Senior QA Executive Validation (1.5 Years Contract)
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Job Location:
Monthly Salary:
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
You will support and lead quality assurance activities at our Singapore site. You will maintain and improve quality systems guide document and training processes and work closely with manufacturing and cross-functional teams. We value practical problem solvers who act with integrity communicate clearly and put patient safety first. This role offers clear career growth hands-on impact on compliant supply and a chance to contribute to GSKs mission of uniting science technology and talent to get ahead of disease together.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Provide quality oversight to validation projects for facilities equipment cleaning analytical methods and computerized systems.
- Author review and approve validation plans protocols reports and related SOPs.
- Assess validation impact during changes deviations and investigations and define appropriate validation steps.
- QA Approver for deviation CAPA change control SOP
- QA Approver for Engineering activities such as Calibration and maintenance plans and asset master data.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelors degree in science engineering or a related discipline or equivalent experience.
- Minimum 5 years experience in pharmaceutical quality assurance validation or related roles.
- Practical knowledge of current Good Manufacturing Practice (cGMP) and regulatory requirements.
- Experience authoring and approving validation documents and SOPs.
- Experience assessing impact of changes deviations and corrective actions on validation status.
- Strong communication skills with the ability to work effectively across functions and with external regulators.
Preferred Qualification
If you have the following characteristics it would be a plus:
- Experience with computerized system validation MES or electronic batch records implementation.
- Prior role leading validation for new product introduction or technical transfer projects.
- Project management experience and familiarity with continuous process verification approaches.
- Practical understanding of quality management systems and audit processes.
To learn more about Singapore GSK and our people please click on this link: 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 were 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.
We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities contact . Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.
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 GSKs 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 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.
Required Experience:
Senior IC
Key Skills
- IVR
- SOAP
- Avaya
- Solaris
- Cost Accounting Standards
- Database Design
- Hibernate
- ITIL
- Weblogic
- Express.js
- Contracts
- ASP
About Company
About us We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.
