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The Role We have a fantastic opportunity for a Senior Formulation Scientist for our site in Nottingham Quotient Sciences’ formulation teams have vast experience across an array of drug product formats including; solid oral dosage forms, oral liquid dosage forms, nasal dosage forms, solubility-enhanced dosage forms, parenterals, gels, ointments and creams. As a Senior Formulation Scientist, you will lead pre-clinical or stand-alone formulation development programmes requiring s ...Read more about Senior Formulation ScientistMore
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We have a fantastic opportunity for a part-time (15 hours per week) Payroll Specialist, based onsite in Ruddington, Nottingham. Reporting to the People Services Lead, you will be responsible for processing payroll in an accurate and timely manner in adherence to company schedules. Providing generalist support to the People Team and supporting other members of the People Services Team when required. Main tasks and responsibilities To complete any administrative payroll tasks and process ...Read more about Payroll SpecialistMore
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The role The role of the Maintenance Technician will contribute to the success of the business through effective supervision of equipment in the GMP Manufacturing Area (GMP) and Laboratory Facilities. They will directly supervise the Technical Operations equipment team which comprises of two equipment technicians and attend meetings where they are responsible for equipment status updates. Main Tasks and Responsibilities To effectively supervise the GMP and Laboratory equipment To effectively ...Read more about Maintenance TechnicianMore
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The Role We are looking for a Stores Controller to join our procurement department in Nottingham. Reporting to the Procurement Manager, you will be responsible for coordinating activities associated with the Goods-In Area, Stores, Purchase Order Processing function and supporting the wider business in ensuring the correct stock is maintained and supplies are ordered and distributed efficiently. Main tasks and responsibilities Responsible for the organisation and efficient running of the G ...Read more about Stores ControllerMore
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We have a fantastic part-time (22.5 hours per week) opportunity available for a HR Advisor, based onsite in Ruddington, Nottingham. Reporting to the People Services Lead, you will operate as part of the People Team to support human resources activities. You will be responsible for the deployment and effectiveness of a broad range of defined Human Resources processes within Quotient Sciences. Working with managers and employees, you will resolve queries and embed a positive colleague expe ...Read more about HR AdvisorMore
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The RoleDue to business growth, we have an exciting career opportunity available for a Formulation Scientist at our site in AlnwickQuotient Sciences’ formulation teams have vast experience across an array of drug product formats for administration via different routes to include oral,, intravenous, sub-cutaneous nasal and sub-linqual.. Correspondingly, the range of product types include solubility- or permeability-enhancing dosage forms, gels, ointments and creams.As a Formulation Scientist you ...Read more about Senior Formulation ScientistMore
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The Role Due to business growth, we have an exciting career opportunity available for a Formulation Scientist at our site in Nottingham. Quotient Sciences’ formulation teams have vast experience across an array of drug product formats for administration via; solid oral dosage forms, oral and nasal dosage forms, solubility-enhanced dosage forms, parenterals, gels, ointments and creams. As a Formulation Scientist you will conduct formulation development work including pre-formulation and formulati ...Read more about Formulation ScientistMore
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The Role Are you looking for a new challenge? Do you want to work as part of a dynamic team that helps get new medicines to market? As a Healthcare Assistant, you will play a key role in providing a safe and caring environment for our volunteers who take part in our clinical trials. No prior clinical experience is required, a full training programme is provided. Key responsibilities of a Healthcare Assistant include: Collection and recording of high-quality study data in compliance with the Stu ...Read more about Healthcare AssistantMore
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The Role Assist with the planification, preparation of clinical schedules to ensure the effective delivery of clinical studies and volunteer safety at all times. To comply & adhere to GCP guidelines and regulations as required of this role To ensure subject safety at all times Main tasks and Responsibilities: Plan, prepare and manage the clinical schedule to ensure effective delivery of clinical studies Liaise with relevant departments e.g. screening, data, lab, medical an ...Read more about Clinical SchedulerMore
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Main Tasks and Responsibilities Provide QA floor support and oversight to the production of registration batches for clinical and commercial product materials to ensure that product is manufactured in accordance with specifications, customer’s market authorizations and GMP requirements. Conducts floor audits and periodic checks of in process documentation and logbooks for compliance during second shift. Provide guidance to manufacturing and laboratory personnel to proactively ensure GMP compl ...Read more about Senior QA AssociateMore
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The Role The Validation Engineer is responsible for providing engineering support for maintenance and validation activities while managing regulatory requirements around methodology and protocols for pharmaceutical manufacturing. Main Tasks and Responsibilities Manages the scope, deliverables, schedule, budget, and quality of maintenance/engineering projects related to CGMP process equipment, utilities, controls, and physical building. This may include generation/review of design documen ...Read more about Validation EngineerMore
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The Role The Cleaning Validation Specialist is responsible for coordinating the cleaning validation activities , including but not limited to preparing and executing the protocols and reports for cleaning validation. This position will lead all efforts for cleaning method development and will work closely with Analytical Development team for executing the cleanability studies. This position will maintain the “Cleaning validation matrix” and will work with cross functional teams for introduction ...Read more about Cleaning Validation SpecialistMore
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The Role Overall responsibility for quality of laboratory processing for assigned duties To ensure study data is collected to a high quality in accordance with ICH-GCP, protocol and lab manual To ensure subject safety at all times Main tasks and responsibilities Provides encouragement, support, positive reinforcement to laboratory technicians Oversees sample labelling, processing and shipping duties as required Ensures lab set up and cleaning duties are performed on a daily, weekly and monthl ...Read more about Clinical Laboratory LeadMore
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The Role The EHS Manager is responsible for ensuring compliance with federal, state, and local environment, health and safety regulatory requirements and provides strategic leadership and oversight for EHS activities. Main tasks and responsibilities will include: Defines, maintains, and communicates core EHS program requirements and expectations Acts as the owner for site level key performance indicators and metrics Develops and maintains site action plans including annual EHS Plan in accordanc ...Read more about EHS ManagerMore
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The Role The Screening Research Lead is responsible for the performance of screening activities for prospective research volunteers tracks overall study event schedule and participant compliance To comply & adhere to GCP guidelines and regulations as required of this role To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards To ensure subject safety at all times Main tasks and responsibilities Must be able to read and understand protocol ...Read more about Screening Research LeadMore
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The Role Are you looking for a new challenge? Do you want to work as part of a dynamic team that helps get new medicines to market? 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. No prior clinical experience is required, a full training programme is provided. You can also enjoy free and secure on site parking. Key responsibilities of a Clinical Research Technician include: Collection ...Read more about Clinical Research Technician - Night shiftsMore
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The Role The Facilities Maintenance Manager is responsible for managing all aspects of facilities including but not limited to the operations, maintenance, and repair of GMP and non-GMP building infrastructure, assets, utilities, and systems. Duties include management of hard and soft services, contracts, and vendors. Hard Services– HVAC, Water, Electrical, Gases, Sanitary Waste, etc. Soft Services– Pest Control, Garments, Vending, Waste Management, Housekeeping, Reception, Security, Snow Remo ...Read more about Facilities Maintenance ManagerMore
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The Role Responsible for the processing and registration of all screening volunteers, verifying proper identification and maintaining the participant directory. To comply & adhere to GCP guidelines and regulations as required of this role. To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards. To ensure subject safety at all times Main tasks and responsibilities Prepare and assemble screening charts. Register scre ...Read more about Registration CoordinatorMore
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The Role Supervise GMP Operations in the daily execution of Manufacturing processes, cleaning/sanitization procedures of the facility, equipment, and instruments. To comply & adhere to Good Manufacturing Practice (cGMP) standards. Main tasks and responsibilities will include: Support day to day operations with an “on the shop floor” presence. Monitor’s operators and equipment throughout shift to ensure all SOPs are properly followed and executed. Coaches’ operators on proper operation and ad ...Read more about Production SupervisorMore
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The Role Under the direction of the Team Leader, the incumbent is responsible for reviewing, updating, tracking and providing timely processing of all assigned documentation generated or executed within the clinical Manufacturing Department. As an Executed Batch Records (EBR) reviewer, this position is expected to conduct a full, comprehensive and complete EBR review on behalf of Clinical manufacturing group within 72 hours of batch documentation completion. EBRs consist of a stand-alone documen ...Read more about GMP Document ReviewerMore
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The Company 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 help biotech and pharma customers save precious time and money in getting drugs to patients.As a growing and successful business, we employ more than 1,300 talented individuals globally, located at state-of-the-art development, manufacturing and clinica ...Read more about IT Support Specialist (Hybrid- Alnwick)More
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The Role Are you looking for a new challenge? Do you want to work as part of a dynamic team that helps get new medicines to market? As a Clinical Technician, you will play a key role in providing a safe and caring environment for our volunteers who take part in our clinical trials. No prior clinical experience is required, a full training programme is provided. Key responsibilities of a Clinical Technician include: Collection and recording of high-quality study data in compliance with the Study ...Read more about Clinical TechnicianMore
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The Role The QA Associate will support contract of clinical and commercial manufacturing for Pharmaceutical products during second shift. The QA Associate will support the technology transfer for clinical and commercial manufacturing and provide QA oversight of the manufacturing process during second shift. Ensure the implementation and maintenance of an efficient and effective quality management system, maintain open and timely communication across the teams, and visibly demonstrate the behav ...Read more about QA Associate (2nd Shift)More
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The Role The Research Volunteer Liaison (Activities Coordinator) works with the Clinical and Screening Teams to ensure the best possible experience for the volunteers, maximizing the potential for them to maintain compliance during their participation, to complete the trials and return for future studies Coordinates study volunteer activities (transportation to consultation or off-site procedure appointments) and addresses non-study related needs of volunteers during their inpatient stay a ...Read more about Activities CoordinatorMore
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The Role Responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications To comply & adhere to GCP guidelines and regulations as required of this role To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards To ensure subject safety at all times Main tasks and responsibilities Responsible for administering study medication to study participants Familiar with intravenous ...Read more about Clinical Research NurseMore