Join Quotient Sciences as a Senior Manufacturing Scientist
We accelerate drug development by integrating formulation development, clinical testing, data sciences, and manufacturing into one seamless process. Our proprietary platform, Translational Pharmaceutics, shortens timelines by 9–12 months on average.
Arcinova, our specialist arm in Reading and Alnwick, UK, delivers end-to-end drug substance and early drug product services, including bioanalysis and radiolabeling—streamlining early development from candidate selection to proof of concept.
Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.
The Opportunity
We are seeking a Senior Manufacturing Scientist to lead a team of operators and scientists in delivering aseptic and non-sterile manufacturing projects. This is a hands-on leadership role within a GMP cleanroom environment, focused on quality, compliance, and continuous improvement.
Job Purpose
* Lead and develop a team delivering aseptic and non-sterile manufacturing projects.
* Ensure operations comply with cGMP and cEHS best practices.
* Drive timely closure of quality events and foster a culture of continuous improvement.
* Support the Head of Drug Product Manufacturing in maintaining facility qualification status.
* Lead technical transfers of products into the manufacturing facility.
* Deputise for the Head of Drug Product Manufacturing when required.
* Support internal, client, and regulatory audits of GMP manufacturing capabilities.
* Collaborate closely with QA and cross-functional teams to uphold quality standards and share knowledge.
Qualifications & Experience
* Degree or equivalent in a relevant scientific discipline, or extensive pharmaceutical manufacturing experience.
* Proven experience leading and developing technical teams.
* Strong understanding of GMP regulatory requirements.
* Experience partnering with internal and external stakeholders to deliver results.
* Knowledge of the drug development process.
Key Attributes
* Excellent written and verbal communication skills.
* Results-driven with strong planning and prioritisation abilities.
* High attention to detail and ability to work independently and collaboratively.
* Forward-thinking with a continuous improvement mindset.
* Diligent, flexible, and adaptable.
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.
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 organization. We will not discriminate on the basis of race, color, 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.
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