Quality Operations, Global API Intern

at  BristolMyers Squibb

Dublin, County Dublin, Ireland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Dec, 2024Not Specified19 Sep, 2024N/AMemos,Product Reviews,Cmos,Specs,Directives,Training,It,Management SystemNoNo
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Description:

WORKING WITH US

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 .
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!

  • Initiate, revise and evaluate change controls in respect of contract manufacturers
  • Support all activities associated with uploading and approval of protocols, reports, memos and other quality relevant documents in the Document Management System
  • Support preparation of Quality Agreements and purchase specs.
  • Support Annual Product Reviews submitted by the CMO’s and prepare for approval
  • Support in providing information for quality council meeting
  • Follow corporate policies and directives.
  • Support audit observation closure.
  • Review and update CMO Bona Fides as required.
  • Support the update of annual risk assessments for CMOs as required.
  • Support the update of stability protocols as necessary.
  • Support quality related projects as required.
  • Manage the annual Batch Record Review-Re-qualification of CMOs

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Other Industry

Pharma / Biotech / Healthcare / Medical / R&D

Other

Graduate

Proficient

1

Dublin, County Dublin, Ireland