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Quality Tech 2

Biovation Labs LLC
locationWest Valley City, UT, USA
PublishedPublished: 6/14/2022
Technology
Full Time

Job Description

Job Description

Benefits Offered:

  • Medical
  • Dental
  • Vision
  • 401K with company match
  • PTO
  • 11 Paid Holidays

4/10 schedule Monday - Thursday (Maybe asked to work overtime, weekends, or Holidays depending on business needs)

PM Shift 4 PM - 2:30 AM

Job Summary:

The Quality Technician II plays a key role in ensuring product integrity and regulatory compliance throughout the manufacturing process. This position is responsible for performing in-depth inspections, testing, and documentation of raw materials, in-process components, and finished goods. The role supports quality initiatives by enforcing GMP standards, executing internal audits, resolving non-conformances, and implementing corrective actions. Acting as a mentor and indirect lead to junior quality staff, the Quality Technician II collaborates cross-functionally to uphold quality standards, improve processes, and contribute to continuous improvement efforts. This position requires strong analytical skills, attention to detail, and the ability to work independently in a dynamic manufacturing environment.

Job Duties & Responsibilities :

  • Assures consistent quality and oversees inspection, physical test methods and procedures.
  • Enforces good manufacturing practices and systems by verifying processes and reviewing documentation.
  • Achieves quality by contributing information and preparing and completing action plans; identifying and resolving problems; determining system improvements; implementing change, enforcing policies and procedures.
  • Accomplishes quality objectives; analyzes variances and initiates corrective actions.
  • Supports quality processes by documenting evidence, identifying critical control points and preventative measures by monitoring procedures and verification of procedures.
  • Assists in writing and updating quality procedures.
  • Maintains and improves product quality by surveillance audits, company policies, systems, procedures, and compliance.
  • Prepares quality documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.
  • Responsible for conducting testing procedures on equipment during manufacturing processes to ensure that products comply with quality standards.
  • Focuses on various procedures throughout the manufacturing process; Inspection of finished goods to find defects, check weights, etc.
  • Oversees the rework process by inspection and physical test methods and procedures.
  • Pulling incoming raw and finished samples for testing, inspect and verify incoming and outgoing product and paperwork to ensure that products comply with quality standards.
  • Oversees and updates in-process product inspection standards.
  • Maintains product quality by enforcing quality policies and procedures.
  • Accurately update quality logs; Lab submission, skip lot testing, MRB and expired products.
  • Sample, perform and document thorough examinations of all materials and finished products.
  • Conduct and report internal audits and evaluations.
  • Implement and improve quality control operating procedures.
  • Supports the management of outside lab testing, material review, and release procedures.
  • Administers a timely turnaround on OOS, NCR, or CAPA activities especially relating to incoming raw materials and finished product prior to release.
  • Performs in-process or incoming material testing in-house as needed on equipment housed within the sampling laboratory.
  • Acts as an indirect lead of other quality technicians to coach and monitor performance as needed to report up to quality management.
  • Can act in place of quality tech I position to cross cover areas when department might be shorthanded.
  • Can act as a provisional backup for Quality Supervisor if Director or Assistant Manager assign.
  • Other projects as assigned.
  • Adheres to cGMP within production areas of facility, monitors and enforces other team members adherence to requirements.
  • Possesses a higher level of understanding of cGMP requirements and has the ability to coach and train fellow employees on appropriate compliance with standards.
  • Responsible for monitoring and reporting on consumable items and inventory, equipment calibration and performance, and other items as needed to maintain an effective sampling/testing lab and process.
  • As a higher-level employee within the quality unit, this position facilitates interdepartmental cooperation for the purposes of effective production and continuously improving a companywide culture committed to high standards of quality in all aspects of manufacturing.
  • Maintain a clean and safe work environment.

Qualifications:

  • High School Diploma or GED Preferred. Equivalent experience will be considered on a case-by-case basis.
  • Previous work experience in quality control or other related fields
  • Strong attention to detail
  • Strong analytical and critical thinking skills
  • Excellent written and verbal communication skills
  • Proficient in Microsoft Office
  • A proficiency in reading and writing English to meet FDA record keeping requirements.
  • Competency in adding, subtracting, multiplying, dividing, calculating percentages, and determining the simple mathematical formulas to be used.
  • Frequent walking, standing, bending, and reaching throughout the shift.
  • Ability to lift up to 20 pounds.
  • Compliance with GMP environment and PPE requirements.


4/10 schedule 4 PM - 2:30 AM Monday - Thursday

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