What are the responsibilities and job description for the Quality Analyst III position at Mentis Systems?
Role :-Quality Analyst III
Duration : 6 Months
Location: Salt Lake City, UT 84108
Shift schedule: M-F 8/9am to 4:30/5:30pm MST
Temp to Perm: No. Contingent role through March/April 2025
Core Essential Skill Sets Candidates Must Have
Duration : 6 Months
Location: Salt Lake City, UT 84108
Shift schedule: M-F 8/9am to 4:30/5:30pm MST
Temp to Perm: No. Contingent role through March/April 2025
Core Essential Skill Sets Candidates Must Have
- Forklift, Detailed Orientated, Self Starter
- Material Staging and Handling
- Load and unload trucks and other vehicles.
- Ensure adherence to company policies, cGMPs, SOPs, and Batch Record instructions.
- Efficiently stage materials for production areas.
- Drug -11-panel w/Fentanyl
- Basic Background:
- SSN Trace (SSN) – Past Address and AKA Search
- 7-Year County Court Searchoff SSN Trace (Unlimited Counties as revealed by SSN Trace
- 7-Year Statewide Criminal Search (All States as revealed per SSN Trace)
- 7-Year Enhanced Nationwide Criminal Search
- 7-Year Federal Criminal District Criminal Search
- International Criminal Check (If Applicable – Lived Internationally in last 7 years)
- DOJ National Sex Offender Search
- GDS (World Watch) – Global Sanctions and World Watch Lists
- Professional License Verification – (If applicable per the Job Description)
- Employment Verification – 7 Year History
- Education Verification – Highest Level Earned
- Driver’s Abstract – (If applicable per the Job Description)
- Medical Test:
- Vision Screen - Near, Far, Color, Depth and Peripheral
- Vital Signs
- Audiogram & Noise and Hearing Questionnaire
- Spirometry & OSHA Respirator Questionnaire
- Lifting Assessment (manufacturing, maintenance, warehouse, security, or as indicated) - lifting up to 50 pounds
- Performing QA review/approval of investigation reports, change controls, Standard Operating Procedures, investigation documentation, and process/facility change control documents.
- Manage and track tasks for assigned Quality projects, CAPAs, and/or Audit Response commitments, and other initiatives to assure on time completion.
- Responsible for collaborating with appropriate departments to resolve both technical and compliance issues by providing Quality Assurance oversight.
- Bachelor’s Degree, preferably in a scientific discipline (biology, chemistry or closely related field) or equivalent education/experience with a minimum of 10 years relevant progressive experience in the pharmaceutical industry.
- Requires a minimum of 3 years of experience in Quality Assurance, Quality Engineering, or Compliance role within pharmaceutical industry.
- Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems, as well as Quality systems such as Trackwise.
- Self-directed with ability to organize and prioritize work
- Ability to communicate effectively with excellent written and oral communication skills
- Ability to interact positively and collaborate with co-workers and management
