Analytical Scientist II

Join to apply for the Analytical Scientist II role at Quotient Sciences
Join to apply for the Analytical Scientist II role at Quotient Sciences
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.

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. 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.

People join Quotient Sciences because we are a respected member of the drug development community that’s focused on innovation and are driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.

The Role

We are looking for an Analytical Scientist II to join our Reading site on a permanent basis.

As an Analytical Scientist II, you will be responsible for performing routine and project-based analytical testing using a range of techniques. You will support early-stage product development, QC release, stability testing, and method validation, while ensuring compliance with Good Manufacturing Practice (GMP) standards.

Key Responsibilities

Conduct routine daily operations in the analytical laboratory using techniques like HPLC, FTIR, UV, KF, Dissolution and potentially NGI, ED, PSD, XRPD, cleaning verifications etc.
Performing routine early product development, QC release and stability testing and/or analytical method validation and formulation development support.
To comply and adhere to Good Manufacturing Practice (GMP) standards.

Main Tasks And Responsibilities

Perform routine analysis using techniques within the department in timely manner and aware of hours assigned to tasks and the impact on timelines.
Support project activities and contribute in the evaluation of data, problem solving, development and validation activities with minimal supervision.
Accurately follow analysis steps outlined in documentation with minimal errors and ensure laboratory writeups are clear, concise and fully follow the principles of ALCOA+.
Ensure that GMP compliance is maintained in the Analytical laboratory and for all equipment (HPLC, Dissolution bath, KF etc.) and highlights issues and seek advice if problems occur.
Trained to level 2 on most equipment/techniques once experienced in job level and is able to perform routine analysis reliably with increased competency in the use of conventional lab techniques.
Perform some method development, optimization and validation activities under supervision.
Plan and execute daily work allocated activities with minimal supervision and complete work in a timely manner with minimal errors.
Participate in general lab maintenance/calibration tasks.
Troubleshooting analysis and equipment issues with minimal supervision.
To generate, assimilate, trend and evaluate technical and scientific data generated and compile reports/protocols in line with project objectives under minimal supervision.

Additional Tasks/responsibilities

To lead some project activities as appropriate under supervision to meet required project timelines.
Support the performance of lab technician responsibilities when required.
Contribute to the stability chambers call-out rota as required once appropriately trained.
To maintain your own training record and to discuss needs with your line manager.
To proactively employ the principle of continuous improvement and a basis of teamwork in day to day activities. Raise ideas and support operational excellence initiatives across the department.
Ensure all associated QSM activities and analytical documentations are kept up to date. (e.g. SOPs, Read and understood, assigned deviations, CAPA etc.).

Qualifications And Experience

Minimum HND/HNC or equivalent experience in a laboratory focussed discipline.
Basic understanding of or experience of working to cGMP preferable.
Good interpersonal and communication skills.
Experience in the use of HPLC equipment.

Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organisation you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.

Our Commitment to Diversity, Equity and Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organisation. As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today.

Specifically we will not discriminate on the basis of race, colour, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.

This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
Seniority level Seniority level Entry level
Employment type Employment type Full-time
Job function Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing
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