Winter Co-op/R&D Quality and Risk Management

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas
(infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together

The R&D Quality and Risk Management (QuRE) department is responsible for ensuring quality, risk management, and operational excellence across all research and development activities. The team partners strategically with business units to build quality into processes early, proactively manage risks, and support inspection readiness. Key functions include Quality Assurance, Risk & Quality Management Systems, Functional and Process Quality, Therapeutic Area Quality, Third Party Quality, Auditing, Inspection & Intelligence, Governance & Risk, and Quality Services & Solutions.

The department’s objectives are to:

• Accelerate innovation through “Quality by Design”
• Administer robust audit and inspection programs
• Integrate risk management into business planning and performance
• Drive continuous improvement through data analytics and lessons learned
• Support due diligence, M&A, and regulatory compliance

QuRE provides dedicated support for functions and processes, manages quality strategies at the program/asset level, oversees vendor qualifications, and leads cross-functional issue management. The team fosters a culture of quality, compliance, and risk awareness to enable safe, effective, and innovative R&D outcomes.

The R&D Quality and Risk Management Co-op will support the R&D QuRE (Quality, Risk, and Excellence) team in delivering quality assurance, risk management, and operational excellence across research and development functions. This role is designed for a motivated student seeking hands-on experience in pharmaceutical R&D quality and risk management.

Quality Business Partner Support

• Collaborate with functional and process quality teams to provide dedicated quality support for R&D functions and processes.
• Assist in developing and implementing fit-for-purpose quality strategies (e.g., Precision Medicine, Digital Health, AIML, Safety, Regulatory Affairs).
• Support process oversight, advice, and lessons learned initiatives.
• Participate in inspection readiness and preparedness programs.
• Contribute to due diligence activities and M&A support.

Quality Assurance

• Assist in administering audit programs focused on high-risk areas.
• Support the preparation, conduct, and reporting of GLP, GCP, and GVP audits (internal and external).
• Help coordinate pre-inspection visits and sponsor mock inspections.
• Participate in horizon scanning of inspection trends and industry benchmarking.

Risk & Quality Management System

• Support the integration and execution of R&D Quality Management Systems (QMS).
• Assist in risk assessments, issue management, and CAPA (Corrective and Preventive Actions) processes.
• Help gather and analyze risk data and insights to facilitate management reviews and continuous improvement.
• Participate in business operations support, including communication and engagement plans (e.g., newsletters, townhalls).

Quality Services & Solutions

• Contribute to the development and deployment of strategies for quality planning, KPI monitoring, and roadmap execution.
• Support knowledge management and collaboration tools.
• Assist in IT system validation, electronic data integrity, and readiness assessments.

• Pursuing a BS degree in Life Science, Business, Regulatory, Computer Science, Statistics or similar disciplines.
• Strong analytical, organizational, and communication skills.
• Interest in pharmaceutical R&D, quality assurance, and risk management.
• Must be able to work full-time (35-40 hours/week) throughout the duration of the 6-month co-op (January ~ June 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.

• Ability to work collaboratively in a cross-functional team environment.
• Proficiency in PowerBI, Veeva QMS; familiarity with data analytics tools is a plus.

• Must successfully pass a drug screen and background check prior to assignment target start date.  
• Please note: If you do not receive an automated email after submitting your application, be sure to check your spam folder.

• While GSK embraces a flexible work environment, we do require certain positions to be onsite. Candidates who are hired for an on-site role or hybrid role, and reside outside of 50-miles from their assigned work location, are eligible for relocation stipend. This is a one-time payment to help offset housing & relocation expenses. Please refer to the position details for the requirements of each position. 
• GSK Interns and Co-ops are offered a competitive hourly pay rate and benefits. Please note, benefits eligibility determined the month following date of hire.

• This job posting is for a temporary role as an employee of Atrium on assignment at GSK. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on several factors, including skills, competencies, experience, educational degree obtained, location and/or being pursued and other job-related factors permitted by law.

  In addition, this role will be eligible for overtime pay, in accordance with federal and state requirement.

  • Pay Rate Range: $21/hr to $40/hr

Interested in learning more? Register now on our digital learning platform (GSK Get Ahead - Connectr) where you can access interview and assessment hints and tips, speak to a mentor and learn more about life at GSK.