QA Production Associate I

We believe being healthy should not require tradeoffs. SCN BestCo is a leading innovator, developer and manufacturer of Vitamin, Mineral & Supplement (VMS), Over the Counter (OTC) and prebiotics/probiotics in enjoyable forms such as gummies, lozenges and chews. With over 50 years of excellence, our team leads the way in changing how consumers make healthier choices. With unique food science expertise and proprietary processes, we’ve pioneered many firsts. Our passion to create new to the world products has guided and continues to be core to our mission of making health and wellness more enjoyable. Come join us and become a part of our winning formula!

We have openings on 2nd and 3rd shift

(2nd) 3:00pm- 11:00pm

(3rd) 11:00pm - 7:00am

Essential Duties:

• Daily Auditing of the manufacturing and packaging process including acceptable quality limits (AQLs), package inspections for quality defects, check sheets and other required documentation.
• Issue batch records and labels for production.
• Recognize and act upon quality events.
• Initiate holds when a quality event occurs.
• Audit manufacturing floor and logbooks monthly to ensure compliance.
• Assist in product validations by pulling required samples and taking readings as needed.
• Use electronic documentation systems for data entry and issuance of batch records.
• Collect samples as required for retain samples and validation activities.
• Collect samples of raw material and package components.
• Other duties assigned by the QA Supervisor.
• kage components
• Perform other job duties as assigned

Supervisory Responsibility:

This job has no supervisory responsibilities.

Knowledge and Skill Requirements

• Requires daily use of a computer.
• Self-starter with the ability to work under pressure in a fast-paced environment.
• Ability to work within a team on multiple projects simultaneously.
• Must be hygiene and safety oriented, with the highest level of integrity.
• Must be able to complete all required documentation (includes, but is not limited to, batch records, log books, notebooks, raw data (charts, graphs, scans, etc.), validation protocols, labels and cGMP-related forms).

REQUIRED QUALIFICATIONS:

• Minimum of a High School Diploma or GED
• At least 1 year of work experience in a customer service, office or manufacturing setting in a job requiring attention to detail and documentation or an Associates degree or higher.
• Able to stand for long periods of time
• Must be able to work 12-hour shifts day or night.
• Basic Computer Knowledge

PREFERRED:

• Knowledge of FDA regulations and standards
• Prior experience in a cGMP environment
• 1-year experience with AQLs, package inspections for quality defects, check sheets and other required documentation

Education

• High School or better

Behaviors

• Detail Oriented: Capable of carrying out a given task with all details necessary to get the task done well

Motivations

• Self-Starter: Inspired to perform without outside help

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)