QUOTIENT SCIENCES

Responsibility

• company Overview
• collection and recording of high-quality study data in compliance with the Study Protocol and internal procedures
• perform clinical procedures including but not limited to; blood pressure, pulse, temperature, ECG’s/holters and taking blood samples via venepuncture
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• collection and processing of biological samples in line with Study Protocols
• the Role
• quality control checking of eSource and paper source documents
• building collaborative relationships with peers and a wide range of internal stakeholders
• providing the highest level of care and customer service to our volunteers
• healthy volunteers are taking part in clinical trials in the clinical research unit
• no prior clinical experience is required, a full training programme is provided
• immediate Life Support training is provided
• this role offers great career development into ward leading, shift leading, IV cannulation, set-up of clinical study documentation and more
• we offer opportunities to progress into managerial roles such as Deputy Lead and Clinical Lead through internal development programs
• additionally, this role allows you to be trained in dosing and assessing the accountability of study drugs
• this role involves shift and weekend work
• quotient Sciences have a full-time opportunity available for a Sample Processing Technician. This role is based at the clinical research unit at the site in Nottingham
• as a Clinical Research Technician, you will play a key role in providing a safe and caring environment for our volunteers who take part in our clinical trials
• your role is essential to our volunteer experience and crucial to the development of new medicines
• the Candidate
• all clinical procedures are taught to the highest standard by a dedicated in-house training team
• sample analysis is not carried out at Quotient, therefore you will be responsible for the reconciliation of all samples that enter the lab and manage the shipment of these samples to 3rd parties who will conduct the analysis offsite
• are you looking for a new challenge? Would you like to work in clinical research?
• preparation and collection of biological samples in line with the Study Protocol
• your role is to work closely with the clinical staff by handling a large volume of biological samples which are taken from the volunteers on clinical trials
• quality Control checking of source documentation and case report forms
• company Benefits

Trade

• scientific Research & Development
• installation & Maintenance
• Scientific Research & Development
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• Installation & Maintenance

Earnings for position technician

Current offers for the position:

Responsibility

• company Overview
• quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway
• cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients
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• to act at all times in compliance with Good Manufacturing Practice and report any issues
• as guided/requested, manufacture and package oral clinical products specifically on the 3P R1000 robotic capsule filling machine
• execution and review of batch manufacturing records in line with third party and Quotient developed formulation and manufacturing processes
• prepare and complete documentation associated with the manufacture and supply of clinical products specifically manufactured on the 3P R1000 filling machine
• because humanity needs solutions, fast
• perform setups, operation, disassembly, cleaning and monitoring of processing equipment per approved procedures and/or batch manufacturing records
• dispense APIs, excipients, drug products, IMPs and packaging materials for clinical use and maintain GMP stocks as required
• the Role
• preparation, review and revision of manufacturing related documentation such as equipment SOPs, cleaning checklists etc
• participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment, specifically the 3P R1000 filling machine
• ensure that all activities performed are recorded accurately in GMP records
• cleaning process equipment and manufacturing areas following written procedures
• record work in compliance with relevant regulatory requirements, internal policies/procedures and where appropriate, client requirements
• you will support the dispensing, manufacture and packaging of clinical products in accordance with GMP requirements and company procedures
• as a growing and successful business, we employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA
• lead specific continuous improvement activities and highlight any improvements needed for equipment, storage and processes
• supporting continuous improvement activities and highlighting any improvements needed for equipment, storage and processes
• work flexibly across the site to meet business needs
• liaise with Supplies/Warehouse/Management in staging of materials and in the return of properly reconciled materials
• science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it
• full training will be provided by the team
• the Candidate
• working in a safe responsible manner at all times
• the successful candidate will have
• people join Quotient Sciences because we are a respected member of the drug development community, driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast
• your main tasks and responsibilities
• ideally have a degree in a Science subject
• manufacture of pharmaceuticals to GMP standards Clinical Trial Manufacturing and internal SOP standards , utilising a range of different equipment and processes
• performing other duties as reasonably required
• provision of effective and efficient technical support in the scientific aspects of clinical trial manufacturing. Experience of the manufacture of different dosage forms type/manufacturing processes
• contribute to the preparation and completion of documentation associated with the manufacture and supply of clinical products
• experience of clinical trial manufacturing
• higher qualifications in science would be advantageous
• good attention to detail to ensure that all tasks are carried out in a reproducible manner with the minimum number of avoidable errors
• excellent interpersonal and communication skills
• keeping detailed and accurate records of all work undertaken, ensuring that all records are clear, concise and legible at all times to enable for full repetition and traceability as per Good Documentation Practice
• the ideal candidate will have relevant work experience or have substantial work experience in a similar type of work
• support the dispensing of APIs, excipients, drug products, IMPs and packaging materials for clinical use and maintain GMP stock as required
• this is a fantastic opportunity for a Manufacturing Technician Apprentice to join the Drug Product department in Alnwick on a full time and permanent basis
• excellent organisational, problem solving and follow up skills
• participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment
• ability to perform multiple tasks and prioritise effectively
• company benefits
• record work in compliance with relevant regulatory requirements, internal policies/procedures and where appropriate, client’s requirements
• excellent attention to detail
• work with due regards to health and safety of self and others
• applicants must have the right to work in the UK upon being offered employment
• our Commitment to Diversity & Inclusion

Requirements

• good written/oral communication skills
• A high level of personal integrity and commitment
• flexible approach to new work challenges

Current offers for the position:

Responsibility

• ensure that the dignity, health, safety and welfare of study participants is the highest priority at all times
• ensure that the dignity, health, safety, and welfare of study participants is the highest priority at all times
• perform study related procedures such as cannulation, venepuncture, telemetry, holters, vital signs, ECGs, collection of blood samples., in accordance with ICH-GCP
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• utilise your skills, knowledge and clinical judgement to assess vital signs
• respond to emergency situations and lead/participate in training scenarios
• review, check and maintain emergency equipment
• use prior clinical experience and knowledge to assist clinical leads and deputies with the preparation of clinical trials
• review, check and administer concomitant medication
• review, check and maintain compliance of emergency equipment in line with phase 1 accreditation scheme requirements
• administration of dosage forms inclusive of various routes and devices in accordance with the study specific protocol
• to record data obtained in a timely manner according to the protocol
• utilise nursing assessment skills to support general well-being of study participants and potential adverse events. Document adverse events and take appropriate action as needed
• utilise nursing assessment skills to support general well-being of study participants and potential adverse events. Document adverse events and take appropriate action as needed including administration of concomitant medications
• support the clinical team to ensure that source data completion is to a high standard
• perform quality control checks
• provide a lead role in responding to emergency situations. Participate in training scenarios and support the Training and Compliance Team with ILS training of non-clinical staff
• quality control checking of eSource and paper source documents
• to obtain Nurse Led Informed Consent by educating, explaining and informing participants of study procedures in conjunction with ICF
• developing new drugs is key to the future health of the nation. Through our clinical trials, we have helped to improve and develop treatments for asthma, diabetes, heart disease, irritable bowel syndrome and many other conditions
• monitor compliance and support audit readiness at all times
• monitor compliance within the clinical unit and support audit readiness at all times
• lead by example to encourage professional conduct and ensure clinical excellence is maintained across the clinic
• utilise your nurse leadership skills to lead, inspire, influence and motivate the clinical team

Requirements

• we pride ourselves on being a dynamic and supportive company offering full training and career progression opportunities. Immediate Life Support training will also be provided

Trade

• nursing
• Nursing

Current offers for the position:

Responsibility

• manage site cleaning personnel and contract personal hygiene services to ensure that specified standards are maintained
• analyse samples from preclinical and clinical studies by ICP-MS, GC-MS and LC-MS
• manage the site grounds maintenance activities, ensuring high standards are maintained
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• perform ICP-MS, GC-MS and LC-MS bioanalytical assay validations
• manage the contracted Pest Control operations to agreed standards
• on-The-Job training and mentoring of Bioanalyst
• deputise for the Head of Department as required
• manage the site security staff
• supervise a team of Bioanalytical Scientists
• support the commercial enquiry, cost estimation and proposal generation process
• to ensure where appropriate that all activities are carried out in accordance with Regulatory Standards and current Standard Operating Procedures
• identify opportunities for business growth and contribute to
• ensure that goods are received in compliance with company procedures
• the Candidate
• department strategy
• manage the site portering services to ensure that deliveries are provided in accordance with internal customer requirements
• BSc in a relevant scientific discipline
• work with Head of Department to monitor and control costs and resources according to budget
• provide leadership and scientific direction to direct reports. Including the provision of mentoring and development opportunities to facilitate progression opportunities for colleagues
• manage the collection, segregation, packaging, disposal and recording of all waste streams, ensuring compliance with current regulations
• 1 year minimum of experience in bioanalysis
• implement training plans as agreed with Head of Department
• work directly with potential clients and the rest of the organisation to formalise the scope of work requests and to maximise the number and value of awards
• manage dispatches from site in compliance with regulations
• experience in line management would be advantageous
• maintain Laboratory Notebook, ensuring that this is countersigned, and contribute to countersigning others’ books as assigned
• manage the laundry services to ensure employee requirements are met
• good written and oral communication skills
• guide and counsel other department members through synthetic problems they might encounter and contribute to the resolution of same
• ensures work is conducted in compliance with relevant regulatory requirements, internal policies/procedures and client requirements where appropriate
• arrangement of shipments with selection of courier companies, ensuring that client confidentiality is always maintained
• ensure work is completed in compliance with relevant regulatory requirements, internal policies / procedures, and client requirements where appropriate, reviewing and updating supporting documentation as appropriate
• flexible approach to new work challenges
• ensure that self and others using laboratories handle and dispose of materials in accordance with agreed company practices and procedures
• waste solvent collections and entering information on to site spreadsheet, also palletising solvent drums & shrink wrapping
• suggest improvements to site procedures and systems to improve team and department efficiency and compliance
• maintain laboratory systems that have been implemented as a result of GMP action programmes

Requirements

• an excellent record in Synthetic organic chemistry, either at Doctoral level or Graduate with minimum of five or eight years’ relevant industrial experience respectively

Current offers for the position:

Responsibility

• attend appropriate study/ departmental meetings
• providing general administrative support to the medical writing department and other departments based at the Edinburgh Office
• generate query and telephone screening checklists from inclusion/ exclusion criteria listed in the Clinical Protocol and Informed Consent Forms
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• liaising with other Quotient departments at other sites eg Facilities, IT, HR/Training and QA
• set-up study details on the Volunteer Database with new and existing volunteer details
• assisting in the publication of clinical study reports
• to continually update the Volunteer Database
• assisting the Medical Writing staff by performing quality control tasks
• direct communication with volunteers by telephone and face-to-face meetings
• this position will report to our Medical Writing Coordination Team Leader
• run regular Volunteer Database searches to source appropriate volunteers for trials
• archiving of studies as appropriate
• full training will be provided in administration and medical writing publishing and quality control processes and techniques
• provide general administration support as required
• QC of files
• the Candidate
• the successful candidate will be a strong administrator, ideally with experience maintaining databases and a good eye for detail
• working for a research company, laboratory, academic institution, NHS etc.)
• the role also involves working closely with other staff in our Medical Writing department, other departments based at the Edinburgh site and support staff from Facilities, IT, HR/Training and QA
• candidates must also be numerate with an eye for detail but there is no requirement for a degree
• dependent on your development, our career pathway allows you to expand your skills over time and progress to more senior roles and tasks

Requirements

• good organisational skills and the ability to work to deadlines whilst maintaining quality standards
• attention to detail and the ability to multitask are essential
• effective oral and written communication skills
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• company Benefits
• our Commitment to Diversity & Inclusion
• quotient Sciences are advocates for positive change and conscious inclusion
• applicants must have the right to work in the UK at the time of being offered employment. The role will be based in our Edinburgh office and can be full time or part-time over 5 days

Current offers for the position: