QC Chemist

1d1 day ago

No deviation

Singapore, SG · Contract · S$45,000 – S$65,000

About this role

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. The QC Analyst performs timely and accurate testing of bulk products, in-process materials, raw materials, and environmental samples in accordance with cGMP, SOPs, and test methods. This role supports laboratory operations through assay trending, documentation, and general lab maintenance while ensuring compliance.

Daily responsibilities include prioritizing and performing various testing and analysis to support business requirements. Analysts handle analysis of samples according to Standard Operating Procedures and Test Methods, with documentation of results per current Good Manufacturing Practices. Problem-solving of analytical methods and troubleshooting of equipment are key aspects of the work.

The position requires strong technical expertise, attention to detail, and collaborative work in a biotech or life sciences environment. Proficiency in bioassay techniques such as ELISA, potency, PCR, and FACS is essential. Involvement in method transfers, validation, and equipment qualification enhances laboratory capabilities.

We foster a culture of collaboration, inclusion, and continuous development, guided by Empathy, Integrity, and Transparency. Join us to contribute to impactful projects, drive innovation, and make a real difference in the pharmaceutical industry while advancing your career.

Requirements

Degree in a relevant Science field or Equivalent
Relevant lab experience in biotech or development services, R&D, healthcare, and life science field is an advantage
2-4 years experience in QC
Demonstrates an ability and desire to learn from experience
Uses knowledge of business area to make accurate and timely decisions
Ensures quality standards are maintained while delivering results
Bio Assay Area: Understanding and execution of ELISA, potency, PCR, and FACS methods

Responsibilities

Prioritize and perform various testing and analysis in a timely manner to support business requirements
Analyze bulk product, in-process, raw material, or environmental samples according to Standard Operating Procedures and Test Methods
Document results in accordance with current Good Manufacturing Practices (cGMP)
Solve problems with analytical methods and troubleshoot equipment
Participate in method transfers and validation
Support equipment qualification and technical selection of QC equipment, standards, and reagents
Conduct assay trend analysis, document revision, and updates
Provide general lab support including housekeeping, equipment maintenance, inventory management, supplies ordering, glassware management, and autoclaving

Benefits

Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs
Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated
Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career