Quality Specialist

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 - that is 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
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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