Work schedule: 2nd Shift, 100% onsite
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.
The training period will be 3-4 weeks and will be Monday through Friday on 1st shift.
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
Required skills:
- 2+ years-experience in a QA, QC or Manufacturing role
· Associate or Bachelor’s degree
· Previous experience working in a life science, pharmaceutical or medical products GMP environment.
· Prior experience with batch record review.
· Previous experience reviewing and approving deviations or investigations.
· Previous experience with LIMS, QMS or other database for documentation and review of SOP’s: paperless environment
Technology environment the consultant will be working in: SAP B1, eLIMS, Novatek, Master Control
Job Type: Contract
Pay: $36.00 - $40.00 per hour
Experience level:
Schedule:
Work setting:
- In-person
- Manufacturing facility
Education:
Experience:
- Quality control: 3 years (Preferred)
- CAPA: 2 years (Preferred)
- GMP manufacturing: 3 years (Preferred)
- life science or pharma industry: 1 year (Preferred)
Ability to Relocate:
- Philadelphia, PA: Relocate before starting work (Required)
Work Location: In person