No deviation

QC Specialist

No deviation  •  Singapore, SG (Onsite)  •  7 days ago
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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.

Position Overview

This role supports the Quality Control (QC) laboratory in maintaining equipment reliability, documentation integrity, and compliance with GMP requirements. The position assists with calibration, maintenance, and qualification of laboratory instruments, coordinates vendor servicing activities, and supports the broader equipment lifecycle from documentation to qualification. It also plays a key part in ensuring laboratory records, SOPs, and change controls are accurate, current, and compliant, while contributing to investigations, deviations, and CAPA activities as needed. The role further supports continuous improvement efforts, including audit readiness and the adoption of laboratory best practices, to help drive operational excellence within the QC department.

Key Responsibilities

Required Qualifications

  • Diploma or Degree in Science, Chemistry, Biology, Pharmacy, or a related discipline.
  • Prior experience in a QC laboratory or GMP-regulated environment preferred.
  • Familiarity with laboratory equipment calibration, maintenance, and qualification processes.
  • Working knowledge of GMP, Data Integrity, and quality system requirements (e.g., change control, deviations, CAPA).
  • Strong attention to detail and accuracy in documentation.
  • Good organizational and coordination skills, with the ability to liaise with vendors and cross-functional teams.
  • Effective written and verbal communication skills.
  • Proficiency in relevant software/systems (e.g., LIMS, MS Office) is a plus.

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.

No deviation

About No deviation

Founded in 2007, No deviation is a trusted partner to pharmaceutical and biotech companies seeking smarter ways to deliver compliance. From engineering consultancy to CQV execution, regulatory compliance, and digital enablement, we support our clients across the entire project lifecycle in Asia, Europe.

We specialise in:

CQV (Commissioning, Qualification & Validation)

Lean, risk-based approaches aligned with GAMP 5, Annex 15, and ASTM E2500.

Quality, Compliance & Regulatory

Audit readiness, QMS remediation, documentation, and training.

Project Management & Technical Support

From operational readiness to vendor coordination.

Digital Enablement

Implementation of paperless validation (e.g. Kneat Gx), data integrity, and process digitalisation.

Specialised Training & Talent Support

Upskilling programs and resource placement to accelerate project success.

Our approach is rooted in patient safety, process understanding, regulatory compliance, and a constant drive for operational excellence in terms of safety, quality, delivery, and cost.

If you’re troubleshooting a deviation, planning a major CQV deployment, or scaling digital validation tools, we work side-by-side with your teams to deliver meaningful outcomes. Our methodology draws from ICHQ9 risk principles, with a hands-on framework: Understand - Observe - Define - Implement.

Want to learn more about paperless CQV, digital QMS, or project-ready resources? We’re happy to talk. Visit nodeviation.com to explore how we can support you.

Industry
Chemicals & Materials
Company Size
51-200 employees
Headquarters
Singapore, SG
Year Founded
2007
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