Bristol Myers Squibb · 3 hours ago
Calibration Technician
Warren, NJ
Contract
Onsite
Mid Level
$26/hr - $28.48/hr
3+ years expBristol Myers Squibb is a leading biopharmaceutical company, and they are seeking a Calibration Technician to support laboratory and clinical manufacturing operations. The role involves executing equipment calibration, preventative maintenance, and performance verification, while ensuring compliance with safety and quality standards.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Executes equipment calibration, preventative maintenance, performance verification, troubleshooting and repair activities in laboratory and manufacturing areas, as required per current scheduling (CMMS) System
Escorts and supervises vendors for calibration, preventative maintenance, performance verification and repair functions as required per current scheduling (CMMS) System
Reviews and approves vendor executed calibration, maintenance, repair, and performance verification records for accuracy, and completeness
Documents and populates calibration/maintenance information in WPT (Work Plan Template) or MDT (Measurement Data Template) using CMMS system
Modifies or update CMMS documentation as required
Prepares reports and keeps records on calibration inspection, testing, and repairs
Executes requalification on Controlled Temperature Units (ex. Refrigerators, Freezers (which includes -20C / -80C Freezers), Incubators, Cryotanks, Cryopods, and Storage Rooms/Areas)
Supports multiple sites within Warren and Summit
Supports clinical manufacturing on-call equipment troubleshooting activities during weekends as required
Ensures all calibration, PM, and performance verification records are filed appropriately after approval
Contacts supplier for quotation on external calibration/PM of the equipment and calibration standards
Initiates, participates, and assists in resolution of quality investigations
Authors and supports the development, revision, and review of written Standard Operating Procedures (SOP) for calibration, preventive maintenance, and performance verification of instruments/equipment
Supports the development, review and approval of calibration and maintenance plans in site CMMS system
Supports the execution of process improvement studies, as required
Adheres to written policies and procedures governing the LSM department activities and the equipment they manage to ensure compliance with approved standards
Performs inventory of the equipment and/or standards in the labs as required
Maintains a positive relationship with the site customers and outside vendors while promoting a positive team environment
Participates actively in special projects as required
Ensure low cost of the Laboratory Systems Management (LSM) department (Reducing overtime, implementing innovative ideas)
Plans, justify and implement cost reduction small projects
Usage of several test equipment and tools (e.g., pressure gauges, temperature, humidity meters, flow meters, particle counters and temperature mapping equipment etc.)
Follows cGMP (current Good Manufacturing Practices) and ALCOA principles ('ALCOA' defines that data should be Attributable, Legible, Contemporaneous, Original, and Accurate) In addition, 'ALCOA+' guidance recommends that data is also Complete, Consistent, Enduring, and Available
Work with planning group to ensure system is updated as calibration, maintenance and performance verification activities are performed
Perform NCRs investigations
Maintains all required Corporate, Facilities and EHS training as required
Adheres to all safety procedures and hazard communication
Qualification
Required
Knowledge of cGMP and good documentation practices
Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment
Strong problem-solving skills and the ability to work independently
Excellent interpersonal and communication skills with experience dealing with a diverse workforce where individual initiative, accountability to the team, and professional maturity are required
Strong multi-tasking and organizational ability. Ability to effectively manage multiple tasks and activities simultaneously
Proficiency in Microsoft Office Suite Word, Excel, PowerPoint, and Outlook; innate ability to learn new software, such as corporate intranet and enterprise applications
Ability to interact effectively with QC, Manufacturing, QA, and Engineering & Facilities groups
High school Diploma or Associates or Bachelor's degree
3+ years of lab experience preferred in pharma or medical device industry or manufacturing
Occasional stooping, bending, stretching, pushing, pulling, reaching, and/or lifting up to 25 lbs
Ability to sit, stand, walk, and move within workspace for extended periods
Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing, and pulling
Environment may include working in office, laboratory, or manufacturing area
Donning proper gowning and/or PPE such as safety glasses and shoes in an environment with hazardous materials and waste will be required
Working safely and effectively when working alone or working with others will be required
Preferred
Working knowledge of scheduling software and systems, and inventory management systems, e.g., Blue Mountain RAM and/or Maximo Computerized Maintenance Management System (CMMS) preferred
3+ years of lab experience preferred in pharma or medical device industry or manufacturing
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
10001+ employees
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 CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
Recent News
2026-01-16
Pharmaceutical Technology
2026-01-16
Company data provided by crunchbase