ECQ Engineer Q3 jobs in United States
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Bristol Myers Squibb · 2 days ago

ECQ Engineer Q3

Bristol Myers Squibb is a leading biopharmaceutical company transforming patients' lives through science. The Equipment Engineer II, ECQ Operations supports laboratory, clinical, and commercial manufacturing operations, leading projects and ensuring compliance with quality standards.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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H1B Sponsor Likelynote

Responsibilities

Execute equipment calibration, preventive maintenance, performance verification, and repair activities in laboratory and manufacturing areas
Supervise vendors performing calibration, maintenance, and repair functions
Review and approve vendor records for calibration, maintenance, repair, and performance verification for accuracy and compliance with Bristol-Myers Squibb standards
Enter data into the site CMMS system and ensure records are filed appropriately after approval
Write and support deviations resulting from calibration or performance verification failures, including developing and supporting corrective and preventative actions
Support development, revision, and review of procedures for calibration, preventive maintenance, and performance verification
Support development, review, and approval of calibration and maintenance plans, including asset induction requests/modifications in the site CMMS system
Support execution of equipment performance verification and process improvement studies
Adhere to all ECQ team policies and procedures to ensure compliance is held to the highest standard
Promote and provide excellent customer service and support
Regularly review, prioritize, and promptly respond to customer equipment performance verification and support requests
Provide technical support and guidance on calibration, equipment performance verification, and validations issues
Interface with customers to ensure all expectations are being met
Maintain positive relationships with Equipment Commissioning & Qualification department members and site customers, promoting a positive team environment
Work with planning group to ensure the system is updated as calibration, maintenance, and performance verification activities are performed
Maintain required Corporate, Facilities, and EHS training
Adhere to all safety procedures and hazard communication
May act as SME in internal and regulatory audits

Qualification

CGMP knowledgePharmaceutical systemsEquipment performance verificationMicrosoft Office SuiteCalibration managementMulti-tasking skillsCommunication skillsProblem-solving skillsInterpersonal skills

Required

Knowledge of cGMP, GXP, GAMP, SDLC regulations (including 21CFR part 11), computer systems validation requirements, and good documentation practices
Advanced knowledge of pharmaceutical, manufacturing, and laboratory systems and equipment
Strong written and verbal communication skills
Excellent interpersonal skills; experience with diverse workforce, individual initiative, accountability, and professional maturity
Strong multi-tasking and organizational skills; ability to manage multiple tasks and activities simultaneously in a fast-paced environment
Highly proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and database systems
Ability to quickly learn new software applications, such as corporate intranet and enterprise business systems
Working knowledge of scheduling software and inventory management systems, mainly Blue Mountain RAM
Ability to interact effectively with laboratory, QA, and Facilities groups
Bachelor's degree in Engineering or Science-related discipline preferred
Minimum 2 years' experience in FDA-regulated industry
Strong problem-solving skills, verbal and written communication skills, and ability to work independently
Strong interpersonal and team skills; willingness to work in an environment requiring initiative and accountability
2 years of maintenance coordinating/planning experience, preferably in a laboratory environment

Preferred

Bachelor's degree in Engineering or Science-related discipline preferred
Experience working directly with bench top manufacturing and laboratory equipment (cell counters, liquid handlers, Flow Cytometry, UPLC, HPLC, etc.) preferred
Knowledge of cGMP in the pharmaceutical industry
Excellent computer skills, including knowledge of calibration management and environmental monitoring systems
Experience working in a commercial environment preferred

Benefits

Health Coverage Medical, pharmacy, dental, and vision care.
Wellbeing Support Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off
US Exempt Employees flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Company

Bristol Myers Squibb

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At Bristol Myers Squibb, we work every day to transform patients’ lives through science.

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 Company
Total Funding
$29.32B
Key Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B

Leadership Team

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Charles Bancroft
CFO
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Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
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Company data provided by crunchbase