GMP Manufacturing Technician 4- Day Shift

Millipore Corporation; St. Louis (MO); On-site; USD 33,000 - 56,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Retirement contributions

Job summary

MilliporeSigma's Cherokee Site in St. Louis, MO, is hiring a GMP Manufacturing Technician 4 for day shift to support 12‑hour operations (6:00 am–6:30 pm) with a 5% shift differential.

You will prepare buffer formulations, maintain clean manufacturing areas, and execute tasks in compliance with cGMPs, GDP, and Good Documentation Practices. Requirements include a high school diploma or GED and at least 6 months of pharma GMP experience; preferred candidates have prior pharma manufacturing

Qualifications

• High school diploma or GED.
• 6 months' experience in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT, knowledge of Good Documentation Practices).

Responsibilities

• Prepare buffer formulations for Drug Substance manufacturing with emphasis on safety and quality.
• Maintain cleanliness of manufacturing areas and perform routine cleaning.
• Execute and document daily tasks following cGMPs and GDP standards.
• Follow approved SOPs and document activities per GDP guidance.
• Maintain logbooks per procedure.
• Dispose cleaning and process waste safely according to procedures.
• Maintain stock of supplies and gowning using Kanban.
• Assist in quality deviations as needed.
• Perform safety inspections and preventive maintenance.
• Assist in procedures to ensure safety and quality compliance.
• Support process improvements, safety and training of new employees, and daily departmental goals.

Skills

GMP experience

Mechanical aptitude

Process improvement

FDA/EMA familiarity

Good Documentation Practices

Education

High school diploma or GED

Tools

Microsoft Office (Word, Excel)

Job description

Role

The GMP Manufacturing Technician 4 - Day Shift at MilliporeSigma's Cherokee Site (3300 S. Second Ave, St. Louis), located in St. Louis, Missouri.

Job Duties

• Prepare buffer formulations in support of Drug Substance manufacturing, with a focus on safety and quality.
• Maintain cleanliness of manufacturing areas including cleaning during regularly scheduled intervals (daily, weekly, etc.).
• Execution and documentation of daily tasks following current Good Manufacturing Practices (cGMPs).
• Utilize quality approved operating procedures and document activities with adherence to GDP standards.
• Maintaining logbooks in accordance with the procedure.
• Safely and properly dispose cleaning and process waste per approved procedures.
• Maintain safe stock of supplies and gowning utilizing Kanban system.
• Aid/input in quality deviations as needed.
• Perform safety inspections and necessary preventive maintenance.
• Assist 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 6STraining of new employees on department policy, procedure, and processes.
• Assist in a department function and work closely with department supervisor to ensure daily department operating goals are achieved.

Shift Details

This role will support 24/7 manufacturing operations and work 12-hour shifts from 6:00am - 6:30pm, including a 5% shift differential.

Physical Attributes

• Stand for extended periods of time.
• Lift, push, and 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.RSREMD

Pay Range for this position: $24.00 - $41.00. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.