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The Role The Group Leader/ Supervisor is responsible for providing engineering support for maintenance and validation activities while managing regulatory requirements around methodology and protocols for pharmaceutical manufacturing. This will be a hands-on role while managing the team deliverables for engineering support and validation activities. Main Tasks and Responsibilities Manages the scope, deliverables, schedule, budget, and quality of maintenance/engineering projects related to CGMP ...Read more about Validation Group Leader/ SupervisorMore
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The Role GMP operations in the daily execution of Manufacturing GMP, and Clinical batches; cleaning/sanitization procedures and support functions of equipment, facilities and instruments. Main tasks and responsibilities will include: Facility Sanitization & Equipment Cleaning Procedures Weighing and Manufacturing of GMP, R&D and Clinical Batches Equipment Staging, Setup, Operation, Disassembly and Cleaning with no supervision Performance Verification/Calibration of Instruments Material Handlin ...Read more about GMP Operator (2nd Shift)More
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The Role GMP operations in the daily execution of Manufacturing GMP, and Clinical batches; cleaning/sanitization procedures and support functions of equipment, facilities and instruments. Main tasks and responsibilities will include: Facility Sanitization & Equipment Cleaning Procedures Weighing and Manufacturing of GMP, R&D and Clinical Batches Equipment Staging, Setup, Operation, Disassembly and Cleaning with no supervision Performance Verification/Calibration of Instruments Material Handlin ...Read more about GMP Operator (1st Shift)More
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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 Rem ...Read more about Facilities Maintenance ManagerMore
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The RoleWe are looking for a part time Cleaning Operative to work weekends at our clinic. As cleaning operative you will work in Clinical and non-clinical areas providing and maintain the highest standard of cleaning. You will work in accordance with Quotient Sciences Policies and Procedures including COSHH, Manual Handling, Health and Safety, Infection Control and attend annual training. Main tasks and responsibilities The role involves cleaning in Clinical and non-clinical areas, ensuring at ...Read more about Cleaning Operative (part time, weekend opportunity)More
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The Role The People Coordinator aids with and facilitates the human resource processes for the Philadelphia site. This role provides administrative support to the human resource function as needed, including record keeping, file maintenance and HRIS entry and recruitment. • To comply & adhere to GMP guidelines and regulations as required of this role Main Tasks and Responsibilities Support the scheduling of interviews; oversees preparation of interview questions and other hiring related do ...Read more about People Coordinator - Part Time (HR)More
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The Role Responsible for the development and implementation of the People Strategy of all human resource activities for the Quotient Sciences Miami Site including but not limited to employee engagement, talent & succession planning, workforce planning, coaching managers, benefits, compensation & 401k administration, analysis of People Metrics employee relations and policy administration and interpretation Ensure compliance to company policies, procedures and documentation Responsible for proce ...Read more about People Business Partner - Part Time (HR)More
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The Role Responsible for the development and implementation of the People Strategy of all human resource activities for the Quotient Sciences Miami Site including but not limited to employee engagement, talent & succession planning, workforce planning, coaching managers, benefits, compensation & 401k administration, analysis of People Metrics employee relations and policy administration and interpretation Ensure compliance to company policies, procedures and documentation Responsible for proce ...Read more about People Team - People Business PartnerMore
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**Enhanced night rate for this role. For more details please get in touch with sara.bhutta@quotientsciences.com** The Role This is a great opportunity for a nurse looking to take the next step in their career in clinical research In your role as Clinical Research Nurse, you will work on a wide range of leading clinical trials with a multifunctional team, broadening your skills and helping pharmaceutical companies progress new medicines to market. The position will be clinic based at our Nottingh ...Read more about Night Clinical Research Nurse - Enhanced Night RateMore
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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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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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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 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 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 and ...Read more about Clinical SchedularMore
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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 Conduct - Clinical Laboratory LeadMore
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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 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 sc ...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 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 Conduct - Clinical Technician IMore