Description: Providing best practice day-to-day manufacturing pharmaceutical services to manage workflow, production and Document Procedure Compliance so as to ensure safe and efficacious medicines are manufactured. Key Performance Areas: Lead / Champion ...
2 years ago
Description: To provide best practice day-to-day manufacturing pharmaceutical services to manage work flow, production and Document Procedure Compliance so as to ensure safe and efficacious medicines are manufactured. To comply with cGMP, MCC guidelines, ...
2 years ago
Description: You will be responsible for supervising team members in their specific Packaging areas. Setting and maintenance of machines. Ensuring that packaging processes are carried out according to specified procedures and methods. Qualifications and ...
2 years ago
Description: You will be responsible for supervising team members in their specific Packaging areas. Setting and maintenance of machines. Ensuring that packaging processes are carried out according to specified procedures and methods. Qualifications and ...
2 years ago
Description: To ensure that utility systems are maintained in a state of compliance and reliably performs their validated function with maximum availability to support the different production areas. Ensure that operation and maintenance requirements of ...
2 years ago
Description: To support the overall Validation Program by conducting qualifications and preparing and/or executing validation documents. This includes the generation, development, modification, and routing of Validation Protocols, Final Reports, Standard ...
2 years ago
Description: To manage and organise task to ensure shift works efficiently and effectively. Shift leader shares responsibilities with other team members on shift, such as operations, delegating task, troubleshooting, reports, and other administrative ...
2 years ago
Description: Ensure that the scope of practice is met with regard to current Good Laboratory Practice in line with local and international requirements. Key Responsibilities: Perform release analysis on samples Timeous execution of OOS procedure Review ...
2 years ago
Description: You will provide clear direction, identify opportunities, and define the organizational structure of projects. Key Performance Areas: Identify, quantify opportunities and issues through analysis of manufacturing site Oversee production ...
2 years ago
Description: Providing best practice day-to-day manufacturing pharmaceutical services to manage workflow, production and document procedure compliance so as to ensure safe and efficacious medicines are manufactured. Qualifications and Experience: Pharm ...
2 years ago
Description: You will provide clear direction, identify opportunities, and define the organizational structure of projects. Key Performance Areas: Identify, quantify opportunities and issues through analysis of manufacturing site Oversee production ...
2 years ago
Description: Key Outputs: Assist with external audits were necessary; compile reports and follow-up on CAPA Participate in risk assessments on QMS and departmental processes to assess risk and identify mitigating actions and controls Conduct root cause ...
2 years ago