Job description
Description
Zelh is a fast-growing, passionate outsourcing company.
Our mission is to be the most reliable logistics and IT provider in the industry by offering and maintaining consistently high-quality services.
One of our client is engaged in manufacturing dietary supplements of the highest quality, setting industry standards every step of the way. They feel a strong responsibility for every product they make. The company has grown up rapidly - thats why they are looking for a new member - Quality Specialist.
Duties and Responsibilities
•Completes online portal platform and email submissions of testing for raw materials and finished products (for both the internal and external laboratories)
•Saves all results received in portals or emails into the Quality folder(s)
•Manages laboratory tracker in Excel of all results (when sent, due, etc.)
•Certificate of Analysis draft creation
•Investigates out of specification results with their background knowledge in assay test methodology (example: knowledge on interferences with compounds undergoing HPLC, UPLC, LC-MS, GC, etc. testing)
•Performs other duties as assigned
Key Competencies (Knowledge, Skills, and Abilities)
·Superior verbal and written communication and interpersonal skills.
·Excellent interpersonal and organizational skills with strong attention to detail and accuracy.
·Excellent analytical, decision-making, and problem-solving skills.
·Excellent written communication and proofreading skills (essential).
·Ability to work efficiently in a dynamic fast-paced environment.
·Effective time management skills and the ability to meet deadlines.
·Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers,
common fractions, and decimals.
·Extremely focused on personal and food safety.
·Ability to handle frequent interruptions.
·Excellent attendance and reliability.
Experience:
•Extensive experience in a quality environment required.
•High proficiency in computer technology and systems operations.
•Thorough comprehension of U.S. FDA regulations (21CFR 111 & 117), Good Manufacturing Practices, and assays of marker components.
Working conditions:
Work schedule: Mon-Frid, 7am-5pm EST
Competitive Salary in USD
Work type - Remote
10+ business days of paid time off, 15 - after 2 years, 7 days of Public Holidays, 3 sick leaves
Equipment provided
