PAY - $29.08/hr. - ONSITE - TEMP TO PERM - DURATION - 3-6 MONTHS TO CONVERT - SHIFT - MON - FRI 2PM - 10:30PM.

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 Catalent SOP) through document review/approval, real time monitoring/approval of manufacturing activities and testing/approval of in-process and finished product samples.

II. Specific Tasks, Duties and Responsibilities:

RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO:

• 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 Catalent 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 team work 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

III. 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

Job Type: Temp-to-hire

Salary: $20.00 - $29.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Experience level:

• 1 year

Schedule:

• Monday to Friday

Work setting:

• In-person

Experience:

• Quality Assurance: 2 years (Preferred)

Work Location: In person