Engineering Validation Intern (sdpf)

Engineering CQV Intern

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. 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.

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 program 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 program 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!

During your placement as an Engineering CQV Intern, you will get experience of performing commissioning, qualification, and validation (CQV) processes in one of our varied workstreams, which include Cleaning Validation, Computer Systems, Equipment CQV, or Temperature Mapping. You will support the Sterile Drug Product Facility (SDPF) project as part of the CQV team and you will get exposure to various Engineering CQV activities such as:

• Develop and execute commissioning and qualification plans for new and existing equipment and systems.
• Perform equipment and system start-up activities, including functional testing and troubleshooting.
• Develop and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
• Develop and execute validation protocols to support facility/utilities, equipment, and computer systems validation.
• Updating validation operational procedures under guidance from the Senior validation engineer.
• Ensure that validation activities comply with regulatory requirements (e.g., FDA, EMA, ICH) and industry standards (e.g., GAMP 5).
• Maintain validation documentation and ensure it is up-to-date and audit-ready.
• Identify opportunities for process improvements and implement changes to enhance efficiency and compliance.
• Participate in root cause analysis and corrective/preventive action (CAPA) processes.
• Work closely with cross-functional teams, including Quality Assurance, Manufacturing, Engineering, and Regulatory Affairs.
• Communicate validation plans, progress, and results to stakeholders.
• Utilization of LIVES Thermal Mapping Equipment.
• Generate and review thermal mapping reports & PI/PAS trends.
• Informing managers of progress against defined timelines and ensuring accountability of tracking to deadlines.

What Qualities Are We Looking For?

• Pharmaceutical Science, Computer Systems, Biotechnology, Computer Applications Software Engineering discipline of study or a related field.
• 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

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as "Transforming patients' lives through science™", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the company deems critical to collaboration, innovation, productivity, employee well-being, and engagement, and it enhances the company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.