GMP CMMS & Validation Specialist

MilliporeSigma; St. Louis (MO); On-site; USD 64,000 - 100,000; Full time

Benefits offered by this job

Health insurance

Paid time off (PTO)

Retirement contributions

Job summary

MilliporeSigma in St. Louis, MO, seeks a role to support CMMS administration, change control, deviations, CAPAs, and quality documentation. The facility at 3300 South Second Street serves as the base for daily operations.

You will coordinate validation, maintenance, and engineering documentation, track alarms, assist audits, and ensure cGMP compliance with strong communication and document control skills.

Qualifications

• Associate Degree in Chemistry, Biology, Controls Engineering, Mechanical Engineering or other Life Science or Engineering Discipline.
• Vocational degree or certification in industrial maintenance or related field with 1+ years GMP experience.
• High School Diploma/GED with 3+ years GMP manufacturing experience.

Responsibilities

• Coordinate validation, maintenance, and engineering documentation and tasks.
• Author technical reports, quality records, maintenance plans, and operating procedures.
• Manage Change Controls, Deviations, and CAPAs in the QMS across cross-functional teams.

Skills

Cross-functional teamwork

Oral & written communication

Documentation management

Attention to detail

Education

Associates degree in Chemistry/Biology/Engineering

Vocational certification in industrial maintenance

High School Diploma with GMP experience

Tools

TrackWise

Mango

SAP or other QMS/CMMS systems

Job description

MilliporeSigma in St. Louis, MO, seeks a role to support CMMS administration, change control, deviations, CAPAs, and quality documentation. The facility at 3300 South Second Street serves as the base for daily operations.

You will coordinate validation, maintenance, and engineering documentation, track alarms, assist audits, and ensure cGMP compliance with strong communication and document control skills.