Entry-Level Biotech Manufacturing Technician I (cGMP)

ADP, Inc.

Mountain View (CA)

On-site

USD 46,000 - 50,000

Full time

3 days ago
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Benefits offered by this job

401K with match
FSA/HSA
Life/AD&D
Disability insurance
Pet insurance

Job summary

Canon Medical Diagnostics USA, Inc. in Mt. View, CA is seeking a Manufacturing Associate Technician I to perform production line tasks under cGMP, including equipment setup, cleaning, labeling, packaging, and lot accountability in a biotech manufacturing setting.

The role requires attention to detail, ability to read batch records, and strong English communication. Candidates should have a High School Diploma and at least one year of hands-on experience in a cGMP environment; occasional exposure

Qualifications

  • High School Diploma (Prefer AS or equivalent college course work in Chemistry or Life Sciences)
  • Minimum one (1) year hands-on technical experience in a cGMP Manufacturing environment of the biotech or pharmaceutical industry
  • Ability to follow instructions and communicate clearly and concisely in English, both orally and in writing

Responsibilities

  • Assist in equipment, processes, and tools validation in Manufacturing
  • Clean and maintain work area and equipment; perform line clearances and inspect components
  • Communicate effectively with co-workers and supervisor
  • Follow SOPs, batch records, and manufacturing instructions precisely
  • Repair, maintain, operate, and troubleshoot production and test equipment

Skills

cGMP knowledge
English comms
MS Office
Manual dexterity

Education

High School Diploma

Tools

PC basics

Job description

Canon Medical Diagnostics USA, Inc. in Mt. View, CA is seeking a Manufacturing Associate Technician I to perform production line tasks under cGMP, including equipment setup, cleaning, labeling, packaging, and lot accountability in a biotech manufacturing setting.

The role requires attention to detail, ability to read batch records, and strong English communication. Candidates should have a High School Diploma and at least one year of hands-on experience in a cGMP environment; occasional exposure

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