GMP Manufacturing Tech: Filling & Visual Inspection

Boehringer Ingelheim Pharmaceuticals, Inc.

Fremont (CA)

On-site

USD 54,000 - 80,000

Full time

8 days ago

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Benefits offered by this job

Medical, dental, and vision coverage
Retirement savings options
Paid time off

Job summary

Boehringer Ingelheim is seeking a Manufacturing Associate, Filling and Visual Inspection to operate routine unit operations in a multi-product facility. This role requires adherence to cGMP, safety protocols, and strong attention to detail in a collaborative, on-site setting.

Responsibilities include supporting manufacturing processes, maintaining documentation, and helping with training and quality investigations while working with cross-functional teams in Fremont, CA.

Qualifications

  • Minimum 1 year of experience in GMP regulated industry.
  • Experience in a cGMP environment is required.
  • Ability to concentrate on detail-oriented tasks in a technical setting with quality at the forefront.
  • Strong written and verbal communication skills.
  • Ability to work with computer-based systems and read SOPs.

Responsibilities

  • Perform basic Filling or Visual Inspection operations under supervision.
  • Support continuous improvement projects of low to moderate complexity.
  • Document work and maintain batch records in accordance with SOPs and cGMP.
  • Assist in training new technicians and ensure safety standards are followed.
  • Maintain production areas and stock consumables/materials.
  • Report process or equipment anomalies promptly.

Skills

GMP experience
cGMP
Detail-oriented
Strong communication
Teamwork
Computer literacy
SOP reading/writing

Education

High School degree
Associate/Bachelor degree in related field preferred

Job description

Boehringer Ingelheim is seeking a Manufacturing Associate, Filling and Visual Inspection to operate routine unit operations in a multi-product facility. This role requires adherence to cGMP, safety protocols, and strong attention to detail in a collaborative, on-site setting.

Responsibilities include supporting manufacturing processes, maintaining documentation, and helping with training and quality investigations while working with cross-functional teams in Fremont, CA.

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