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JOIN US
Verification Specialist [Quality Department]
Negotiable
Education：
本科
|
Work experience：
1-3年
|
Number of recruits：
1
Job description
1. Responsible for reviewing and drafting the management documents of the quality department, formulating the drafting and verification guidelines, verification master plan, verification SOP, annual verification summary, etc., and complete the classification and filing of verification documents.
2. Carry out periodic verification of equipment in each production workshop, track and analyze abnormal conditions in the workshop.
3. Organize the implementation of process verification and cleaning verification in each workshop, coordinate with relevant departments, track the verification implementation process; and draft plans and reports. Participate in the confirmation of the first and post-renovation equipment and facilities led by the equipment department.
4. Review the FAT and SAT documents of the equipment prepared by the supplier, and participate in the implementation process of FAT and SAT.
5. Responsible for reviewing/drafting various verification guidelines and URS drafted by the user department, participating in the bidding and inspection of engineering and equipment projects to ensure compliance with the latest regulatory requirements.
Education background: Biochemistry, bioengineering, pharmacy and other related majors, bachelor degree or above.
Work experience: have work experience in the verification of pharmaceutical preparation companies
Skills and skills: Familiar with GMP, GSP, national standards and pharmacopoeia and other regulations, able to use verification equipment.
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Maybe you want to know more:
Jilin Province GenPEG Pharmaceutical Co.,Ltd.
Service Hotline：400-8200469
Company email：jinpg@genscigroup.com
PEG Sales Dedicated Email：salespeg@genscigroup.com
Company address: Xiashi Economic and Technological Development Zone, Dunhua City, Yanbian Prefecture, Jilin Province
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