QC Biochem Analyst

About No deviation

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 Biochem Analyst is responsible for executing biochemical and analytical testing to support product quality and manufacturing operations. This role involves performing routine and non-routine laboratory analyses in accordance with approved SOPs, test methods, and cGMP requirements. The analyst ensures accurate documentation of results, supports troubleshooting of analytical methods and laboratory equipment, and contributes to overall laboratory efficiency through 5S practices and inventory management. Working collaboratively within the Quality Control team, the QC Biochem Analyst plays a key role in maintaining quality standards while meeting operational timelines in a regulated life sciences environment.

Key Responsibilities

• Prioritize and perform various testing and analyses in a timely manner to support business requirements.
• Analyze product samples according to Standard Operating Procedures (SOPs) and Test Methods.
• Document results in compliance with current Good Manufacturing Practices (cGMP).
• Troubleshoot analytical methods and perform basic equipment troubleshooting.
• Provide general 5S laboratory support, including housekeeping, equipment maintenance, inventory management of supplies, and glassware handling.
• Perform any other duties as assigned by your Supervisor/Manager.

Required Qualifications

• Diploma or Degree in a relevant Science field or equivalent.
• Relevant laboratory experience in life sciences is an advantage.
• 1–3 years of experience in Quality Control (QC).
• Demonstrates ability and willingness to learn from experience.
• Maintains quality standards while delivering results.
• Understanding and execution of ELISA, potency assays, PCR, and FACS methods.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• 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.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.