QC Specialist

You will carry out and oversee quality control testing in our analytical laboratories in Singapore. You will work closely with lab colleagues manufacturing teams and quality partners to ensure accurate compliant and timely release of materials. We value people who are curious reliable and who take pride in doing work that protects patient safety. This role offers clear growth paths hands-on technical learning and a chance to make meaningful impact by helping GSK unite 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:

• Perform routine analytical and biochemistry testing of raw materials manufacturing processes utilities/environmental monitoring and finished materials using approved methods and laboratory instruments.

• Review and approve test data ensuring accuracy and timely availability of results for release decisions and ensure that the tests are analyzed in accordance with corporate regulatory and external agency regulations.

• Support investigations for deviations out-of-specifications and environmental incidents and help implement corrective actions.

• Contribute to method and equipment validation revalidation and qualification activities including execution and documentation.

• Prepare and update laboratory documents such as quality and safety related standard operating procedures test protocols and technical reports.

• Coach and train colleagues on methods instrumentation and data integrity expectations to build team capability.

• Provide support for all laboratory-related activities (e.g. Tiers Gemba DMAIC 5S standard work data reviews etc).

Why You
This role is on-site in Singapore. Hybrid and remote working are not available due to the hands-on laboratory nature of the role.

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Bachelors degree in Life Science Chemistry Biochemistry Microbiology or a related field or Diploma with equivalent relevant experience.

• Minimum 2 years laboratory experience in a regulated environment preferably pharmaceutical or biopharma.

• Practical experience with analytical techniques or biochemistry methods relevant to quality control.

• Knowledge of Good Manufacturing Practice and laboratory quality systems.

• Strong record keeping report writing and basic investigation skills.

• Capability in strong problem-solving skills is recommended (e.g. Identifies / reports /resolve / escalate issues promptly and appropriately and implement appropriate corrective actions.)

• Good teamwork communication skills and ability to organise daily laboratory work.

• Able to work independently and as part of a team under shift patterns (including weekends) when required.

Preferred Qualification
If you have the following characteristics it would be a plus:

• Experience in method validation equipment qualification and computer system validation.

• Hands-on skills with chemistry biochemical or microbiological assays such as Chromatographic analysis and ELISA.

• Practical experience leading investigations root cause analysis and implementing CAPA.

• Familiarity with data integrity principles and electronic laboratory systems.

• Basic knowledge of statistical tools or data analytics for laboratory data review.

• Prior experience supporting audits or acting as a technical subject matter expert.

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.

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