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QC
1
Undergraduate
Price negotiable
Key Responsibilities:
1. Perform a range of standard and specialized physicochemical laboratory tests using both standard and proprietary laboratory equipment, and provide analytical results.
2. Maintain high standards of safety, environmental protection, and hygiene in the laboratory, in compliance with relevant quality systems and current GMP requirements.
3. Responsible for analyzing and resolving any abnormal results that arise during experiments.
4. Responsible for completing batch test records and related equipment usage logs throughout the experimental process.
5. Carry out other tasks assigned by departmental management.
Job Requirements:
1. Bachelor’s degree or above in biology, pharmaceutical sciences, or a related field; outstanding recent graduates will be considered.
2. Candidates with experience in the pharmaceutical industry, physicochemical testing, and GMP compliance are preferred.
3. Strong proficiency in chemical analysis techniques.
4. Team-oriented mindset, excellent interpersonal skills, and strong communication abilities.
5. Proficient in Microsoft Word and other Office applications.
Verification QA
1
Undergraduate
Price negotiable
Job Responsibilities:
1. Review and revise relevant documentation, and draft validation master plans and validation summaries.
2. Organize the preparation of validation-related protocols.
3. Oversee the implementation of validations for various utility systems and ensure the issuance of validation reports.
4. Draft and revise validation management documents and SOPs for validation equipment and instruments.
5. Coordinate and advance the work of validation teams across related departments; compile, review, and verify validation data and reports completed by these teams.
6. Supervise and manage changes and deviations arising during validation activities, and review change and deviation reports generated during the validation process.
7. Participate in validation activities for new construction and renovation projects, as well as in the process validation of new products and equipment.
8. Implement the equipment qualification process for new facilities and issue corresponding validation reports.
Job Requirements:
1. Major in pharmaceutical or biological sciences.
2. Bachelor’s degree or above.
3. At least 2 years of experience in GMP certification, process and equipment validation, production management, or on-site QA, particularly in biologics or injectable products.
4. Preference will be given to candidates with experience in quality system training, on-site monitoring, or production management.
Service Hotline
Address: No. 8, Tongxing West Road, Touqiao Town, Guangling District, Yangzhou City, Jiangsu Province
Postal Code: 225109
Phone: +86-514-87480888 87486888 87484509
Fax: 0514-87487508
Email: rui-jing@163.com
Website: www.rui-jing.com
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