Enable job alerts via email!
A leading biotechnology company based in Singapore is seeking a Quality Control Analyst to conduct testing of samples and ensure compliance with cGMP regulations. The ideal candidate will hold a relevant Bachelor's degree and possess 1-3 years of experience in a biotech or pharmaceutical environment. Join the team to contribute to quality and safety in manufacturing operations while supporting a positive safety culture.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.
As a Quality Control Analyst based in Singapore, you will join our Microbiology/Environmental Monitoring (EM) team. You'll be responsible for testing environmental and product stream samples, ensuring we meet release timelines and maintain compliance with cGMP regulations. Your work will directly support our manufacturing operations and contribute to a culture of continuous improvement, helping us deliver safe and effective diagnostic solutions.
The Opportunity
You will perform routine and non-routine testing of environmental, raw material, and product samples in accordance with Standard Operating Procedures (SOPs) and Test Methods.
You will conduct Environmental Monitoring (EM), including sampling HVAC systems, biological safety cabinets, and compressed gases, as well as monitoring fingertips.
You will document and review results in our Laboratory Information Management System (LIMS) and other documents to ensure compliance.
You will perform problem-solving and troubleshooting for testing-related issues and equipment.
You will support investigations into microbial contamination and help implement corrective actions.
You will contribute to projects, validation, and process improvement works, and assist in preparing EM reports for lot release and trend analysis.
You will cooperate with the team to foster a strong team spirit and embody our lean principles and continuous improvement mindset.
Who You Are
You hold a Bachelor's degree in Microbiology, Biology, Biochemistry, or a related Life Sciences discipline.
You have 1-3 years of relevant work experience, preferably in a biotech or pharmaceutical environment.
You have knowledge of cGMP standards and laboratory safety procedures.
You possess strong communication skills, both written and verbal, in English.
You are a collaborative and proactive team player with the ability to work effectively with others.
You are organized and can plan your work effectively to meet deadlines.
You demonstrate initiative and a proactive attitude, turning ideas into action to support team goals.
You are committed to promoting a positive safety culture and complying with all Safety, Health & Environment (SHE) requirements.
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.