SQA Services

Pharma/Med Device

QualityAuditor-Pharma/MedDevice

$1–1k Beijing, China Audit - Multiple Events
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Quality Auditor - Pharma/Med Device at SQA Services. Skills: supplier quality audits, regulatory knowledge, audit reports. Perform supplier audits at various sites within your region of residence. Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries”

What You'll Achieve.

Assure quality in the supply chains of various clients

Industry & Context.

Pharma/Med Device
Eligibility Requirements

Willingness to travel regionally

What They're Looking For.

Must Have

5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries, Has been the lead auditor in at least 10 audits, Direct audit experience to 21 CFR part 210/211, EU Vol 4, China GMP, 21 CFR part 820, and ISO 13485, communication and writing skills, Proven ability to deescalate workplace conflicts effectively, Ability to adapt to new technology and software., Willingness to travel regionally

Nice to Have

Direct audit experience to ISO 17025, ISO 15378, IPEC, ICH Q7 and/or Canada GMP, ISO certifications are a plus but not mandatory

What You'll Do.

Perform supplier audits at various sites within your region of residence

Assure quality in the supply chains of various clients within the pharmaceutical

and/or animal health industries

and deliver supplier audits based on your own and the client schedule

Utilize your regulatory knowledge of various standards from ISO

Respond to the Content team in a timely manner regarding edits/questions to your audit report

Write audit reports in accordance with client specifications

How You'll Work.

Team & Collaboration

Respond to the Content team in a timely manner regarding edits/questions to your audit report

Communication Scope

communication and writing skills

Process & Methodology

Coordinate, prepare, execute, and deliver supplier audits

Full Job Description

## Description For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.   We’re hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform supplier quality  audits at various suppliers in the Beijing area. These audits are generally 1-2 days long. You are given the flexibility to accept or reject these assignments according to your own availability.  ## Key Responsibilities Perform supplier audits at various sites within your region of residence Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc… Respond to the Content team in a timely manner regarding edits/questions to your audit report Write audit reports in accordance with client specifications ## Required Qualifications 5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries Has been the lead auditor in at least 10 audits Direct audit experience to 21 CFR part 210/211, EU Vol 4, China GMP, 21 CFR part 820, and ISO 13485 Strong communication and writing skills Proven ability to deescalate workplace conflicts effectively Ability to adapt to new techn

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