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Quality Control Technician

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: JobRx, Inc.
Full Time position
Listed on 2026-05-18
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 50000 - 70000 USD Yearly USD 50000.00 70000.00 YEAR
Job Description & How to Apply Below
Location: Indianapolis

Overview

Spherion is hiring Pharmaceutical Production Technicians in Indianapolis, IN for a mid‑level position in the aseptic filling group within the Manufacturing department. The role requires a GMP‑certified individual to perform aseptic filling operations, equipment calibration, and lead teams where necessary.

Responsibilities
  • Become certified for entry into the GMP cleanroom space to perform sanitization, stock/replenish supplies, equipment setup, and related aseptic filling operations.
  • Execute aseptic fill processes using batch records and SOPs.
  • Verify the calibration of all related equipment and sanitization of supplies to support production.
  • Increase competency in manufacturing area procedures, including aseptic and cleanroom areas, component preparation, filling and capping.
  • Operate equipment in the fill suite.
  • Perform tasks with minimal supervisor direction.
  • Provide training for new team members.
  • Understand the manufacturing schedule and coordinate tasks to achieve the schedule.
  • Provide floor leadership in the absence of a supervisor or PT3 technicians.
  • Transport and/or dispose of hazardous chemicals.
  • Perform all other duties as assigned.
  • Immediately notify supervisor if affected by an infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist.
Working Hours

7:00 AM - 3:30 PM

Requirements Education
  • High School diploma (B.S. degree in chemistry/biology/life sciences is a plus).
Experience
  • 1–4 years of experience in a cGMP pharmaceutical manufacturing setting.
  • Minimum 3–5 years of aseptic filling experience in a cGMP pharmaceutical manufacturing facility.
  • Isolator experience.
Skills & Knowledge
  • Extensive knowledge of bulk formulation, equipment cleaning, preparation, and assembly.
  • Experience in stopper prep, capping, and packaging.
  • Computer skills in Microsoft Office (Word, Excel).
  • College coursework preferred.
  • Knowledge of GMP compliance regulations.
  • Ability to comprehend and follow detailed procedural instructions.
  • Adequate working knowledge of arithmetic functions for calculations in product documentation.
Benefits

Health, prescription, dental, vision, AD&D, life insurance, short‑term disability, and a 401(k) plan available (subject to eligibility).

Equal Opportunity Employer

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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