{"id":3022755,"url":"https://alion.io/job/bristol-myers-squibb-manager-quality-engineering-change-controldocument-review","title":"Manager, Quality Engineering, Change Control/Document Review","company":{"id":7994,"name":"Bristol Myers Squibb","domain":"bms.com","url":"https://alion.io/company/bms","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":97,"open_postings":46,"ghost_share":0,"stale_share":0.304,"repost_share":0,"time_to_fill_p50_days":21,"computed_at":"2026-10-29T05:49:05Z"}},"role":"Management","role_family":"Management","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Madison, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":116660,"max":141368,"currency":"USD","period":"year","gross":null,"usd_annual":141368},"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-10-21T18:12:51Z","employer_posted_date":"2026-10-21","last_verified_at":"2026-10-29T05:45:55Z","board_verified":true,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"At Bristol Myers Squibb, our employees often ask, “Who are you working for?”-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.\nPosition Summary\nThe Manager, Quality Engineering, Change Control/Document Review at the Summit Cell Therapy Manufacturing facility is responsible for supporting the business process owner for Change Control module and the associated governing local procedures and supporting processes. This is a highly visible role with site responsibility and cross-functional influence that has impact on departmental performance and broad quality change control management. The incumbent will serve as the subject matter expert for the Change Control process across the site.\nDuties/Responsibilities\nManages the change control quality process for all GMP activities and works with responsible cross functional areas ensure timely completion.\nReview and approve change controls and associated documents for appropriateness and to ensure records are in compliance with regulatory requirements and internal procedures.\nDrive or support process improvement initiatives.\nSME support during internal and health authority inspections of facility\nCommunicates effectively with cross functional stakeholders on matters related to change control process.\nMust be action-oriented and customer-focused and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking.\nAble to prepare written communications and communicate problems to management with clarity and accuracy.\nHas advanced computer skills to increase department's productivity, as well as broadening technical and scientific knowledge.\nRoutinely recognizes and resolves Quality issues; Informs management of proposed solutions. Seeks management guidance on complex issues; develops procedures.\nAbility to fully interpret complex results and situations and articulate recommendations for resolution.\nQualifications\nMust have experience with cGMP manufacturing, Quality, and Compliance.\nMust have strong authorship and be able to critically evaluate change controls and generate technical conclusions consistent with Quality risk management principles\nMust be able to routinely recognize quality issues and interpret problems, as well as proposed solutions for complex issues. \nMust understand continuous improvement and be able improve the compliance and efficiency of the quality system.\nMust be able to effectively prepare and convey data analysis to management and others within the group with clarity and accuracy.\nMust be self-directed, complete routine tasks independently and be confident in making decisions in respective subject matter area, consulting with management for decisions outside of established processes.\nRequires moderate direction to complete more complex tasks.\nComfortable providing input/guidance to others within the department and across the organization in change control technical writing.\nPropose solutions for issues and work with management to resolve.\nAble to recognize conflict and notify management with proposed recommendations for resolution.\nAble to prepare written communications and communicate problems to management with clarity and accuracy.\nAble to support internal and health authority inspections of facility.\nUnderstanding of Change Controls and why they are required.\nAble to write and review reports with clarity and brevity.\nBachelor of Science degree required.\nMinimum of eight years of experience in the pharmaceutical or related industry.\nCollege or university degree required.\nAn equivalent combination of education and experience may be substituted.undefined\nWe hire for skills and capabilities, not just credentials - if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.\nCompensation Overview:\nMadison - Giralda - NJ - US: $116,660 - $141,368\nThe starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.\nBenefits:\nSubject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).\nU.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.\nNon-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.\nDepending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.\nU.S.-based job seekers can explore full benefit offerings athttps://careers.bms.com/benefits\nHow We Work\nWhere you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.\nSupporting People with Disabilities\nBMS 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 . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.\nCandidate Rights\nBMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.\nFor roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/\nData Protection\nWe will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.\nAny data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.\nIf this posting is missing required information required by local law or incorrect, contact BMS at  with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.\nR1607570 : Manager, Quality Engineering, Change Control/Document Review","description_format":"text","description_chars":8229,"description_truncated":false,"requirements":{"experience_years_min":8,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":["Equity","Flexible time off"],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Prescription Drugs","Biologics & Biosimilars","Oncology Therapeutics","Cardiometabolic Therapeutics"],"lifecycle":[{"event":"open","at":"2026-10-21T18:12:51Z"}],"visa":[{"country":"US","licensed_sponsor":true,"evidence":"green card filings: 26","filings_12m":0,"filings_prev_12m":40,"green_card_filings_12m":26,"median_offered_wage_usd":132500,"route":null,"cap_exempt":false,"checked_at":"2026-10-15T11:24:14+00:00","sources":["US Department of Labor: LCA disclosure data (H-1B, H-1B1, E-3)","US Department of Labor: PERM disclosure data (green cards)"],"filings_for_role_12m":0}],"liveness":{"score":79,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.883,"p_room":0.9,"age_days":7,"expected_fill_days":21,"reasons":["conf:0","velocity","win:mid","comp:brand"],"computed_at":"2026-10-29T05:49:05Z"},"pay":{"stated_usd_annual":141368,"is_top_pay":false},"html_url":"https://alion.io/job/bristol-myers-squibb-manager-quality-engineering-change-controldocument-review","json_url":"https://alion.io/job/bristol-myers-squibb-manager-quality-engineering-change-controldocument-review.json","meta":{"generated_at":"2026-10-29T09:00:13Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":13599,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-30T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":7994},"rest":"https://alion.io/mcp/rest/get_company?id=7994"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fbristol-myers-squibb-manager-quality-engineering-change-controldocument-review"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fbristol-myers-squibb-manager-quality-engineering-change-controldocument-review"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fbristol-myers-squibb-manager-quality-engineering-change-controldocument-review"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/bristol-myers-squibb-manager-quality-engineering-change-controldocument-review\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fbristol-myers-squibb-manager-quality-engineering-change-controldocument-review"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3022755}},{"tool":"search_jobs","arguments":{"company":"bms.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3022755},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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