Quality Compliance & Regulatory Ops Intern

Bristol Myers Squibb; Fingal; On-site; EUR 21,000 - 28,000; Part time

Job summary

Bristol Myers Squibb invites you to join its Internship Programme as an Intern, Quality Compliance, External Manufacturing, in Ireland. You will contribute to quality and regulatory activities, gain broad exposure to GMP practices, and support day-to-day operations in a dynamic, cross-functional environment.

The six, nine or twelve month internship adapts to degree requirements, offering hands-on experience, training, and insight into how we operate to ensure patient safety and product quality.

Qualifications

• 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 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.

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.

Skills

Time management

Interpersonal skills

Communication skills

Presentation skills

Teamwork

Education

Undergraduate degree in a relevant scientific discipline

Tools

Word

Excel

Access

PowerPoint

Job description

Bristol Myers Squibb invites you to join its Internship Programme as an Intern, Quality Compliance, External Manufacturing, in Ireland. You will contribute to quality and regulatory activities, gain broad exposure to GMP practices, and support day-to-day operations in a dynamic, cross-functional environment.

The six, nine or twelve month internship adapts to degree requirements, offering hands-on experience, training, and insight into how we operate to ensure patient safety and product quality.