Not a regular QA role but Pharma QA Engineer role
No Fake candidates, Only genuine with Valid LinkedIn Profile and Manager references need
QA Specialist
Onsite in Philadelphia
Length Of Contract Assignment
- 6 months with possible extensions
Work Schedule/typical Work Week/daily Start And End Time - 2nd Shift
- Wed - Sat, 12pm – 10pm (2)
- Sun – Wed, 12pm – 10pm (1)
- Some flexibility with the start time if we had a candidate who wanted to start at 1pm or 2pm. Cannot start before noon and need to finish up by midnight.
- 100% onsite
- The training period will be 3-4 weeks and will be Monday through Friday on 1st shift.
Project Description
Describe the project and why the client is doing it?
- Our client is expanding 2nd shift production due to an increase in customer demand. Currently does not have approval to hire FTE.
- As a result of the increase in production staff and activity on the second shift, QA needs to have additional resources in the manufacturing suites.
- These resources will be handling QA operations and provide QA support to the manufacturing team.
Technology Environment The Consultant Will Be Working In
SAP B1, eLIMS, Novatek, Master Control
Consultant’s Day To Day Responsibilities
- Initiating investigations resulting from product deviations and non-conformance issues.
- Assisting with the development of CAPA’s
- Visual inspection and observation of production process and staff in the GMP manufacturing suites. Participation in walk throughs.
- Review and approve deviations.
- Compile and review raw data and sample test results, including Final Reports and CoA’s
- Review and approve executed batch records.
- Reviewing environmental monitoring trend reports and generating environmental summaries
If you are interested or have any references please share resume at mukul@brightmindsol.com.