowledge and practical experience with GMP and validation principles as well as fluent in both English and French.
Key Words:
MSAT / Packaging Engineer / Life Sciences / Pharmaceutical / Biotechnology / GMP / Validation / Closure Integrity / Shipping Validation / Product Quality
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from 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: Verviers,Belgium
Start: 01/11/2024
Salary / Rate: Dependent on experience
Posted: 2024-11-01 15:27:03
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We are currently looking for a Quality Director to join a leading pharmaceutical company in the South East of the UK.
As the Quality Director, you will manage, maintain, and improve quality and compliance across multiple global entities, ensuring strategic alignment with the companys business plan.
You will be accountable for compliance with legal requirements, including Manufacturers/Importers Authorisation, Wholesale Dealers Authorisation, and Good Manufacturing and Distribution Practices (GMP/GDP).
KEY DUTIES AND RESPONSIBILITIES
Your key responsibilities as the Quality Director will be:
1.
Lead and manage the global Quality, Technical, and Compliance teams to ensure adherence to GMP and GDP standards.
You will oversee Qualified Persons (QPs) and manage product certification across multiple locations.
2.
Review and optimise the Quality Management System (QMS) and ensure all quality systems are compliant with regulatory bodies like MHRA and foreign authorities.
3.
As the Quality Director, you will provide expert advice to the board on quality matters and collaborate with senior leadership on business strategy and quality improvement plans.
4.
Manage regulatory inspections and customer audits, while driving continuous improvement initiatives based on performance metrics
ROLE REQUIREMENTS:
To be successful in your application for the Quality Director role, we are looking for the following experience:
1.
A Degree or higher level in Chemistry / Pharmaceutical Management / Quality Assurance, with extensive experience in pharmaceutical quality management, including leadership and team management within a GMP environment.
2.
Extensive experience with regulatory compliance in the UK, EU, and international markets, including expertise in handling audits and managing the performance of quality teams.
3.
Ability to engage cross-functional teams, drive continuous improvement initiatives, and provide strategic leadership in quality matters.
WHATS IN IT FOR YOU?
As a Quality Director, you will be part of the key site senior leadership team in a global pharmaceutical company, with the opportunity to shape the quality strategy and ensure compliance with regulatory bodies.
You will benefit from career development opportunities, a competitive benefits package, and the chance to lead high-impact quality initiatives across multiple global entities.
Key Words: Quality Director / Head of Quality / GMP / GDP / Pharmaceutical / Compliance / QP / Quality Assurance / Continuous Improvement / Regulatory Compliance / MHRA / Audits
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development.
We welcome applications for any applicant 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 East England,England
Start: 29/10/2024
Salary / Rate: Experience Dependent
Posted: 2024-10-29 14:29:03
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Are you an experienced Chemistry Team Leader looking for an exciting new job opportunity?
We are currently looking for a Chemistry Team Leader to join a leading pharmaceutical company based in the Hertfordshire area.
As the Chemistry Team Leader, you will be responsible for overseeing a defined section of the laboratory, ensuring that samples are taken and tested according to plan, results are checked and progressed, and that Good Manufacturing Practice (GMP) and standards are met.
This is a first-line management role, providing an excellent platform to demonstrate your leadership skills and make a significant impact.
Key Duties and Responsibilities:
Your duties as the Chemistry Team Leader will be varied; however, the key duties and responsibilities are as follows:
1.
Organise and schedule departmental work to ensure batch progression targets are met.
2.
Ensure calibration or validation of laboratory equipment and automated systems is performed.
3.
Deliver training to all members of the department and ensure all staff are working in accordance with Standard Operating Procedures and GMP.
4.
Act as a subject matter expert in relation to the work of the section and produce reports covering laboratory results.
Role Requirements:
To be successful in your application to this exciting role as the Chemistry Team Leader, we are looking to identify the following on your profile and past history:
1.
Relevant degree in Chemistry or a related field.
2.
Extensive industry experience in a laboratory setting, with demonstrated competency in managing others.
3.
A working knowledge and practical experience with cGMP/GLP and laboratory instrumentation, ideally chromatography (GC and HPLC).
Key Words:
Chemistry Team Leader / Pharmaceutical / Laboratory Management / GMP / GLP / Quality Control / Analytical Chemistry / Laboratory Supervisor / Team Leadership / Pharmaceutical Testing / Laboratory Operations
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from 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: Hertfordshire,England
Start: 18/10/2024
Salary / Rate: Dependent on experience
Posted: 2024-10-18 16:04:12
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We are currently looking for a QC Analyst to join a leading company based in the Essex area.
As the QC Analyst you will be responsible for conducting Quality Control testing and documenting laboratory testing in accordance with the MHRA and EU GMP Guidelines.
As the QC Analyst will also be responsible for performing and assisting in the OOS investigations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1.
As the QC Scientist you will be competing analysis of Pharmaceutical products using analytical techniques such as HPLC, UV-Vis, GC and IR.
2.
You will comply with cGMP and carrying out routine tasks accurately and following strict methodologies to carry out analyses.
As well as complying with company Health & Safety Policy and Procedures.
3.
As the QC Analyst you will perform method validations and method transfers where needed, whilst maintaining and operating standard laboratory equipment, for example titrators, pH meters etc.
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 discipline or equivalent industry experience.
2.
Proven industry experience in working with a GMP or GLP environment within a pharmaceutical, chemical or food laboratory.
3.
A working knowledge and practical experience with HPLC as well as other analytical methods such as GC, IR and UV-VIS.
Key Words: HPLC, QC, Quality Control, GMP, GLP, Pharmaceuticals, Essex, GC, ICH, MHRA.
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: 11/10/2024
Salary / Rate: £25000 - £32000 per annum
Posted: 2024-10-11 10:05:35
