Senior / QA Executive at GSK

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

14 Feb, 26

Salary

0.0

Posted On

16 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, GMP Compliance, Root Cause Analysis, Auditing, Change Control, CAPA, Coaching, Communication, SAP, Veeva Systems, Risk Assessment, Quality Risk Management, Technical Documentation, Investigations, Manufacturing Oversight, Collaboration

Industry

Pharmaceutical Manufacturing

Description

Site Name: Singapore - Tuas Posted Date: Nov 14 2025 You will join a committed quality team in Singapore to protect product quality and patient safety. You will provide material and operational quality oversight during manufacturing and support investigations, audits and batch documentation. We value curiosity, clear communication, and a practical, solutions-focused mindset. This role offers growth through hands-on experience, cross-functional collaboration, and meaningful impact aligned with our mission of uniting science, technology and talent to get ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Provide QA oversight of supplier management activities. Support incoming material documentation review and release Provide day-to-day quality oversight on the production floor to ensure compliance with GMP and site procedures. Support investigations for deviations, non-conformances and customer complaints, including data gathering and root cause analysis. Participate in internal auditing and inspection readiness activities and support responses to audit findings. Support change control, CAPA and periodic product review activities to drive timely closure and continuous improvement. Coach and work closely with manufacturing, laboratory and engineering teams to embed quality practices. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals. Degree in Life Sciences, Chemistry, Engineering or a related discipline. At least 2 years of experience in a GMP-regulated manufacturing environment; experience in pharmaceuticals preferred. Practical knowledge of current Good Manufacturing Practices and quality systems. Experience with SAP or Veeva systems Experience supporting health authority inspections or major audits. Familiarity with risk assessment and quality risk management tools. Demonstrated ability to coach or mentor colleagues and to influence cross-functional teams. Strong written and verbal communication skills in English. Ability to review technical documentation and perform basic investigations. Comfortable working on-site and engaging directly with production teams. To learn more about Singapore GSK and our people, please click on this link: https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore #Li-GSK Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Responsibilities

The role involves providing quality oversight during manufacturing and supporting investigations, audits, and batch documentation. You will also coach and collaborate with cross-functional teams to ensure compliance with quality practices.