Night-Shift On-the-Floor QA Specialist

Bristol-Myers Squibb Co; New Jersey; On-site; USD 48,000 - 58,000; Full time

Benefits offered by this job

Comprehensive benefits

Wellbeing support

Retirement plan

Paid time off and holidays

Job summary

Bristol Myers Squibb is seeking a Quality Assurance Shop Floor professional for 24x7 oversight in NJ. The role supports Manufacturing, QC Labs, Label Operations and Warehouse Operations, ensuring adherence to cGMP and internal standards.

The position requires interpreting events, verifying batch records, and guiding CAPA and investigations. Shifts are Wed-Sat Nights, 5:00pm-5:30am, with responsibilities spanning quality control, process improvement, and cross-functional collaboration in a

Qualifications

• Must be action-oriented and proficient in decision-making, building relationships, problem-solving, and analytical thinking.
• Ability to understand, follow, and apply internal policies, procedures, and quality principles.
• Prior experience with quality processes, including batch record review, change control, product complaints, deviations, investigations, and CAPA management.
• Ability to assess unfolding situations, diagnose problems, and propose practical solutions.
• Detail-oriented and task-focused with the ability to meet deadlines and priorities.

Responsibilities

• Provide routine Quality on-the-floor oversight and triage unexpected events with Manufacturing, Quality Labs, Label Operations and Supply Chain operations.
• Interpret problems and communicate clearly to management and groups with brevity and accuracy.
• Identify departures from procedures and escalate complex issues to senior members.
• Perform and document operational verification within MES per approved procedures.
• Observe manufacturing operations for deviations and aseptic practices.
• Review manufacturing batch records for compliance and provide feedback on documents.

Job description

Bristol Myers Squibb is seeking a Quality Assurance Shop Floor professional for 24x7 oversight in NJ. The role supports Manufacturing, QC Labs, Label Operations and Warehouse Operations, ensuring adherence to cGMP and internal standards.

The position requires interpreting events, verifying batch records, and guiding CAPA and investigations. Shifts are Wed-Sat Nights, 5:00pm-5:30am, with responsibilities spanning quality control, process improvement, and cross-functional collaboration in a