Chemist[ Map Ta Phut ]
Solvay Asia Pacific Company Limited- About the role
- Our team, is integrated in the production department and focuses on chemistry products.
- As a Job title, you will work on chemistry support .You will get the opportunity to contribute to Solvay and have a positive impact on chemistry.
- You will be accountable for:
- To ensure that the Solvay Sodium Bicarbonate MTP product and manufacturing plant comply with all relevant regulations and customer requirement, conformity of these new activities to the GxP regulation
- Bicar product ( TEC, Feed, FOOD ,and Pharma grade) batch record review, release and batch certification management ( CoC and CoA)
- Develop and maintain manual, procedures, work instruction and all quality related document within the department
- Corrective action and preventive action request (CAPA) and Deviation management.
- Audit management. Internal audit, Customer audit, Authority and certified body audit and Supplier audit
- Quality trial, monitoring and report management
- Customer complaint management (By delegated). Complaint receiving and response to ensuring that relevant customer complaints are dealt with effectively.
- Ensure that the product are keep for stability and retained sample
- FDA annual report and Annual product review
- Special project as assigned
- Ensuring that a quality management system is implemented, Up to date and maintained
- Ensuring that initial and continuous training programmes are implemented and maintained
- Ensuring that the service provider and supplier are correctly approved as per procedure by coordination with the purchasing department and End-user.
- Ensuring that self-inspections are performed at appropriate regular intervals following a prearranged programme and necessary corrective measures are put in place
- Deciding on the final disposition of rejected products (By delegated).
- Approving any returns to saleable stock
- Bicar product ( TEC, Feed, FOOD ,and Pharma grade) batch record review, release and batch certification management ( CoC and CoA)
- Develop and maintain manual, procedures, work instruction and all quality related document within the department
- Corrective action and preventive action request (CAPA) and Deviation management.
- Audit management. Internal audit, Customer audit, Authority and certified body audit and Supplier audit
- Quality trial, monitoring and report management
- Customer complaint management (By delegated). Complaint receiving and response to ensuring that relevant customer complaints are dealt with effectively.
- Ensure that the product are keep for stability and retained sample
- FDA annual report and Annual product review
- Special project as assigned
- Ensuring that a quality management system is implemented, Up to date and maintained
- Ensuring that initial and continuous training programmes are implemented and maintained
- Ensuring that the service provider and supplier are correctly approved as per procedure by coordination with the purchasing department and End-user.
- Ensuring that self-inspections are performed at appropriate regular intervals following a prearranged programme and necessary corrective measures are put in place
- Deciding on the final disposition of rejected products (By delegated).
- Approving any returns to saleable stock
- Ensuring that any additional requirements imposed on certain products by national legislation are adhered to and communicate the action or requirement to the related person
- Focusing on the management of authorized activities and the accuracy and quality of records
- Keeping appropriate records of any delegated duties
- About you
- Bachelor degree in pharmaceutical science or related field or higher education qualified
- 1-3 years experience in pharmaceutical function
- Adaptability, capability to address multitasks, ability to interact with the other departments of the company
- English skills is requested
- 5-day work week
- Social security
- Health insurance
- Accident Insurance
- Annual trip or party
- Annual bonus