Bristol Myers Squibb

Bristol Myers Squibb

Posted via Workday

Senior Materials Management Associate

Apply by Oct 6, 2026

Posted Oct 2, 2026

Role at a glance

Job function
Supply Chain, Procurement & Trade Inventory & Materials Management
Salary
Not Disclosed
Location
Devens, Massachusetts, United States
Employment
Full-time
Experience
Experience in a Regulated environment such as FDA, Pharma, Bio-Pharma required
Education
High School diploma required. Associates or some college, or trade school preferred

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Role Summary

AI-generated

This role manages receiving, inspection, inventory transactions, and shipping of materials in a GMP-regulated environment. It handles raw materials, supplies, packaging components, and other received materials.

What You'll Do

  • Receive purchased materials, visually inspect them, verify identification and quantities, and record the information in inventory systems.
  • Process transactions in SAP and resolve damaged, short, excess, or missing orders according to the stated procedure.
  • Inspect and sample raw materials and packaging components for analysis or reevaluation, following procedures and GMP requirements.
  • Complete and review GMP forms and batch records for receiving and shipping activities.
  • Maintain accurate inventory records, including freight containers, and participate in cycle counting.
  • Prepare materials for shipment, verify correct picking and status, and load trucks.

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

High school diploma, a driver's license, completion of an MVR with an acceptable driving record, and experience in a regulated environment such as FDA, pharma, or biopharma are required.

Preferred

  • Associates degree, some college, or trade school.
  • Forklift driving experience; training will be provided.

Original job description

Content provided by the employer

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.



Key Responsibilities:

  • Receives purchased materials (raw materials, supplies, packaging components, narcotics, and dangerous substances), makes visual inspections to the cargo, verifies (by counting and / or weighing) proper identification and records the information in the inventory control systems(s).
  • Maintains and generates transactions in the SAP environment and handles damaged / shortages / excess / or missing orders following the Materials Damages & Claim Procedure.
  • Conducts raw material inspection and sampling, following established procedures and GMP requirements.
  • Removes the samples to be used for analysis of raw materials and packaging components received and the samples used for re-evaluation of the existing materials.
  • Completes GMP forms and batch records for material receiving and shipping activities, reviewing work to ensure accuracy and compliance.
  • Plans and organizes work to respond to changing workloads and maintain effective operations.
  • Maintains a safe work environment and resolves routine issues without supervisory approval.
  • Keeps data in the inventory control systems (manual and /or computerized) update and accurate, including the freight containers inventory. Participates in Cycle Counting process as per Inventory Control Procedure. Prepares physically materials for shipment and ensure that materials are correctly picked for shipping, as per their applicable status and according to the current GMP’s and loading of trucks.

Education and Requirements:

  • High School diploma required. Associates or some college, or trade school preferred
  • Driver's license required--MVR must be completed, and acceptable driving record is required
  • Experience driving a forklift preferred, not required (will train)
  • Experience in a Regulated environment such as FDA, Pharma, Bio-Pharma required
  • Position Handles Hazardous Materials

We 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.

Compensation Overview:

Devens - MA - US: $30.81 - $37.33per hour

The 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.


Benefits:


Subject 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).


U.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.


Non-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.


Depending 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.


U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits


How We Work

Where 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.


Supporting People with Disabilities

BMS 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 [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For 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/


Data Protection

We 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.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


If this posting is missing required information required by local law or incorrect, contact BMS at [email protected]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.



R1607092 : Senior Materials Management Associate
Bristol Myers Squibb

About the company

Bristol Myers Squibb

Large Enterprise

Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, immunology, and cardiovascular health, the company leverages advanced science and technology to create transformative therapies that address critical unmet medical needs. Operating in more than 70 countries, Bristol Myers Squibb emphasizes collaborative efforts and strong partnerships in research and development to drive advancements in healthcare and improve patient outcomes worldwide.