JOB FUNCTION: Scientific
JOB TYPE: Direct Hire
LOCATION: Pennsville, NJ
JOB TYPE: Direct Hire
LOCATION: Pennsville, NJ
COMPENSATION: $85k
REMOTE / ONSITE: Onsite
POSTED: May 26, 2023
REMOTE / ONSITE: Onsite
POSTED: May 26, 2023
Our client reviews and approves executed production records, production investigations, Master Production Records, COAs and DMFs. Knowledge of cGMP’s and ICH guidelines (Q7, Q8, ect), decision maker and someone who can adapt well to a changing environment. They are seeking a QA Specialist to join their team!
Salary/Hourly Rate:
$85,000
Position Overview:
The QA Specialist reviews lab sample results and manufacturing records relative to qualification/validation activities. The QA Specialist conducts, writes, and reviews quality related investigations.
Responsibilities of the QA Specialist:
- Writes and reviews Product Validation/Qualification/Assessments documents, Equipment Qualifications
- Assessments documents Computerized Systems Validations/Assessments documents
- Responsible for cGMP compliance of assigned manufacturing operations/areas and conducts cGMP inspections
Qualifications for the QA Specialist:
- 3 to 5 years of experience in auditing in a pharmaceutical manufacturing environment is required
- Excellent communication skills
- Conscientious and detail-oriented
- Excellent computer skills (MS Office, WinLIMS, SAP)
- Team player
- Self-manage daily work and set priorities
- Manage projects and prioritize appropriately
Education Requirements:
- Bachelor’s degree in microbiology (preferred), biology, chemistry, or engineering is required
Benefits:
- Client provided benefits, upon eligibility
EOE/M/F/D/V/SO
Position ID: 124005