Quality Assurance Specialist
Job Description
R&D Partners is seeking to hire a Quality Assurance Specialist in Frederick, MD.
Your main responsibilities as a Quality Assurance Specialist:
Reads, understands, and follows SOP s and complies with cGMP s
Writes new standard operating procedures or revises existing documentation utilizing document management systems.
Supports the evaluation and disposition of labelling, raw materials, intermediates and finished products through timely evaluation of batch records, laboratory results and other cGMP documents.
Supports the issuance and reconciliation of GMP documentation
Electronic system usage with tools such as Trackwise, GQCLIMS, Pas-X, FileTrail and SAP.
What we are looking for in a Quality Assurance Specialist:
Bachelor's in biology, engineering or related field is required
Minimum of 2 to 3 years of biopharmaceutical/pharmaceutical experience
Minimum of 1 year of QA/QC or validation experience
Understanding of basic scientific principles. Understanding of basic biotech manufacturing processes. Good understanding of cGMPs, Regulatory standards and concepts.
Develops solutions to a variety of compliance problems of moderate scope and complexity.
Why Choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including:
Medical insurance PPO, HMO & HSA
Dental & Vision insurance
401k plan
Employee Assistance Program
Long-term disability
Weekly payroll
Expense reimbursement
Online timecard approval
Pay Scale:
$41,600 $52,000 (Dependent on Experience)
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal-opportunity employer.