QC Chemist (10 months contract)

No deviation Pte Ltd.; Singapore; On-site; SGD 45,000 - 65,000; Full time

Job summary

A leading pharmaceutical solutions provider in Singapore is seeking a QC Chemist for a 10-month contract. This role involves testing bulk products, raw materials, and environmental samples in compliance with quality standards. Ideal candidates will have 2-4 years of QC experience and a degree in a relevant Science field, as well as proficiency in bioassay techniques like ELISA and PCR. Join us and contribute to impactful projects within a collaborative environment.

Qualifications

• 2-4 years experience in QC.
• Relevant work experience in biotech or life sciences.
• Demonstrates an ability to learn from experience.

Responsibilities

• Perform various testing/analysis in a timely manner.
• Document results according to cGMP.
• Troubleshoot analytical methods and equipment.

Skills

Attention to detail

Problem solving

Collaboration

Proficiency in bioassay techniques

Education

Degree in a relevant Science field

Tools

ELISA

PCR

FACS

Job description

About the job QC Chemist (10 months contract)

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally.

Position Overview

The QC Analyst is responsible for performing 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 involves method validation and transfer, equipment qualification, and troubleshooting of analytical methods and instruments. The QC Analyst supports laboratory operations through assay trending, documentation, and general lab maintenance while ensuring compliance with regulatory and quality standards. The position requires strong technical expertise, attention to detail, and the ability to work collaboratively in a biotech or life sciences environment, with proficiency in bioassay techniques such as ELISA, potency, PCR, and FACS.

Key Responsibilities

• To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
• Analysis of bulk product, in-process, raw material or environmental samples according to Standard Operating Procedures and Test Methods.
• Documentation of results in accordance with current Good Manufacturing Practices (cGMP).
• Problem solving of analytical methods as well as troubleshooting of equipment.
• Involvement in method transfers and validation.
• Involved in equipment qualification and technical selection of QC equipment and/or standards and reagents.
• Assay trend analysis, document revision and update.
• General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
• Any other duties as assigned by your Supervisor/Manager.

Required Qualifications

• Degree in a relevant Science field or Equivalent
• Relevant work experience in a biotech or development services, R&D, healthcare and life science field would be advantageous
• 2-4 years experience in QC
• Demonstrates an ability and desire to learn from experience
• Uses knowledge of their 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