"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact. Your Role: Perform analyses using industry-standard techniques such as HPLC, GC, Spectrophotometry, Dissolution, and Microbiological testing. Ensure that all testing is performed according to established analytical methods, SOPs, and regulatory requirements, and that all data are recorded accurately in compliance with Good Documentation Practices (GDP). Conduct and monitor stability studies to evaluate product shelf life and performance under various storage conditions. Collaborate with cross-functional teams to support investigations, root cause analysis, and implementation of CAPAs. Carry out sampling of raw materials, intermediates, and finished pharmaceutical products in accordance with approved procedures. Maintain compliance with Good Laboratory Practice (GLP) and Health & Safety protocols to ensure a safe, efficient, and reliable laboratory environment. Your Profile: A degree in Chemistry, Pharmaceutical Sciences, Microbiology or a related scientific discipline. Experience in a pharmaceutical QC laboratory, preferably within a GMP-regulated environment. Proven competence in analytical techniques such as HPLC, GC, and Spectroscopy, or Microbiological analysis. Strong attention to detail, excellent problem-solving abilities, and the capability to work effectively under pressure. Good communication skills in English, both verbally and in writing. Your Benefits: Additional Job Description (Your Benefits) We offer a competitive remuneration and benefits package, including performance-related incentives, health insurance, and opportunities for professional development. The successful candidate will benefit from a collaborative working environment, flexible arrangements where applicable, and career progression within an international organisation. Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry. Application Submission & Screening: Share your qualifications and enthusiasm through our application process. We review each submission to identify candidates whose skills best match the role. Initial Interview: We’ll explore your background, aspirations, and how you could contribute to our mission and culture. On-Site Interview: If possible, we invite you to meet us in person, connect with future colleagues, and get a feel for our workspace. Offer Stage: Congrats! If selected, you'll receive a detailed offer including compensation, benefits, and the exciting opportunities ahead. Onboarding: After you accept, we’ll guide you through a smooth, tailored onboarding experience to help you settle into your new role. Feedback & Improvement: Your feedback helps us continuously improve and enhance the candidate experience for others. Create an account by clicking ‘Sign In’ at the top of the page to set up personalized email alerts when new roles that match your aspirations become available.