Quality Assurance Associate - Newtown, United States - Onsite Personnel LLC

Onsite Personnel LLC Newtown, United States

4 weeks ago

Description

Job Description

Job Description
Role Purpose:
QMS (Quality Management Systems)

Associate:The QA Associate ensures quality and compliance of the facility with applicable regulatory requirements.

These activities may include reviewing documents and data, conducting systems or process-focused audits and inspections, consulting on quality and compliance issues, maintaining quality databases, performing trend analyses and reporting metrics where required, as well as performing quality / compliance training, as needed.

Provide support during regulatory inspections. Assists with the development of SOPs, specifications, and other quality document control activities as needed.

Key Duties & Responsibilities:
QMS (Quality Management Systems)

Associate:· Conduct routine walk-throughs of manufacturing areas for adherence with SOPs and good documentation practices including but not limited to sample management and accountability, data integrity (manufacturing, calibration and maintenance logbooks, batch record documentation) and adherence with applicable safety requirements.

Review documentation, results and reports from raw material and finished product analysis for accuracy and completeness.· Perform regularly scheduled, formalized internal audits of manufacturing areas for adherence with SOPs, cGMPs, FDA, OSHA, EPA and DEA regulations.· Review SOPs, Specifications, Batch Record Documentation.· Maintain KPIs related to manufacturing accuracy and conformance with SOPs, regulations and Guidelines and present to the Quality Council.· Review and maintain Quality Management Records (Change control, Deviation, CAPA, Root cause Investigations, Market complaints, Product recall, OOS and Outliers) to ensure compliance with procedures and assurance of due date requirements.· Review validation reports for aseptic manufacturing, filling and support processes, equipment, and utilities for compliance against approved protocols.· Ensure manufacturing compliance for adherence with aseptic technique, process validations, hold time studies, and media fill simulation studies.· Preparation and review of Standard Operating Procedures· Review executed documents for adherence with batch record, SOPs and protocol requirements.· Perform quality on-floor audits, area inspections, room and line clearances.· Assists with quality improvement initiatives as needed.· Assists with development/ writing of SOPs or other quality documents and/or reports as needed.· Provides consultation on quality and compliance topics in areas of expertise.· Performs other duties as assigned.· Complies with company polices, SOPs, and data integrity requirements.

Technical Competencies:
QMS (Quality Management Systems)

Associate:· Bachelor's Degree is preferred· Ability to read, identify, transcribe, and communicate details accurately.· Ability to perform daily work assignments accurately, timely and in a safe manner with moderate supervision.· Must be able to multi-task and work in a fast-paced environment.· Self-motivated & exceptional organizational skills.· Ability and willingness to work cooperatively with others.· Knowledge of Microsoft Office products (Word, Excel) .· High degree of discretion dealing with confidential information.· Prior experience with electronic quality systems is preferred.· Manage time effectively to complete assignments in expected period.· Ability to communicate effectively and follow detailed written and verbal instruction.· Ability to train on SOPs, regulatory guidelines, and storage requirements.

Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment.

Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws.

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