Raw Material Scientist

Lonza; Slough; On-site; Confidential; Full time

Benefits offered by this job

Global benefits list available

Agile working culture

Inclusive workplace

Job summary

Lonza in United Kingdom dedicated to QC Raw Materials is seeking a detail-oriented Raw Material Scientist. You will perform testing and ensure data integrity within a GMP manufacturing setting, while mentoring junior team members and supporting deviation investigations.

You will work on ensuring timely results, maintaining compliance, and driving continuous improvement across the quality systems. This site-based role emphasizes collaboration and precision to manufacture medicines to the highest

Qualifications

• Experience in QC laboratory environments and GMP manufacturing.
• Proven ability to review data, ensure accuracy, and maintain data integrity.
• Involvement with investigations, deviations, CAPAs, and quality system activities.

Responsibilities

• Perform testing of raw material samples and document results per GMP and procedures.
• Evaluate analytical data, identify issues or trends, and elevate findings to QC management.
• Review data and results generated by others for accuracy and compliance.
• Lead and support deviations, change controls, OOS/OOT investigations, CAPAs and other GMP records.
• Drive continuous improvement to GMP compliance, lab efficiency, and safety.
• Communicate risks to timelines and manage changing priorities.

Skills

QC laboratory

GMP

Analytical testing

Data integrity

Mentoring

Regulatory compliance

Education

Bachelor's or Master's in Life Sciences

Job description

The Role

United Kingdom, Slough

Job Title: Raw Material Scientist

Location: Slough

We are seeking a motivated and detail-oriented professional to join our QC Raw Materials team. In this role, you will be responsible for delivering high-quality analytical and operational support while ensuring activities are completed within agreed timelines and in accordance with GMP requirements. Working with general guidance from senior team members, you will demonstrate a strong commitment to quality, continuous improvement, and operational excellence within a fast-paced custom manufacturing environment.

As a key member of the team, you will be expected to execute work accurately and efficiently, adapt to changing priorities, and contribute to maintaining the highest standards of compliance and quality. You will also play an important role in supporting and mentoring junior colleagues, helping to foster a collaborative culture and ensure consistent performance across the department.

This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What You Will Get

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• A variety of benefits dependant on role and location
• The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits

What You Will Do

• Perform testing of raw material samples and accurately document results in accordance with GMP requirements, approved procedures, and established timelines.
• Critically evaluate analytical data, identify potential issues or trends, and elevate findings to QC Management as appropriate.
• Review and approve data, records, and results generated by other team members, ensuring accuracy, compliance, and data integrity.
• Lead and support quality system activities, including the investigation and completion of Deviations, Change Controls, OOS/OOT investigations, CAPAs, and other GMP quality records.
• Drive continuous improvement initiatives to enhance GMP compliance, laboratory efficiency, safety, and overall quality performance.
• Effectively manage changing priorities, proactively communicate risks to timelines, and elevate delays or operational challenges when required.
• Support raw material disposition activities and collaborate with cross-functional stakeholders to ensure timely decision-making.
• Provide guidance and mentorship to junior team members, promoting best practices and ensuring consistently high standards of work within the QC function.
• Champion a culture of quality, compliance, and continuous improvement, ensuring all activities are performed in accordance with GMP standards and company procedures.

What We Are Looking For

• Degree or Master's qualification in Life Sciences or a related scientific discipline.
• Experience working within a QC laboratory and/or GMP manufacturing environment.
• Previous involvement in investigations, deviations, CAPAs, and continuous improvement initiatives.
• Proven experience in chemical and/or biochemical testing techniques, with the ability to generate, interpret, and report analytical data accurately and effectively.
• Strong understanding of GMP principles and quality systems, with a track record of maintaining compliance, completing quality documentation, and adhering to regulatory requirements.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Reference: R78574