Project Manager I in Alnwick

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process.

As Project Manager I, you will manage the planning, execution, and delivery of customer and non‑customer projects at Alnwick—ensuring timelines, budgets, and quality standards are met. You’ll be the primary point of contact for clients and internal teams, driving communication, governance, and issue resolution throughout the project lifecycle, while supporting portfolio visibility, commercial performance, and continuous improvement initiatives.

What You’ll Do

• Project Planning & Delivery: Develop and maintain project plans, timelines, and resource schedules. Coordinate internal kick‑off meetings and external client meetings. Ensure project documentation is accurate and up to date.
• Client Communication: Act as the primary point of contact for clients across the project lifecycle. Provide timely updates and manage expectations on deliverables and timelines. Address client queries and elevate issues when needed.
• Governance & Compliance: Maintain risk registers and issue logs for assigned projects. Ensure adherence to governance frameworks and contractual obligations. Support change‑order management and documentation.
• Financial & Commercial Support: Monitor project budgets and track actual vs. planned hours. Identify scope changes and initiate change orders. Contribute to profitability analysis and cost control.
• Reporting & Visibility: Update PSA systems and dashboards with accurate project status. Prepare progress reports for internal stakeholders and clients. Support lessons‑learned reviews and continuous improvement initiatives.

What You’ll Bring

• Experience in project management within pharmaceutical, biotech, or scientific services.
• Strong organizational and time‑management skills.
• Ability to manage multiple projects simultaneously under strict deadlines.
• Excellent communication and stakeholder‑engagement skills.
• Familiarity with project‑management tools (e.g., PSA systems, Gantt charts).
• Commercial awareness with an understanding of cost‑control principles.

Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organization 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 organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.