Huntsville, Alabama, United States · On-site
Job Title Accounting Generalist Company TriRx Pharmaceutical Services Function A/P, A/R & Cost System Maintenance, Payroll Location(s) Huntsville, AL Department Finance Direct Reports (list) None Reports to (title) Finan…
Skills: Accounts Payable, Accounts Receivable, Payroll Processing, Financial Reporting, SAP By Design
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The Accounting Generalist manages accounts payable, accounts receivable, and payroll processing to ensure financial accuracy and compliance. This role collaborates with internal departments to support operational efficiency and maintains accurate financial records within the ERP system.
Candidates must have a high school diploma or GED and at least 5 years of experience in finance, specifically in accounts payable, accounts receivable, and payroll. Proficiency in Microsoft Office is required, and experience with SAP By Design is considered a plus.
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Job Title | Accounting Generalist | Company | TriRx Pharmaceutical Services | ||||
Function | A/P, A/R & Cost System Maintenance, Payroll | Location(s) | Huntsville, AL | ||||
Department | Finance | Direct Reports (list) | None | ||||
Reports to (title) | Finance Director | Date Submitted | 04/09/2025 | ||||
To be completed by Corporate Compensation: | |||||||
FLSA (USA only) | Non-Exempt |
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| Date Reviewed |
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Job Summary - a concise overview of the job | |||||||
The Accounting Generalist is responsible for performing a variety of accounting functions with a focus on accounts payable, accounts receivable, payroll, and financial reporting. This position ensures timely and accurate processing of vendor and customer transactions, payroll accuracy, and compliance with internal policies and external regulations. The role collaborates closely with internal departments, suppliers, and customers to support the company’s financial health and operational efficiency. Accounts Payable
Payroll/HR
Accounts Receivable
Perform other accounting and administrative duties as assigned.
All incumbents are responsible for following applicable Division & Company policies and procedures. | |||||||
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. | |||||||
Interfaces with departments across the facility to ensure proper handling of accounts payable and payroll. Supports the site’s financial integrity by managing vendor payments, payroll accuracy, and compliance with financial policies. Contributes to financial accuracy through timely payroll management. | |||||||
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Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time | |||||||
Accountability | Responsibilities | % of Time | |||||
Floor Operations |
| 97 % | |||||
Non-Conforming Events |
| 0 % | |||||
Process Improvement |
| 3 % | |||||
Compliance |
| continuous | |||||
Safety |
| continuous | |||||
Total | 100% | ||||||
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Qualifications | |
Education & Experience | Minimal acceptable level of education, work experience and certifications required for the job |
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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. |
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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. |
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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. |
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Your Product. Your facility. Your team. A CDMO you can trust.
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.
Offices: 101 Merritt 7, Norwalk, Connecticut 06851, US · 120 Vintage Dr NE, Huntsville, Alabama 35811, US · 2, Allée de la Grindolière, Segré, Pays de la Loire 49500, FR · 12707 Shawnee Mission Pkwy, Shawnee, Kansas 66216, US · Fleming Road, Liverpool, England L24 9LN, GB
Your Product. Your facility. Your team. A CDMO you can trust.
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.
Offices: 101 Merritt 7, Norwalk, Connecticut 06851, US · 120 Vintage Dr NE, Huntsville, Alabama 35811, US · 2, Allée de la Grindolière, Segré, Pays de la Loire 49500, FR · 12707 Shawnee Mission Pkwy, Shawnee, Kansas 66216, US · Fleming Road, Liverpool, England L24 9LN, GB
