Aseptic Fill/Finish Technician

elanco; Iowa City (IA); On-site; USD 38,000 - 52,000; Full time

Job summary

Elanco Iowa City, IA is seeking a Fill/Finish Operator to fill serials of antigen and perform aseptic product processing in accordance with SOPs and Manufacturing Directions. You will work with sterile solutions and parenteral products, maintaining strict aseptic technique and product sterility.

Responsibilities include equipment setup, operation, and cleaning; assembling antigens into final formulations; and documenting component identities per cGMP guidelines.

Qualifications

• High School Diploma/GED.
• Ability to perform calculations and conversions involving weights, volumes, and percentages.
• Computer aptitude that allows the person to adapt to future platforms and software.

Responsibilities

• Responsible for manufacturing and compounding sterile solutions and other parenteral classed products, including obtaining, weighing, measuring, and adding all raw materials as per production procedures.
• Set-up, operate, and dismantle for cleaning all equipment involved in the production process, and perform inspections and assessments of equipment and material condition prior to use.
• Assemble antigens into final product formulations and preparation of adjuvants or other intermediates, with a focus on maintaining product sterility.
• Verify and document the identity of all components used in formulation and adhere to cGMP documentation practices.
• Follow Standard Operating Procedures/Filling Manufacturing Directions.

Skills

Calculations

Computer literacy

Education

High school diploma or GED

Job description

Elanco Iowa City, IA is seeking a Fill/Finish Operator to fill serials of antigen and perform aseptic product processing in accordance with SOPs and Manufacturing Directions. You will work with sterile solutions and parenteral products, maintaining strict aseptic technique and product sterility.

Responsibilities include equipment setup, operation, and cleaning; assembling antigens into final formulations; and documenting component identities per cGMP guidelines.