OLSA Resources, Inc.

A leading staffing firm in Santa Ana is seeking a Documentation Specialist to ensure compliance with corporate policies. Responsibilities include creating and revising procedures, managing version control, and supporting document integrity. The ideal candidate should have over 5 years of experience in documentation, especially within the medical device sector, and be proficient in Agile document management. This position is crucial for maintaining quality standards in documentation throughout the organization. #J-18808-Ljbffr

Overview Must have a technical background, be familiar with applicable US and foreign regulations, standards, corporate and divisional standards. Specifically, the individual must have a working knowledge of Quality Systems Regulations (QSR) and International Standards (ISO13485). Additionally, the individual must understand a variety of quality/operational systems that support facility, product design, development, production, distribution, installation, and understand the principals of quality management. Bachelor degree (in Engineering preferred) or equivalent experience and sufficient exposure to pharmaceutical or medical device related industries required along with 4+ years relevant experience as Internal Auditor, Quality Engineer and/or Manufacturing Engineer in an R & D and /or manufacturing environment in pharmaceutical or medical device related industries. Position requires significant product and systems related knowledge. Must have excellent oral and written...

A leading resources company in Temecula seeks a qualified professional with a technical background in quality management for the pharmaceutical or medical device sectors. The position requires a Bachelor's degree in Engineering or equivalent experience, alongside 4+ years relevant experience. Applicants must be adept in Quality Systems Regulations (QSR) and ISO13485, possessing excellent communication skills. This is an on-site role in California. #J-18808-Ljbffr