Our Quality Control Department is looking for a full-time Compliance Specialist who is committed and passionate about dietary supplements and understands the importance of upholding a commitment to quality.
The Compliance Specialist will ensure that the organization’s products and services are consistent. They check the quality of incoming and outgoing products manufactured in our cGMP-compliant facility by conducting tests, monitoring production processes, and ensuring products meet the company’s quality standards. We manufacture pure, all-natural health solutions that change lives in a genuine, caring, and positive environment.
Must possess outstanding verbal & written communication skills and work effectively with others along with true integrity. On-the-job training is provided. cGMP, FDA, FSMA and/or quality control experience preferred but willing to train the right candidate. If you are a dedicated Quality Control Specialist we encourage you to apply.
Essential Duties and Responsibilities:
Establish, approve, and maintain all controlled documents which include but are not limited to SOPs (standard operating procedures), Master Manufacturing Record, Master Batch Record, and Packaging documents.
Establish, approve, and test (organoleptic quality) per QC specifications for all starting materials, finished products, packaging materials and labels.
Evaluate procedures for document change control including but not limited to revising and approving the revision of all established quality control specifications, sampling, and testing instructions as necessary, replacing superseded versions, and maintaining a complete written collection of the current version and historical record of all amendments.
Participate in all investigations of deviations, discrepancies, or test failure. Evaluate and authorize any deviations from standard processing and procedures, reprocessing, and /or re-working of products or materials.
Manufacturing Floor support: Provide routine, real-time floor support to manufacturing teams, ensuring adherence to cGMPs and established internal documentation including SOPs, Master Batch Record (MBRs), and Test Methods. Reports errors in a timely manner.
Batch Record Review: Perform batch record review. Coordinate completion of batch record review in a timely manner to support clinical product availability. Work with operators and technicians to correct deficiencies and mentor to assure understanding.
Review and approve CofAs (Certificates of Analysis).
Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues in a timely manner.
Develop effective working relationships with functional area peers and managers.
Wage: $21
Benefits include:
PTO
Paid Holidays Off
Employee Discounts
Simple IRA
M-F Shift
Cafe on-site with Employee Discounts
Paid Lunch Breaks
Costco Membership Reimbursed
The position is available immediately. Send resume by email.