Job description

Must not be allergic to Cephalosporins or Penicillin.

This position is responsible supporting the execution of projects for manufacturing equipment and manufacturing processes. This position will work under the direct supervision of a validation engineer and/or manufacturing supervisor.

Essential Duties and Responsibilities:

Responsible for set up, start up, operation, and tear down of manufacturing equipment (filling equipment, packaging machines, and production tanks) needed for validation execution.

Responsible performing tasks related to drug formulation, weighing, cleaning the complex, tanks, equipment, filter integrity testing, and completing documentation necessary for traceability to specifications and procedures.

Responsible for building embossing, issuing ports, cleaning pressure vessels for studies or runs.

Responsible for responding to alarm conditions, documenting data into records, performing air volume, filling volume testing, adjusting during the run. May be required to perform intermediate level maintenance on equipment in conjunction with a trained mechanic.

Responsible for performing container testing, which include seal integrity testing, burst testing, tensile strength testing, closure force testing.

Responsible for cross functional coordination with personnel such as manufacturing, quality, maintenance, and laboratories.

Work Environment: Work with pressurized equipment, work with hot surfaces, wet environment, work with chemicals and drug compounds. May require the individual to pickup materials up to 50 lbs. Will be required to wear personal protective equipment, which may include PAPR equipment. Some work may be required to be performed during off-shift or weekend hours.

Qualification Requirements:

• Ability to work independently and ability to interact successfully in teams.
• Requires strong documentation, communication, and interpersonal skills.
• Knowledge of standard operating procedures, specifications, and job-specific training materials.
• Ability to receive training from several departments, such as maintenance, manufacturing, and engineering.
• Proficient Use of Computers
• Adherence to site's attendance policy

Education and/or Experience: High School Diploma required with 3 or more years of experience. Associates degree or 2-year technical degree with 2 or more years of experience preferred. Experience in pharmaceutical manufacturing preferred.

#IND2

Job Type: Contract

Pay: $15.00 - $22.00 per hour

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Ability to commute/relocate:

• Round Lake, IL: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

• "Please state your work authorization / visa status/ US CITIZEN."
• "Please mention your personal email address and contact number."

Education:

• High school or equivalent (Preferred)

Experience:

• Manufacturing: 3 years (Preferred)
• Maintenance: 3 years (Preferred)
• Documentation review: 3 years (Preferred)

Shift availability:

• Day Shift (Preferred)

Work Location: In person

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