Description
Position Summary:
Professional in Chemical Engineering or Pharmaceutical Chemistry to support and ensure regulatory compliance, manage quality documentation, and handle sanitary registrations.
Key Highlights:
1. Experience in regulatory affairs and quality management
2. Ensure compliance with GMP and applicable regulations
3. Management of quality documentation and processes
A Chemical Engineer or Pharmaceutical Chemist with experience in regulatory affairs and quality management in food and/or dietary supplement manufacturing facilities. The candidate will be responsible for supporting and ensuring compliance with GMP, sanitary requirements, and applicable regulations, as well as managing documentation and processes related to quality, sanitary registrations, audits, and regulatory matters of the company.
**Working Hours:**
* **Monday:** 8:00 a.m. to 4:30 p.m.
* **Tuesday to Friday:** 8:00 a.m. to 5:00 p.m.
Workplace: On-site employment