Quality Compliance Intern — Regulatory Operations

Bristol Myers Squibb UK & Ireland; Dublin; Vor Ort; EUR 19.000 - 25.000; Vollzeit

Zusammenfassung

Bristol Myers Squibb Ireland offers an internship in Quality Compliance within External Manufacturing. You will gain hands-on experience supporting quality and regulatory activities across multiple teams.

The six to twelve month program provides exposure to GMP practices, regulatory documents, and cross-functional collaboration, with an hourly rate of €14.94 and local benefits. This role is based in Dublin and is ideal for an undergraduate pursuing a scientific degree.

Qualifikationen

• Undergraduate degree in a relevant scientific discipline.
• 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.

Aufgaben

• 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.

Ausbildung

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

Tools

Word

Excel

Access

PowerPoint

Jobbeschreibung

Bristol Myers Squibb Ireland offers an internship in Quality Compliance within External Manufacturing. You will gain hands-on experience supporting quality and regulatory activities across multiple teams.

The six to twelve month program provides exposure to GMP practices, regulatory documents, and cross-functional collaboration, with an hourly rate of €14.94 and local benefits. This role is based in Dublin and is ideal for an undergraduate pursuing a scientific degree.