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External Quality Bio Sterile Operations Intern

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Bristol Myers Squibb

Oct 18, 2024

  • Internship
    Full-time
    Summer Internship
  • Research & Development
    Healthcare
  • New Brunswick
  • Quick Apply

AI generated summary

  • You should be motivated, team-oriented, and passionate about biopharma. A background in biomedical sciences, strong communication skills, and US work authorization are essential.
  • You will support quality investigations, compliance tracking, metrics analysis, document management, procedure reviews, and engage in quality culture and operational excellence initiatives.

Requirements

  • We are looking for highly motivated individuals who can collaborate in teams and have the willingness to learn.
  • Biomedical Sciences, Biotechnology, Analytical Science, Pharmaceutical & Biomedical Chemistry or Pharmaceutical & Industrial Chemistry discipline of study, or related applicable fields
  • Passionate about the biopharma sector and innovation in healthcare
  • Strong communication skills
  • Ability to work as a member of a team
  • Energetic, collaborative, and dedicated
  • All candidates must be authorized to work in the US at the time of hire. Please note that immigration or visa sponsorship is not available for this position.

Responsibilities

  • Support the Bristol Myers Squibb (BMS) Market Action Fact Finding Meetings (FIT / FIRM) and Product Review Committee processes for major / critical investigations involving Third Party products.
  • Support compliance and tracking of Field Alert Reports, Biological Product Defect Reports, Quality Defect Notifications and all other Health Authority notifications associated with CMOS managed by ExM
  • Support improvement projects as needed
  • Support the compilation & analysis of the Quality Performance metrics of the various business units of EXM Bio-Sterile Quality for Quality Council, Annual Product Quality Reviews (APQRs) and Business Operations, ensuring timely escalations and actions as required,
  • Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements support the progression of GMP documents within the Documentation Management System
  • Authoring, review and approval of QA-related procedures & Quality Agreements
  • Support the review and approval of site procedures
  • Engage in Quality Culture initiatives
  • Engage in Operational Excellence initiatives
  • Due to the nature of the role, you may work in other and/or multiple OA areas once the appropriate training has been completed.

FAQs

What is the duration of the internship program?

The internship program lasts for 10 weeks.

What kind of experience will I gain during this internship?

You will gain experience in BioPharma, leadership exposure, career mentorship, and have the opportunity to make an impact on meaningful work.

What are the key responsibilities of the External Quality Bio Sterile Operations Intern?

Responsibilities include supporting compliance and tracking of quality reports, engaging in quality culture initiatives, authoring and reviewing QA-related procedures, and participating in improvement projects.

What qualifications are required for this internship?

Candidates should be highly motivated individuals with a background in Biomedical Sciences, Biotechnology, Pharmaceutical Chemistry, or related fields, along with strong communication skills and teamwork capabilities.

Is this position open to all applicants?

All candidates must be authorized to work in the US at the time of hire, and immigration or visa sponsorship is not available for this position.

Will I be working solely in the Bio-Sterile Operations area?

Due to the nature of the role, you may work in other and/or multiple operational areas once the appropriate training has been completed.

Are there opportunities for networking during the internship?

Yes, the program includes formal and informal networking opportunities, focusing on mentorship and professional development.

What values does Bristol Myers Squibb prioritize in its workplace?

BMS prioritizes passion, innovation, urgency, accountability, inclusion, and integrity, fostering an inclusive culture that encourages diversity.

What is the on-site work protocol for this internship?

The occupancy type assigned for this internship will depend on the nature of the responsibilities, which could include site-essential or hybrid work models.

Does BMS support disabled individuals in the recruitment process?

Yes, BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process and offers reasonable workplace accommodations.

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Bristol Myers Squibb

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.