Manufacturing Technician

Fladger Associates

Fremont (CA)

On-site

USD 49,300 - 65,700

Full time

14 days+

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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

1 week ago Be among the first 25 applicants

Direct message the job poster from Fladger Associates

Professional Recruiter @ Fladger Associates | Pharmaceutical & Technical Recruiting

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.