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About
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. RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. Job Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned: Assist in day-to-day QA Operations activities to ensure compliance with GMP and regulatory requirements. Support Quality disposition process by ensuring that all required documents are accurately and properly completed and compiled against approved procedures and specifications, including all related deviations. Support internal manufacturing processes through shop floor monitoring and documentation review. Participate in external manufacturing oversight activities, including review of batch records and quality documentation. Aid in incoming material release by verifying documentation and performing quality checks. Contribute to continuous improvement initiatives within QA Operations. Maintain accurate records and ensure timely completion of assigned tasks. Assist in drafting Standard Operating Procedures (SOPs), batch records, technical documents, and other document types utilized at the site. Contribute to continuous improvement initiatives by identifying opportunities to enhance process efficiency, reduce costs, or improve product quality. Maintain accurate and detailed documentation for all activities in compliance with regulatory standards. This is a position that requires working in a GMP cleanroom environment, wearing protective clothing, and handling of radioactive materials. Ability to climb ladders and lift up to 50 lbs. Learning Opportunities
Exposure to QA processes in a regulated manufacturing environment. Hands-on experience with compliance and quality systems. Understanding of radiopharmaceutical production and associated quality standards. Skills and Qualifications
Eagerness to learn and adapt in a dynamic, regulated environment. Strong organizational skills and ability to manage multiple tasks. Commitment to maintaining high standards of safety, quality, and compliance. Strong analytical and problem-solving skills with attention to detail. Proficiency in Microsoft Office. Ability to work independently and collaboratively in a team-oriented environment. Excellent written and verbal communication skills. Ability to climb ladders and lift up to 50 lbs. Education and Experience
Current enrollment in a Bachelor's or Master's degree program in engineering, science, or a related field. Basic understanding of pharmaceutical manufacturing processes, validation principles and regulatory requirements is preferred. Prior internship or coursework in pharmaceutical manufacturing, process engineering, or quality assurance is desirable but not required. All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment. Please note that immigration or visa sponsorship is not available for this position. This is a temporary, time-bound position intended for the duration of the internship or co-op program. Employment in this role does not imply or guarantee ongoing or permanent employment with BMS. The starting hourly compensation for this assignment is within the range of $23.00 to $42.00/hr. Please note that the final individual compensation and any applicable benefits will be determined by your employer of record (and not BMS). Factors influencing this decision may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location of the job. Compensation details are subject to change.
Languages
- English
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