Job Summary: We are seeking a Biochemistry and Pharmacy student for a Quality internship, supporting daily operations, document reviews, and inspections to ensure compliance and global health. Key Highlights: 1. You will gain valuable global work experience. 2. You will advance your career with genuine impact. 3. You will develop skills in a learning environment. **Help us get ahead of disease alongside our Quality team** **Required Education:** Currently enrolled in a Biochemistry and Pharmacy degree program Minimum 1 year remaining to graduation. **Other Requirements:** Must be enrolled at a Peruvian university during the internship. **Language Requirement:** Advanced English **Expected Start Date:** August 2026 **Internship Duration:** 1 year *Hybrid model: 2 days onsite* **Application Deadline:** We recommend applying as soon as possible. This vacancy will close once we receive sufficient applications, so apply early to ensure your application is considered. **Are you looking to gain valuable global work experience and help positively impact the health of billions of people? Apply today for an internship at GSK!** An internship at GSK offers you the opportunity to advance your career: you’ll take on a real role with genuine impact! You’ll perform demanding and meaningful work on real projects or assignments. You’ll also learn with us, develop your skills, and gain valuable experience for wherever your future may lead. **What will you do?** Support the team in daily customer service and logistics operations.* Review Internal Quality Agreements (IQAs) and Quality Agreements against registered product details, and coordinate with manufacturing sites for approval and signature.* Coordinate with third parties for certified translation of Certificates of Analysis (CoA) (for tender processes) and GxP documents.* Support maintenance of validity for regulatory master templates and product inspection documentation, in accordance with regulatory approval communications.* Inspection and sampling of imported products (role: inspector).* Verification of primary and secondary components, leaflets, and Certificates of Analysis against documentation provided by Regulatory Affairs (registered details), as part of product inspection (role: inspector).* Inspection and sampling of packaging materials (role: inspector).* Inspection and sampling of reconditioned products (role: inspector).* Tracking shipment of samples for analysis to third-party laboratories.* Support the Quality Approver in preparing documentation and responding to DIGEMID inspections as part of the certification process for release of biological product batches.* Review master documentation for reconditioned products (role: inspector).* Review temperature monitoring device data received during product imports (role: inspector).* Support the Quality Approver in managing product returns.* Support management of quality complaints.* Support activities related to report generation, recordkeeping, and key performance indicators (KPIs).* Support specific Quality activities as defined by the Process Owner’s priorities, e.g., tracking logistics operator (3PL) programs impacting GSK’s service, participation in audit teams for BPA/BPDT inspections, among others. * (\*) "Inspector": A person who conducts a comprehensive review of the product and related documentation, and submits the documentation and review results for verification by GSK’s Quality Approval team, which ultimately decides whether to release or reject the product. **What are we looking for?** Proficiency in Office 365 (Intermediate Excel and PowerPoint)* Final-year student in Pharmacy and Biochemistry.* Advanced English proficiency.* Intermediate knowledge of Microsoft Word, Excel, PowerPoint, and Outlook.* High attention to detail and strong organizational skills. * Desirable: The following qualifications are not mandatory but will contribute to your success and development in this role: Interest in using data analytics and digital tools to support quality processes and decision-making.* Familiarity with Artificial Intelligence (AI) tools (e.g., Microsoft Copilot) for documentation drafting, report generation, and process optimization.* Basic knowledge of Good Storage Practices (GSP) and Good Distribution and Transportation Practices (GDP/GDTP) or Quality Management Systems.* Curiosity and willingness to learn about emerging technologies and their application in Quality and Compliance. * **What will you learn?** You will support GSK’s Quality team in Peru in managing local BPA/BPDT activities and contribute to maintaining compliance of the Quality Management System (QMS). You will collaborate with colleagues from Quality, Regulatory Affairs, and Logistics. **What do we offer?** Financial remuneration* Meal vouchers* Open and friendly team * **Let’s make it happen!** You’ll find tips, suggestions, and guidance about our selection process on our website. Learn more about the application process at gsk.to/ECprocess (optional). You can learn more about GSK and our careers here: https://www.gsk.com/en\-gb/careers/ **Apply now!** ***Need help with your application?*** *Please write to* AM.EarlyTalentRecruitment@gsk.com *and let us know how we can assist you.* \#EarlyCareers **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. If you require any adjustments or accommodation during the selection process to better showcase your abilities, please let our team know as soon as we contact you. We're here to support you. **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. Our inclusive workplace makes our employees feel engaged by the contribution they make, by affording them equal treatment regardless of actual or perceived characteristics. As so, when you apply for a job at GSK, it is not necessary to include on your resume information such as: race, color, ethnicity, age, gender, sexual orientation, marital status, religion, origin, photographs or any other personal characteristics. Find out what life at GSK is really like www.gsk.com
María García
Indeed · HR
María García
Indeed · HR
