Stay up-to-date on Baxter careers

Apply Now    

Manufacturing Tech 1

Req #: 180004ME_en
Location: St Paul, MN US
Job Category: Manufacturing
Date Posted: 3/1/2018 6:52:47 PM
Baxter International


About Baxter

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.


The Manufacturing Technician I is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply.  He/She is expected to fully participate in both departmental projects and any quality working teams which may be applicable.  Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands on execution of all activities in the production area.

Essential Duties and Responsibilities

  • Supports all local manufacturing operations.
  • Supply components, small parts, glassware, tubing, etc. to cell culture and purification areas.

  • Operate general production equipment (such as parts washers, autoclave, stir plates, etc.)

  • Complete relevant paperwork following GDP/GMP guidelines.

  • Manually clean all portable equipment and small parts.

  • Participate on Continuous Improvement Teams.

  • Receive and distribute supplies into the production area as necessary.

  • Perform daily cleaning of the production area to maintain in GMP fashion.

  • May perform other duties as assigned.


Qualifications for this role


  • Must have good written and verbal communication skills and understanding of cGMP regulations.
  • Familiarity with medical device production equipment including but not limited to autoclave, DP oven and CIP/SIP.
  • Must be able to read and follow detailed written instructions.
  • Good interpersonal skills and be able to work effectively and efficiently in a team environment.
  • This position requires shift, weekend and holiday work.  Overtime may be required at times.
  • The incumbent must work in a clean room environment wearing special garments.  Additionally, personal protective equipment must be worn due to safety requirements.
  • Knowledge of basic chemical and biological safety procedures.
  • Ability to work closely with others in high demand situations.  Every employee is responsible for performing his/her job safely and for calling to managements attention of unsafe conditions, practices, or equipment.  May require overtime to meet production schedule. 
  • This job also involves hazardous materials and hazardous waste responsibilities  which include understanding and complying with hazardous materials and hazardous waste regulations for job duties such as:
  • proper handling, storage, hazardous waste in-house treatment using neutralization and dilution systems, and labeling requirements for hazardous materials and hazardous waste.
  • May require immunization before performing work within the manufacturing area.

 Education and Experience

 Requires high school diploma or equivalent with 0-2 years related manufacturing experience.



Apply Now    
Link for schema