Autoclave & Cleanroom Technician I

American Regent, Inc.; Hilliard (OH); On-site; USD 36,000 - 48,000; Full time

Job summary

American Regent, Inc. in Ohio is seeking an entry level Component Prep, Sanitization and Sterilization Technician I to join the Manufacturing Team.

You will assist with component prep, cleaning, sterilization, and documentation to support the production of sterile pharmaceuticals in a cGMP environment. Responsibilities include following SOPs, maintaining cleanroom standards, and contributing to production planning while working under supervision.

Qualifications

• Proven ability to follow SOPs and cGMP requirements.
• Excellent communication and teamwork.
• Ability to perform repetitive lifting and standing.

Responsibilities

• Performs sanitary cleaning activities as defined by established operating procedures and as directed by Manager/Supervisor.
• Performs a variety of production prep activities including deboxing, staging, equipment and component sterilization and post fill sterilization.
• Complete production documentation including logbooks, cleaning tags, batch records, etc. per quality and cGMP requirements.
• Ensure strict adherence to and compliance with SOP's and protocols.
• Ensure all work is performed and documented in accordance with existing company policies, procedures (SOP's), Current Good Manufacturing Practices (cGMPs), and health and safety requirements.
• Provides feedback to supervisor and peers about cycle status, equipment condition, and other issues that would affect the production schedule or relate to continuous improvement.

Skills

Attention to detail

Team collaboration

Reading & interpreting English docs

Lift up to 50 lbs

Manual dexterity

Adherence to safety & cGMP

Education

High School Diploma or GED

1 year manufacturing experience (preferred)

Job description

American Regent, Inc. in Ohio is seeking an entry level Component Prep, Sanitization and Sterilization Technician I to join the Manufacturing Team.

You will assist with component prep, cleaning, sterilization, and documentation to support the production of sterile pharmaceuticals in a cGMP environment. Responsibilities include following SOPs, maintaining cleanroom standards, and contributing to production planning while working under supervision.