Quality Compliance - Inspection Readiness & Risk Intern

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Inspire and be inspired. We offer a variety of opportunities for undergraduate and post-graduate students to use your talent, skills, education and passion to help make an impact on patient’s lives – all while growing your career and earning academic credit.

Our Internship Programme gives you a real opportunity to gain practical ‘hands-on’ experience, training and shadow the experts of your chosen field. It also provides you with insight into what it’s like to work with us.

We will place you in a six-, nine-, or twelve-month Internship Programme depending on the requirements of your degree course. So, are you ready to embark on a new adventure? We can’t wait to see what you’re made of!

Position Summary

The Intern, Quality Compliance, External Manufacturing, will participate in and

provide support for a wide range of quality compliance activities within External

Manufacturing. This includes contributing to quality compliance, quality services,

inspection readiness and risk management efforts, and assisting with general

departmental needs as required. The role provides broad exposure to quality

practices and supports day-to-day operations in a dynamic, cross functional

environment.

Responsibilities:

• Support the compilation, tracking, and follow up of quality and regulatory

performance metrics across External Manufacturing.

• Where applicable, assist with the compilation of Regulatory Restriction

Forms and support regulatory requests received for filing applications.

• Work with Virtual Plant Teams to support progression of change controls

and other quality system activities, including deviations, CAPAs, product

quality complaints, documentation, audits, and inspections.

• Support the preparation of regulatory summaries for Annual Product

Quality Reports.

• Provide quality and regulatory support to Contract Manufacturing

Operations within a cross functional team, contributing to the

management of CMOs and ensuring alignment with applicable GMP,

corporate policies, and regulatory requirements.

• Support ongoing quality and regulatory projects, continuous improvement

initiatives, and Operational Excellence efforts.

• Assist with the progression of GMP and regulatory documents within the

Documentation Management System, including review, processing, and

authorship of quality or regulatory related procedures.

• Support the review and approval of site procedures and associated

documents as required.

• Engage in Quality Culture initiatives across External Manufacturing.

• Provide routine administrative support such as scheduling meetings,

preparing presentations, issuing meeting minutes, and maintaining action

logs.

• Collaborate with relevant departments to support compliance and ensure

effective communication across teams.

• Perform other ad hoc tasks as assigned by management or relevant

quality representatives in support of team and departmental goals.

Qualifications, Knowledge and Skills Required

• Currently undertaking an undergraduate degree in a relevant scientific

discipline such as General Science, Biomedical Sciences, Biotechnology,

Analytical Science, Pharmaceutical and Biomedical Chemistry, or

Pharmaceutical and Industrial Chemistry.

• Strong time management and organisational skills, with the ability to

manage multiple tasks and work independently using initiative.

• Effective interpersonal, communication, presentation, and teamwork skills.

• Proficiency in key computer applications including Word, Excel, Access

and PowerPoint, with the ability to collect, analyse, interpret and present

information clearly.

• Demonstrated ability to work in a fast-paced environment, balancing

several projects at once.

• Flexible, motivated, energetic and collaborative, with the ability to meet

targets and milestones.

• Confident public speaking skills and the ability to engage effectively with

others.

• Passion for the pharmaceutical sector and innovation in healthcare.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

2, 213.90 € per month

Pay for this internship/co‑op position is provided in accordance with local market practices and applicable laws. Pay may be offered as an hourly rate and/or monthly stipend, or other locally compliant structure. Pay is determined based on objective factors such as academic level, relevant experience, skills, and work location.

Interns and co‑op participants may be eligible for limited benefits depending on program structure, work location, and local requirements. Eligibility and offerings are governed by applicable policies and employment regulations.

This is a temporary, time‑bound position intended for the duration of the internship or co‑op program and does not guarantee continued or permanent employment following program completion.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1606998 : Quality Compliance - Inspection Readiness & Risk Intern