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Contractor Quality Control Technician

Job in Noblesville, Hamilton County, Indiana, 46060, USA
Listing for: Curium Pharma
Contract position
Listed on 2026-07-06
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Quality Engineering, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 50000 - 70000 USD Yearly USD 50000.00 70000.00 YEAR
Job Description & How to Apply Below
Position: (Contractor) Quality Control Technician

(Contractor) Quality Control Technician

Date:
Jun 2, 2026

Location:

Noblesville, IN, United States, 46060

About Curium

Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world‑class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life‑threatening diseases to over 14 million patients annually.

The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: an enhanced quality of care for our patients. A trusted partner to our customers.

A supportive employer to our valued team.

Job Summary

The (Contractor) Quality Control Technician role is responsible for performing analytical testing of raw materials, in‑process samples, and finished pharmaceutical products to ensure compliance with regulatory and company standards. This role is critical to maintaining product quality, supporting production timelines, and ensuring regulatory compliance.

Work Schedule: Saturday‑Wednesday 12:00 AM — 8:30 AM (Times subject to change)

Essential Functions
  • Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, DEA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
  • Perform routine and non‑routine analytical testing using techniques such as HPLC, GC, UV‑Vis, FTIR, titration, ICP‑MS etc.
  • Conduct testing on raw materials, intermediates, and finished products in accordance with cGMP and SOPs.
  • Review and interpret analytical data; prepare detailed and accurate reports and documentation.
  • Maintain laboratory equipment, including calibration, qualification, and troubleshooting.
  • Participate in method development, method validation, and stability studies as required.
  • Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal quality standards.
  • Support investigations (OOS, OOT, deviations) and assist in root cause analysis and CAPA implementation.
  • Maintain a clean and organized laboratory environment and adhere to safety guidelines.
  • Participate in audits and inspections and support documentation requests from regulatory authorities.
Requirements
  • Associate Degree in life science or a related field or completion of 4 college‑level life science courses required. Bachelor Degree in life science or a related field preferred. Work experience is considered in lieu of degree.
  • 1 or more years of relevant experience required.
  • Solid knowledge of analytical techniques and instrumentation (HPLC, GC, etc.).
  • Familiarity with cGMP, GLP, and regulatory guidelines.
  • Must be able to resolve problems, handle conflict and make effective decisions under pressure, and conduct Root Cause Analysis.
  • Ability to do simple to complex math calculations, input data into the computer and analyze data as required.
  • Ability to multitask projects.
  • Must be proficient in use of Microsoft suite office products.
  • Good computer skills, including utilizing personal computers and data entry programs Good hands on, analytical, and problem solving and decision making skills.
  • Excellent writing and verbal communications skills.
  • Ability to work independently and with others to accomplish goals and priorities High level of energy and regular, consistent attendance.
  • Verifiable working knowledge of cGMP guidelines and their application in a pharmaceutical manufacturing environment.
Working Conditions
  • Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
  • Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending,…
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