GMP Manufacturing Technician 4- Day Shift

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

Benefits offered by this job

Health insurance

PTO

Retirement contributions

Other perquisites

Job summary

MilliporeSigma is seeking a GMP Manufacturing Technician 4 for Day Shift at the Cherokee Site in St. Louis, MO. You will support API manufacturing in a cGMP environment, performing established procedures and contributing to process improvements.

Emphasis on compliance, safety, equipment maintenance, and accurate documentation. Shift details include 12-hour days (6:00am–6:30pm) with a 5% shift differential. Requires a HS diploma and 6 months GMP experience, with benefits such as health insurance,

Qualifications

• High school diploma or GED required.
• 6 months’ experience in a pharmaceutical GMP environment.
• Ability to follow cGMP and GDP procedures.

Responsibilities

• Carry out established GMP procedures safely in a cGMP setting.
• Assist in buffer preparation, equipment maintenance, and material staging.
• Document tasks using approved SOPs and maintain logbooks.
• Support safety inspections and quality deviations as needed.

Skills

GMP operations

Education

High school diploma or GED

Job description

Work Location: St. Louis, Missouri

Shift:

Department: LS-SC-UYKMEB

Recruiter: Erin Wilson

This information is for internals only. Please do not share outside of the organization.

Your Role:

The GMP Manufacturing Technician 4 - Day Shiftat MilliporeSigma's Cherokee Site (3300 S. Second Ave, St. Louis), you will play a key role in supporting API (Active Pharmaceutical Ingredients) manufacturing within a cGMP-regulated environment.This role is responsible for safely carrying out established procedures, contributing to the development of improved operational approaches, and providing essential manufacturing support. Day-to-day activities will encompass equipment maintenance, solution preparation, equipment and supply staging, and a variety of other manufacturing support tasks. Expectations to ensure “Compliance “and “Readiness” within our GMP Operations teams, ultimately enabling high manufacturing success. Job duties include:

• 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.
• 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 6S
• Training 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.

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.

Who you are:

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 experiencein 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.