Job description

Job Description:
1. Conduct tasks that provide the data required to demonstrate that pharmaceutical products meet regulatory requirements. The primary responsibilities for this position include, but are not limited to:
a. Perform Quality Assurance inspections for operations within the Clean Room environment.
b. Execute AQL Sampling and Inspection activities for raw materials, packaging components, and finished products.
c. Perform Area Clearance, in-process inspections, and labeling material issuance.
d. Execute and manage the Retains and Returned Goods processes.
e. Periodically summarize status and progress of assigned activities as requested by Supervisor.
2. Function as primary administrator and/or back up for at least one Quality system, to include but not limited to: Document Control process, Quality Training System, and/or the Material Identity Control System (Part number List), etc.
3. Draft and/or contribute to QA documentation, including deviation reports, standard operating procedures (SOP), and Quality metrics/trend data.

Requirements:

• High School Diploma with 3-5 years’ experience; or undergraduate degree in a scientific-related field with 0-2 years of experience in the Pharmaceutical/Biotech industry,
• Experience in a GMP regulated environment preferred.

Job Type: Contract

Salary: $20.00 - $25.00 per hour

Schedule:

• Day shift
• Monday to Friday

Ability to commute/relocate:

• Baltimore, MD 21224: Reliably commute or planning to relocate before starting work (Required)

Work Location: One location

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