Bristol Myers Squibb
pharmaceutical
GraduateValidationAssociateScientist/Engineer(Manufacturing,Science&Technology)
“Graduate Validation Associate Scientist / Engineer (Manufacturing, Science & Technology) at Bristol Myers Squibb. Skills: validation protocols, Standard Operating Procedures (SOPs), validation reports, risk assessments, validation studies, cycle development, sampling, testing, data analysis, technical reports. Gain hands-on experience with different manufacturing equipment and process areas within a sterile drug product facility. Support cleaning validation, process validation, and equipment-rel”
What You'll Achieve.
Takes ownership of assigned tasks and delivers to agreed timelines and quality standards
Industry & Context.
Good problem-solving and analytical skills; Approaches challenges with a structured, logical, and data-driven mindset; Support investigations, root cause analysis, and continuous improvement activities
2-year fixed term contract, Site-essential roles require 100% of shifts onsite at your assigned facility., Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility., ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
What They're Looking For.
Must Have
Bachelor’s or Master’s degree in Engineering, Science, or a related discipline, Recent graduate or early-career professional, Interest in pharmaceutical or biotechnology manufacturing
What You'll Do.
Gain hands-on experience with different manufacturing equipment and process areas within a sterile drug product facility
Support cleaning validation
and equipment-related activities
Develop and write validation protocols
Standard Operating Procedures (SOPs)
and validation reports
Support risk assessments to identify critical parameters and acceptance criteria
Execute validation studies
including cycle development
Assist in the preparation and execution of validation protocols
and technical reports
Learn how regulatory requirements (e.g. EU GMP
FDA) are applied in day-to-day manufacturing environments
Participate in cross-functional teams with Manufacturing
Engineering and other functions
Support investigations
and continuous improvement activities
Build knowledge of aseptic manufacturing
risk management and good documentation practices
How You'll Work.
Team & Collaboration
work as part of a multidisciplinary team; Participate in cross-functional teams with Manufacturing, Quality, Engineering and other functions
Communication Scope
Clear written and verbal communication
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