Shift Quality Officer
2 weeks ago
**Site Name**: Singapore - Jurong
**Posted Date**: May 6 2025
**_
Purpose_**
To ensure that products manufactured are in full compliance with current Good Manufacturing Practices (cGMP) and regulatory requirements so as to meet stipulated product quality standards in line with the established specifications of the organisation.
To operate within the framework of safety, occupational hygiene, responsible environmental protection and in a dynamic business environment.
**_Responsibilities_**
- Review documents/analytical test results and assess all attributes/elements contributing to product release to determine if product/equipment is fit for release.
- Assess, review and approve changes that may have an impact on product quality, validation and/or cGMP compliance to ensure timely product release to customers.
- Inspect and release process equipment/plant after turnaround
- Co-ordinate Periodic Product Review (PPR) activities and compile the report.
- Lead or participate in investigations arising from customer complaints, returned goods or product failure etc, and accurately assess the impact of the complaint/failure/investigation so as to make appropriate recommendations on remedial actions for follow-up.
- Participate as an audit team member in the preparation of site audits by corporate and external groups such as the Food and Drug Administration (US), Health Sciences Authority (HSA), etc to ensure GMP and regulatory compliance. Conduct internal (Level 1 or 2) audits.
- Draft, compile, review and update appropriate procedures and listing relating to GMP and operational quality.
- Mentor and train new hires of Quality Officers as required
**Knowledge, Skills & Experience**
- At least a honours degree in a relevant science/engineering discipline
- Open to fresh graduates
- Good interpersonal skills
- Good oral and written communication skills
- Good investigation skills
- At least 3 years of relevant experience in the pharmaceutical industry
- Extensive knowledge on GMP, validation, quality, and manufacturing processes
- Good knowledge of corporate management systems
- Good audit skills
- Good knowledge of regulatory processes
Li-GSK
**Why GSK?**
**Uniting science, technology and talent to get ahead of disease together.**
GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
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