Position Description: The QC Inspector tasks pertain to Quality Control Compliance including the review of batch records and inspection of production at every stage from Blending, Encapsulation to Packaging.

EDUCATION/EXPERIENCE:

At least 1 year of experience in production batch record review and/or incoming inspection
Experience in Quality and/or Manufacturing in a cGMP environment
Knowledge of quality systems, cGMP, and Good Documentation Practice (GDP)
Proficient computer skills including Microsoft Office applications
Able to work in a timely manner in a fast-paced environment
Strong organizational skills, multitasking, and attention to detail
Strong experience of Microsoft Excel
Excellent communication skills and ability to work in a team
Strong willingness to learn and grow
Basic math skills, keen observation ability
Bilingual, must be able to read and write English and Spanish
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Adhere to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices.
Conduct thorough inspections of staged raw materials in pharmacy, in-process components in manufacturing and packaging, and finished products to ensure they meet quality standards.
Perform routine in-process checks using established methods in manufacturing and packaging to verify product quality, integrity, and safety.
Inspect the lines and/or room clearance for pharmacy, blending, manufacturing, and packaging.
Inspects all processes of the departments as assigned.
Inspects the information white board at each phase of the process to confirm the work-in-process products match records on hand.
Review the batch record and the batch record reconciliation in all phases of the manufacturing process.
Accurately document in-process checks, inspection results, and deviations from approved standards like batch records.
Monitor temperatures of entire facility as needed.
Maintain comprehensive and up-to-date records of quality control activities like sample logs, retains, temperature logs, cleaning logs for rooms/lines etc.
Ensure the inspection and sample retention of all processes are being taken, at the actual manufacturing process, and documented on the correct forms and retained correctly.
Collaborate with cross-functional teams as needed.
Responsible for communicating quality defects with supervisors.
Assist as needed in providing information or retain samples required to complete investigations for customer complaints, deviations and/or CAPA.
Work at different stations as production requires.
Maintain a clean and safe work environment.
Show a desire and willingness to learn and succeed.
Complete all required training activities.
Demonstrate a commitment to the organization by maintaining regular, on-site attendance, act in a reliable manner and follow through on responsibilities.
Other duties as assigned.