Quality Assurance Expert
3 days ago
About No deviation Pte Ltd
We revolutionize the pharmaceutical landscape by delivering patient-centric solutions.
Our team of experts in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services is seeking individuals who are passionate about contributing to impactful projects and driving 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.
Job Description:As a detail-oriented QA Specialist in Singapore, you will support Quality Assurance activities in a cGxP manufacturing facility.
You will ensure compliance with SOPs and regulatory standards, conduct routine QA tasks, and provide oversight for batch records and validation protocols.
This role is ideal for someone with 1-3 years of QA/Validation experience in a GMP environment, eager to contribute to a dynamic and collaborative team.
Key Responsibilities:- Conduct routine QA activities, including SOP reviews, deviation investigations, and change controls.
- Provide QA oversight for batch records, validation protocols, and CAPA implementation.
- Ensure real-time decision-making during manufacturing processes and escalate issues as needed.
- Participate in regulatory inspections and customer audits, offering SME support when required.
- Lead small projects and provide cross-functional QA guidance.
- Education: Degree in a science-related or engineering field.
- Experience: 1–3 years in QA/Validation within a GMP environment.
- Familiarity with cGMP, manufacturing processes, and quality management systems is essential.
- Strong problem-solving, interpersonal, and communication skills.
- Agility, collaboration, customer focus, and the ability to drive results in a dynamic environment.
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