Demonstrates entry level knowledge of QA systems, Document Control routing, issuance and sampling techniques.
Ability to complete Oracle transactions.
Demonstrates entry level knowledge of current Good Manufacturing Practices (GMPs)
Demonstrates entry-level proficiency in Microsoft Office applications.
Demonstrates ability to work effectively in a team environment.
Demonstrates solid verbal, written, and interpersonal communication skills.
Following detailed instructions under supervision, assists with raw material sampling and testing.
Performs routine inspections of incoming, intermediate, and outgoing materials for proper identification and conformance to approved specifications.
Assists with the sampling and identification (quarantine, approved, on hold, or rejected) of all materials in accordance with current Good Manufacturing Practices (GMPs) requirements.
Documents, files and maintains inspection records.
Performs basic tasks in support of the collection, retention and storage of finished product and packaging component retain samples.
Performs basic tasks in support of the distribution, retrieval, and filing of controlled documents (SOPs, Specifications, and Test Methods) as well as other Quality Assurance documents).
3 years of relevant administrative experience and a High School diploma OR 2 years of relevant administrative experience and AA degree.
Good oral and written communication skills
Attention to detail a must
Use of a respirator a must.
Standing for extended periods of time to perform floor inspections/sampling and weekly/monthly room recovery.
Pharma experience in QA and an AA degree preferred.
Previous GMP experience preferred.