Job Description

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.

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 Lab experience in a biotech or development services, R&D, healthcare and lifescience field would be advantage
• 2-4 years experience in QC
• Demonstrates an ability and desire to learn from experience
• Uses knowledge of his/her business area to make accurate and timelydecisions
• Ensures quality standards are maintained while delivering results
• Bio Assay Area: Understanding and execution of ELISA, potency , PCR and FACS methods

Why join us?

• 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.

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.