assigned portfolio of products: Assisting with internal product queries from relevant departments Assisting products Conduct dossier due diligence to ensure all data gaps are addressed Prepare the registration applications regulatory authorities Work in collaboration with internal and external stakeholders to assess regulator's Guidelines pertaining to the pharmaceutical industry. Internal training and mentoring Establish and maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate or implement
manufacturing processes, ingredient and product analysis and verification, problem identification, modification Information on product labels and product technical data sheets. Liaise with "Toll manufacturing" customers Management. To build and maintain product formulation data base (spread sheet with hyperlink references). Background function To build an approved, supplier/ ingredient data base. To Create Procedures and Works Instructions documented and investigated. Main Working Relationships Internal Company Directors Laboratory Staff Plant personnel
manufacturing processes, ingredient and product analysis and verification, problem identification, modification Information on product labels and product technical data sheets. Liaise with "Toll manufacturing" customers Management. To build and maintain product formulation data base (spread sheet with hyperlink references). Background function To build an approved, supplier/ ingredient data base. To Create Procedures and Works Instructions documented and investigated. Main Working Relationships Internal Company Directors Laboratory Staff Plant personnel
manufacturing processes, ingredient and product analysis and verification, problem identification, modification Information on product labels and product technical data sheets.
manufacturing processes, ingredient and product analysis and verification, problem identification, modification Information on product labels and product technical data sheets.
verbal communication with all interested parties (internal & external). SHEQ observation and coaching coaching (SOC's) weekly. Report complaints (internal and external) on mySHEQ system and Construction Manager Manager. Ensure good relationship with Clients (internal and external) and build on it. Compile, update, and product release inspection records. Compile product data pack in accordance with the Company or Client requirements Review and maintain PQMP, ITP's, QCS's, product data packs and revise when required. Report changes needed
position works on complex problems requiring data analysis and the ability to perform an in-depth evaluation and vendors. Provide LDMS (centralized laboratory data management system) support to sites; provide program establishment of equipment maintenance programs, and proper data and specimen management. Review and analyze clinical Quality Control (EQC) program support including analysis, interpretation and reporting to sites. Review
scientifically defendable national and international field surveys for data collection in support of specialist
to research designs, methods, data management strategies, data analysis, and publication writing. Organise Ensure all research activities align with international best practice with regards to research ethics update of NPO's internal organisational Monitoring and Evaluation systems, analysing data and providing
to research designs, methods, data management strategies, data analysis, and publication writing. Organise Ensure all research activities align with international best practice with regards to research ethics update of NPO's internal organisational Monitoring and Evaluation systems, analysing data and providing