Continuous Improvement Specialist, 3rd Shift (GMP Pharma)

Trillium Staffing; Berlin (OH); On-site; USD 27,674 - 39,414; Full time

Job summary

Trillium Staffing is seeking a Continuous Improvement Specialist for the Berlin/Millersport area in the United States. You will support manufacturing operations, drive process improvements, and focus on reducing waste, improving efficiency, quality and safety in a GMP pharma packaging setting.

The ideal candidate has GMP manufacturing experience, strong Lean knowledge, and solid MS Office skills. Lift requirements and the ability to read technical documentation are included in the role.

Qualifications

• 1+ yrs experience in a GMP manufacturing environment
• HS Degree or equivalent required; Associate in manufacturing, Industrial Tech or Engineering Tech a plus
• Understanding of performance metrics in relation to manufacturing (scrap, downtime, yield)
• Familiarity with Lean Manufacturing (Kaizen, 6S)
• Proficient in MS Office
• Experience reading technical documentation such as Batch records, SOPs
• Basic math skills
• Ability to lift 50 lbs

Responsibilities

• Support manufacturing operations and drive process improvements.
• Reduce waste and enhance efficiency, quality and safety in a GMP pharma packaging environment.
• Go through batch records and SOPs to ensure compliance and accuracy.

Skills

GMP manufacturing experience

Process improvement

Quality and safety awareness

Basic math

Reading technical docs

Lift 50 lbs

Education

High school diploma

Associate degree in manufacturing/Engineering Tech

Tools

MS Office

Job description

Trillium Staffing is seeking a Continuous Improvement Specialist for the Berlin/Millersport area in the United States. You will support manufacturing operations, drive process improvements, and focus on reducing waste, improving efficiency, quality and safety in a GMP pharma packaging setting.

The ideal candidate has GMP manufacturing experience, strong Lean knowledge, and solid MS Office skills. Lift requirements and the ability to read technical documentation are included in the role.