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Manufacturing QA Chemist; Day Shift

Job in Brownsburg, Hendricks County, Indiana, 46112, USA
Listing for: Antech Diagnostics
Full Time position
Listed on 2026-01-27
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 24 USD Hourly USD 24.00 HOUR
Job Description & How to Apply Below
Position: Manufacturing QA Chemist (Day Shift)

Overview

We understand that the world we want tomorrow starts with how we do business today. Antech is dedicated to creating a better world for pets. Our culture centers on our guiding philosophy, The Five Principles:
Quality, Responsibility, Mutuality, Efficiency and Freedom. Antech is part of Mars Science & Diagnostics, a family-owned company focused on veterinary care.

Work Shift: Monday - Friday, start time between 7:00 am and 8:30 am

Target Pay: $24.00 per hour. At Antech, pay decisions are determined using factors such as relevant job-related skills, experience, education, training and budget.

Job Purpose / Overview

The Manufacturing QC Chemist is responsible for supporting Quality Control and Quality Assurance functions to ensure all products and manufacturing processes meet established quality standards and regulatory requirements. This role maintains product integrity, compliance, and continuous improvement within the manufacturing environment.

Essential Duties and Responsibilities
  • Perform visual inspections and laboratory analyses to verify product quality and compliance.
  • Perform laboratory assays (e.g., PCR, ELISA, radioactive/fluorescent assays) and support validation of new and existing products and processes.
  • Document, report, and investigate non-conformance issues; perform root cause analysis and recommend corrective actions.
  • Monitor QC parameters using statistical tools (e.g., Levy-Jennings charts) and maintain accurate records in QA databases.
  • Calibrate, maintain, and troubleshoot laboratory equipment and instrumentation.
  • Handle hazardous chemicals and small quantities of radioactive materials in accordance with safety and regulatory guidelines (e.g., NRC regulations).
  • Assist with sample collection, validation studies, and initial data review for new and existing products.
  • Support method and assay validation, including analytical testing and documentation.
  • Participate in internal audits and continuous improvement initiatives within manufacturing and Biobank facilities.
  • Ensure compliance with SOPs, Batch Production Records (BPR), and company/industry quality standards.
  • Implement and track corrective and preventive actions (CAPA).
  • Maintain positive working relationships and effective communication across departments.
  • Adhere to all safety regulations and company policies.
  • Prepare detailed inspection and audit reports for management review.
  • Perform other related duties as assigned.

We share a collaborative obligation to conduct ourselves ethically and hold each other accountable to the values and standards of the organization. Every employee is expected to ask questions, seek guidance, and report concerns and/or violations of company policy or ethical standards. Antech Diagnostics has processes to communicate with leadership and expects commitment to integrity and uncompromising values.

Education and Experience
  • Associates degree required; bachelor’s degree in science-related discipline preferred.
  • Experience with general laboratory and IVD manufacturing equipment.
Knowledge,

Skills and Abilities
  • Knowledge of GMP, GLP, and GDP standards.
  • Experience handling hazardous chemicals.
  • Experience in general reagent compounding or buffer preparation.
  • Proficiency in laboratory techniques, including precision filling and pipetting.
  • Familiarity with molecular assays (PCR, ELISA, radioactive, fluorescent).
  • Strong statistical analysis skills.
  • High attention to detail and commitment to work quality.
  • Effective problem-solving abilities.
  • Strong verbal and written communication skills; ability to collaborate across teams.
  • Basic computer proficiency (Excel, Word, familiar with MRP system software).
Working Conditions
  • Laboratory environment with exposure to biohazards and hazardous chemicals (per National Hazard Communication Standards).
  • Handling of small quantities of radioactive materials.
  • The associate may need to review a comprehensive list of chemicals with department supervision.
  • Manual dexterity for computer keyboarding; typical office environment with cubicles, computers and overhead lighting.
  • Physical requirements include sitting, standing, walking, and reaching; may lift and/or move up to 15 pounds.
  • Temperature extremes are…
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