If you are passionate about delivering excellence, and think you are a great fit with our organization, we'd love to hear from you. To apply for any of our openings, click on the desired position and complete your application online.
For any jobs listed below without a specific city and/or state, they are considered REMOTE opportunities. If you do not see a position that fits your particular skill set, please click here to apply for GENERAL CONSIDERATION. Balchem Corporation, and its subsidiaries, offers a competitive salary and benefits package and is an Equal Opportunity Employer.
Quality Assurance Specialist - Night ShiftResponsible for activities involving quality assurance at Albion's Utah Facilities.
ESSENTIAL FUNCTIONS: Inspect, sample, and release or reject incoming components and materials.Review all receiving records for components, packaging, and labels.Determine whether all components, packaging, and labels conform to specifications.Approve and release from quarantine all components, packaging, and labels before they are used.Determine whether all in-process specifications are met.Determine whether each finished batch conforms to product specifications.Approve and release or reject each finished batch for distribution including and reprocessed finished batch.Ensure that manufacturing, packaging, labeling, and holding operations ensure the quality of product and that the product is packaged and labeled as specified in the master manufacturing record.Approve or reject all processes, specifications, written procedures, controls, tests, and examinations, and deviations from or modifications to them, that may affect product quality.Ensure that required representative samples are collected.Ensure that all tests and examinations required are conducted.Review and approve the results of all required tests and examinations.Ensure compliance with all local, state, and federal regulatory requirements.Ensure compliance with all internal programs and requirements designed for production of safe, quality products.Review and approve batch production related records.Periodically review all records for calibration of instruments and controls.Write, revise, and review standard operating procedures and work instructions.Inspect and conduct GMP facility audits.Conduct QA involvement with production teams to improve manufacturing systems.REQUIREMENTS: Possess a High School diploma or GED with two (2) years of relevant manufacturing experience in the food, dietary supplement, or pharmaceutical industry.Considerable knowledge of various aspects of basic computer operations and systems such as Word, Excel and Outlook.Communicate clearly, concisely, and effectively.Meticulous nature, displaying a penchant for detail and precision.Strong organization skills and the ability to manage multiple tasks concurrently.Work independently while developing effective working relationships with managers and fellow employees.Ability to follow GMP standards and guidelines.Ability to review, understand and apply information set forth in Standard Operating Procedures (SOPs).Ability to handle confidential information.WORKING CONDITIONS: Manufacturing environment with exposure to mineral powder products.Must be able to work in a corrosive environment with exposure to acid fumes, caustic and toxic substances.
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