Second-Shift Microbiology Manufacturing Operator

Oxoid Remel Microbiology

Lenexa (KS)

On-site

USD 22,000 - 33,000

Full time

14 days+
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Benefits offered by this job

Competitive hourly pay
Shift differential (2nd/3rd shifts)
Annual performance bonus
Annual merit increase
Medical, Dental, Vision benefits
Paid Time Off
Tuition Reimbursement
Employee Referral Bonus
Career Advancement Opportunities

Job summary

Oxoid Remel Microbiology is seeking a Manufacturing Operator for the second shift in Lenexa, KS. You will follow SOPs, operate and maintain equipment, and ensure safe handling of materials in a GMP environment.

Responsibilities include following procedures, wearing PPE as required, documenting activities, and contributing to process improvements while upholding a culture of teamwork and quality.

Qualifications

  • High school diploma or equivalent required.
  • No previous work experience required.
  • Experience in manufacturing, operations, production or lab setting preferred.

Responsibilities

  • Follow all written procedures and report discrepancies in procedures (SOP’s, DHR’s, etc.) to the Area Supervisor.
  • Wear Personal Protective Equipment (PPE) when needed. Refer to job specific job Safety Analysis.
  • Perform all work activities in a safe manner. Maintain a safe and clutter free work area. Clean up all spills immediately.
  • Read, understand, and complete required documentation. All paperwork shall be accurately and neatly completed in accordance with established policies and procedures.
  • Set up and adjust machine to operate a variety of sizes and types using tools to adjust machine.
  • Actively engage in making suggestions for process improvement.
  • Encourage an atmosphere of partnership.

Skills

English communication
Math skills

Education

High school diploma or equivalent

Job description

Oxoid Remel Microbiology is seeking a Manufacturing Operator for the second shift in Lenexa, KS. You will follow SOPs, operate and maintain equipment, and ensure safe handling of materials in a GMP environment.

Responsibilities include following procedures, wearing PPE as required, documenting activities, and contributing to process improvements while upholding a culture of teamwork and quality.

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