GMP Manufacturing Technician 4- Day Shift
Job Summary
The GMP Manufacturing Technician 4 - Day Shift at MilliporeSigma's Cherokee Site supports API manufacturing within a cGMP-regulated environment. Key responsibilities include preparing buffer formulations, maintaining cleanliness, executing tasks according to cGMPs, and assisting in process improvement.
Shift Details
This role supports 24/7 manufacturing operations and works 12-hour shifts from 6:00am – 6:30pm. Responsibilities include preparing buffer formulations, maintaining cleanliness, and performing safety inspections.
Job Duties
- Prepare buffer formulations in support of Drug Substance manufacturing, ensuring safety and quality.
- Maintain cleanliness of manufacturing areas, including cleaning during regularly scheduled intervals.
- Execute and document daily tasks following current Good Manufacturing Practices (cGMPs).
- Utilize quality approved operating procedures and document activities with adherence to GDP standards.
- Maintain logbooks in accordance with the procedure.
- Safely and properly dispose cleaning and process waste per approved procedures.
- Maintain safe stock of supplies and gowning using a Kanban system.
- Aid/input in quality deviations as needed.
- Perform safety inspections and necessary preventive maintenance.
- Aid in preparation of and follow procedures to ensure compliance with applicable Safety and Quality guidelines.
- Develop, assist in the implementation of process improvement, safety, quality, and 6S training of new employees.
- Assist in a department function and work closely with department supervisor to achieve daily department operating goals.
Physical Attributes
- Stand for extended periods of time.
- Lift, push, or pull up to 35lbs.
- Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment.
Minimum Qualifications
- High school diploma or GED.
- 6 months’ experience in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT).
- Knowledge of Good Documentation Practices.
Preferred Qualifications
- Prior experience in pharmaceutical manufacturing environment.
- Strong mechanical aptitude.
- Demonstrated process improvement experience.
- Familiarity with FDA, EMA, and other regulatory standards.
- Demonstrated knowledge and experience in various computer skills, including Windows (Word, Excel, PowerPoint, etc.).
Pay Range
The pay range for this position is $24.00 - $41.00 per hour. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors.
Benefits
- Health insurance
- Paid time off (PTO)
- Retail contributions
- Other perquisites
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