What are the responsibilities and job description for the QA Analyst position at The Staffing Resource Group, Inc?
QA ASSOCIATE 1
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
- Title : QA ASSOCIATE 1
- Location : Winchester , KY
- Industry : Pharmaceutical
- Hours : SHIFT - MON-FRI - 2PM-10 : 30PM
- Salary : up to $26.44 (Paid Weekly - Benefits Available)
- Employment Type : Contract to hire
Position Summary :
The QA Associate is responsible for the Quality support functions associated with the manufacturing
of solid oral dosage products for a given business unit. The essential responsibilities associated with
this position are oversight of the manufacturing operations (as dictated by cGMP, CFR, and SOP)
through document review / approval, real time monitoring / approval of manufacturing activities
and testing / approval of in-process and finished product samples.
Responsibilities :
Recommend SOP and batch record changes as needed
Review proposed SOP revisions and provide feedback to management
Real-time audit of batch records in the production suites for completeness, documentation,
calculation errors and conformance to critical process parameters
Perform room and equipment clearances per procedure following cleaning conducted by
production.
Perform microbial swabbing of equipment and room surfaces for environmental monitoring.
Maintain a full understanding of all SOPs and policies along with all cGMP and CFR
guidance that are applicable to the manufacturing of solid oral dosage pharmaceutical
products.
Perform routine testing of in-process and finished product samples including particle size, bulk
density, moisture analysis, appearance, and AQL testing real-time.
Monitor production manufacturing areas for compliance to SOP / cGMP / batch record and safety
requirements in order to identify and resolve routine errors and prevent possible deviations
that affect production real-time.
Works cross functionally to assess impact for potential deviations and assist in identifying if an
investigation is required.
Initiate deviation problem reports in Trackwise for issues discovered by QA, providing
sufficient detail of the incident so that a full investigation by the responsible department can be
conducted.
Manage quality status of WIP and finished good materials on physical inventory and in
inventory system (JD Edwards)
Other assignments as needed within the scope of QA Associate training curriculum.
Assist in investigations for deviations by supporting data gathering and root cause analysis
Enforcement of GMP Compliance.
Promotes teamwork and good communication.
Provide training and coaching to manufacturing staff as needed
Support site process improvements (training, efficiency projects, implementation of CAPAs)
Supports customer complaint investigation by performing inspection of retains and complaint
samples
Essential Skills and Experience :
Education or Experience :
Bachelor s Degree in related science or technical field preferred with 2 years prior work
experience
Minimum of High School Diploma with 4 years of relevant experience in a regulated GMP
manufacturing environment.
Additional qualifications desired are Lean Six Sigma, ASQ certification or other professional certification.
Knowledge / Skills Requirements :
Familiarity with basic laboratory instrumentation
Safe work habits
Basic math and computer skills
Good communication skills
Ability to follow written and verbal instructions
Able to work with limited supervision for routine tasks
Excellent documentation and handwriting skills
Proficient reading and comprehension skills
Sound decision-making, technical and problem-solving skills
Good time management skills
Expert technical writing and problem-solving skills
Good Laboratory Practices
Experienced with continuous improvement techniques
EOE / ADA
IND123
LI-SRG14
Salary : $26
