Document Control Specialist jobs in United States
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Bristol Myers Squibb · 3 days ago

Document Control Specialist

Bristol Myers Squibb is a dynamic biotechnology company focused on improving survival for cancer patients through innovative drugs. The Document Control Specialist will oversee the document control system for a new Radiopharmaceutical facility, ensuring compliance and quality in document management and supporting clinical development and GMP operations.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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H1B Sponsor Likelynote

Responsibilities

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

Qualification

Quality assurance experienceGMP experienceDocument management system21 CFR complianceFDA regulatory experienceHighly organizedProfessional ethicsCommunication skills

Required

BS/MS in a Science related discipline preferred
3-5 years of quality assurance experience
Experience working with FDA or other federal and state regulatory bodies
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

Preferred

Pharmaceutical and GMP experience preferred

Benefits

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Company

Bristol Myers Squibb

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At Bristol Myers Squibb, we work every day to transform patients’ lives through science.

H1B Sponsorship

Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)

Funding

Current Stage
Public Company
Total Funding
$29.32B
Key Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B

Leadership Team

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Charles Bancroft
CFO
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Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
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Company data provided by crunchbase