QC Equipment Lifecycle Specialist – Cell Therapy

Bristol Myers Squibb; United States; On-site; USD 91,000 - 110,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Flexible Time Off

Paid holidays

Disability insurance

Job summary

Bristol Myers Squibb is hiring a Senior Specialist to manage the lifecycle activities of QC laboratory equipment at Devens, MA. You may serve as the QC equipment system owner, ensuring GMP-compliant documentation and calibration processes.

Responsibilities include creating validation protocols, coordinating with cross-functional teams, and maintaining records and equipment databases in a regulated environment. This role reports to QC management and offers comprehensive benefits.

Qualifications

• Understand and apply Global Regulatory and cGMP requirements.
• Demonstrate strong problem-solving and technical writing skills.
• Communicate task status with cross-functional teams.
• Work well in a fast-paced team and meet deadlines.

Responsibilities

• Manage lifecycle activities of QC lab equipment.
• Create equipment User Requirements and validation documents.
• Collaborate with QC labs, Site Engineering, Facility Services for commissioning/decommissioning.

Skills

Regulatory compliance

cGMP knowledge

Documentation

Communication

Education

Bachelor’s degree in science

Advanced degree preferred

Tools

SAP

Valgenesis

Maximo

Job description

Bristol Myers Squibb is hiring a Senior Specialist to manage the lifecycle activities of QC laboratory equipment at Devens, MA. You may serve as the QC equipment system owner, ensuring GMP-compliant documentation and calibration processes.

Responsibilities include creating validation protocols, coordinating with cross-functional teams, and maintaining records and equipment databases in a regulated environment. This role reports to QC management and offers comprehensive benefits.