Quality Control Chemist II

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TriRx Shawnee LLC

Posted 3 months ago

Full Time

Huntsville, Alabama

In Person

Smart Summary

Responsibilities

The Chemist II evaluates chemical and physical properties of raw materials and finished products using various analytical techniques under cGMP guidelines. Responsibilities include performing method transfers, conducting laboratory investigations, and maintaining equipment calibration.

Qualifications

You have a Bachelor's degree in Chemistry or a related field and a minimum of 1 year of analytical laboratory experience. You are proficient with chromatographic equipment, Microsoft Office Suite, and possess knowledge of FDA regulations and Good Manufacturing Practices (GMPs).

Must Have Skills for ATS

Chemistry

cGMP

analytical testing

wet chemistry

chromatographic analysis

thin-layer chromatography

gas chromatography

high performance liquid chromatography

Mass Spectroscopy

ultra performance chromatography

GC

HPLC

UPLC

FDA regulations

GMP

GLP

GCP

Lean Manufacturing

Six-Sigma

Microsoft Office Suite

Excel

Teams

Job Description

Job Summary - a concise overview of the job

A Chemist II evaluates the chemical and physical properties of various raw materials and finished products under cGMP guidelines. Utilizes established methods and procedures and laboratory equipment to perform the analytical testing and ensure all products released are safe and efficacious.  Performs method transfer and validations, and conducts laboratory investigations.

Scope of Authority - span of control (work unit, site, department, division, etc.), monetary value of budget/spend authority ( capital, operating, etc.), P&L responsibility, etc.

The Chemist II operates within the Analytical Quality Control Laboratory, under the direction of the Quality Organization.

The Chemist II has no budget/spend authority, but may act as SME in the selection of materials and equipment.

Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time

Accountability

Responsibilities

% of Time

Floor 

Operations

  • Maintain a clean, organized, and safe work area.
  • Perform daily calibrations and maintenance on analytical equipment, such as analytical balances, pH meters, density meters, etc.
  • Prepare test solutions, compounds, or reagents for analysis of raw materials and finished products.
  • Accurately and precisely perform analytical testing using a variety of wet chemistry techniques, such as  weighing and measuring, density, specific gravity, pH, viscosity, titration, and conductivity.
  • Perform assay, impurity/degradant, and solvent determinations by chromatographic analysis via thin-layer, gas (GC), high performance (HPLC), Mass Spectroscopy, and ultra performance chromatography (UPLC).  
  • Perform minor maintenance and troubleshooting on chromatographic equipment.
  • Multitask projects while maintaining high levels of accuracy
  • Other duties as assigned

75%

Non-Conforming Events

  • Complete basic laboratory investigations with a thorough understanding of root cause analysis and required CAPAs

15%

Process Improvement

  • Work in cross functional teams as necessary to complete projects, transfers, and investigations

10%

Compliance

  • Maintain current training compliance on assigned SOPs and company policies.
  • Accurately and legibly document and record all work completed so that analyses may be fully traceable and reproducible.
  • Identify as an expert on at least one type of laboratory equipment, and acts as a SME for that instrument

continuous

Safety

  • Operate under all corporate safety requirements at all times, including use of PPEs and adherence to company policies in handling of hazardous substances

continuous

Total

100%

Qualifications

Education & Experience

Minimal acceptable level of education, work experience and  certifications required for the job

  • Bachelor’s degree in Chemistry or Related Field
  • Minimum of 1 year experience in an analytical laboratory

  

Knowledge

Proficiency in a body of information required for the job    

e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc.

  • Knowledge of FDA regulations
  • Familiarity with Good Manufacturing Practices (GMPs)
  • Familiarity with analytical laboratory operations and associated safety requirements
  • Possesses an expanded understanding of column chemistry with ability to troubleshoot most problems without support.

Skills 

Abilities

Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc.

  • Experience with chromatographic equipment and integration software
  • Experience with Microsoft Office Suite of Products, including Word, Excel, and Teams
  • Analytical laboratory experience

Physical Requirements

Physical & mental requirements     e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.

  • Must be capable of wearing all appropriate PPEs correctly during handling of hazardous substances
  • Some work may require extended periods of time standing at a lab bench
  • Must be visually capable of accurately measuring and reading volumes of solution in volumetric apparatus (i.e. accurately read meniscus)

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TriRx Shawnee LLC

TriRx Pharmaceutical Services is a leading global contract development and manufacturing organization (CDMO) that provides comprehensive solutions for the animal health and human pharmaceutical industries. TriRx provides integrated development, manufacturing, and supply services from our network of state-of-the-art facilities across the United States and Europe. Founded by industry veterans, TriRx understands what it means to outsource development and manufacturing of your drug product, and that we are committed to delivering CDMO services at a higher standard of performance. Built on honesty, openness, and integrity, TriRx gives our clients total access to our people and processes, treating your product like its own. TriRx is your partner for advancing products to market. We provide comprehensive development, manufacturing, and packaging capabilities from the clinical- to commercial-scale for both sterile and non-sterile pharmaceutical drug products. Our expertise spans a wide range of services and modalities including: - Biologics - Biotech API - Solid Dose - Drug Development - Analytical Testing - Solutions, Suspensions, and Colloidal Dispersions - Liquids, Creams, Ointments - Fill/Finish - Packaging - Aseptic Compounding - Animal Health Products TriRx maintains strict adherence to the regulatory standards required by the FDA, EMA, and other global health authorities. This, coupled with our rigorous quality control processes, ensures that every product we manufacture meets the highest quality standards. We are more than just a CDMO; we are a trusted partner in the pharmaceutical industry. Whether you are a startup biotech or a multinational pharmaceutical company, TriRx is dedicated to helping you achieve your objectives and bring vital medications to the markets and patients who need them most. Your Product. Your Facility. Your Team. A CDMO You Can Trust.
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