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Manufacturing Operator

Meet Life Sciences

Fremont (CA)

On-site

USD 49,000 - 74,000

Full time

Yesterday
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Job summary

An established industry player is seeking a Manufacturing Operator to join its dynamic team. This entry-level role involves executing routine operations in a multi-product pharmaceutical manufacturing facility, focusing on assembly and packaging of drug products. You'll be responsible for setting up machines, troubleshooting equipment, and ensuring compliance with SOPs and GMP standards. Join a collaborative environment where your contributions will directly impact the quality of life-saving products. If you're passionate about biotechnology and eager to grow in the manufacturing sector, this opportunity is perfect for you.

Qualifications

  • 1+ years in a GMP-regulated environment preferred in biotech or pharma.
  • Physical ability to lift up to 40 lbs and stand for long periods.

Responsibilities

  • Set up and troubleshoot automated and semi-automated machines.
  • Document all work according to SOPs and maintain production areas.

Skills

GMP Compliance
Equipment Setup
Documentation Practices
Problem Solving
Safety Standards

Education

High School Diploma
Associate's Degree
Bachelor's Degree

Job description

*This position requires employees to be fully vaccinated against COVID-19 or have an approved medical or religious accommodation.*

Job Summary:

The Manufacturing Operator executes routine unit operations within the Assembly and Packaging areas of a multi-product pharmaceutical manufacturing facility. This role supports the assembly and packaging of drug products, assists with equipment setup and troubleshooting, and ensures adherence to SOPs and GMP standards for manufacturing operations.

Responsibilities:

  • Assist in setting up automated and semi-automated machines (e.g., autoinjector, pre-filled syringe assembly machines).
  • Support minor equipment repairs, adjustments, and changeovers.
  • Identify and address operational issues, including mechanical or component problems, in real-time.
  • Document all work in accordance with SOPs, including batch records and logbooks.
  • Perform cleaning and sanitization of production areas, including waste disposal and room preparation.
  • Verify equipment calibration and ensure controlled document compliance.
  • Assist with assembly, packaging, and visual inspection/filling operations.
  • Maintain inventory of components and materials to ensure readiness for production.
  • Ensure adherence to safety standards and escalate unsafe conditions or behaviors.
  • Maintain production areas following 5S standards.
  • Communicate effectively with shift personnel during hand-offs and changes.

Qualifications:

  • High school diploma required; Associate's/Bachelor's degree or biotechnology vocational training preferred.
  • Minimum of 1 year of experience in a GMP-regulated environment, preferably within the biotechnology or pharmaceutical industry.
  • Must adhere to SOPs, proper documentation practices, and cGMP regulations.
  • Physical ability to stand and walk for extended periods, and lift up to 40 lbs as required.
Seniority level
  • Seniority level
    Entry level
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Manufacturing
  • Industries
    Pharmaceutical Manufacturing

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