Bristol-Myers Squibb
Document Control Specialist
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. Summary
The Document Control Specialist is responsible for the tactical oversight and maintenance of document control system for a new Radiopharmaceutical facility in Indianapolis, IN. The Document Control Specialist will be a primary contact point for document control support. This position will utilize quality assurance knowledge in maintaining the quality program to be ready for clinical development and GMP commercial operations. Additional responsibilities may include providing support for corporate activities. Job Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned. Manage the process for the creation, review, approval, and issuance of GxP controlled site documents and records including batch records, logbooks, forms, procedures, protocols, templates, and reports. Manage electronic document management system (EDMS) document lifecycle workflows and assignment of reviewers / approvers and training tasks. Review the format and metadata of new documents to ensure compliance with approved templates, procedures and EDMS requirements. Provide guidance to document initiators, owners, and users to ensure compliance with all applicable procedures / regulations and assist users with EDMS workflow related issues. Manage the periodic review of controlled documents and partner with document owners to ensure periodic reviews are completed within the required timelines. Coordinate and liaise with other departments to facilitate uniform quality standards for the site. Ensure that compliance to the training program is maintained and updated as needed. Process DCR packages and review for correctness and completeness; monitor and update in-process documents. Create, assign, and archive QA controlled lab notebooks and logbooks. Education and Experience
BS/MS in a Science related discipline preferred 3-5 years of quality assurance experience Pharmaceutical and GMP experience preferred. Experience working with FDA or other federal and state regulatory bodies. Skills and Qualification
Highly motivated and organized professional with the ability to work independently. Working knowledge of 21 CFR Parts 11, 210, and 211 Very personable with strong communication skills Excellent professional ethics, integrity, and ability to maintain confidential information. Physical Demands
While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close and distance vision. This is a position that requires working in a laboratory environment. Protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials. Work Environment
The noise level in the work environment is usually moderate. Compensation Overview: $34.05 - $41.26 per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
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. Summary
The Document Control Specialist is responsible for the tactical oversight and maintenance of document control system for a new Radiopharmaceutical facility in Indianapolis, IN. The Document Control Specialist will be a primary contact point for document control support. This position will utilize quality assurance knowledge in maintaining the quality program to be ready for clinical development and GMP commercial operations. Additional responsibilities may include providing support for corporate activities. Job Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned. Manage the process for the creation, review, approval, and issuance of GxP controlled site documents and records including batch records, logbooks, forms, procedures, protocols, templates, and reports. Manage electronic document management system (EDMS) document lifecycle workflows and assignment of reviewers / approvers and training tasks. Review the format and metadata of new documents to ensure compliance with approved templates, procedures and EDMS requirements. Provide guidance to document initiators, owners, and users to ensure compliance with all applicable procedures / regulations and assist users with EDMS workflow related issues. Manage the periodic review of controlled documents and partner with document owners to ensure periodic reviews are completed within the required timelines. Coordinate and liaise with other departments to facilitate uniform quality standards for the site. Ensure that compliance to the training program is maintained and updated as needed. Process DCR packages and review for correctness and completeness; monitor and update in-process documents. Create, assign, and archive QA controlled lab notebooks and logbooks. Education and Experience
BS/MS in a Science related discipline preferred 3-5 years of quality assurance experience Pharmaceutical and GMP experience preferred. Experience working with FDA or other federal and state regulatory bodies. Skills and Qualification
Highly motivated and organized professional with the ability to work independently. Working knowledge of 21 CFR Parts 11, 210, and 211 Very personable with strong communication skills Excellent professional ethics, integrity, and ability to maintain confidential information. Physical Demands
While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close and distance vision. This is a position that requires working in a laboratory environment. Protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials. Work Environment
The noise level in the work environment is usually moderate. Compensation Overview: $34.05 - $41.26 per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.