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We are currently looking for a QA Document Controller to join a leading Biotechnology company based in the North of the UK.
As the QA Document Controller you will be responsible for assisting in the development and on-going management of the companies Quality Management Systems.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Document Controller will be varied however the key duties and responsibilities are as follows:
1.
Responsible for the development and implementation of the Quality Management System (QMS), carrying out day to day activities such as CAPAs, deviations, change controls and supplier qualification.
2.
Make sure that the CMO batch documentation are compliant to GXP standards, including the review of GMP documentation.
3.
You will work closely with the Quality Specialist, and assist in regulatory inspections and customer audits.
4.
You will generate, retrieve, manage, and follow-up quality documents generated both internally and generated by vendors in the QMS.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QA Document Controller we are looking to identify the following on your profile and past history:
1.
Relevant degree in a relevant life sciences discipline
2.
Proven industry experience working in a GxP environment - (GMP, GLP, GDP preferred)
3.
A working knowledge and practical experience with document / Quality Management Systems, and Electronic Document Management Systems
Key Words: QA | Quality Assurance | QMS | Quality Management Systems | Clinical | GMP | GxP | Biotechnology | QDM | Quality Document Management Systems | Electronic Document Management Systems | Drug Discovery | CAPA | Deviations |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: United Kingdom,United Kingdom
Start: 26/03/2024
Salary / Rate: £26000 - £30000 per annum
Posted: 2024-03-26 18:16:03
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We are currently looking for a QC Analyst to join a leading company based in the Kent area.
As the QC Analyst you will be responsible for the analysis of pharmaceutical raw materials, APIs, and finished products to ensure compliance with internal and regulatory specifications.
Daily tasks will involve general chemical analysis including stability testing, various laboratory support activities, documenting analytical data, writing reports and SOPs all in accordance with cGMP.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1.
As a QC Analyst you will be involved in Performing analytical testing using GC, HPLC, KF, FTIR and other required techniques in accordance with written procedures.
2.
You will be required to record data into appropriate records and notify the line manager of any OOS, OOT, OOE or questionable results
3.
You will create and update documents in accordance with cGMP and company procedures
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1.
Relevant degree in a chemistry or related science discipline.
2.
Proven industry experience in Pharmaceutical QC testing and GMP (ideally small molecule) and analytical testing using GC, HPLC, KF, FTIR.
3.
Experience in completing OOS investigations, deviations, CAPA, and Change Controls
Key Words: GC / HPLC / TLC / FTIR / QC / Quality Control/ QC Scientist/ GMP / API / Raw materials / Chemistry / analytical /
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Kent,England
Start: 25/03/2024
Salary / Rate: £27000 - £29000 per annum
Posted: 2024-03-25 14:32:15
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We have an exciting new opportunity for a Study Manager Team Lead to join a leading international CRO based in the North Yorkshire area.
As the Study Manager Team Lead you will be responsible for directly line managing a team of Study Managers for regulatory and non-regulatory small molecule bioanalytical studies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Study Manager Team Lead will be varied however the key duties and responsibilities are as follows:
1.
As the Study Manager Team Lead you will directly line manage a team of study managers to ensure the successful execution of small molecule bioanalytical studies.
2.
You will collaborate with cross-functional teams, including sponsors and clients, to plan and coordinate study activities, acting as departmental lead for bioanalytical activities conducted on assigned studies.
3.
As the Study Manager Team Lead you will oversee LC-MS/MS method development and troubleshooting including reviewing protocols, study plans, SOPs or reports as required.
4.
You will document and complete any quality documentation (quality issue, CAPA, deviation, change control) as appropriate and within required time frames.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Study Manager Team Lead we are looking to identify the following on your profile and past history:
1.
Hold a degree in a Chemistry based subject or equivalent (e.g.
Biochemistry)
2.
Proven industry experience in study management leading small molecule bioanalytical studies.
3.
A working knowledge and practical experience using LC-MS/MS.
Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: North Yorkshire,England
Start: 25/03/2024
Salary / Rate: £45000 - £60000 per annum
Posted: 2024-03-25 09:44:03
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We are currently looking for a GLP Study Director to join a leading CRO company based in the Oxfordshire area.
As the GLP Study Director you will be responsible for overseeing GLP studies, executing sample preparation for analysis using various techniques and tools, and collaborating closely with the Laboratory Manager and team to ensure timely project delivery.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the GLP Study Director will be varied however the key duties and responsibilities are as follows:
1.
To apply your experience using chromatographic techniques using HPLC, IC,GC and LC for the analysis of various analytical samples.
2.
Conducting the design of study plans, method validation, method development and to ensure timely project delivery, setting and maintaining high personal standards for study quality.
3.
Oversee GLP studies in strict adherence to guidelines, ensuring compliance with standard operating procedures, and maintaining accurate data records.
4.
Taking an active role in the up-skilling and supervision of Analysts whilst effectively communicating with management to ensure the constant development of the overall Analytical function / team.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the GLP Study Director we are looking to identify the following on your profile and past history:
1.
Relevant degree in Analytical Chemistry OR relevant disciplines
2.
Proven industry experience in working in a CRO GLP environment.
Experience working across agrochemical, biocide, industrial chemical and animal health industries is advantageous
3.
A working knowledge and practical experience with chromatographic techniques such as HPLC, IC, GC, LC.
Key Words: Analytical Chemistry | GLP Studies | Laboratory Equipment | Sample Preparation | Chromatographic Techniques | Project Delivery | Standard Operating Procedures | Data Records | Calibration | Preventive Maintenance | SOP | Study Director | Method Validation | Method Development | CRO | HPLC | LC | GC | Oxfordshire
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Oxfordshire,England
Start: 25/03/2024
Salary / Rate: Competitive
Posted: 2024-03-25 09:36:08
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We are currently looking for a Calibration Engineer to join a leading Pharmaceutical company based in the Wiltshire area.
As the Calibration Engineer you will be responsible for Maintenance, calibration, repair, and continuous development of all process and utility equipment within the mechanical, electrical, instrumentation and control remit within the Engineering Department.
This is a Monday to Friday role and is site based.
KEY DUTIES AND RESPONSIBILITIES:
Your duties will be varied however the key duties and responsibilities are as follows:
1.
As the Calibration Engineer you will conduct requalification and calibration activities in adherence to the schedule and procedures.
2.
Maintain and use GMP documentation for all aspects of the job in accordance with working in a pharmaceutical environment.
3.
Aid with Installation, Operational, and Process Qualification processes for new and existing equipment.
4.
Organise and evaluate calibration data, looking for adverse trends and identifying failures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity, we are looking to identify the following on your profile and past history:
1.
Qualification in an engineering discipline or closely related.
2.
Proven industry experience working to GMP guidelines.
3.
A working knowledge and practical experience within calibration of Pharmaceutical equipment.
Key Words: Engineer | Technician | Calibration | Pharmaceutical | GMP
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Wiltshire,England
Start: 25/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-25 09:26:11
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We are currently looking for a Calibration Engineer to join a leading biopharmaceutical company based in the Hertfordshire area.
As the Calibration Engineer you will be responsible for Maintenance, calibration, repair, and continuous development of all process and utility equipment within the mechanical, electrical, instrumentation and control remit within the Engineering Department.
KEY DUTIES AND RESPONSIBILITIES:
Your duties will be varied however the key duties and responsibilities are as follows:
1.
Calibration of utility, process and laboratory instrumentation.
2.
Maintain and use GMP documentation for all aspects of the job in accordance with working in a pharmaceutical environment.
3.
Aid with Installation, Operational, and Process Qualification processes for new and existing equipment.
4.
Organise and evaluate calibration data, looking for adverse trends and identifying failures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity, we are looking to identify the following on your profile and past history:
1.
Qualification in at least one engineering discipline
2.
Proven industry experience in the calibration of equipment, such as pressure, temperature, flow, pH, UV, conductivity, level and weight sensors.
3.
A working knowledge and practical experience within the highly regulated manufacturing industries:
Key Words: Engineer | Technician | Calibration | Pharmaceutical | GMP
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Hertfordshire,England
Start: 25/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-25 09:14:03
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We are currently looking for a Regional Sales Specialist to join a Global Life Science company covering the London territory.
As the Regional Sales Specialist you will maintain the company's CRM database for the territory in terms of all activity and customer contacts, customer information and sales opportunities, strictly on a regular basis.
This is a remote role which requires around 80% travel to both clients and customers, with frequent visits to the Head Office in Milton Keynes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Regional Sales Specialist will be varied however the key duties and responsibilities are as follows:
1.
The Regional Sales Specialist will interact professionally with all other field personnel that will from time to time be actively supporting you in the territory e.g.
Technical/Market Specialists, Service Engineers, Sales/Technical Managers.
2.
You will fully comply to and operate within the pricing and discount directives set in place by the company whilst operating within the operational guidelines for quotations.
3.
Another responsibility will be to attend and fully represent the company at any trade or media event e.g.
exhibitions, which you may from time to time be asked to attend.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Regional Sales Specialist we are looking to identify the following on your profile and past history:
1.
It is essential to have a strong understanding of the Pharmaceutical or Clinical Market industry along with relevant Sales experience.
2.
The ideal candidate will effectively organise themselves to maximise time in front of a customer via in person and remote meetings.
They will also be a motivated individual with the drive to succeed.
Key Words: Sales Specialist | Analytical | HPLC | GC | Spectroscopy | MS | Mass Spectroscopy | Chromatography | Analytical Instrumentation | BD Executive | Business Development | Regional Sales |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: London,England
Start: 22/03/2024
Salary / Rate: Competitive
Posted: 2024-03-22 15:43:03
