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ECQ Engineer
Job in
Summit, Union County, New Jersey, 07902, USA
Listed on 2026-07-16
Listing for:
Bristol-Myers Squibb
Full Time
position Listed on 2026-07-16
Job specializations:
-
Engineering
Quality Engineering, Manufacturing Engineer
Job Description & How to Apply Below
You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:
Title:
Equipment Engineer, ECQ Operations – Day Shift
Location:
Summit WestPURPOSE AND SCOPEThe Equipment Engineer, Equipment Commissioning & Qualification (ECQ) Operations supports laboratory, clinical and commercial manufacturing operations at their home site. Working with minimum supervision, this individual executes routine tasks, applies analytical skills to solve problems, and may lead small to medium-sized projects. The incumbent will write deviations, support investigations, and assist with change control implementation. Must be available to support 8-hour day shift operations, 5 days per week.
REQUIRED COMPETENCIES Knowledge of cGMP, GXP, GAMP, SDLC regulations, 21 CFR Part 11, computer systems validation, and good documentation practices.
Advanced knowledge of pharmaceutical, manufacturing and laboratory systems and equipment.
Strong written, verbal, and interpersonal communication skills.
Strong multi-tasking, organizational, and time management abilities in a fast-paced environment.
Highly proficient in Microsoft Office Suite; ability to learn new software and enterprise systems quickly.
Working knowledge of scheduling and inventory management systems, including Blue Mountain RAM.Ability to interact effectively with Laboratory, QA and Facilities groups.
EDUCATION AND EXPERIENCEBS in Engineering or Science related discipline preferred.
Minimum 2 years' experience in an FDA-regulated industry.
Minimum 2 years of maintenance coordinating/planning experience, preferably in a laboratory environment.
Experience with benchtop manufacturing and laboratory equipment (cell counters, liquid handlers, Flow Cytometry, UPLC, HPLC, etc.) preferred.
Knowledge of cGMP in the pharmaceutical industry.
Knowledge of calibration management and environmental monitoring systems.
Experience working in a commercial environment preferred.
DUTIES AND RESPONSIBILITIES Execute and supervise equipment calibration, preventative maintenance, performance verification and repair activities in laboratory and manufacturing areas.
Review and approve vendor-executed calibration, maintenance and repair records for accuracy, completeness and BMS compliance.
Enter and maintain data in the site CMMS system; ensure all records are filed appropriately.
Write and support deviations, investigations, and corrective/preventative actions related to calibration or performance verification failures.
Support development, revision and review of procedures, calibration plans, and maintenance plans.
Respond to customer equipment support requests; provide technical guidance on calibration and validation issues.
Maintain all required Corporate, Facilities and EHS training; adhere to all safety procedures.
May serve as SME during internal and regulatory audits.
WORKING CONDITIONS (US Only)
Occasional lifting up to 25 lbs.; ability to sit, stand, walk and perform repetitive tasks for extended periods.
Will spend 70% of time in a laboratory or manufacturing environment; proper gowning/PPE required.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Summit West - NJ - US: $35.76 - $43.33per hour
The starting compensation range(s) for…
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