Manufacturing QA Chemist (Day Shift)

Antech•Brownsburg, IN

7d•$24•Onsite

About The Position

We understand that the world we want tomorrow starts with how we do business today, and that’s why we’re inspired to make A Better World for Pets. Antech is comprised of a diverse team of individuals who are committed to each other’s growth and development. Our culture is centered on our guiding philosophy, The Five Principles: Quality, Responsibility, Mutuality, Efficiency and Freedom. Today Antech is driving the future of pet health as part of Mars Science & Diagnostics, a family-owned company focused on veterinary care. Current Associates will need to apply through the internal career site. Please log into Workday and click on Menu or View All Apps, select the Jobs Hub app, then click the magnifying glass to Browse Jobs. Work Shift: Monday - Friday start time between 7-8:30 am The Target Pay for this position is $24.00 an 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 plays a key part in maintaining product integrity, compliance, and continuous improvement within the manufacturing environment.

Requirements

Associates degree required/ bachelor’s degree in science related discipline preferred.
Experience with general laboratory and IVD manufacturing equipment.
Knowledge of GMP, GLP, & 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).

Responsibilities

Perform visual inspections and laboratory analyses to verify product quality and compliance.
Perform laboratory assays (e.g., PCR, ELISA, radioactive/fluorescent assay) and support validation of new & 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 & 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 ensure that we conduct ourselves in the utmost ethical manner and that we hold each other accountable to the values and standards of the organization.
Every employee is responsible for asking questions, seeking guidance, and reporting concerns and/or violations of company policy or ethical standards.