QA Technician - Production

NEW GENERATION WELLNESSColorado Springs, CO
4d$20 - $26Onsite

About The Position

The Quality Assurance Technician will primarily be responsible for supporting canning room operations, gummy manufacturing and softgel manufacturing in a quality assurance capacity. This includes but is not limited to room inspections, in-process checks, record reviews, inspections of finish products, and release or rejection of batches. In addition to coverage of production areas, they will be responsible for maintenance and archival of completed records, including batch records, packaging records, training records, and any other records needing to be maintained for GMP compliance.

Requirements

  • High School Diploma or equivalent
  • Basic knowledge of Good Manufacturing Practices (GMPs).
  • Knowledge of good documentation practices.
  • Experience in a manufacturing environment is desirable.
  • Ability to read and interpret technical procedures, SOP’s GMP’s, and government regulations.
  • Strong communication skills, both written and verbal.
  • Ability to work as a team and independently.
  • Strong attention to detail.
  • Knowledge of Microsoft suite applications (Excel, Word, Outlook)
  • Knowledge of basic office functions such as filing and scanning
  • Ability to function well in a high-paced and at times, stressful environment.
  • Excellent time management skills with a proven ability to meet deadlines.
  • Using fingers and palm on an object
  • Especially where one must frequently convey detailed or important instructions or ideas accurately, loudly, or quickly.
  • Able to hear average or normal conversations and receive ordinary information.
  • Movements frequently and regularly required using the wrists, hands, and/or fingers.
  • Average, ordinary, visual activity necessary to inspect, prepare documents and products or operate machinery.
  • Frequent walking, and occasional standing and sitting.
  • Ability to lift up to 25 lbs. occasional bending, squatting, climbing, and kneeling.

Nice To Haves

  • Prior experience in quality assurance is preferred but not required.

Responsibilities

  • Follows all employee guidelines, practices, policies, and Standard Operating Procedures (SOPs) to ensure that customer requirements and FDA regulations are met.
  • Performs equipment and room clearances based on cleanliness and adherence to SOP’s.
  • Performs in-process inspections and physical testing of products to ensure compliance with specifications.
  • Performs product release based on physical characteristics, compliance with in-process control limits and finished product specifications.
  • Performs and/or assists with batch record review for accuracy and completeness.
  • Coordinates the collection of finished goods samples for reserve/retain samples.
  • Complies with cGMP regulations and follows all standard operating procedures.
  • Assist in ensuring all personnel comply with cGMP regulations and follow standard operating procedures.
  • Other duties as assigned.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service