Senior QC Specialist ASAT

Your Responsibilities:
Job Description:

•You will participate and support GMP audits and be the Subject Matter Expert (SME) audit frontier for assigned topics.
•You will be leading and managing site/department projects and initiatives.
•You will be responsible to ensure all in-use procedures are current and compliant.
•You will be writing, review and approving all required GMP documentation such as protocols, SOP and reports.
•You will be writing, review and approving notifications (events/deviations) and /OR CAPAs.
•You will be writing, review and approving changes.
•You will also be supporting the local compendium system.
•You will be responsible to lead the problem identification and solving.
•You will be performing development, validation and verification activities where it is required.
•You will be performing methods/knowledge transfer to the routine testing team.
•You will also be responsible to assist the QC lead or QC Manager to manage the operations of the team, and from time to time, provide leadership and guidance to the team.

*LI-GSK

GSK's dedication to the wellbeing of our employees is reflected in the benefits we offer; including healthcare for yourself and dependents, performance related bonus, long term incentives and a host of other flexible offerings you can tailor to your own preferences. We also offer a range of employee health and wellbeing programs including our truly unique Partnership for Prevention program, a global commitment by GSK to provide all employees with up to 40 preventative healthcare services bringing to life our mission to: do more, feel better and live longer.

At GSK we value diversity and treat all candidates equally. We aim to create an inclusive workplace where all employees feel engaged, supportive of one another, and know their work makes an important contribution.

If you would like to join us in innovating and inspiring changes in the industry, we urge you to apply.

Closing date for applications: 15th November 2018

Why You?

Basic qualifications:
Requirements:

•You should have a relevant University degree in Science discipline with 6 years of relevant working experience, or a Diploma with at least 10 years of working experience.
•Preferably having worked in biology or chemistry lab, with experience in method validation, development and transfer.
•Good knowledge in cGLP and cGMP.

Preferred qualifications:
•Knowledge in SAP and compendium would be an advantage.
•Effective report writing skills
•A good team player with a drive to lead a team.
•Good analytical and problem solving skills.

Why GSK?:
GlaxoSmithKline (GSK) is a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have three global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products. Our goal is to be one of the world's most innovative, best performing and trusted healthcare companies.
We are proud of the difference we make.

GSK has ranked 1st in the Access to Medicines Index all five times since its launch in 2008 and FORTUNE Magazine ranked us #1 on its 'Change the World list' which recognizes companies that have made significant progress in sustainable, scalable approaches to addressing societal problems as part of their company strategy.

GSK Vaccines has a broad portfolio and innovative pipeline of vaccines to protect people of all ages. We deliver over two million vaccine doses per day to people living in 160 countries, preventing a range of diseases such as; hepatitis, rotavirus and HPV infections, diphtheria, tetanus, whooping cough, measles, mumps, rubella, bacterial meningitis and influenza. Our Tuas site, one of only two GSK global vaccines manufacturing facilities worldwide, operates around-the-clock to manufacture the active ingredient used to make a GSK vaccine that protects children against pneumonia.

Contact information:
You may apply for this position online by selecting the Apply now button.
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