Technician I, QC Sample Management, Cell Therapy

Bristol-Myers Squibb; Harvard (MA); On-site; USD 37,000 - 45,000; Full time

Job summary

Bristol Myers Squibb in Devens, MA is seeking a Technician I, QC Sample Management, to handle test samples through the lifecycle, maintain inventory, and support distribution to functional groups.

The role requires an Associate's degree or higher (or a high school diploma with 2+ years of relevant experience) and involves following procedures, working in a fast-paced team, and ensuring lab safety and accurate labeling.

Qualifications

• Associate's degree or higher.
• High school diploma/GED with 2+ years of relevant work experience.
• Knowledge of basic electronic systems (email, MS Office, etc.)

Responsibilities

• Handle test samples and retains throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal.
• Facilitate cold chain transfers of samples.
• Label and track samples and materials per procedures including chain of custody records.
• Maintain inventory and support distribution of QC samples and materials to functional groups as scheduled or requested.
• Record performance metrics for the sample management group.
• Follow lab procedures to maintain a safe and organized lab.

Skills

Detail oriented

Follow procedures

Team environment

Meet deadlines

Effective communication

Education

Associate degree or higher

High school diploma + 2+ years experience

Job 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.

Position Summary

Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal. Maintains inventory and support distribution of QC sample and materials to appropriate functional groups as scheduled or requested.

Shift/Days/Hours

This role works from 6AM to 6PM following a 12-hour rotating shift (36/48 hours over a 2-week period) which includes working every other weekend, holidays falling on scheduled workdays, and during adverse weather conditions in support of QC and the manufacturing facility. Flexibility to work irregular hours and short notice overtime may be required.

Duties/Responsibilities

• Handle test samples and retains throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal.
• Facilitate cold chain transfers of samples.
• Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with written procedures.
• Maintain inventory and support distribution of QC samples and materials to functional groups as scheduled or requested.
• Record performance metrics for the sample management group.
• Follow lab procedures to maintain a safe and organized lab.
• Perform other tasks as assigned.

Reporting Relationship

This position will report to QC management.

Qualifications

Specific Knowledge, Skills, Abilities: Reliable and detail oriented with organizational skills. Ability to understand and follow procedures. Ability to work in a fast-paced team environment, meet deadlines, and adjust to changing priorities. Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.

Education/Experience/ Licenses/Certifications

Associate's degree or higher. High school diploma/GED with 2+ years of relevant work experience will be considered. Netherlands: MLO level 3 is preferred. An equivalent combination of education and experience, preferably in a regulated environment, will be considered. Knowledge of basic electronic systems (email, MS Office, etc.) required.

Job Safety Requirements & Essential Physical Demands

Ability to perform lifting tasks up to 20 lbs (9 kg) at floor and waist height. Ability to lift up to 10 lbs (4.5 kg) overhead as well as push or maneuver carts to transport materials between locations. Ability to perform frequent pipetting and related laboratory tasks within a biological safety cabinet, including extended periods of seated work. Ability to independently don, doff, and wear required personal protective equipment such as but not limited to lab coat/frock, gloves, safety glasses/face shield for prolonged periods while performing laboratory work. Ability to safely handle and use chemical disinfectants, flammable materials, and hazardous chemicals. Work may involve handling of dry ice, liquid nitrogen, and cryogenically cooled materials. Ability to use step stools while reaching and handling materials. Ability to work in a Biosafety Level 2 (BSL-2) environment. The laboratory employee is responsible for performing work safely in accordance with EHSS procedures. This includes identifying and controlling risks, proper use of personal protective equipment (PPE), safe handling of chemicals and biological agents, compliance with waste and emergency procedures, and active participation in training and safety programs.

Compensation Overview

Devens - MA - US: $27.35 - $33.14per 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 [e-mail]. 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 [e-mail] 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.

R1605956 : Technician I, QC Sample Management, Cell Therapy Data Privacy Link

We're creating innovative medicines for patients fighting serious diseases. We're also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.