The QA Associate is responsible of inspecting products at different phases in their development to ensure they meet a set of consistent standards. Their duties include performing visual inspections, recording quality issues and planning processes to decrease the instance of defects in products.

The following responsibilities would characterize the requirements of this position. Must possess the skills necessary to perform the majority of the listed functions:

1. Create new Batch Control Worksheets from. signed off customer SPECs;

2. Compile and maintain master formulas and bill of material documentation to ensure accurate and quality finished product that meet and/or exceed GMP standards;

3. Complete ERP entries for item Master keys, bills of material, and lab releases;

4. Review manufacturing batch records prior to being released to Production;

5. Compile, implement, and maintain deviation records and QA releases;

6. Compile and maintain records of document form changes, deviation records, and QA releases;

7. Create and maintain various Microsoft Access database files;

8. Update Batch Control Worksheets from change request received from Sales department;

9. Perform any other related duties as assigned.

Competencies

1. Minimum 1-2 years in a comparable clerical or manufacturing position;

2. High School Diploma required; some college experience preferred;

3. Intermediate mathematical, problem-solving and communication skills;

4. General computer concepts;

5. Working knowledge in Microsoft Outlook, Excel, and Word;

6. Working knowledge of ERP or other inventory tracking software.

7. Ability to multi-task.

8. Ability to adjust work schedule as business needs require

DISCLAIMER & ACKNOWLEDGEMENT:

The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.

4Excelsior provides full turnkey service contract manufacturing of dietary supplements and sports nutrition products. Our NSF Current Good Manufacturing Practices (cGMP) facility adheres only to the highest standards in procurement, formulation, manufacturing, and product testing.

At 4Excelsior, we’re committed to the highest standards of quality in the dietary supplement and sports nutrition industry. In an industry plagued by quality control issues, 4Excelsior has gone beyond and implemented a number of additional certifications and quality control processes that exceed industry standards.

Our goal as a contract manufacturer is provide our clients with complete confidence in our manufacturing capabilities and the product that we produce on their behalf. We believe in an ethical and transparent approach to manufacturing, from start to finish.

At 4Excelsior, we believe that a diverse, equal and inclusive working culture strengthens any business model and brings it greater success. We ensure fair treatment and opportunity for all. We strive to minimize prejudice and discrimination on the basis of an individual or group of individual's protected characteristics, no matter their sexual orientation, culture, religion, race, age, gender or disability.