QC Specialist

Are you an experienced Quality Control professional eager to ensure the safety and compliance of vital pharmaceutical packaging and raw materials? Join our dedicated QC team in Basel to perform critical analytical testing and support cGMP quality operations that bring life-changing therapies to patients.

Onsite role

This is an onsite role. Working together in person supports close, real-time collaboration and team alignment, enabling us to deliver our best work. 

Start Date: September / October 2026

Contract details: 12 months | 80% - 100% (41h/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:

• Perform analytical testing of primary packaging materials, raw materials (such as excipients), and consumables in accordance with strict cGMP guidelines to support safe drug manufacturing.

• Execute thorough laboratory investigations for out-of-specification or unexpected results and support technical troubleshooting.

• Support analytical method implementation, qualification, verification, and validation activities.

• Author, review, and update QC-related documentation including SOPs, testing procedures, specifications, validation protocols, and lab records.

• Liaise with suppliers and qualified external laboratories to obtain and verify Certificates of Analysis (CoAs) and essential GMP documentation.

• Collaborate cross-functionally with Quality Assurance, Supply Chain, and Operations to maintain project timelines and compliance.

• Drive continuous improvement initiatives to enhance efficiency and accuracy across laboratory operations.

What we are looking for:

• Completed vocational training as a Laboratory Technician with 4+ years of QC experience in a cGMP environment; or a Bachelor's/Master's degree in Chemistry or a related scientific discipline with relevant QC experience.

• Solid practical experience in analytical testing of raw materials, excipients, and consumables (e.g., wet chemistry, FTIR, or physical/chemical assays).

• Practical experience testing primary packaging materials is highly desirable.

• Sound working knowledge of cGMP regulations, pharmacopeial standards, and quality control systems.

• Strong analytical mindset, methodical problem-solving skills, and precise documentation practices.

• Excellent communication skills in English; proficiency or working knowledge of German is a strong advantage.

• Self-motivated and organized professional who thrives both independently and as part of a collaborative team.

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.

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.