QC Analyst 3

QC Analyst – Technical Transfer & Validations

This is an office-first role. Working together in person supports close, real-time collaboration and team alignment, enabling us to deliver our best work. You will work primarily in the office and laboratory, with the flexibility to work remotely for 20% of your time (one day per week).

What you will get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Competitive hourly rate.

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do:

• Support production operations by actively executing technical transfer activities and method/software validations within the Quality Control department.

• Serve as a Subject Matter Expert (SME) for at least one core laboratory software system (e.g., SoftmaxPro, Empower, SoloVPE).

• Draft and revise GMP procedures, validation documentation, and execute test scripts for analytical software and methods.

• Perform technical root-cause analysis for routine software issues and data deviations.

• Collaborate closely with cross-functional teams to interpret technical needs, project priorities, and system requirements.

• Strictly apply Data Integrity (DI) principles across all documentation and testing in compliance with site guidelines.

• Maintain complete training compliance and perform semi-routine analytical tasks to meet project deadlines.

What we are looking for:

• High School Diploma or equivalent required; Bachelor’s or Associate’s degree in Chemistry, Biology, or a related scientific discipline preferred.

• Proven Quality Control (QC) laboratory experience within a GMP-regulated biopharmaceutical environment.

• Hands-on experience with analytical software systems (e.g., SoftmaxPro, Empower, SoloVPE) and electronic quality systems (e.g., TrackWise, LIMS).

• Demonstrated background in method or software validations, test script execution, and technical writing.

• Strong problem-solving skills with the ability to interpret analytical data independently and perform root-cause analysis.

• Excellent written and verbal communication skills with a self-motivated, collaborative mindset.

About Lonza

At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

Ready to play your part in shaping the future of life sciences? Apply now.