About Us

Headquartered in Denmark, NNIT Singapore Pte Ltd is a rapidly expanding leader in life science consulting, delivering innovative solutions across Singapore and the broader Asian region since 2011. We provide comprehensive, end-to-end services tailored to life science clients, covering every aspect of the value chain-from laboratory environments and clinical operations to regulatory affairs, manufacturing, and supply chain management.

Guided by our core values-Open & Honest, Conscience Driven, and Value Adding-our approach ensures that these principles are reflected in every interaction. With a dedicated team of 1,700 consultants across Europe, Asia, and the USA, we are committed to supporting our clients in bringing vital medicinal products to patients.

Role Overview

NNIT is seeking professionals from the life sciences industry for full-time, on-site roles at our client locations in Tuas, Singapore. As a Junior/Consultant (Quality Assurance), you'll be providing oversight for Quality on-the-floor and operations support. You will support manufacturing operations and IPC testing through purposeful presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations.

In this role, you will report to your Line Manager and work closely with key stakeholders on-site. Your expertise and proactive approach will be crucial in driving and delivering high-quality service.

* Required to perform 12-hour shift (day / night)

Key Responsibilities

• Provide direct Quality Assurance support for all GMP activities (including on-the-floor quality oversight, deviations, change control and CAPAs)

• Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicators meet targeted metrics

• Participate in root cause investigations for deviations

• Review of deviations, change controls, and other quality records (with focus on highly complex records) such as electronic batch records, SOPs, logbooks and work orders

• Support in regulatory inspections, and interact directly with regulatory inspectors

• Supporting other QA initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation

Essential Qualifications

• Bachelor's Degree in Science or related technological field and 2 years of directly related experience OR

• Associate's Degree in Science or related technological field and 4 years of directly related experience OR

• High School Diploma in Science or related technological field / GED and 6 years of directly related experience

Valuable Experience

• 1-3 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical/biopharmaceutical industry with progressively increasing responsibility and demonstrated experience in quality assurance, and quality systems.

• Direct experience with bulk manufacturing of biopharmaceuticals

• Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff

What We Offer

Impactful Projects: Consulting roles with international healthcare clients on strategically significant projects.

Professional Environment: Work within a motivated team in a professional consultancy setting.

Leadership Opportunities: Take on leadership roles and contribute to shaping our organization.

Career Development: Excellent opportunities for career advancement within a leading consulting firm.

Training & Mentoring: Structured training programs and peer mentoring to support your professional growth.

If you're ready to make a significant impact in the life sciences field and advance your career with a rapidly growing firm, we invite you to apply for this exciting opportunity.