all - especially pharma products). Implement thew SOPs, GMP structures, ISO 9001 and other ISO standards
deadlines are met as per SOP.
knowledge of cGxP regulations You will be proficient in SOP and master QA document compilation/control with an Environment Oversee and update all departmental SOPs and manage QA document control, Site Master File comprehensive training for all employees in GxP and relevant SOPs Bilingual: English and Afrikaans Strong computer
knowledge of cGxP regulations You will be proficient in SOP and master QA document compilation/control with an Environment Oversee and update all departmental SOPs and manage QA document control, Site Master File comprehensive training for all employees in GxP and relevant SOPs Bilingual: English and Afrikaans Strong computer
for use as per relevant SOP Ensure documentation/materials are checked as per SOP Ensure sign off on process: manufacturing methods Performs training of staff on SOPs, safety, cGMP related requirements, etc. Initiates Accountable for product and data integrity Writing up of SOPs Generation and close out of deviations and change Review and improve current documents (BMR/BPRs, SOPs, Logbooks, etc.) Drawing up of new BMR/BPRs Plan/organise/conduct non-conformances reports to QA Ensures that cGMP and SOP procedures are strictly adhered to Monitors quality
pharmaceutical manufacturing environment Experience in SOP compilation 3 years of manufacturing experience Proven departments are fully trained on GxP and all approved SOPs relevant to their roles. Good computer literacy Controls Validations Product Quality Review SOPs and SOP Training Administration Internal and External
pharmaceutical manufacturing environment Experience in SOP compilation 3 years of manufacturing experience Proven departments are fully trained on GxP and all approved SOPs relevant to their roles. Good computer literacy Controls Validations Product Quality Review SOPs and SOP Training Administration Internal and External
knowledgeable on implementing strategies and SOP's
review of Event Documentation aligned to OEC and SOP requirements prior to approval submission by AMI Event Documentation aligned to OEC requirements and SOPs post-events Filing of all pre and post-event documentation transactional report Timelines related to event schedule and SOP process requirements; Audit documentation maintained
review of Event Documentation aligned to OEC and SOP requirements prior to approval submission by AMI Event Documentation aligned to OEC requirements and SOPs post-events Filing of all pre and post-event documentation transactional report Timelines related to event schedule and SOP process requirements; Audit documentation maintained