QA Shop Floor

American Laboratories is a growing (yet, still small, think family-like feel) multi-industry supplier for the extensive products it manufactures. We were founded in 1967 based on the knowledge of manufacturing enzymes, proteins, and flavors to various industries. Today, American Laboratories’ food and pharmaceutical divisions employ over 125 people, offering an extensive listing of over 300 products to the Human Pharmaceuticals, Human Nutritional, Food Processing, and Animal Health industries in the United States and 45 countries around the world.

At ALI-PM, we are looking for candidates with varied backgrounds and skills. Diverse ideas come from diverse people, and we are devoted to offering an all-encompassing work environment where everyone feels valued and respected. Our pace of work enables fast learning and fosters an environment where you can stretch yourself and make an impact. We offer a variety of job specific and business skills programs and trainings to our employees. As a member of our team, you’ll have an opportunity to draw from those resources when you need them, and likewise, contribute your expertise when you have something to share.

We offer a highly competitive compensation package (salary and bonus) as well as a comprehensive, family-friendly benefits package including:

• Exceptional family medical, dental, and vision benefits (100% company paid premiums). 100% paid deductible/out of pocket expenses for Medical
• Paid time off and sick leave
• 9 paid holidays
• Exceptional 401k fund contributions (up to 9%)
• Great schedules
• Wellness incentives

Pay is based on experience.

Position Overview

We are seeking a dedicated and detail-oriented Quality Assurance Technician to join our team in Omaha, NE. In this role, you will play a crucial part in ensuring that our manufacturing processes meet the highest standards of quality and compliance. If you have a background in pharmaceuticals and a passion for quality control, we want to hear from you!

Responsibilities

• Conduct regular inspections (including cleaning checks) and audits of manufacturing processes to ensure compliance with Standard Operating Procedures (SOPs).
• Assist in the development and implementation of Manufacturing Instructions (MI) to enhance product quality.
• Perform quality control tests and document results accurately.
• Collaborate with production teams to identify and resolve quality issues promptly.
• Maintain accurate records of quality assurance activities and report findings to management.
• Participate in training sessions to stay updated on industry standards and best practices.
• Support continuous improvement initiatives to enhance product quality and operational efficiency.

Qualifications

• Experience in a manufacturing environment, preferably within the pharmaceutical industry.
• Basic understanding of manufacturing in cGMP environment, documentation and data integrity requirements.
• Highly strategic as well as hands on and metric driven.
• Strong understanding of Standard Operating Procedures (SOPs) and Manufacturing Instructions (MI).
• Experience with Current Good Manufacturing Process (cGMP) regulations
• Proven quality control experience with a keen eye for detail.
• Basic computer skills, including proficiency in data entry and documentation.
• Excellent communication and teamwork skills.
• Ability to work independently and manage multiple tasks effectively.
• High school diploma or equivalent; additional certifications in quality assurance are a plus.

You should be proficient in:

• Manufacturing Instruction (MI)
• Pharmaceuticals
• Standard Operating Procedures (SOPs)
• Quality Control Experience
• Experience in a Manufacturing Environment
• Basic Computer Skills