Qa Operations Intern

Description:

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us.

BMS is seeking to recruit a QA Operations Intern to join the QA Laboratory Operations and QA Technical Operations teams at Multi-Product Cell Culture Drug Substance Facility in Cruiserath, Dublin .

Compliance and administrative support for QA Laboratory Operations and QA Technical Operations teams

Roles And Responsibilities

• Engagement in Quality Culture and EOHSS initiatives
• Generation of data and metrics relating to Investigations
• Visual management of data and metrics relating to Investigations
• Analysis of RFT data
• Author/update departmental documentation including Standard Operating Procedures (SOPs), work instructions (WIs), Forms and training documents.
• Support QA activities for both QC laboratories and Biological Drug Substance Manufacturing, as applicable, for
  • New Product Introduction - Method validations and Technical Transfer
  • Change controls
  • Deviations/Investigations
  • CAPAs
  • Qualification/Validation protocols & reports for instruments, equipment, utilities, computer systems, Computer Software Validation (CSV)
  • Other associated documentation
  • Asset management (Maximo Service Requests)
  • Automation Change Requests
• Support improvement initiatives within the QA Laboratory Operations / QA Technical Operations teams
• Support the site inspection readiness program for internal and external regulatory inspections
• Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements