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  • Virtual ● Req #120
    20 February 2024
    The Role A senior member of a high performing, cross-functional commercial team. Accountable for driving both new client acquisition and expansion of existing customer relationships into our Drug Product business portfolio. Accountable for achieving individual commercial objectives and enabling those of the wider commercial team. You will develop and execute a nimble territory strategy via your deep and early understanding of market-place dynamics and trends. You will self-build a robust drug ... More
  • Nottingham, UK ● Req #100
    20 February 2024
    Key responsibilities of a Clinical Research Physician include: To act as a medically qualified person responsible for medical aspects of Phase I and II activities To manage the process by which a volunteer is screened for a specific study, to determine their eligibility to take part in the study To take medical responsibility for the everyday running of studies including the welfare of volunteers under the direction of the Principle Investigator To liaise with the Principal Investigators, Lead ... More
  • Nottingham, UK ● Req #27
    20 February 2024
    Due to growth and expansion, we are hiring a PBPK Modelling Research Fellow to join our Scientific consulting group. The role will provide hands-on modelling and simulation (M&S) scientific support to Quotients clients including first-in-human predictions, biopharmaceutic and formulation evaluations and drug drug interaction modelling. Key Tasks Build and rigorously test PBPK models including performing parameter sensitivity analysis where appropriate using GastroPlus and other relevant modelli ... More
  • Boothwyn, PA, USA ● Req #111
    19 February 2024
    The Role The QA Specialist will interact with Quotient Sciences’ customers and ensure that contracted manufacturing and testing activities are conducted in accordance with current Good Manufacturing Practices (cGMP), Data Integrity requirements, other applicable standards and regulations, customer’s market authorization, and Quotient’s policies and procedures. The QA Specialist will ensure efficient and effective implementation of quality requirements into the quality management system, proactiv ... More
  • Boothwyn, PA, USA ● Req #112
    19 February 2024
    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 ... More
  • Reading, UK ● Req #102
    06 February 2024
    An opportunity has arisen for a Senior Analytical Scientist to join the Analytical Services (QC) team in Reading.   You will be responsible for support and leading project activities and contribute to the evaluation of data, problem solving, development and validation activities. Collaborating with line manager to provide the analytical requirement for allocated projects, including the set of tests required for the given formulation type and proactively liaising with the relevant department for ... More
  • The Role A senior member of a high performing, cross-functional commercial team. Accountable for driving both new client acquisition and expansion of existing customer relationships into our Drug Product business portfolio. Accountable for achieving individual commercial objectives and enabling those of the wider commercial team. You will develop and execute a nimble territory strategy via your deep and early understanding of market-place dynamics and trends. You will self-build a robust drug ... More
  • Alnwick NE66, UK ● Req #93
    26 January 2024
    The Role As Site EHS Lead, you will support the Site Head and Site Leadership Team with the necessary advice and support to ensure a safe working environment is maintained. Work effectively with the EHS teams at other Quotient’s site to ensure a consistent, harmonised approach to EHS. This is a site based role at our Alnwick facility.   Main tasks and responsibilities: Provide support to the regional Executive Director, EHS in ensuring the effective implementation of Quotient’s ... More
  • Miami, FL, USA ● Req #81
    24 January 2024
    Summary of job purpose  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 the ... More
  • Boothwyn, PA, USA ● Req #95
    24 January 2024
    The Role The Analytical Scientist III is responsible for analytical release and stability testing under the supervision of the Group Leader within the Clinical Quality Control Team. Main tasks and responsibilities will include: Operates and troubleshoots the following instruments and equipment to test and evaluate pharmaceutical samples HPLC/UPLC, dissolution apparatus, Karl-Fischer water content titrator, GC, FTIR, UV, and any other instruments as directed Follows analytical testing methods, c ... More
  • Alnwick NE66, UK ● Req #77
    24 January 2024
    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 ... More
  • Alnwick NE66, UK ● Req #26
    24 January 2024
      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 yo ... More
  • Nottingham, UK ● Req #87
    22 January 2024
    In this role you will provide general practical support on a day to day basis for the Facilities management and Stores functions  You will need: IT knowledge Full UK driving licence Practical experience and the ability to perform general handyman type jobs Be physically fit You will be involved in: Distribute booked in packages to end users around the Nottingham buildings Carry out routine repairs and maintenance around site e.g. painting, varnishing, changing lightbulbs, minor repairs Carry ... More
  • Boothwyn, PA, USA ● Req #75
    12 January 2024
    The Role The QC Scientist II is responsible for analytical release and stability testing under the supervision of the Group Leader within the Clinical Quality Control Team. Main tasks and responsibilities will include: Operates and troubleshoots the following instruments and equipment to test and evaluate pharmaceutical samples HPLC/UPLC, dissolution apparatus, Karl-Fischer water content titrator, GC, FTIR, UV, and any other instruments as directed Follows analytical testing methods, compend ... More
  • Miami, FL, USA ● Req #63
    10 January 2024
    Summary of job purpose 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 Qualifications and experience required for competent performance BSN or RN with experience preferably within a ... More
  • Boothwyn, PA, USA ● Req #66
    03 January 2024
    The Role Develop stable and bioavailable pharmaceutical dosage forms. Develop and optimize manufacturing processes and manufacture clinical supplies To comply & adhere to Good Manufacturing Practice (GMP) standards. Main tasks and responsibilities Formulate oral solid dosage forms in a fast-paced contract manufacturing environment. Developed a wide array of formulations including immediate and modified release for Phase I – III. Scaled up formulation and processes from lab to pilot scale to ... More
  • Miami, FL, USA ● Req #58
    15 December 2023
    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. 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 U ... More
  • Miami, FL, USA ● Req #55
    15 December 2023
    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. 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 U ... More
  • Miami, FL, USA ● Req #54
    15 December 2023
    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. 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 U ... More
  • Miami, FL, USA ● Req #53
    15 December 2023
    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. 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 U ... More
  • Boothwyn, PA, USA ● Req #51
    15 December 2023
    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 ... More
  • Boothwyn, PA, USA ● Req #52
    15 December 2023
    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 ... More
  • Boothwyn, PA, USA ● Req #60
    15 December 2023
    The Role To conduct lab scale formulation development and clinical manufacturing (GMP Batch Manufacturing) related activities. To comply & adhere to Good Manufacturing Practice (GMP) standards. Main tasks and responsibilities Conduct lab work as planned by the supervisor that involves development of pharmaceutical formulations such as tablets, capsules and liquids. Conduct pharmaceutical manufacturing of oral dosage forms using small to large scale equipment for development and process scale ... More
  • Boothwyn, PA, USA ● Req #61
    14 December 2023
    The Role Responsible for providing leadership and functional oversight of Philadelphia Site Quality Operations functions (Quality Assurance and Quality Control) and ensuring company’s adherence to quality policies, practices, standard operating procedures (SOPs) and regulatory requirements, as described in current Good Manufacturing Practices (cGMPs). Ensure effective implementation, maintenance and continuous improvement of GxP Quality programs and infrastructure to support Contract Developme ... More
  • Nottingham, UK ● Req #40
    14 December 2023
    The Role This is a fantastic opportunity for a Registered Nurse looking to take the next step in their career in clinical research. 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 Nottingham site and our facility is made up of 85 beds across 6 wards which has recently undergone extensive refurbishment and operates 24 hours a ... More