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 have a full-time Microbiologist role available based at our site in Alnwick. This is a pivotal role working in a busy team. As the Microbiologist, you will: Develop, validate, and apply microbiological methodologies. Apply microbiological methodologies during the quality control and stability evaluation of a range of materials. Conduct environmental monitoring of the GMP manufacturing facility and during the manufacture of sterile products. Comply with GxP guidelines and regulations as required for this role. Main tasks and responsibilities
Develop, validate, and report microbiological methodology as guided/requested. Apply microbiological methodologies during the quality control and stability evaluation of a range of materials. Participate in environmental monitoring of the GMP manufacturing facility and during the manufacture of products. Prepare work protocols for approval, critically assess data generated, and review data from peers. Prepare and review reports, quality documents, and training documentation. Acquire/record data in a manner that complies with GxP and internal policies/procedures. Perform assigned roles such as equipment responsible operator, equipment hardware/software validation, and the ordering of consumable items. Work with due regard to health and safety of self and others. Work flexibly across the site to meet business needs. Qualifications and experience required for competent performance
BSc or equivalent in a relevant scientific discipline. Experience in the application of microbiological methodologies in a pharmaceutical environment is advantageous. Good written and oral communication skills. The ability to critically assess data. A flexible approach to new work challenges. Application Requirements
When applying for a position with Quotient Sciences, 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, your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences 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. 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.
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We have a full-time Microbiologist role available based at our site in Alnwick. This is a pivotal role working in a busy team. As the Microbiologist, you will: Develop, validate, and apply microbiological methodologies. Apply microbiological methodologies during the quality control and stability evaluation of a range of materials. Conduct environmental monitoring of the GMP manufacturing facility and during the manufacture of sterile products. Comply with GxP guidelines and regulations as required for this role. Main tasks and responsibilities
Develop, validate, and report microbiological methodology as guided/requested. Apply microbiological methodologies during the quality control and stability evaluation of a range of materials. Participate in environmental monitoring of the GMP manufacturing facility and during the manufacture of products. Prepare work protocols for approval, critically assess data generated, and review data from peers. Prepare and review reports, quality documents, and training documentation. Acquire/record data in a manner that complies with GxP and internal policies/procedures. Perform assigned roles such as equipment responsible operator, equipment hardware/software validation, and the ordering of consumable items. Work with due regard to health and safety of self and others. Work flexibly across the site to meet business needs. Qualifications and experience required for competent performance
BSc or equivalent in a relevant scientific discipline. Experience in the application of microbiological methodologies in a pharmaceutical environment is advantageous. Good written and oral communication skills. The ability to critically assess data. A flexible approach to new work challenges. Application Requirements
When applying for a position with Quotient Sciences, 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, your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences 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. 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.
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