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Quality Control Technician

Advanced Resources

  • Noblesville, IN
  • 2 days ago
  • $20–$24 Per Hour
  • Contractor
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Skills

  • Biotech and Pharmaceuticalunmatched
  • Maintain Complianceunmatched
  • Materials Analysisunmatched
  • Materials Testingunmatched
  • Product Supportunmatched
  • Production Supportunmatched
  • Quality Controlunmatched
  • Quality Managementunmatched
  • Regulatory Complianceunmatched
  • Sample/Specimen Processingunmatched
  • Testingunmatched

Description

Summary of Position

The 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.

 

Job Responsibilities

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.

Numbers & Facts

LocationNoblesville, IN
Job TypeContractor
IndustryStaffing/Employment Agencies
Salary$20–$24 Per Hour
Year Founded2002
Websitehttp://www.advr.com

Qualifications

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, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment.
Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury.
Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed.
May be required to sit or stand for long periods of 8+ hours a day while performing duties.
Must possess good hand-eye coordination; close attention to detail is required.
Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants.
Willingness to complete safety training within allotted timeframes, and work in a team-based environment.
Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.

Skills

  • Quality Control
  • HPLC
  • Gas Chromatography
  • Liquid Chromatography
  • GMP (Good Manufacturing Practices)
  • Current Good Manufacturing Practice (cGMP)
  • Root Cause Analysis
  • CAPA

About Company

Get to know Advanced Resources.

We are a group of hard working, dedicated professionals who are committed to providing quality staffing solutions to our clients and creating opportunities for our candidates. We have different interests, like cooking, baseball, traveling, golf, volunteering, teaching and even an appreciation for 80s music – just like you, we are multi-dimensional. Regardless of where our personal passions lie, one thing is universal, our desire to create solutions and to find a great career fit for you!

Our company goal.

 

Since 2002, many of the nation's most respected Fortune 500 companies have turned to us for innovative, cost-effective workforce solutions. Our goal is to be a strategic business partner delivering staff augmentation resources, direct hires, contract to hire and training solutions across multiple verticals throughout the country. Resources you want, when you need them, from people you trust and want to work with.

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