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Quality Operations, Global API Intern

  • Internship
    Full-time
    Placement Program
  • Healthcare
  • Dublin
  • Quick Apply

AI generated summary

  • You must manage change controls, support document uploads, assist in quality agreements, prepare reviews, ensure audit closure, and update risk assessments and stability protocols as needed.
  • You will manage change controls, support document uploads, prepare Quality Agreements, assist in audits, update assessments, and handle annual Batch Record Reviews for CMOs.

Requirements

  • 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

Responsibilities

  • 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

FAQs

What kind of experience can I expect to gain from the internship?

You will gain practical hands-on experience, training, and the opportunity to shadow experts in the field, as well as insight into what it's like to work at Bristol Myers Squibb.

How long is the internship program?

The internship program can range from six to twelve months, depending on the requirements of your degree course.

What specific responsibilities will I have as a Quality Operations, Global API Intern?

You will be involved in initiating and evaluating change controls, supporting document management activities, assisting in quality agreement preparation, and managing audit observation closures, among other tasks.

Is the internship paid?

The job description does not specify whether the internship is paid; please check with the hiring department for details.

Are there opportunities for academic credit during this internship?

Yes, the internship program offers opportunities for students to earn academic credit while gaining experience.

What type of work environment does Bristol Myers Squibb promote?

Bristol Myers Squibb promotes a diverse and inclusive work environment, recognizing the importance of balance and flexibility, alongside providing a range of competitive benefits.

Are there any specific qualifications or skills required for this internship?

While specific qualifications are not listed in the job description, candidates should possess relevant educational background, skills, and a passion for quality operations in the pharmaceutical industry.

Is the internship location-based, or can it be done remotely?

The specific occupancy type for this role is not mentioned, but it typically requires being onsite at your assigned facility for site-essential or site-by-design roles.

What are the corporate values at Bristol Myers Squibb?

Bristol Myers Squibb's shared values include passion, innovation, urgency, accountability, inclusion, and integrity.

Is there support for individuals with disabilities during the recruitment process?

Yes, BMS provides support for individuals with disabilities through a transparent recruitment process and reasonable workplace accommodations.

Manufacturing & Electronics
Industry
10,001+
Employees

Mission & Purpose

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome. Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients. Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do.