GSK · 1 day ago
Summer Intern/QA Specialist
GSK is a global biopharma company focused on uniting science, technology, and talent to advance health. The role of Summer Intern/QA Specialist involves supporting the quality strategy for QA systems, ensuring compliance, and driving continuous improvement initiatives at the site level.
BiotechnologyHealth CarePharmaceutical
Responsibilities
Ensure compliance of the site-level QMS to regulatory requirements, continuous improvement and simplifying compliance processes
Follow a standardized QMS approach tailored to the site’s operations
Support strategy deployment and performance management processes for site-specific Quality Systems and Improvements such as change control, deviation, CAPA, and GMP training
Develop and deploy strategies to improve quality culture and ensure QMS compliance at the site level
Support digital innovation to enhance accessibility and relevance of QMS content for the site
Collaborate with site local process owners to deploy quality systems such as VQMS and SAP/ERP quality modules
Identify and manage risks associated with site QA systems
Assess and translate site-specific user requirements to define optimal functionality for systems
Lead continuous improvement projects to drive operational excellence for critical quality processes at the site through the site Quality Improvement Plan (QIP)
Analyze and interpret site-level quality system metrics to propose and implement process improvements
Ensure alignment, compliance, and effectiveness of site-level processes within the QMS framework
Support site inspections and issue resolution, ensuring alignment with local regulations
Build strong partnerships across site functions (e.g., QC, DDA, Engineering, and Operations) to identify, escalate, and mitigate compliance risks
Engage with site stakeholders to prioritize support and risk mitigation
Qualification
Required
Pursuing a BS or MS degree in any Scientific, Engineering, Computing field (e.g. Chemistry, Biology, Biotechnology, Data Science, Chemical Engineering, Industrial Engineering, etc.)
Record of leadership, project management, continuous improvement, decision-making, and communication
Must be able to work full-time (35-40 hours/week) throughout the durations of the 10-12 week internship (May/June ~ August 2026)
Must have an active student status and/or within 12 months post-graduation from a BS or MS degree program. Post-doctoral candidates are not eligible
Strong interpersonal & leadership skills
Experience in a regulated environment and/or knowledge of regulated quality, manufacturing, GMP/GDP requirements
Ability to drive manage change, lead complex projects, and make independent decisions
Experience with operational excellence and continuous improvement techniques
Must successfully pass a drug screen and background check prior to assignment target start date
Completion of the immersive GSK Digital Assessment is required to proceed in the application process
Benefits
Relocation stipend
Competitive hourly pay rate
Overtime pay
Company
GSK
We are uniting science, technology and talent to get ahead of disease together. Our community guidelines: https://gsk.to/socialmedia
H1B Sponsorship
GSK has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (45)
2024 (56)
2023 (54)
2022 (53)
2021 (54)
2020 (72)
Funding
Current Stage
Public CompanyTotal Funding
$25.51MKey Investors
CARB-X
2021-03-02Grant· $18M
2020-09-23Grant· $7.51M
1978-01-13IPO
Recent News
EIN Presswire
2025-11-24
Company data provided by crunchbase