Analytical Technical Services Analyst
AI in this role
Validate analytical methods and perform laboratory testing to ensure product and material quality at GSK.
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Analytical Technical Services Analyst
You will validate and support analytical methods that ensure product and material quality. You will work closely with laboratory colleagues, quality and production teams. We value practical problem-solving, clear communication, and a focus on data integrity. This role offers hands-on technical work, chances to grow into wider technical leadership, and the opportunity to contribute to GSK’s 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:
- Validate analytical methods and cleaning verification methods according to approved protocols and regulatory expectations.
- Perform routine and non-routine testing of raw materials, packaging, intermediates, finished products and stability samples using validated methods.
- Operate, maintain and troubleshoot laboratory instruments such as HPLC, GC, UV/Vis, IR, atomic absorption and analytical balances.
- Prepare and standardize reference standards, reagents and solutions; keep accurate laboratory records and maintain data integrity.
- Support technical investigations, root cause analysis and corrective actions for out-of-specification results or equipment issues.
- Contribute to method transfers, prepare or update SOPs, and support knowledge sharing during product launches.
Why you?
Working arrangement: This position is on-site in Egypt. You will be based in our laboratory and regularly collaborate with cross-functional colleagues.
Basic Qualification:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology or a related science field.
- 0 to 3 years of practical laboratory experience in analytical testing, preferably in a regulated industry.
- Practical experience or training with common analytical instrumentation and laboratory techniques.
- Knowledge of good laboratory practice (GLP), good manufacturing practice (GMP) and basic environmental, health and safety (EHS) expectations.
- Basic computer skills and ability to use laboratory systems and standard office software.
- Effective communication skills in English and ability to work well in diverse teams.
Preferred Qualification:
If you have the following characteristics, it would be a plus:
- Hands-on experience operating HPLC and GC with basic method troubleshooting skills.
- Experience with stability sample handling, stability programs or stability storage management.
- Experience in raw materials or packaging testing and supplier certificate of analysis review.
- Familiarity with Quality Management Systems and experience following or writing SOPs and technical protocols.
- Previous experience in a multinational or highly regulated environment.
- Strong attention to detail and a clear commitment to data integrity.
What we value
We look for people who are curious, reliable and ready to learn. You will be supported with coaching and practical experience. Our team values respect, transparency, accountability and collaboration. If you want to build technical skills and make a meaningful impact, we encourage you to apply.
Ready to apply?
If this role feels like the next step for you, please apply. Tell us how your experience and mindset will help the team deliver high-quality results. We look forward to learning about you.
Skills
Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations
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.
Contact information:
You may apply for this position online by selecting the Apply now button.
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.
How we rate this
Analytical Technical Services Analyst at GSK rates 10 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
Prepare for this job
A free preview built only from this posting: what it asks for, what you could be asked in an interview, and how to adjust your resume.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where analytical validation was part of your work. What did you do?
- Tell me about a project where laboratory testing was part of your work. What did you do?
- Tell me about a project where root cause analysis was part of your work. What did you do?
- Tell me about a project where data integrity was part of your work. What did you do?
- Tell me about a project where sop compliance was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Analytical Validation, Laboratory Testing, Root Cause Analysis, Data Integrity, and Sop Compliance. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them — a tool named with nothing behind it rarely survives a human read.
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