Manufacturing Technician

Fladger Associates; Fremont (CA); On-site; USD 49,000 - 66,000; Full time

Job summary

A leading company in pharmaceutical manufacturing seeks a Manufacturing Technician for the Fremont area. The role involves executing visual inspections and supporting drug product operations in a GMP environment. Candidates should have at least a High School Diploma and relevant industry experience, demonstrating the ability to work in high-detail technical tasks with a focus on quality.

Qualifications

• Minimum 1 year work experience in a GMP regulated industry.
• Experience in logistics coordination and batch record executions.

Responsibilities

• Executes routine operations in Visual Inspection related to drug product manufacturing.
• Performs internal support duties including drug product filling and packaging.
• Adheres to safety standards and maintains production areas according to predefined standards.

Skills

Detail-oriented

Strong communication skills

Collaboration

Education

High School Diploma

Associates/Bachelor's degree or Biotechnology vocational training

Job description

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Responsibilities:

• Excellent employment opportunity for a Manufacturing Visual Inspection in the Fremont, CA area.
• 2nd Shift: Monday to Friday, 2:00PM-10:30PM
• Executes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility.
• Performs duties under limited supervision and according to standard operating and manufacturing procedures.
• Executes independently with adequate training, complex fundamental operations as visual inspection, advance visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES Operations and Exceptions.
• Performs internal support duties including assisting drug product filling and packaging.
• Executes independently with adequate training fundamental operations:

Experience:

• High School Diploma + minimum 1 year work experience in GMP regulated industry
• Associates/Bachelor's degree or Biotechnology vocational training preferred
• Logistics Coordination
• Batch record executions
• Work order initiation and tracking
• Support Projects
• Support Creation/Maintain Training Kits Documents work according to cGMP and cGDP.
• Adheres to established regulations and follows cGMP established by site.
• Reports abnormalities and deviations in a timely and accurate manner.
• Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.
• Maintains production areas according to predefined standards (5s).
• Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.
• Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs.
• Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and “Right the first-time” mindset.
• Strong written and verbal communication skills.
• Ability to work with computer-based systems and manufacturing execution systems (MES).
• Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards.
• Ability to work as part of a high performing team and collaborate effectively with staff.
• Must be able to read and see clearly.
• Duties of this position may require the incumbent to exert some physical effort.
• Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity.
• Weight is typically no more than 25 pounds.
• Employees required to participate and have acceptable result from vision testing including color blindness.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Manufacturing and Production

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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