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QA Data Reviewer-Pharmaceutical

Job in New Brunswick - Middlesex County - NJ New Jersey - USA , 08933
Company: ProStaff Solutions Inc
Full Time position
Listed on 2021-04-15
Job specializations:
  • Pharmaceutical
    Pharmaceutical QA
  • Quality Control
    Pharmaceutical QA, Quality Supervisor
Job Description & How to Apply Below
ProStaff Solutions is looking for a QA Data Reviewer to work with a pharmaceutical company in New Brunswick, NJ.

Pay Rate: $28/hr
1st shift
Contract (between 3-12 months)

Job Summary:
The QA Data Reviewer is accountable for reviewing analytical data critically per current in-house and compendial requirements.

Area of Responsibility:  Data Review of Raw Material, Finished Product, Packaging Material, and Stability
Comply with GDPs, GLPs, and cGMPs
Adhere to the Safety and Health Program and associated plans
Educate analytical chemists to improve analytical data reporting
Audit lab on a routine basis and report directly to department head
Continuously improve documentation system to increase efficiency and GLP compliance
Completion of work within the assigned time frame
Coordinate and discuss with other team members for continuous improvement of review
Discussions and provide suggestions to QC analysts for continuous improvement of the documentation process within cGMP requirements and applicable written test procedures and methods
Interaction with QC Analysts and Group Leaders as well as managers of other departments as needed
Able to work as a team member in QC Lab environment
Any other responsibilities which are assigned by the manager or department head.

Education:  Bachelor s degree in Chemistry, Pharmacy, Biochemistry, or a related field is required

Experience:  5+ years experience within a Quality Assurance/Quality Control environment
Knowledge of QC laboratory test procedures, cGMP requirements, ICH/USFDA guidelines, raw material analysis, method validation guidelines, analytical method transfers, finished products and stability testing procedures
Review of standard operating procedures, test procedures, and validation protocols
 
 
 
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