Key Responsibilities
- Perform supplier audits at various sites within Japan
- Assure quality in the supply chains of various clients within the animal health, pharmaceutical, medical device, cosmetics, 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 animal health, pharmaceutical, medical device, cosmetics, and/or biologics industries
- Direct audit experience to EffCI, EU GMP, EU Vol 4, and ISO 22716
- Strong communication and writing skills
- Proven ability to deescalate workplace conflicts effectively
- Ability to adapt to new technology and software
- Willingness to travel
Preferred Qualifications
- Strong experience with 21 CFR part 58, 21 CFR part 820, EU GDP, ISO 15378, ISO 17025
- ISO certifications are a plus but not mandatory
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What We Do
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WHAT IS SQA SERVICES, INC.?
SQA provides global supplier quality services for quality-critical industries. With quality, manufacturing, and regulatory experts located in over 50 countries, SQA provides a cost-effective, local supplier presence.
Managed, on-demand services include supplier quality audits, supplier remediation, quality engineering, source inspection, corrective action management, and real-time supplier quality data via SQA's world-class STEPQ technology.
HOW CAN I GET IN TOUCH WITH SQA?
We look forward to connecting with you and discovering how Team SQA can help you and your team reach your quality goals. Contact our team by heading over to http://www.sqaservices.com/contact
If you think you or someone you know would be a great fit for our team, please send your resume to our Associate Development team at: [email protected]