Responsibilities
- Collaborate in weekly meetings, work with stakeholders for quality implementations
- Ensure SOP's and polices are executed to plan.
- Write technical SOP's as necessary.
- Implement GMP QMS at a corporate level.
- Manage projects and be the middle person for coordination; excellent communication skills in Japanese and English.
Qualifications
- 4+ years of experience in the pharmaceutical, consumer, quasi drugs, and/or medical device industries
- Good knowledge of GMP's, investigations, corrective actions, lab management, etc.
- Experience working in a laboratory or understanding of laboratory controls
- Quality Engineering experience preferred
- Bilingual English and Japanese
- Experience with ISO 9001, ISO 22000, ISO 22716, GDP, and 21 CFR part 210/211
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What We Do
Welcome to the SQA Services, Inc. home on LinkedIn! Follow us to stay up to date on all things quality - including industry events, news, and ways to get involved with #TeamSQA. Also, keep an eye out for job postings! SQA is always looking for quality professionals and new team members! 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]
