What are the responsibilities and job description for the Quality Control Analyst position at Kaztronix LLC?
Job Description: Job Title: Quality Control Analyst
Shift/Schedule Details: Sunday-Wednesday (4 10-hour shifts, flexible start time)
*Training will be Mon-Fri 8am-5pm*
Location: Holly Springs, NC
Job Description
Reporting to the QC Team Leader you will perform tasks associated with release testing and reviewing laboratory data.
The Role
" You will ensure that the Environmental Monitoring samples are collected and tested for aseptic facilities, such as surface, water, and air sampling.
" You will review Environmental monitoring samples according to quality requirements and ensure results reported are valid, accurate, and documented per applicable regulatory and corporate requirements.
" Document test results in appropriate records and computer systems.
" Support documentation and records, distributing, and filing all manufacturing procedures, and deviations.
" Follow Standard Operating Procedures (SOPs) and maintain compliance with current Good Manufacturing Practice (cGMP) regulatory guidelines.
" This role requires up to 10 hours of standing, some light inventory/stocking work, and gowning into Zone B, C, and D areas.
" Must be able to adjust to schedule changes, be able to problem solve, have critical thinking skills, and be equally able to work with a team and independently.
Minimum Required Qualifications
Shift/Schedule Details: Sunday-Wednesday (4 10-hour shifts, flexible start time)
*Training will be Mon-Fri 8am-5pm*
Location: Holly Springs, NC
Job Description
Reporting to the QC Team Leader you will perform tasks associated with release testing and reviewing laboratory data.
The Role
" You will ensure that the Environmental Monitoring samples are collected and tested for aseptic facilities, such as surface, water, and air sampling.
" You will review Environmental monitoring samples according to quality requirements and ensure results reported are valid, accurate, and documented per applicable regulatory and corporate requirements.
" Document test results in appropriate records and computer systems.
" Support documentation and records, distributing, and filing all manufacturing procedures, and deviations.
" Follow Standard Operating Procedures (SOPs) and maintain compliance with current Good Manufacturing Practice (cGMP) regulatory guidelines.
" This role requires up to 10 hours of standing, some light inventory/stocking work, and gowning into Zone B, C, and D areas.
" Must be able to adjust to schedule changes, be able to problem solve, have critical thinking skills, and be equally able to work with a team and independently.
Minimum Required Qualifications
- Associate's Degree or Biowork Certificate
- Min 1-year experience in Pharma
- GDP experience
- Experience with Environmental Monitoring, Water collection, aseptic gowning and technique, and plate reading
- This role requires up to 10 hours of standing, some light inventory/stocking work, and gowning into Zone B, C, and D areas.
- Must be able to adjust to schedule changes, be able to problem solve, have critical thinking skills, and be equally able to work with a team and independently.
- LIMS experience is a plus
- MetOne particle counter
- SAS air sampler
Salary : $28 - $32
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