Compliance Auditor III-28984

OLSA Resources, Inc.; Temecula (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

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.

Qualifications

• Bachelor's degree or equivalent experience in pharmaceutical or medical device industries.
• 4+ years as Internal Auditor, Quality Engineer, or Manufacturing Engineer.
• Familiarity with applicable US and foreign regulations and standards.

Skills

Quality Systems Regulations (QSR)

ISO13485

Excellent oral and written communication skills

Education

Bachelor's degree in Engineering or equivalent experience

Job description

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 communication skills.

Qualifications

• Bachelor's degree (in Engineering preferred) or equivalent experience with exposure to pharmaceutical or medical device related industries.
• 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.
• Working knowledge of Quality Systems Regulations (QSR) and International Standards (ISO13485); familiarity with applicable US and foreign regulations, standards, corporate and divisional standards.
• Understanding of quality/operational systems that support facility, product design, development, production, distribution, installation, and the principles of quality management.
• Excellent oral and written communication skills.