Junior QA Operations

No deviation Pte Ltd.; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A pharmaceutical solutions provider in Singapore seeks a Quality Assurance professional to support QA operations, participate in improvement projects, and ensure effective communication with stakeholders. Applicants should have 1-2 years of QA experience in a GMP environment and excel in attention to detail and collaboration. This role offers comprehensive health coverage and a culture of inclusion and innovation.

Benefits

Comprehensive Health & Wellness Coverage

Inclusive Culture

Career Advancement Opportunities

Qualifications

• 1-2 years of Quality Assurance experience in a GMP environment.
• Strong attention to detail; meticulous in document review and record-keeping.
• Good communication skills; able to collaborate effectively with stakeholders.

Responsibilities

• Provide support for routine QA operations, including quality reviews of logbooks and SOPs.
• Participate in and contribute to continuous improvement projects.
• Liaise with cross-functional stakeholders to ensure alignment of QA tasks.

Skills

Quality Assurance experience

Attention to detail

Good communication skills

Ability to learn quickly

Ability to work independently

Job description

Position Overview

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.

Key Responsibilities

• Provide support for routine QA operations, including quality reviews of: Logbooks, Periodic reviews & SOPs.
• Participate in and contribute to continuous improvement projects
• Liaise with cross-functional stakeholders to ensure alignment and timely execution of QA tasks

Required Qualifications

• 1-2 years of Quality Assurance experience in a GMP environment
• Strong attention to detail; meticulous in document review and record-keeping
• Good communication skills; able to collaborate effectively with stakeholders
• Fast learner who can pick up new systems and processes quickly
• Able to work independently with minimal supervision

Benefits

• Comprehensive Health & Wellness Coverage: Receive medical 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.